[{"date_published":"2016-10-02T00:00:00Z","issue":"2","status":"public","publication_identifier":{"eissn":["1532-2548"],"issn":["0032-0889"]},"doi":"10.1104/pp.16.00415","quality_controlled":"1","department":[{"_id":"EvBe"}],"fulldoi":"https://doi.org/10.1104/pp.16.00415","main_file_link":[{"open_access":"1","url":"https://doi.org/10.1104/pp.16.00415"}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","publication_status":"published","publication":"Plant Physiology","language":[{"iso":"eng"}],"type":"journal_article","publisher":"American Society of Plant Biologists","_id":"1331","oa_version":"Published Version","scopus_import":"1","isi":1,"month":"10","ddc":["580"],"page":"1249 - 1258","external_id":{"isi":["000391147700047"]},"oa":1,"acknowledgement":"This work was financially supported by the following: The Alabama Agricultural Experiment Station HATCH grants 370222-310010-2055 and 370225-310006-2055 for funding to P.J.Z., E.A.K, A.M.P., and A.M.R. P.J.Z. and E.A.K were supported by an Auburn University Cellular and Molecular Biosciences Research Fellowship. I.D.C. is a postdoctoral fellow of the Research Foundation Flanders (FWO) (FWO/PDO14/043) and is also supported by FWO travel\r\ngrant 12N2415N. F.V.B. was supported by grants from the Interuniversity Attraction Poles Programme (IUAP P7/29 MARS) initiated by the Belgian Science Policy Office and Ghent University (Multidisciplinary Research Partnership Biotechnology for a Sustainable Economy, grant 01MRB510W).","article_type":"original","year":"2016","date_created":"2018-12-11T11:51:25Z","article_processing_charge":"No","date_updated":"2026-06-18T17:30:26Z","title":"Cytokinin response factor 6 represses cytokinin-associated genes during oxidative stress","abstract":[{"text":"Cytokinin is a phytohormone that is well known for its roles in numerous plant growth and developmental processes, yet it has also been linked to abiotic stress response in a less defined manner. Arabidopsis (Arabidopsis thaliana) Cytokinin Response Factor 6 (CRF6) is a cytokinin-responsive AP2/ERF-family transcription factor that, through the cytokinin signaling pathway, plays a key role in the inhibition of dark-induced senescence. CRF6 expression is also induced by oxidative stress, and here we show a novel function for CRF6 in relation to oxidative stress and identify downstream transcriptional targets of CRF6 that are repressed in response to oxidative stress. Analysis of transcriptomic changes in wild-type and crf6 mutant plants treated with H2O2 identified CRF6-dependent differentially expressed transcripts, many of which were repressed rather than induced. Moreover, many repressed genes also show decreased expression in 35S:CRF6 overexpressing plants. Together, these findings suggest that CRF6 functions largely as a transcriptional repressor. Interestingly, among the H2O2 repressed CRF6-dependent transcripts was a set of five genes associated with cytokinin processes: (signaling) ARR6, ARR9, ARR11, (biosynthesis) LOG7, and (transport) ABCG14. We have examined mutants of these cytokinin-associated target genes to reveal novel connections to oxidative stress. Further examination of CRF6-DNA interactions indicated that CRF6 may regulate its targets both directly and indirectly. Together, this shows that CRF6 functions during oxidative stress as a negative regulator to control this cytokinin-associated module of CRF6- dependent genes and establishes a novel connection between cytokinin and oxidative stress response.","lang":"eng"}],"author":[{"full_name":"Zwack, Paul","last_name":"Zwack","first_name":"Paul"},{"full_name":"De Clercq, Inge","last_name":"De Clercq","first_name":"Inge"},{"first_name":"Timothy","last_name":"Howton","full_name":"Howton, Timothy"},{"first_name":"H Tucker","last_name":"Hallmark","full_name":"Hallmark, H Tucker"},{"last_name":"Hurny","id":"4DC4AF46-F248-11E8-B48F-1D18A9856A87","first_name":"Andrej","full_name":"Hurny, Andrej","orcid":"0000-0003-3638-1426"},{"full_name":"Keshishian, Erika","last_name":"Keshishian","first_name":"Erika"},{"last_name":"Parish","first_name":"Alyssa","full_name":"Parish, Alyssa"},{"full_name":"Benková, Eva","orcid":"0000-0002-8510-9739","last_name":"Benková","id":"38F4F166-F248-11E8-B48F-1D18A9856A87","first_name":"Eva"},{"last_name":"Mukhtar","first_name":"M Shahid","full_name":"Mukhtar, M Shahid"},{"first_name":"Frank","last_name":"Van Breusegem","full_name":"Van Breusegem, Frank"},{"first_name":"Aaron","last_name":"Rashotte","full_name":"Rashotte, Aaron"}],"publist_id":"5937","volume":172,"citation":{"chicago":"Zwack, Paul, Inge De Clercq, Timothy Howton, H Tucker Hallmark, Andrej Hurny, Erika Keshishian, Alyssa Parish, et al. “Cytokinin Response Factor 6 Represses Cytokinin-Associated Genes during Oxidative Stress.” Plant Physiology. American Society of Plant Biologists, 2016. https://doi.org/10.1104/pp.16.00415.","short":"P. Zwack, I. De Clercq, T. Howton, H.T. Hallmark, A. Hurny, E. Keshishian, A. Parish, E. Benková, M.S. Mukhtar, F. Van Breusegem, A. Rashotte, Plant Physiology 172 (2016) 1249–1258.","mla":"Zwack, Paul, et al. “Cytokinin Response Factor 6 Represses Cytokinin-Associated Genes during Oxidative Stress.” Plant Physiology, vol. 172, no. 2, American Society of Plant Biologists, 2016, pp. 1249–58, doi:10.1104/pp.16.00415.","apa":"Zwack, P., De Clercq, I., Howton, T., Hallmark, H. T., Hurny, A., Keshishian, E., … Rashotte, A. (2016). Cytokinin response factor 6 represses cytokinin-associated genes during oxidative stress. Plant Physiology. American Society of Plant Biologists. https://doi.org/10.1104/pp.16.00415","ieee":"P. Zwack et al., “Cytokinin response factor 6 represses cytokinin-associated genes during oxidative stress,” Plant Physiology, vol. 172, no. 2. American Society of Plant Biologists, pp. 1249–1258, 2016.","ista":"Zwack P, De Clercq I, Howton T, Hallmark HT, Hurny A, Keshishian E, Parish A, Benková E, Mukhtar MS, Van Breusegem F, Rashotte A. 2016. Cytokinin response factor 6 represses cytokinin-associated genes during oxidative stress. Plant Physiology. 172(2), 1249–1258.","ama":"Zwack P, De Clercq I, Howton T, et al. Cytokinin response factor 6 represses cytokinin-associated genes during oxidative stress. Plant Physiology. 2016;172(2):1249-1258. doi:10.1104/pp.16.00415"},"intvolume":" 172","day":"02"},{"date_updated":"2025-09-22T08:22:19Z","title":"Pervasive selection for and against antibiotic resistance in inhomogeneous multistress environments","abstract":[{"lang":"eng","text":"Antibiotic-sensitive and -resistant bacteria coexist in natural environments with low, if detectable, antibiotic concentrations. Except possibly around localized antibiotic sources, where resistance can provide a strong advantage, bacterial fitness is dominated by stresses unaffected by resistance to the antibiotic. How do such mixed and heterogeneous conditions influence the selective advantage or disadvantage of antibiotic resistance? Here we find that sub-inhibitory levels of tetracyclines potentiate selection for or against tetracycline resistance around localized sources of almost any toxin or stress. Furthermore, certain stresses generate alternating rings of selection for and against resistance around a localized source of the antibiotic. In these conditions, localized antibiotic sources, even at high strengths, can actually produce a net selection against resistance to the antibiotic. Our results show that interactions between the effects of an antibiotic and other stresses in inhomogeneous environments can generate pervasive, complex patterns of selection both for and against antibiotic resistance."}],"author":[{"first_name":"Remy P","id":"3464AE84-F248-11E8-B48F-1D18A9856A87","last_name":"Chait","orcid":"0000-0003-0876-3187","full_name":"Chait, Remy P"},{"last_name":"Palmer","first_name":"Adam","full_name":"Palmer, Adam"},{"first_name":"Idan","last_name":"Yelin","full_name":"Yelin, Idan"},{"full_name":"Kishony, Roy","last_name":"Kishony","first_name":"Roy"}],"article_number":"10333","publist_id":"5936","intvolume":" 7","citation":{"ama":"Chait RP, Palmer A, Yelin I, Kishony R. Pervasive selection for and against antibiotic resistance in inhomogeneous multistress environments. Nature Communications. 2016;7. doi:10.1038/ncomms10333","mla":"Chait, Remy P., et al. “Pervasive Selection for and against Antibiotic Resistance in Inhomogeneous Multistress Environments.” Nature Communications, vol. 7, 10333, Nature Publishing Group, 2016, doi:10.1038/ncomms10333.","short":"R.P. Chait, A. Palmer, I. Yelin, R. Kishony, Nature Communications 7 (2016).","chicago":"Chait, Remy P, Adam Palmer, Idan Yelin, and Roy Kishony. “Pervasive Selection for and against Antibiotic Resistance in Inhomogeneous Multistress Environments.” Nature Communications. Nature Publishing Group, 2016. https://doi.org/10.1038/ncomms10333.","ista":"Chait RP, Palmer A, Yelin I, Kishony R. 2016. Pervasive selection for and against antibiotic resistance in inhomogeneous multistress environments. Nature Communications. 7, 10333.","apa":"Chait, R. P., Palmer, A., Yelin, I., & Kishony, R. (2016). Pervasive selection for and against antibiotic resistance in inhomogeneous multistress environments. Nature Communications. Nature Publishing Group. https://doi.org/10.1038/ncomms10333","ieee":"R. P. Chait, A. Palmer, I. Yelin, and R. Kishony, “Pervasive selection for and against antibiotic resistance in inhomogeneous multistress environments,” Nature Communications, vol. 7. Nature Publishing Group, 2016."