[{"doi":"10.1039/d5cc03194j","type":"journal_article","publication_status":"published","publication_identifier":{"eissn":["1364-548X"],"issn":["1359-7345"]},"issue":"87","_id":"20755","OA_type":"hybrid","intvolume":"        61","article_processing_charge":"Yes (in subscription journal)","quality_controlled":"1","has_accepted_license":"1","fulldoi":"https://doi.org/10.1039/d5cc03194j","article_type":"original","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)"},"title":"Efficient optimization and synthesis of diverse azaarenes via nitrogen atom insertion under continuous flow conditions","status":"public","date_updated":"2026-03-16T08:31:23Z","volume":61,"oa_version":"Published Version","OA_place":"publisher","ddc":["540"],"oa":1,"language":[{"iso":"eng"}],"abstract":[{"text":"We report the development of a continuous flow approach to nitrogen atom insertion. The setup is modular, enabling the rapid optimization of reaction conditions for a wide range of substrates. The milder reaction conditions led to an improved substrate scope and functional group tolerance compared to batch conditions. The reactions can also be safely scaled up to preparative scale.","lang":"eng"}],"publisher":"Royal Society of Chemistry","author":[{"full_name":"Moon, Sooyeon","last_name":"Moon","first_name":"Sooyeon"},{"full_name