},"volume":7,"day":"20","oa":1,"external_id":{"isi":["000369021700002"]},"acknowledgement":"This work was partially supported by US National Institutes of Health grant R01-GM081617, Israeli Centers of Research Excellence I-CORE Program ISF Grant No. 152/11, and the European Research Council FP7 ERC Grant 281891.","tmp":{"name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","image":"/images/cc_by.png","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","short":"CC BY (4.0)"},"date_created":"2018-12-11T11:51:25Z","year":"2016","article_processing_charge":"No","language":[{"iso":"eng"}],"publication":"Nature Communications","user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","publication_status":"published","publisher":"Nature Publishing Group","type":"journal_article","pubrep_id":"662","isi":1,"oa_version":"Published Version","_id":"1332","scopus_import":"1","month":"01","ddc":["570","579"],"has_accepted_license":"1","date_published":"2016-01-20T00:00:00Z","status":"public","file_date_updated":"2020-07-14T12:44:44Z","file":[{"file_id":"5039","access_level":"open_access","date_updated":"2020-07-14T12:44:44Z","creator":"system","file_name":"IST-2016-662-v1+1_ncomms10333.pdf","file_size":1844107,"checksum":"ef147bcbb8bd37e9079cf3ce06f5815d","relation":"main_file","content_type":"application/pdf","date_created":"2018-12-12T10:13:52Z"}],"doi":"10.1038/ncomms10333","quality_controlled":"1","department":[{"_id":"CaGu"},{"_id":"GaTk"}],"fulldoi":"https://doi.org/10.1038/ncomms10333"},{"doi":"10.1038/ncomms10915","file":[{"file_name":"IST-2016-661-v1+1_ncomms10915.pdf","checksum":"9ea0d7ce59a555a1cb8353d5559407cb","file_size":1432577,"file_id":"4834","date_updated":"2020-07-14T12:44:44Z","creator":"system","access_level":"open_access","content_type":"application/pdf","date_created":"2018-12-12T10:10:44Z","relation":"main_file"}],"quality_controlled":"1","corr_author":"1","department":[{"_id":"KrCh"}],"fulldoi":"https://doi.org/10.1038/ncomms10915","date_published":"2016-03-07T00:00:00Z","has_accepted_license":"1","status":"public","file_date_updated":"2020-07-14T12:44:44Z","_id":"1333","scopus_import":"1","oa_version":"Published Version","isi":1,"ddc":["519","530","599"],"month":"03","user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","publication_status":"published","language":[{"iso":"eng"}],"publication":"Nature Communications","type":"journal_article","publisher":"Nature Publishing Group","pubrep_id":"661","date_created":"2018-12-11T11:51:25Z","year":"2016","article_processing_charge":"No","external_id":{"isi":["000371720200001"]},"oa":1,"acknowledgement":"We thank the students for participation; H.-J. Krambeck for writing the software for the game; H. Arndt, T. Bakker, L. Becks, H. Brendelberger, S. Dobler and T. Reusch for support; and the Max Planck Society for the Advancement of Science for funding.","tmp":{"name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","image":"/images/cc_by.png","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","short":"CC BY (4.0)"},"article_number":"10915","publist_id":"5935","volume":7,"intvolume":" 7","citation":{"ama":"Milinski M, Hilbe C, Semmann D, Sommerfeld R, Marotzke J. Humans choose representatives who enforce cooperation in social dilemmas through extortion. Nature Communications. 2016;7. doi:10.1038/ncomms10915","apa":"Milinski, M., Hilbe, C., Semmann, D., Sommerfeld, R., & Marotzke, J. (2016). Humans choose representatives who enforce cooperation in social dilemmas through extortion. Nature Communications. Nature Publishing Group. https://doi.org/10.1038/ncomms10915","ieee":"M. Milinski, C. Hilbe, D. Semmann, R. Sommerfeld, and J. Marotzke, “Humans choose representatives who enforce cooperation in social dilemmas through extortion,” Nature Communications, vol. 7. Nature Publishing Group, 2016.","ista":"Milinski M, Hilbe C, Semmann D, Sommerfeld R, Marotzke J. 2016. Humans choose representatives who enforce cooperation in social dilemmas through extortion. Nature Communications. 7, 10915.","chicago":"Milinski, Manfred, Christian Hilbe, Dirk Semmann, Ralf Sommerfeld, and Jochem Marotzke. “Humans Choose Representatives Who Enforce Cooperation in Social Dilemmas through Extortion.” Nature Communications. Nature Publishing Group, 2016. https://doi.org/10.1038/ncomms10915.","short":"M. Milinski, C. Hilbe, D. Semmann, R. Sommerfeld, J. Marotzke, Nature Communications 7 (2016).","mla":"Milinski, Manfred, et al. “Humans Choose Representatives Who Enforce Cooperation in Social Dilemmas through Extortion.” Nature Communications, vol. 7, 10915, Nature Publishing Group, 2016, doi:10.1038/ncomms10915."},"day":"07","date_updated":"2025-09-22T08:21:34Z","title":"Humans choose representatives who enforce cooperation in social dilemmas through extortion","author":[{"last_name":"Milinski","first_name":"Manfred","full_name":"Milinski, Manfred"},{"orcid":"0000-0001-5116-955X","full_name":"Hilbe, Christian","first_name":"Christian","id":"2FDF8F3C-F248-11E8-B48F-1D18A9856A87","last_name":"Hilbe"},{"full_name":"Semmann, Dirk","first_name":"Dirk","last_name":"Semmann"},{"full_name":"Sommerfeld, Ralf","last_name":"Sommerfeld","first_name":"Ralf"},{"full_name":"Marotzke, Jochem","first_name":"Jochem","last_name":"Marotzke"}],"abstract":[{"text":"Social dilemmas force players to balance between personal and collective gain. In many dilemmas, such as elected governments negotiating climate-change mitigation measures, the decisions are made not by individual players but by their representatives. However, the behaviour of representatives in social dilemmas has not been investigated experimentally. Here inspired by the negotiations for greenhouse-gas emissions reductions, we experimentally study a collective-risk social dilemma that involves representatives deciding on behalf of their fellow group members. Representatives can be re-elected or voted out after each consecutive collective-risk game. Selfish players are preferentially elected and are hence found most frequently in the "representatives" treatment. Across all treatments, we identify the selfish players as extortioners. As predicted by our mathematical model, their steadfast strategies enforce cooperation from fair players who finally compensate almost completely the deficit caused by the extortionate co-players. Everybody gains, but the extortionate representatives and their groups gain the most.","lang":"eng"}]},{"date_created":"2018-12-11T11:51:26Z","year":"2016","article_processing_charge":"No","external_id":{"isi":["000378007300001"]},"oa":1,"tmp":{"name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","image":"/images/cc_by.png","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","short":"CC BY (4.0)"},"article_number":"11824","publist_id":"5934","volume":7,"project":[{"grant_number":"281511","_id":"257A4776-B435-11E9-9278-68D0E5697425","name":"Memory-related information processing in neuronal circuits of the hippocampus and entorhinal cortex","call_identifier":"FP7"},{"call_identifier":"FWF","grant_number":"I2072-B27","name":"Interneuron plasticity during spatial learning","_id":"257D4372-B435-11E9-9278-68D0E5697425"}],"intvolume":" 7","citation":{"ama":"Schönenberger P, O’Neill J, Csicsvari JL. Activity dependent plasticity of hippocampal place maps. Nature Communications. 2016;7. doi:10.1038/ncomms11824","chicago":"Schönenberger, Philipp, Joseph O’Neill, and Jozsef L Csicsvari. “Activity Dependent Plasticity of Hippocampal Place Maps.” Nature Communications. Nature Publishing Group, 2016. https://doi.org/10.1038/ncomms11824.","mla":"Schönenberger, Philipp, et al. “Activity Dependent Plasticity of Hippocampal Place Maps.” Nature Communications, vol. 7, 11824, Nature Publishing Group, 2016, doi:10.1038/ncomms11824.","short":"P. Schönenberger, J. O’Neill, J.L. Csicsvari, Nature Communications 7 (2016).","ieee":"P. Schönenberger, J. O’Neill, and J. L. Csicsvari, “Activity dependent plasticity of hippocampal place maps,” Nature Communications, vol. 7. Nature Publishing Group, 2016.","apa":"Schönenberger, P., O’Neill, J., & Csicsvari, J. L. (2016). Activity dependent plasticity of hippocampal place maps. Nature Communications. Nature Publishing Group. https://doi.org/10.1038/ncomms11824","ista":"Schönenberger P, O’Neill J, Csicsvari JL. 2016. Activity dependent plasticity of hippocampal place maps. Nature Communications. 7, 11824."},"day":"10","date_updated":"2025-09-22T08:20:24Z","title":"Activity dependent plasticity of hippocampal place maps","abstract":[{"text":"Hippocampal neurons encode a cognitive map of space. These maps are thought to be updated during learning and in response to changes in the environment through activity-dependent synaptic plasticity. Here we examine how changes in activity influence spatial coding in rats using halorhodopsin-mediated, spatially selective optogenetic silencing. Halorhoposin stimulation leads to light-induced suppression in many place cells and interneurons; some place cells increase their firing through disinhibition, whereas some show no effect. We find that place fields of the unaffected subpopulation remain stable. On the other hand, place fields of suppressed place cells were unstable, showing remapping across sessions before and after optogenetic inhibition. Disinhibited place cells had stable maps but sustained an elevated firing rate. These findings suggest that place representation in the hippocampus is constantly governed by activity-dependent processes, and that disinhibition may provide a mechanism for rate remapping.","lang":"eng"}],"author":[{"full_name":"Schönenberger, Philipp","last_name":"Schönenberger","id":"3B9D816C-F248-11E8-B48F-1D18A9856A87","first_name":"Philipp"},{"full_name":"O'Neill, Joseph","id":"426376DC-F248-11E8-B48F-1D18A9856A87","last_name":"O'Neill","first_name":"Joseph"},{"first_name":"Jozsef L","id":"3FA14672-F248-11E8-B48F-1D18A9856A87","last_name":"Csicsvari","full_name":"Csicsvari, Jozsef L","orcid":"0000-0002-5193-4036"}],"doi":"10.1038/ncomms11824","file":[{"file_id":"5196","access_level":"open_access","creator":"system","date_updated":"2020-07-14T12:44:44Z","file_name":"IST-2016-660-v1+1_ncomms11824.pdf","checksum":"e43307754abe65b840a21939fe163618","file_size":1793846,"relation":"main_file","content_type":"application/pdf","date_created":"2018-12-12T10:16:10Z"}],"quality_controlled":"1","corr_author":"1","department":[{"_id":"JoCs"}],"ec_funded":1,"fulldoi":"https://doi.org/10.1038/ncomms11824","date_published":"2016-06-10T00:00:00Z","has_accepted_license":"1","status":"public","file_date_updated":"2020-07-14T12:44:44Z","scopus_import":"1","_id":"1334","oa_version":"Published Version","isi":1,"month":"06","ddc":["570"],"user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","publication_status":"published","publication":"Nature Communications","language":[{"iso":"eng"}],"type":"journal_article","publisher":"Nature Publishing Group","pubrep_id":"660"},{"user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","publication_status":"published","language":[{"iso":"eng"}],"main_file_link":[{"open_access":"1","url":"https://arxiv.org/abs/1604.06764"}],"conference":{"start_date":"2016-09-08","end_date":"2016-09-10","location":"Edinburgh, United Kingdom","name":"SAS: Static Analysis Symposium"},"type":"conference","publisher":"Springer","month":"08","scopus_import":"1","_id":"1335","oa_version":"Preprint","isi":1,"page":"23 - 38","date_published":"2016-08-31T00:00:00Z","status":"public","quality_controlled":"1","corr_author":"1","doi":"10.1007/978-3-662-53413-7_2","fulldoi":"https://doi.org/10.1007/978-3-662-53413-7_2","ec_funded":1,"department":[{"_id":"KrCh"},{"_id":"ToHe"}],"title":"Quantitative monitor automata","date_updated":"2025-09-22T08:19:49Z","abstract":[{"lang":"eng","text":"In this paper we review various automata-theoretic formalisms for expressing quantitative properties. We start with finite-state Boolean automata that express the traditional regular properties. We then consider weighted ω-automata that can measure the average density of events, which finite-state Boolean automata cannot. However, even weighted ω-automata cannot express basic performance properties like average response time. We finally consider two formalisms of weighted ω-automata with monitors, where the monitors are either (a) counters or (b) weighted automata themselves. We present a translation result to establish that these two formalisms are equivalent. Weighted ω-automata with monitors generalize weighted ω-automata, and can express average response time property. They present a natural, robust, and expressive framework for quantitative specifications, with important decidable properties."}],"author":[{"last_name":"Chatterjee","id":"2E5DCA20-F248-11E8-B48F-1D18A9856A87","first_name":"Krishnendu","full_name":"Chatterjee, Krishnendu","orcid":"0000-0002-4561-241X"},{"first_name":"Thomas A","id":"40876CD8-F248-11E8-B48F-1D18A9856A87","last_name":"Henzinger","orcid":"0000−0002−2985−7724","full_name":"Henzinger, Thomas A"},{"full_name":"Otop, Jan","id":"2FC5DA74-F248-11E8-B48F-1D18A9856A87","last_name":"Otop","first_name":"Jan"}],"publist_id":"5932","arxiv":1,"alternative_title":["LNCS"],"day":"31","volume":9837,"intvolume":" 9837","citation":{"chicago":"Chatterjee, Krishnendu, Thomas A Henzinger, and Jan Otop. “Quantitative Monitor Automata,” 9837:23–38. Springer, 2016. https://doi.org/10.1007/978-3-662-53413-7_2.","mla":"Chatterjee, Krishnendu, et al. Quantitative Monitor Automata. Vol. 9837, Springer, 2016, pp. 23–38, doi:10.1007/978-3-662-53413-7_2.","short":"K. Chatterjee, T.A. Henzinger, J. Otop, in:, Springer, 2016, pp. 23–38.","ieee":"K. Chatterjee, T. A. Henzinger, and J. Otop, “Quantitative monitor automata,” presented at the SAS: Static Analysis Symposium, Edinburgh, United Kingdom, 2016, vol. 9837, pp. 23–38.","apa":"Chatterjee, K., Henzinger, T. A., & Otop, J. (2016). Quantitative monitor automata (Vol. 9837, pp. 23–38). Presented at the SAS: Static Analysis Symposium, Edinburgh, United Kingdom: Springer. https://doi.org/10.1007/978-3-662-53413-7_2","ista":"Chatterjee K, Henzinger TA, Otop J. 2016. Quantitative monitor automata. SAS: Static Analysis Symposium, LNCS, vol. 9837, 23–38.","ama":"Chatterjee K, Henzinger TA, Otop J. Quantitative monitor automata. In: Vol 9837. Springer; 2016:23-38. doi:10.1007/978-3-662-53413-7_2"},"project":[{"call_identifier":"FWF","name":"Rigorous Systems Engineering","_id":"25832EC2-B435-11E9-9278-68D0E5697425","grant_number":"S 11407_N23"},{"grant_number":"Z211","_id":"25F42A32-B435-11E9-9278-68D0E5697425","name":"Formal methods for the design and analysis of complex systems","call_identifier":"FWF"},{"grant_number":"279307","_id":"2581B60A-B435-11E9-9278-68D0E5697425","name":"Quantitative Graph Games: Theory and Applications","call_identifier":"FP7"},{"grant_number":"ICT15-003","name":"Efficient Algorithms for Computer Aided Verification","_id":"25892FC0-B435-11E9-9278-68D0E5697425"}],"external_id":{"arxiv":["1604.06764"],"isi":["000388924600002"]},"oa":1,"article_processing_charge":"No","date_created":"2018-12-11T11:51:26Z","year":"2016"},{"article_type":"original","article_processing_charge":"No","date_created":"2026-01-29T21:36:22Z","year":"2016","author":[{"orcid":"0000-0001-5996-956X","full_name":"Mandal, Pradeep K","last_name":"Mandal","id":"6a3def15-d4b4-11ef-9fa9-a24c1f545ec3","first_name":"Pradeep K"},{"full_name":"Baptiste, Benoît","last_name":"Baptiste","first_name":"Benoît"},{"full_name":"Langlois d'Estaintot, Béatrice","last_name":"Langlois d'Estaintot","first_name":"Béatrice"},{"first_name":"Brice","last_name":"Kauffmann","full_name":"Kauffmann, Brice"},{"last_name":"Huc","first_name":"Ivan","full_name":"Huc, Ivan"}],"abstract":[{"lang":"eng","text":"Quinoline‐based oligoamide foldamers have been identified as a potent class of ligands for G‐quadruplex DNA. Their helical structure is thought to target G‐quadruplex loops or grooves and not G‐tetrads. We report a co‐crystal structure of the antiparallel hairpin dimeric DNA G‐quadruplex (G4T4G4)2 with tetramer 1a helically folded oligo‐quinolinecarboxamide bearing cationic side chains—that is consistent with this hypothesis. Multivalent foldamer-DNA interactions that modify the packing of (G4T4G4)2 in the solid state are observed."}],"title":"Multivalent interactions between an aromatic helical foldamer and a DNA G‐quadruplex in the solid state","extern":"1","date_updated":"2026-02-23T09:21:50Z","day":"17","volume":17,"intvolume":" 17","citation":{"short":"P.K. Mandal, B. Baptiste, B. Langlois d’Estaintot, B. Kauffmann, I. Huc, ChemBioChem 17 (2016) 1911–1914.","mla":"Mandal, Pradeep K., et al. “Multivalent Interactions between an Aromatic Helical Foldamer and a DNA G‐quadruplex in the Solid State.” ChemBioChem, vol. 17, no. 20, Wiley, 2016, pp. 1911–14, doi:10.1002/cbic.201600281.","chicago":"Mandal, Pradeep K, Benoît Baptiste, Béatrice Langlois d’Estaintot, Brice Kauffmann, and Ivan Huc. “Multivalent Interactions between an Aromatic Helical Foldamer and a DNA G‐quadruplex in the Solid State.” ChemBioChem. Wiley, 2016. https://doi.org/10.1002/cbic.201600281.","ista":"Mandal PK, Baptiste B, Langlois d’Estaintot B, Kauffmann B, Huc I. 2016. Multivalent interactions between an aromatic helical foldamer and a DNA G‐quadruplex in the solid state. ChemBioChem. 17(20), 1911–1914.","apa":"Mandal, P. K., Baptiste, B., Langlois d’Estaintot, B., Kauffmann, B., & Huc, I. (2016). Multivalent interactions between an aromatic helical foldamer and a DNA G‐quadruplex in the solid state. ChemBioChem. Wiley. https://doi.org/10.1002/cbic.201600281","ieee":"P. K. Mandal, B. Baptiste, B. Langlois d’Estaintot, B. Kauffmann, and I. Huc, “Multivalent interactions between an aromatic helical foldamer and a DNA G‐quadruplex in the solid state,” ChemBioChem, vol. 17, no. 20. Wiley, pp. 1911–1914, 2016.","ama":"Mandal PK, Baptiste B, Langlois d’Estaintot B, Kauffmann B, Huc I. Multivalent interactions between an aromatic helical foldamer and a DNA G‐quadruplex in the solid state. ChemBioChem. 2016;17(20):1911-1914. doi:10.1002/cbic.201600281"},"status":"public","issue":"20","date_published":"2016-10-17T00:00:00Z","has_accepted_license":"1","fulldoi":"https://doi.org/10.1002/cbic.201600281","OA_type":"closed access","quality_controlled":"1","doi":"10.1002/cbic.201600281","publication_identifier":{"eissn":["1439-7633"],"issn":["1439-4227"]},"type":"journal_article","publisher":"Wiley","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","publication_status":"published","publication":"ChemBioChem","language":[{"iso":"eng"}],"page":"1911-1914","month":"10","oa_version":"None","_id":"21099"},{"issue":"60","status":"public","date_published":"2016-06-28T00:00:00Z","has_accepted_license":"1","fulldoi":"https://doi.org/10.1039/c6cc04466b","OA_type":"closed access","quality_controlled":"1","doi":"10.1039/c6cc04466b","publication_identifier":{"eissn":["1364-548X"],"issn":["1359-7345"]},"type":"journal_article","publisher":"Royal Society of Chemistry","publication_status":"published","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","language":[{"iso":"eng"}],"publication":"Chemical Communications","page":"9355-9358","month":"06","_id":"21100","oa_version":"None","article_type":"original","article_processing_charge":"No","year":"2016","date_created":"2026-01-29T21:42:03Z","author":[{"first_name":"Pradeep K","id":"6a3def15-d4b4-11ef-9fa9-a24c1f545ec3","last_name":"Mandal","orcid":"0000-0001-5996-956X","full_name":"Mandal, Pradeep K"},{"last_name":"Kauffmann","first_name":"Brice","full_name":"Kauffmann, Brice"},{"last_name":"Destecroix","first_name":"Harry","full_name":"Destecroix, Harry"},{"full_name":"Ferrand, Yann","first_name":"Yann","last_name":"Ferrand"},{"last_name":"Davis","first_name":"Anthony P.","full_name":"Davis, Anthony P."},{"last_name":"Huc","first_name":"Ivan","full_name":"Huc, Ivan"}],"abstract":[{"lang":"eng","text":"Using commercial screens for crystallization of biomolecules and taking advantage of the use of racemic crystallography allowed the production of X-ray quality single crystals and the elucidation at 1.08 Å resolution of the solid state structure of a difficult target: the complex between glucopyranose and a water soluble macrocyclic receptor equipped with dendritic multianionic solubilizing chains."}],"title":"Crystal structure of a complex between β-glucopyranose and a macrocyclic receptor with dendritic multicharged water solubilizing chains","extern":"1","date_updated":"2026-02-23T09:18:46Z","day":"28","volume":52,"intvolume":" 52","citation":{"ieee":"P. K. Mandal, B. Kauffmann, H. Destecroix, Y. Ferrand, A. P. Davis, and I. Huc, “Crystal structure of a complex between β-glucopyranose and a macrocyclic receptor with dendritic multicharged water solubilizing chains,” Chemical Communications, vol. 52, no. 60. Royal Society of Chemistry, pp. 9355–9358, 2016.","apa":"Mandal, P. K., Kauffmann, B., Destecroix, H., Ferrand, Y., Davis, A. P., & Huc, I. (2016). Crystal structure of a complex between β-glucopyranose and a macrocyclic receptor with dendritic multicharged water solubilizing chains. Chemical Communications. Royal Society of Chemistry. https://doi.org/10.1039/c6cc04466b","ista":"Mandal PK, Kauffmann B, Destecroix H, Ferrand Y, Davis AP, Huc I. 2016. Crystal structure of a complex between β-glucopyranose and a macrocyclic receptor with dendritic multicharged water solubilizing chains. Chemical Communications. 52(60), 9355–9358.","chicago":"Mandal, Pradeep K, Brice Kauffmann, Harry Destecroix, Yann Ferrand, Anthony P. Davis, and Ivan Huc. “Crystal Structure of a Complex between β-Glucopyranose and a Macrocyclic Receptor with Dendritic Multicharged Water Solubilizing Chains.” Chemical Communications. Royal Society of Chemistry, 2016. https://doi.org/10.1039/c6cc04466b.","short":"P.K. Mandal, B. Kauffmann, H. Destecroix, Y. Ferrand, A.P. Davis, I. Huc, Chemical Communications 52 (2016) 9355–9358.","mla":"Mandal, Pradeep K., et al. “Crystal Structure of a Complex between β-Glucopyranose and a Macrocyclic Receptor with Dendritic Multicharged Water Solubilizing Chains.” Chemical Communications, vol. 52, no. 60, Royal Society of Chemistry, 2016, pp. 9355–58, doi:10.1039/c6cc04466b.","ama":"Mandal PK, Kauffmann B, Destecroix H, Ferrand Y, Davis AP, Huc I. Crystal structure of a complex between β-glucopyranose and a macrocyclic receptor with dendritic multicharged water solubilizing chains. Chemical Communications. 2016;52(60):9355-9358. doi:10.1039/c6cc04466b"}},{"year":"2016","date_created":"2026-01-29T21:46:40Z","article_processing_charge":"No","tmp":{"name":"Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)","image":"/images/cc_by_nc.png","legal_code_url":"https://creativecommons.org/licenses/by-nc/4.0/legalcode","short":"CC BY-NC (4.0)"},"article_type":"original","oa":1,"intvolume":" 44","citation":{"chicago":"Mandal, Pradeep K, Gavin W. Collie, Suresh C. Srivastava, Brice Kauffmann, and Ivan Huc. “Structure Elucidation of the Pribnow Box Consensus Promoter Sequence by Racemic DNA Crystallography.” Nucleic Acids Research. Oxford University Press, 2016. https://doi.org/10.1093/nar/gkw367.","mla":"Mandal, Pradeep K., et al. “Structure Elucidation of the Pribnow Box Consensus Promoter Sequence by Racemic DNA Crystallography.” Nucleic Acids Research, vol. 44, no. 12, Oxford University Press, 2016, pp. 5936–43, doi:10.1093/nar/gkw367.","short":"P.K. Mandal, G.W. Collie, S.C. Srivastava, B. Kauffmann, I. Huc, Nucleic Acids Research 44 (2016) 5936–5943.","apa":"Mandal, P. K., Collie, G. W., Srivastava, S. C., Kauffmann, B., & Huc, I. (2016). Structure elucidation of the Pribnow box consensus promoter sequence by racemic DNA crystallography. Nucleic Acids Research. Oxford University Press. https://doi.org/10.1093/nar/gkw367","ieee":"P. K. Mandal, G. W. Collie, S. C. Srivastava, B. Kauffmann, and I. Huc, “Structure elucidation of the Pribnow box consensus promoter sequence by racemic DNA crystallography,” Nucleic Acids Research, vol. 44, no. 12. Oxford University Press, pp. 5936–5943, 2016.","ista":"Mandal PK, Collie GW, Srivastava SC, Kauffmann B, Huc I. 2016. Structure elucidation of the Pribnow box consensus promoter sequence by racemic DNA crystallography. Nucleic Acids Research. 44(12), 5936–5943.","ama":"Mandal PK, Collie GW, Srivastava SC, Kauffmann B, Huc I. Structure elucidation of the Pribnow box consensus promoter sequence by racemic DNA crystallography. Nucleic Acids Research. 2016;44(12):5936-5943. doi:10.1093/nar/gkw367"},"volume":44,"day":"08","abstract":[{"lang":"eng","text":"It has previously been shown that the use of racemic mixtures of naturally chiral macromolecules such as protein and DNA can significantly aid the crystallogenesis process, thereby addressing one of the major bottlenecks to structure determination by X-ray crystallographic methods—that of crystal growth. Although previous studies have provided convincing evidence of the applicability of the racemic crystallization technique to DNA through the study of well-characterized DNA structures, we sought to apply this method to a historically challenging DNA sequence. For this purpose we chose a non-self-complementary DNA duplex containing the biologically-relevant Pribnow box consensus sequence ‘TATAAT’. Four racemic crystal structures of this previously un-crystallizable DNA target are reported (with resolutions in the range of 1.65–2.3 Å), with further crystallographic studies and structural analysis providing insight into the racemic crystallization process as well as structural details of this highly pertinent DNA sequence."}],"author":[{"last_name":"Mandal","id":"6a3def15-d4b4-11ef-9fa9-a24c1f545ec3","first_name":"Pradeep K","full_name":"Mandal, Pradeep K","orcid":"0000-0001-5996-956X"},{"last_name":"Collie","first_name":"Gavin W.","full_name":"Collie, Gavin W."},{"first_name":"Suresh C.","last_name":"Srivastava","full_name":"Srivastava, Suresh C."},{"first_name":"Brice","last_name":"Kauffmann","full_name":"Kauffmann, Brice"},{"full_name":"Huc, Ivan","first_name":"Ivan","last_name":"Huc"}],"date_updated":"2026-02-23T09:16:14Z","extern":"1","title":"Structure elucidation of the Pribnow box consensus promoter sequence by racemic DNA crystallography","OA_place":"publisher","OA_type":"gold","fulldoi":"https://doi.org/10.1093/nar/gkw367","doi":"10.1093/nar/gkw367","publication_identifier":{"eissn":["1362-4962"],"issn":["0305-1048"]},"quality_controlled":"1","status":"public","issue":"12","has_accepted_license":"1","date_published":"2016-07-08T00:00:00Z","page":"5936-5943","DOAJ_listed":"1","oa_version":"Published Version","_id":"21101","month":"07","ddc":["570"],"publisher":"Oxford University Press","type":"journal_article","main_file_link":[{"url":"https://doi.org/10.1093/nar/gkw367","open_access":"1"}],"publication":"Nucleic Acids Research","language":[{"iso":"eng"}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","publication_status":"published"},{"date_created":"2026-03-30T12:22:47Z","year":"2016","article_processing_charge":"No","external_id":{"pmid":["27791380"]},"article_type":"original","citation":{"short":"M. Khorasaninejad, A.Y. Zhu, C. Roques-Carmes, W.T. Chen, J. Oh, I. Mishra, R.C. Devlin, F. Capasso, Nano Letters 16 (2016) 7229–7234.","mla":"Khorasaninejad, M., et al. “Polarization-Insensitive Metalenses at Visible Wavelengths.” Nano Letters, vol. 16, no. 11, American Chemical Society, 2016, pp. 7229–34, doi:10.1021/acs.nanolett.6b03626.","chicago":"Khorasaninejad, M., A. Y. Zhu, Charles Roques-Carmes, W. T. Chen, J. Oh, I. Mishra, R. C. Devlin, and F. Capasso. “Polarization-Insensitive Metalenses at Visible Wavelengths.” Nano Letters. American Chemical Society, 2016. https://doi.org/10.1021/acs.nanolett.6b03626.","ista":"Khorasaninejad M, Zhu AY, Roques-Carmes C, Chen WT, Oh J, Mishra I, Devlin RC, Capasso F. 2016. Polarization-insensitive metalenses at visible wavelengths. Nano Letters. 16(11), 7229–7234.","apa":"Khorasaninejad, M., Zhu, A. Y., Roques-Carmes, C., Chen, W. T., Oh, J., Mishra, I., … Capasso, F. (2016). Polarization-insensitive metalenses at visible wavelengths. Nano Letters. American Chemical Society. https://doi.org/10.1021/acs.nanolett.6b03626","ieee":"M. Khorasaninejad et al., “Polarization-insensitive metalenses at visible wavelengths,” Nano Letters, vol. 16, no. 11. American Chemical Society, pp. 7229–7234, 2016.","ama":"Khorasaninejad M, Zhu AY, Roques-Carmes C, et al. Polarization-insensitive metalenses at visible wavelengths. Nano Letters. 2016;16(11):7229-7234. doi:10.1021/acs.nanolett.6b03626"},"intvolume":" 16","volume":16,"day":"24","date_updated":"2026-04-15T11:53:17Z","extern":"1","title":"Polarization-insensitive metalenses at visible wavelengths","author":[{"full_name":"Khorasaninejad, M.","first_name":"M.","last_name":"Khorasaninejad"},{"full_name":"Zhu, A. Y.","last_name":"Zhu","first_name":"A. Y."},{"full_name":"Roques-Carmes, Charles","last_name":"Roques-Carmes","id":"e2e68fc9-6505-11ef-a541-eb4e72cc3e82","first_name":"Charles"},{"first_name":"W. T.","last_name":"Chen","full_name":"Chen, W. T."},{"full_name":"Oh, J.","first_name":"J.","last_name":"Oh"},{"full_name":"Mishra, I.","last_name":"Mishra","first_name":"I."},{"full_name":"Devlin, R. C.","first_name":"R. C.","last_name":"Devlin"},{"full_name":"Capasso, F.","first_name":"F.","last_name":"Capasso"}],"abstract":[{"text":"In this Letter, we demonstrate highly efficient, polarization-insensitive planar lenses (metalenses) at red, green, and blue wavelengths (λ = 660, 532, and 405 nm). Metalenses with numerical apertures (NA) of 0.85 and 0.6 and corresponding efficiencies as high as 60% and 90% are achieved. These metalenses are less than 600 nm-thick and can focus incident light down to diffraction-limited spots as small as ∼0.64λ and provide high-resolution imaging. In addition, the focal spots are very symmetric with high Strehl ratios. The single step lithography and compatibility with large-scale fabrication processes make metalenses highly promising for widespread applications in imaging and spectroscopy.","lang":"eng"}],"publication_identifier":{"eissn":["1530-6992"],"issn":["1530-6984"]},"doi":"10.1021/acs.nanolett.6b03626","quality_controlled":"1","OA_type":"closed access","fulldoi":"https://doi.org/10.1021/acs.nanolett.6b03626","date_published":"2016-10-24T00:00:00Z","issue":"11","status":"public","keyword":["Metasurface","polarization-insensitive metalenses","visible wavelength","titanium dioxide"],"pmid":1,"_id":"21522","oa_version":"None","scopus_import":"1","ddc":["530"],"month":"10","page":"7229-7234","publication":"Nano Letters","language":[{"iso":"eng"}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","publication_status":"published","publisher":"American Chemical Society","type":"journal_article"},{"status":"public","date_published":"2016-10-01T00:00:00Z","article_processing_charge":"No","fulldoi":"https://doi.org/10.1364/fio.2016.jw4a.63","OA_type":"closed access","date_created":"2026-03-30T12:22:48Z","year":"2016","quality_controlled":"1","doi":"10.1364/fio.2016.jw4a.63","publication_identifier":{"eisbn":["9781943580194"],"issnl":["2162-2701"]},"abstract":[{"lang":"eng","text":"We report high numerical aperture meta-lenses in the visible spectrum with focal spots as small as 0.65λ. Meta-lenses are based on ultra-thin titanium dioxide metasurface phase masks. They operate in transmission mode and are polarization-insensitive."}],"author":[{"full_name":"Khorasaninejad, M.","first_name":"M.","last_name":"Khorasaninejad"},{"full_name":"Chen, W. T.","last_name":"Chen","first_name":"W. T."},{"first_name":"A.","last_name":"Zhu","full_name":"Zhu, A."},{"full_name":"Oh, J.","first_name":"J.","last_name":"Oh"},{"first_name":"Charles","id":"e2e68fc9-6505-11ef-a541-eb4e72cc3e82","last_name":"Roques-Carmes","full_name":"Roques-Carmes, Charles"},{"last_name":"Mishra","first_name":"I.","full_name":"Mishra, I."},{"full_name":"Devlin, R. C.","first_name":"R. C.","last_name":"Devlin"},{"last_name":"Capasso","first_name":"F.","full_name":"Capasso, F."}],"conference":{"start_date":"2016-10-17","end_date":"2016-10-21","location":"Rochester, NY, United States","name":"FiO: Frontiers in Optics"},"publisher":"Optica Publishing Group","type":"conference","publication":"Frontiers in Optics 2016","title":"High numerical aperture meta-lenses at visible wavelengths","language":[{"iso":"eng"}],"publication_status":"published","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","date_updated":"2026-05-05T07:04:29Z","extern":"1","day":"01","citation":{"ama":"Khorasaninejad M, Chen WT, Zhu A, et al. High numerical aperture meta-lenses at visible wavelengths. In: Frontiers in Optics 2016. Optica Publishing Group; 2016. doi:10.1364/fio.2016.jw4a.63","chicago":"Khorasaninejad, M., W. T. Chen, A. Zhu, J. Oh, Charles Roques-Carmes, I. Mishra, R. C. Devlin, and F. Capasso. “High Numerical Aperture Meta-Lenses at Visible Wavelengths.” In Frontiers in Optics 2016. Optica Publishing Group, 2016. https://doi.org/10.1364/fio.2016.jw4a.63.","mla":"Khorasaninejad, M., et al. “High Numerical Aperture Meta-Lenses at Visible Wavelengths.” Frontiers in Optics 2016, JW4A.63, Optica Publishing Group, 2016, doi:10.1364/fio.2016.jw4a.63.","short":"M. Khorasaninejad, W.T. Chen, A. Zhu, J. Oh, C. Roques-Carmes, I. Mishra, R.C. Devlin, F. Capasso, in:, Frontiers in Optics 2016, Optica Publishing Group, 2016.","ieee":"M. Khorasaninejad et al., “High numerical aperture meta-lenses at visible wavelengths,” in Frontiers in Optics 2016, Rochester, NY, United States, 2016.","apa":"Khorasaninejad, M., Chen, W. T., Zhu, A., Oh, J., Roques-Carmes, C., Mishra, I., … Capasso, F. (2016). High numerical aperture meta-lenses at visible wavelengths. In Frontiers in Optics 2016. Rochester, NY, United States: Optica Publishing Group. https://doi.org/10.1364/fio.2016.jw4a.63","ista":"Khorasaninejad M, Chen WT, Zhu A, Oh J, Roques-Carmes C, Mishra I, Devlin RC, Capasso F. 2016. High numerical aperture meta-lenses at visible wavelengths. Frontiers in Optics 2016. FiO: Frontiers in Optics, JW4A.63."},"month":"10","article_number":"JW4A.63","_id":"21635","oa_version":"None","scopus_import":"1"},{"page":"7242-7246","scopus_import":"1","_id":"21812","oa_version":"None","month":"06","ddc":["540"],"publisher":"Wiley","type":"journal_article","language":[{"iso":"eng"}],"publication":"Angewandte Chemie International Edition","publication_status":"published","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","fulldoi":"https://doi.org/10.1002/anie.201601048","OA_type":"closed access","publication_identifier":{"eissn":["1521-3773"],"issn":["1433-7851"]},"doi":"10.1002/anie.201601048","quality_controlled":"1","issue":"25","status":"public","pmid":1,"date_published":"2016-06-13T00:00:00Z","intvolume":" 55","citation":{"ama":"Frisch H, Fritz E, Stricker FJ, et al. Kinetically controlled sequential growth of surface‐grafted chiral supramolecular copolymers. Angewandte Chemie International Edition. 2016;55(25):7242-7246. doi:10.1002/anie.201601048","short":"H. Frisch, E. Fritz, F.J. Stricker, L. Schmüser, D. Spitzer, T. Weidner, B.J. Ravoo, P. Besenius, Angewandte Chemie International Edition 55 (2016) 7242–7246.","mla":"Frisch, Hendrik, et al. “Kinetically Controlled Sequential Growth of Surface‐grafted Chiral Supramolecular Copolymers.” Angewandte Chemie International Edition, vol. 55, no. 25, Wiley, 2016, pp. 7242–46, doi:10.1002/anie.201601048.","chicago":"Frisch, Hendrik, Eva‐Corinna Fritz, Friedrich J Stricker, Lars Schmüser, Daniel Spitzer, Tobias Weidner, Bart Jan Ravoo, and Pol Besenius. “Kinetically Controlled Sequential Growth of Surface‐grafted Chiral Supramolecular Copolymers.” Angewandte Chemie International Edition. Wiley, 2016. https://doi.org/10.1002/anie.201601048.","ista":"Frisch H, Fritz E, Stricker FJ, Schmüser L, Spitzer D, Weidner T, Ravoo BJ, Besenius P. 2016. Kinetically controlled sequential growth of surface‐grafted chiral supramolecular copolymers. Angewandte Chemie International Edition. 55(25), 7242–7246.","apa":"Frisch, H., Fritz, E., Stricker, F. J., Schmüser, L., Spitzer, D., Weidner, T., … Besenius, P. (2016). Kinetically controlled sequential growth of surface‐grafted chiral supramolecular copolymers. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201601048","ieee":"H. Frisch et al., “Kinetically controlled sequential growth of surface‐grafted chiral supramolecular copolymers,” Angewandte Chemie International Edition, vol. 55, no. 25. Wiley, pp. 7242–7246, 2016."},"volume":55,"day":"13","author":[{"full_name":"Frisch, Hendrik","first_name":"Hendrik","last_name":"Frisch"},{"last_name":"Fritz","first_name":"Eva‐Corinna","full_name":"Fritz, Eva‐Corinna"},{"id":"7aca2cfc-46cf-11f0-abd3-8c96b5186745","last_name":"Stricker","first_name":"Friedrich J","full_name":"Stricker, Friedrich J"},{"last_name":"Schmüser","first_name":"Lars","full_name":"Schmüser, Lars"},{"full_name":"Spitzer, Daniel","last_name":"Spitzer","first_name":"Daniel"},{"full_name":"Weidner, Tobias","last_name":"Weidner","first_name":"Tobias"},{"full_name":"Ravoo, Bart Jan","first_name":"Bart Jan","last_name":"Ravoo"},{"full_name":"Besenius, Pol","last_name":"Besenius","first_name":"Pol"}],"abstract":[{"lang":"eng","text":"We report a facile strategy to grow supramolecular copolymers on Au surfaces by successively exposing a surface‐anchored monomer to solutions of oppositely charged peptide comonomers. Charge regulation on the active chain end of the polymer sufficiently slows down the kinetics of the self‐assembly process to produce kinetically trapped copolymers at near‐neutral pH. We thereby achieve architectural control at three levels: The β‐sheet sequences direct the polymerization away from the surface, the height of the supramolecular copolymer brushes is well‐controlled by the stepwise nature of the alternating copolymer growth, and 2D spatial resolution is realized by using micropatterned initiating monomers. The programmable nature of the resulting architectures renders this concept attractive for the development of customized biomaterials or chiral interfaces for optoelectronics and sensor applications."}],"date_updated":"2026-05-11T07:15:50Z","extern":"1","title":"Kinetically controlled sequential growth of surface‐grafted chiral supramolecular copolymers","date_created":"2026-05-06T10:51:04Z","year":"2016","article_processing_charge":"No","article_type":"original","external_id":{"pmid":["26989886"]}},{"month":"05","ddc":["540"],"oa_version":"None","_id":"21815","day":"20","volume":55,"page":"7009-7264","citation":{"chicago":"Frisch, Hendrik, Eva‐Corinna Fritz, Friedrich J Stricker, Lars Schmüser, Daniel Spitzer, Tobias Weidner, Bart Jan Ravoo, and Pol Besenius. Inside Back Cover: Kinetically Controlled Sequential Growth of Surface‐grafted Chiral Supramolecular Copolymers (Angew. Chem. Int. Ed. 25/2016). Angewandte Chemie International Edition. Vol. 55. Wiley, 2016. https://doi.org/10.1002/anie.201604416.","mla":"Frisch, Hendrik, et al. “Inside Back Cover: Kinetically Controlled Sequential Growth of Surface‐grafted Chiral Supramolecular Copolymers (Angew. Chem. Int. Ed. 25/2016).” Angewandte Chemie International Edition, vol. 55, no. 25, Wiley, 2016, pp. 7009–264, doi:10.1002/anie.201604416.","short":"H. Frisch, E. Fritz, F.J. Stricker, L. Schmüser, D. Spitzer, T. Weidner, B.J. Ravoo, P. Besenius, Inside Back Cover: Kinetically Controlled Sequential Growth of Surface‐grafted Chiral Supramolecular Copolymers (Angew. Chem. Int. Ed. 25/2016), Wiley, 2016.","ieee":"H. Frisch et al., Inside back cover: Kinetically controlled sequential growth of surface‐grafted chiral supramolecular Copolymers (Angew. Chem. Int. Ed. 25/2016), vol. 55, no. 25. Wiley, 2016, pp. 7009–7264.","apa":"Frisch, H., Fritz, E., Stricker, F. J., Schmüser, L., Spitzer, D., Weidner, T., … Besenius, P. (2016). Inside back cover: Kinetically controlled sequential growth of surface‐grafted chiral supramolecular Copolymers (Angew. Chem. Int. Ed. 25/2016). Angewandte Chemie International Edition (Vol. 55, pp. 7009–7264). Wiley. https://doi.org/10.1002/anie.201604416","ista":"Frisch H, Fritz E, Stricker FJ, Schmüser L, Spitzer D, Weidner T, Ravoo BJ, Besenius P. 2016. Inside back cover: Kinetically controlled sequential growth of surface‐grafted chiral supramolecular Copolymers (Angew. Chem. Int. Ed. 25/2016), Wiley,p.","ama":"Frisch H, Fritz E, Stricker FJ, et al. Inside Back Cover: Kinetically Controlled Sequential Growth of Surface‐grafted Chiral Supramolecular Copolymers (Angew. Chem. Int. Ed. 25/2016). Vol 55. Wiley; 2016:7009-7264. doi:10.1002/anie.201604416"},"intvolume":" 55","user_id":"ba8df636-2132-11f1-aed0-ed93e2281fdd","publication_status":"published","language":[{"iso":"eng"}],"title":"Inside back cover: Kinetically controlled sequential growth of surface‐grafted chiral supramolecular Copolymers (Angew. Chem. Int. Ed. 25/2016)","publication":"Angewandte Chemie International Edition","extern":"1","date_updated":"2026-05-12T08:07:49Z","abstract":[{"text":"A modular strategy for the synthesis of surface-confined supramolecular copolymers is reported by P. Besenius, B. J. Ravoo, and co-workers in their Communication on page 7242 ff. The sequential addition of aqueous solutions containing the anionic or cationic comonomer enables the stepwise growth of alternating copolymers from gold surfaces. Charge regulation passivates the growing chain end and yields kinetically trapped chiral copolymers with a tunable height of 5–19 nm.","lang":"eng"}],"author":[{"full_name":"Frisch, Hendrik","first_name":"Hendrik","last_name":"Frisch"},{"full_name":"Fritz, Eva‐Corinna","first_name":"Eva‐Corinna","last_name":"Fritz"},{"first_name":"Friedrich J","id":"7aca2cfc-46cf-11f0-abd3-8c96b5186745","last_name":"Stricker","full_name":"Stricker, Friedrich J"},{"first_name":"Lars","last_name":"Schmüser","full_name":"Schmüser, Lars"},{"full_name":"Spitzer, Daniel","last_name":"Spitzer","first_name":"Daniel"},{"full_name":"Weidner, Tobias","last_name":"Weidner","first_name":"Tobias"},{"full_name":"Ravoo, Bart Jan","first_name":"Bart Jan","last_name":"Ravoo"},{"first_name":"Pol","last_name":"Besenius","full_name":"Besenius, Pol"}],"type":"other_academic_publication","publisher":"Wiley","publication_identifier":{"issn":["1433-7851"],"eissn":["1521-3773"]},"doi":"10.1002/anie.201604416","article_processing_charge":"No","fulldoi":"https://doi.org/10.1002/anie.201604416","year":"2016","date_created":"2026-05-06T10:53:03Z","date_published":"2016-05-20T00:00:00Z","status":"public","issue":"25"},{"volume":8,"intvolume":" 8","citation":{"ama":"Kundu PK, Das S, Ahrens J, Klajn R. Controlling the lifetimes of dynamic nanoparticle aggregates by spiropyran functionalization. Nanoscale. 2016;8(46):19280-19286. doi:10.1039/c6nr05959g","apa":"Kundu, P. K., Das, S., Ahrens, J., & Klajn, R. (2016). Controlling the lifetimes of dynamic nanoparticle aggregates by spiropyran functionalization. Nanoscale. Royal Society of Chemistry. https://doi.org/10.1039/c6nr05959g","ieee":"P. K. Kundu, S. Das, J. Ahrens, and R. Klajn, “Controlling the lifetimes of dynamic nanoparticle aggregates by spiropyran functionalization,” Nanoscale, vol. 8, no. 46. Royal Society of Chemistry, pp. 19280–19286, 2016.","ista":"Kundu PK, Das S, Ahrens J, Klajn R. 2016. Controlling the lifetimes of dynamic nanoparticle aggregates by spiropyran functionalization. Nanoscale. 8(46), 19280–19286.","chicago":"Kundu, Pintu K., Sanjib Das, Johannes Ahrens, and Rafal Klajn. “Controlling the Lifetimes of Dynamic Nanoparticle Aggregates by Spiropyran Functionalization.” Nanoscale. Royal Society of Chemistry, 2016. https://doi.org/10.1039/c6nr05959g.","mla":"Kundu, Pintu K., et al. “Controlling the Lifetimes of Dynamic Nanoparticle Aggregates by Spiropyran Functionalization.” Nanoscale, vol. 8, no. 46, Royal Society of Chemistry, 2016, pp. 19280–86, doi:10.1039/c6nr05959g.","short":"P.K. Kundu, S. Das, J. Ahrens, R. Klajn, Nanoscale 8 (2016) 19280–19286."},"day":"19","abstract":[{"lang":"eng","text":"Novel light-responsive nanoparticles were synthesized by decorating the surfaces of gold and silver nanoparticles with a nitrospiropyran molecular photoswitch. Upon exposure to UV light in nonpolar solvents, these nanoparticles self-assembled to afford spherical aggregates, which disassembled rapidly when the UV stimulus was turned off. The sizes of these aggregates depended on the nanoparticle concentration, and their lifetimes could be controlled by adjusting the surface concentration of nitrospiropyran on the nanoparticles. The conformational flexibility of nitrospiropyran, which was altered by modifying the structure of the background ligand, had a profound impact on the self-assembly process. By coating the nanoparticles with a spiropyran lacking the nitro group, a conceptually different self-assembly system, relying on a reversible proton transfer, was realized. The resulting particles spontaneously (in the dark) assembled into aggregates that could be readily disassembled upon exposure to blue light."}],"author":[{"full_name":"Kundu, Pintu K.","first_name":"Pintu K.","last_name":"Kundu"},{"first_name":"Sanjib","last_name":"Das","full_name":"Das, Sanjib"},{"last_name":"Ahrens","first_name":"Johannes","full_name":"Ahrens, Johannes"},{"full_name":"Klajn, Rafal","last_name":"Klajn","id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b","first_name":"Rafal"}],"extern":"1","date_updated":"2024-10-14T12:16:21Z","title":"Controlling the lifetimes of dynamic nanoparticle aggregates by spiropyran functionalization","year":"2016","date_created":"2023-08-01T09:42:22Z","article_processing_charge":"No","article_type":"original","external_id":{"pmid":["27830865"]},"oa":1,"page":"19280-19286","scopus_import":"1","_id":"13385","oa_version":"Published Version","month":"10","type":"journal_article","publisher":"Royal Society of Chemistry","main_file_link":[{"url":"https://doi.org/10.1039/C6NR05959G","open_access":"1"}],"publication_status":"published","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","language":[{"iso":"eng"}],"publication":"Nanoscale","fulldoi":"https://doi.org/10.1039/c6nr05959g","doi":"10.1039/c6nr05959g","publication_identifier":{"eissn":["2040-3372"],"issn":["2040-3364"]},"quality_controlled":"1","issue":"46","keyword":["General Materials Science"],"status":"public","pmid":1,"date_published":"2016-10-19T00:00:00Z"},{"page":"10795-10801","month":"10","oa_version":"None","_id":"13386","scopus_import":"1","publisher":"American Chemical Society","type":"journal_article","language":[{"iso":"eng"}],"publication":"Langmuir","publication_status":"published","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","fulldoi":"https://doi.org/10.1021/acs.langmuir.6b01690","quality_controlled":"1","publication_identifier":{"issn":["0743-7463"],"eissn":["1520-5827"]},"doi":"10.1021/acs.langmuir.6b01690","pmid":1,"status":"public","issue":"42","keyword":["Electrochemistry","Spectroscopy","Surfaces and Interfaces","Condensed Matter Physics","General Materials Science"],"date_published":"2016-10-25T00:00:00Z","day":"25","intvolume":" 32","citation":{"ama":"Moldt T, Przyrembel D, Schulze M, et al. Differing isomerization kinetics of azobenzene-functionalized self-assembled monolayers in ambient air and in vacuum. Langmuir. 2016;32(42):10795-10801. doi:10.1021/acs.langmuir.6b01690","ista":"Moldt T, Przyrembel D, Schulze M, Bronsch W, Boie L, Brete D, Gahl C, Klajn R, Tegeder P, Weinelt M. 2016. Differing isomerization kinetics of azobenzene-functionalized self-assembled monolayers in ambient air and in vacuum. Langmuir. 32(42), 10795–10801.","apa":"Moldt, T., Przyrembel, D., Schulze, M., Bronsch, W., Boie, L., Brete, D., … Weinelt, M. (2016). Differing isomerization kinetics of azobenzene-functionalized self-assembled monolayers in ambient air and in vacuum. Langmuir. American Chemical Society. https://doi.org/10.1021/acs.langmuir.6b01690","ieee":"T. Moldt et al., “Differing isomerization kinetics of azobenzene-functionalized self-assembled monolayers in ambient air and in vacuum,” Langmuir, vol. 32, no. 42. American Chemical Society, pp. 10795–10801, 2016.","short":"T. Moldt, D. Przyrembel, M. Schulze, W. Bronsch, L. Boie, D. Brete, C. Gahl, R. Klajn, P. Tegeder, M. Weinelt, Langmuir 32 (2016) 10795–10801.","mla":"Moldt, Thomas, et al. “Differing Isomerization Kinetics of Azobenzene-Functionalized Self-Assembled Monolayers in Ambient Air and in Vacuum.” Langmuir, vol. 32, no. 42, American Chemical Society, 2016, pp. 10795–801, doi:10.1021/acs.langmuir.6b01690.","chicago":"Moldt, Thomas, Daniel Przyrembel, Michael Schulze, Wibke Bronsch, Larissa Boie, Daniel Brete, Cornelius Gahl, Rafal Klajn, Petra Tegeder, and Martin Weinelt. “Differing Isomerization Kinetics of Azobenzene-Functionalized Self-Assembled Monolayers in Ambient Air and in Vacuum.” Langmuir. American Chemical Society, 2016. https://doi.org/10.1021/acs.langmuir.6b01690."},"volume":32,"abstract":[{"lang":"eng","text":"Azobenzenealkanethiols in self-assembled monolayers (SAMs) on Au(111) exhibit reversible trans–cis photoisomerization when diluted with alkanethiol spacers. Using these mixed SAMs, we show switching of the linear optical and second-harmonic response. The effective switching of these surface optical properties relies on a reasonably large cross section and a high photoisomerization yield as well as a long lifetime of the metastable cis isomer. We quantified the switching process by X-ray absorption spectroscopy. The cross sections for the trans–cis and cis–trans photoisomerization with 365 and 455 nm light, respectively, are 1 order of magnitude smaller than in solution. In vacuum, the 365 nm photostationary state comprises 50–74% of the molecules in the cis form, limited by their rapid thermal isomerization back to the trans state. In contrast, the 455 nm photostationary state contains nearly 100% trans-azobenzene. We determined time constants for the thermal cis–trans isomerization of only a few minutes in vacuum and in a dry nitrogen atmosphere but of more than 1 day in ambient air. Our results suggest that adventitious water adsorbed on the surface of the SAM stabilizes the polar cis configuration of azobenzene under ambient conditions. The back reaction rate constants differing by 2 orders of magnitude underline the huge influence of the environment and, accordingly, its importance when comparing various experiments."}],"author":[{"full_name":"Moldt, Thomas","first_name":"Thomas","last_name":"Moldt"},{"full_name":"Przyrembel, Daniel","first_name":"Daniel","last_name":"Przyrembel"},{"first_name":"Michael","last_name":"Schulze","full_name":"Schulze, Michael"},{"first_name":"Wibke","last_name":"Bronsch","full_name":"Bronsch, Wibke"},{"full_name":"Boie, Larissa","first_name":"Larissa","last_name":"Boie"},{"full_name":"Brete, Daniel","last_name":"Brete","first_name":"Daniel"},{"last_name":"Gahl","first_name":"Cornelius","full_name":"Gahl, Cornelius"},{"full_name":"Klajn, Rafal","last_name":"Klajn","id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b","first_name":"Rafal"},{"full_name":"Tegeder, Petra","first_name":"Petra","last_name":"Tegeder"},{"full_name":"Weinelt, Martin","last_name":"Weinelt","first_name":"Martin"}],"title":"Differing isomerization kinetics of azobenzene-functionalized self-assembled monolayers in ambient air and in vacuum","date_updated":"2023-08-07T12:27:06Z","extern":"1","article_processing_charge":"No","date_created":"2023-08-01T09:42:37Z","year":"2016","article_type":"original","external_id":{"pmid":["27681851"]}},{"publisher":"Wiley","type":"journal_article","publication":"Advanced Optical Materials","language":[{"iso":"eng"}],"publication_status":"published","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","page":"1373-1377","oa_version":"None","_id":"13387","scopus_import":"1","month":"09","keyword":["Atomic and Molecular Physics","and Optics","Electronic","Optical and Magnetic Materials"],"issue":"9","status":"public","date_published":"2016-09-01T00:00:00Z","fulldoi":"https://doi.org/10.1002/adom.201600364","publication_identifier":{"eissn":["2195-1071"]},"doi":"10.1002/adom.201600364","quality_controlled":"1","abstract":[{"text":"Come on in, the water's fine! Non-photoresponsive nanoparticles can be reversibly assembled using light by placing them in an aqueous solution of a photo­acid. Upon exposure to visible light, the photoacid reduces the pH of the solution, which induces attractive interactions between the nanoparticles. In the dark, the resulting nanoparticle aggregates spontaneously disassemble. The process can be repeated many times.","lang":"eng"}],"author":[{"full_name":"Samanta, Dipak","first_name":"Dipak","last_name":"Samanta"},{"first_name":"Rafal","id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b","last_name":"Klajn","full_name":"Klajn, Rafal"}],"date_updated":"2024-10-14T12:16:34Z","extern":"1","title":"Aqueous light-controlled self-assembly of nanoparticles","intvolume":" 4","citation":{"ama":"Samanta D, Klajn R. Aqueous light-controlled self-assembly of nanoparticles. Advanced Optical Materials. 2016;4(9):1373-1377. doi:10.1002/adom.201600364","ista":"Samanta D, Klajn R. 2016. Aqueous light-controlled self-assembly of nanoparticles. Advanced Optical Materials. 4(9), 1373–1377.","apa":"Samanta, D., & Klajn, R. (2016). Aqueous light-controlled self-assembly of nanoparticles. Advanced Optical Materials. Wiley. https://doi.org/10.1002/adom.201600364","ieee":"D. Samanta and R. Klajn, “Aqueous light-controlled self-assembly of nanoparticles,” Advanced Optical Materials, vol. 4, no. 9. Wiley, pp. 1373–1377, 2016.","short":"D. Samanta, R. Klajn, Advanced Optical Materials 4 (2016) 1373–1377.","mla":"Samanta, Dipak, and Rafal Klajn. “Aqueous Light-Controlled Self-Assembly of Nanoparticles.” Advanced Optical Materials, vol. 4, no. 9, Wiley, 2016, pp. 1373–77, doi:10.1002/adom.201600364.","chicago":"Samanta, Dipak, and Rafal Klajn. “Aqueous Light-Controlled Self-Assembly of Nanoparticles.” Advanced Optical Materials. Wiley, 2016. https://doi.org/10.1002/adom.201600364."},"volume":4,"day":"01","article_type":"original","year":"2016","date_created":"2023-08-01T09:42:49Z","article_processing_charge":"No"},{"oa":1,"article_processing_charge":"No","year":"2016","date_created":"2023-08-01T09:43:07Z","title":"Inside cover: Reversible photoisomerization of spiropyran on the surfaces of Au25 nanoclusters (ChemPhysChem 12/2016)","extern":"1","date_updated":"2024-10-14T12:16:44Z","author":[{"full_name":"Udayabhaskararao, T.","last_name":"Udayabhaskararao","first_name":"T."},{"full_name":"Kundu, Pintu K.","last_name":"Kundu","first_name":"Pintu K."},{"full_name":"Ahrens, Johannes","last_name":"Ahrens","first_name":"Johannes"},{"last_name":"Klajn","id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b","first_name":"Rafal","full_name":"Klajn, Rafal"}],"abstract":[{"text":"The Inside Cover picture illustrates the fluorescent properties of a gold nanocluster functionalized with several copies of a red-emitting merocyanine (image by Ella Marushchenko). The red fluorescence can be turned on and off reversibly by using an external stimulus.","lang":"eng"}],"day":"17","volume":17,"intvolume":" 17","citation":{"ama":"Udayabhaskararao T, Kundu PK, Ahrens J, Klajn R. Inside Cover: Reversible Photoisomerization of Spiropyran on the Surfaces of Au25 Nanoclusters (ChemPhysChem 12/2016). Vol 17. Wiley; 2016:1711-1711. doi:10.1002/cphc.201600480","apa":"Udayabhaskararao, T., Kundu, P. K., Ahrens, J., & Klajn, R. (2016). Inside cover: Reversible photoisomerization of spiropyran on the surfaces of Au25 nanoclusters (ChemPhysChem 12/2016). ChemPhysChem (Vol. 17, pp. 1711–1711). Wiley. https://doi.org/10.1002/cphc.201600480","ieee":"T. Udayabhaskararao, P. K. Kundu, J. Ahrens, and R. Klajn, Inside cover: Reversible photoisomerization of spiropyran on the surfaces of Au25 nanoclusters (ChemPhysChem 12/2016), vol. 17, no. 12. Wiley, 2016, pp. 1711–1711.","ista":"Udayabhaskararao T, Kundu PK, Ahrens J, Klajn R. 2016. Inside cover: Reversible photoisomerization of spiropyran on the surfaces of Au25 nanoclusters (ChemPhysChem 12/2016), Wiley,p.","chicago":"Udayabhaskararao, T., Pintu K. Kundu, Johannes Ahrens, and Rafal Klajn. Inside Cover: Reversible Photoisomerization of Spiropyran on the Surfaces of Au25 Nanoclusters (ChemPhysChem 12/2016). ChemPhysChem. Vol. 17. Wiley, 2016. https://doi.org/10.1002/cphc.201600480.","short":"T. Udayabhaskararao, P.K. Kundu, J. Ahrens, R. Klajn, Inside Cover: Reversible Photoisomerization of Spiropyran on the Surfaces of Au25 Nanoclusters (ChemPhysChem 12/2016), Wiley, 2016.","mla":"Udayabhaskararao, T., et al. “Inside Cover: Reversible Photoisomerization of Spiropyran on the Surfaces of Au25 Nanoclusters (ChemPhysChem 12/2016).” ChemPhysChem, vol. 17, no. 12, Wiley, 2016, pp. 1711–1711, doi:10.1002/cphc.201600480."},"date_published":"2016-06-17T00:00:00Z","status":"public","keyword":["Physical and Theoretical Chemistry","Atomic and Molecular Physics","and Optics"],"issue":"12","quality_controlled":"1","doi":"10.1002/cphc.201600480","publication_identifier":{"issn":["1439-4235"],"eissn":["1439-7641"]},"fulldoi":"https://doi.org/10.1002/cphc.201600480","publication_status":"published","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","publication":"ChemPhysChem","language":[{"iso":"eng"}],"main_file_link":[{"open_access":"1","url":"https://doi.org/10.1002/cphc.201600480"}],"type":"other_academic_publication","publisher":"Wiley","month":"06","_id":"13388","oa_version":"Published Version","page":"1711-1711"},{"year":"2016","date_created":"2023-08-01T09:43:18Z","article_processing_charge":"No","article_type":"original","external_id":{"pmid":["26593975"]},"volume":17,"citation":{"ama":"Udayabhaskararao T, Kundu PK, Ahrens J, Klajn R. Reversible photoisomerization of spiropyran on the surfaces of Au25 nanoclusters. ChemPhysChem. 2016;17(12):1805-1809. doi:10.1002/cphc.201500897","ista":"Udayabhaskararao T, Kundu PK, Ahrens J, Klajn R. 2016. Reversible photoisomerization of spiropyran on the surfaces of Au25 nanoclusters. ChemPhysChem. 17(12), 1805–1809.","ieee":"T. Udayabhaskararao, P. K. Kundu, J. Ahrens, and R. Klajn, “Reversible photoisomerization of spiropyran on the surfaces of Au25 nanoclusters,” ChemPhysChem, vol. 17, no. 12. Wiley, pp. 1805–1809, 2016.","apa":"Udayabhaskararao, T., Kundu, P. K., Ahrens, J., & Klajn, R. (2016). Reversible photoisomerization of spiropyran on the surfaces of Au25 nanoclusters. ChemPhysChem. Wiley. https://doi.org/10.1002/cphc.201500897","short":"T. Udayabhaskararao, P.K. Kundu, J. Ahrens, R. Klajn, ChemPhysChem 17 (2016) 1805–1809.","mla":"Udayabhaskararao, T., et al. “Reversible Photoisomerization of Spiropyran on the Surfaces of Au25 Nanoclusters.” ChemPhysChem, vol. 17, no. 12, Wiley, 2016, pp. 1805–09, doi:10.1002/cphc.201500897.","chicago":"Udayabhaskararao, T., Pintu K. Kundu, Johannes Ahrens, and Rafal Klajn. “Reversible Photoisomerization of Spiropyran on the Surfaces of Au25 Nanoclusters.” ChemPhysChem. Wiley, 2016. https://doi.org/10.1002/cphc.201500897."},"intvolume":" 17","day":"17","abstract":[{"text":"Au25 nanoclusters functionalized with a spiropyran molecular switch are synthesized via a ligand-exchange reaction at low temperature. The resulting nanoclusters are characterized by optical and NMR spectroscopies as well as by mass spectrometry. Spiropyran bound to nanoclusters isomerizes in a reversible fashion when exposed to UV and visible light, and its properties are similar to those of free spiropyran molecules in solution. The reversible photoisomerization entails the modulation of fluorescence as well as the light-controlled self-assembly of nanoclusters.","lang":"eng"}],"author":[{"full_name":"Udayabhaskararao, T.","last_name":"Udayabhaskararao","first_name":"T."},{"full_name":"Kundu, Pintu K.","last_name":"Kundu","first_name":"Pintu K."},{"last_name":"Ahrens","first_name":"Johannes","full_name":"Ahrens, Johannes"},{"full_name":"Klajn, Rafal","first_name":"Rafal","last_name":"Klajn","id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b"}],"extern":"1","date_updated":"2024-10-14T12:16:54Z","title":"Reversible photoisomerization of spiropyran on the surfaces of Au25 nanoclusters","fulldoi":"https://doi.org/10.1002/cphc.201500897","publication_identifier":{"issn":["1439-4235"],"eissn":["1439-7641"]},"doi":"10.1002/cphc.201500897","quality_controlled":"1","keyword":["Physical and Theoretical Chemistry","Atomic and Molecular Physics","and Optics"],"status":"public","issue":"12","pmid":1,"date_published":"2016-06-17T00:00:00Z","page":"1805-1809","_id":"13389","oa_version":"None","scopus_import":"1","month":"06","type":"journal_article","publisher":"Wiley","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","publication_status":"published","publication":"ChemPhysChem","language":[{"iso":"eng"}]},{"day":"08","volume":59,"intvolume":" 59","citation":{"ama":"Klajn R. Borrowing titania’s photoinduced electrons for molecular switching. Science China Chemistry. 2016;59(4):420-421. doi:10.1007/s11426-016-5573-4","apa":"Klajn, R. (2016). Borrowing titania’s photoinduced electrons for molecular switching. Science China Chemistry. Springer Nature. https://doi.org/10.1007/s11426-016-5573-4","ieee":"R. Klajn, “Borrowing titania’s photoinduced electrons for molecular switching,” Science China Chemistry, vol. 59, no. 4. Springer Nature, pp. 420–421, 2016.","ista":"Klajn R. 2016. Borrowing titania’s photoinduced electrons for molecular switching. Science China Chemistry. 59(4), 420–421.","chicago":"Klajn, Rafal. “Borrowing Titania’s Photoinduced Electrons for Molecular Switching.” Science China Chemistry. Springer Nature, 2016. https://doi.org/10.1007/s11426-016-5573-4.","mla":"Klajn, Rafal. “Borrowing Titania’s Photoinduced Electrons for Molecular Switching.” Science China Chemistry, vol. 59, no. 4, Springer Nature, 2016, pp. 420–21, doi:10.1007/s11426-016-5573-4.","short":"R. Klajn, Science China Chemistry 59 (2016) 420–421."},"author":[{"full_name":"Klajn, Rafal","first_name":"Rafal","id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b","last_name":"Klajn"}],"title":"Borrowing titania’s photoinduced electrons for molecular switching","extern":"1","date_updated":"2024-10-14T12:17:06Z","article_processing_charge":"No","date_created":"2023-08-01T09:43:33Z","year":"2016","article_type":"original","page":"420-421","month":"03","scopus_import":"1","_id":"13390","oa_version":"None","type":"journal_article","publisher":"Springer Nature","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","publication_status":"published","language":[{"iso":"eng"}],"publication":"Science China Chemistry","fulldoi":"https://doi.org/10.1007/s11426-016-5573-4","quality_controlled":"1","publication_identifier":{"eissn":["1869-1870"],"issn":["1674-7291"]},"doi":"10.1007/s11426-016-5573-4","keyword":["General Chemistry"],"status":"public","issue":"4","date_published":"2016-03-08T00:00:00Z"},{"article_processing_charge":"No","date_created":"2023-08-01T09:43:46Z","year":"2016","external_id":{"pmid":["31968727"]},"article_type":"original","day":"01","volume":81,"citation":{"ama":"Amdursky N, Kundu PK, Ahrens J, Huppert D, Klajn R. Noncovalent interactions with proteins modify the physicochemical properties of a molecular switch. ChemPlusChem. 2016;81(1):44-48. doi:10.1002/cplu.201500417","short":"N. Amdursky, P.K. Kundu, J. Ahrens, D. Huppert, R. Klajn, ChemPlusChem 81 (2016) 44–48.","mla":"Amdursky, Nadav, et al. “Noncovalent Interactions with Proteins Modify the Physicochemical Properties of a Molecular Switch.” ChemPlusChem, vol. 81, no. 1, Wiley, 2016, pp. 44–48, doi:10.1002/cplu.201500417.","chicago":"Amdursky, Nadav, Pintu K. Kundu, Johannes Ahrens, Dan Huppert, and Rafal Klajn. “Noncovalent Interactions with Proteins Modify the Physicochemical Properties of a Molecular Switch.” ChemPlusChem. Wiley, 2016. https://doi.org/10.1002/cplu.201500417.","ista":"Amdursky N, Kundu PK, Ahrens J, Huppert D, Klajn R. 2016. Noncovalent interactions with proteins modify the physicochemical properties of a molecular switch. ChemPlusChem. 81(1), 44–48.","ieee":"N. Amdursky, P. K. Kundu, J. Ahrens, D. Huppert, and R. Klajn, “Noncovalent interactions with proteins modify the physicochemical properties of a molecular switch,” ChemPlusChem, vol. 81, no. 1. Wiley, pp. 44–48, 2016.","apa":"Amdursky, N., Kundu, P. K., Ahrens, J., Huppert, D., & Klajn, R. (2016). Noncovalent interactions with proteins modify the physicochemical properties of a molecular switch. ChemPlusChem. Wiley. https://doi.org/10.1002/cplu.201500417"},"intvolume":" 81","title":"Noncovalent interactions with proteins modify the physicochemical properties of a molecular switch","extern":"1","date_updated":"2024-10-14T12:17:16Z","abstract":[{"lang":"eng","text":"It is reported that spiropyran—a widely investigated molecular photoswitch—can be stabilized in aqueous environments in the presence of a variety of proteins, including human serum albumin, insulin fibrils, lysozyme, and glucose oxidase. The optical properties of the complexed photoswitch are protein dependent, with human serum albumin providing the spiropyran with emission features previously observed for a photoswitch confined in media of high viscosity. Despite being bound to the protein molecules, spiropyran can undergo a ring-opening reaction upon exposure to UV light. This photoisomerization process can affect the properties of the proteins: here, it is shown that the electrical conduction through human serum albumin to which the spiropyran is bound increases following the ring-opening reaction."}],"author":[{"last_name":"Amdursky","first_name":"Nadav","full_name":"Amdursky, Nadav"},{"last_name":"Kundu","first_name":"Pintu K.","full_name":"Kundu, Pintu K."},{"first_name":"Johannes","last_name":"Ahrens","full_name":"Ahrens, Johannes"},{"last_name":"Huppert","first_name":"Dan","full_name":"Huppert, Dan"},{"id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b","last_name":"Klajn","first_name":"Rafal","full_name":"Klajn, Rafal"}],"quality_controlled":"1","doi":"10.1002/cplu.201500417","publication_identifier":{"eissn":["2192-6506"]},"fulldoi":"https://doi.org/10.1002/cplu.201500417","date_published":"2016-01-01T00:00:00Z","pmid":1,"issue":"1","keyword":["General Chemistry"],"status":"public","month":"01","oa_version":"None","_id":"13391","scopus_import":"1","page":"44-48","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","publication_status":"published","language":[{"iso":"eng"}],"publication":"ChemPlusChem","type":"journal_article","publisher":"Wiley"},{"project":[{"_id":"25832EC2-B435-11E9-9278-68D0E5697425","name":"Rigorous Systems Engineering","grant_number":"S 11407_N23","call_identifier":"FWF"},{"_id":"25892FC0-B435-11E9-9278-68D0E5697425","name":"Efficient Algorithms for Computer Aided Verification","grant_number":"ICT15-003"},{"call_identifier":"FP7","name":"Quantitative Graph Games: Theory and Applications","_id":"2581B60A-B435-11E9-9278-68D0E5697425","grant_number":"279307"}],"citation":{"mla":"Hansen, Kristoffer, et al. The Big Match in Small Space. Vol. 9928, Springer, 2016, pp. 64–76, doi:10.1007/978-3-662-53354-3_6.","short":"K. Hansen, R. Ibsen-Jensen, M. Koucký, in:, Springer, 2016, pp. 64–76.","chicago":"Hansen, Kristoffer, Rasmus Ibsen-Jensen, and Michal Koucký. “The Big Match in Small Space,” 9928:64–76. Springer, 2016. https://doi.org/10.1007/978-3-662-53354-3_6.","ista":"Hansen K, Ibsen-Jensen R, Koucký M. 2016. The big match in small space. SAGT: Symposium on Algorithmic Game Theory, LNCS, vol. 9928, 64–76.","ieee":"K. Hansen, R. Ibsen-Jensen, and M. Koucký, “The big match in small space,” presented at the SAGT: Symposium on Algorithmic Game Theory, Liverpool, United Kingdom, 2016, vol. 9928, pp. 64–76.","apa":"Hansen, K., Ibsen-Jensen, R., & Koucký, M. (2016). The big match in small space (Vol. 9928, pp. 64–76). Presented at the SAGT: Symposium on Algorithmic Game Theory, Liverpool, United Kingdom: Springer. https://doi.org/10.1007/978-3-662-53354-3_6","ama":"Hansen K, Ibsen-Jensen R, Koucký M. The big match in small space. In: Vol 9928. Springer; 2016:64-76. doi:10.1007/978-3-662-53354-3_6"},"intvolume":" 9928","volume":9928,"day":"01","alternative_title":["LNCS"],"arxiv":1,"publist_id":"5927","author":[{"full_name":"Hansen, Kristoffer","first_name":"Kristoffer","last_name":"Hansen"},{"orcid":"0000-0003-4783-0389","full_name":"Ibsen-Jensen, Rasmus","last_name":"Ibsen-Jensen","id":"3B699956-F248-11E8-B48F-1D18A9856A87","first_name":"Rasmus"},{"first_name":"Michal","last_name":"Koucký","full_name":"Koucký, Michal"}],"abstract":[{"lang":"eng","text":"We study repeated games with absorbing states, a type of two-player, zero-sum concurrent mean-payoff games with the prototypical example being the Big Match of Gillete (1957). These games may not allow optimal strategies but they always have ε-optimal strategies. In this paper we design ε-optimal strategies for Player 1 in these games that use only O(log log T) space. Furthermore, we construct strategies for Player 1 that use space s(T), for an arbitrary small unbounded non-decreasing function s, and which guarantee an ε-optimal value for Player 1 in the limit superior sense. The previously known strategies use space Ω(log T) and it was known that no strategy can use constant space if it is ε-optimal even in the limit superior sense. We also give a complementary lower bound. Furthermore, we also show that no Markov strategy, even extended with finite memory, can ensure value greater than 0 in the Big Match, answering a question posed by Neyman [11]."}],"date_updated":"2025-09-22T08:18:27Z","title":"The big match in small space","year":"2016","date_created":"2018-12-11T11:51:28Z","article_processing_charge":"No","oa":1,"external_id":{"arxiv":["1604.07634"],"isi":["000389020400006"]},"page":"64 - 76","isi":1,"oa_version":"Preprint","_id":"1340","scopus_import":"1","month":"09","publisher":"Springer","type":"conference","conference":{"end_date":"2016-09-21","start_date":"2016-09-19","name":"SAGT: Symposium on Algorithmic Game Theory","location":"Liverpool, United Kingdom"},"main_file_link":[{"url":"https://arxiv.org/abs/1604.07634","open_access":"1"}],"language":[{"iso":"eng"}],"user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","publication_status":"published","department":[{"_id":"KrCh"}],"ec_funded":1,"fulldoi":"https://doi.org/10.1007/978-3-662-53354-3_6","doi":"10.1007/978-3-662-53354-3_6","quality_controlled":"1","status":"public","date_published":"2016-09-01T00:00:00Z"}]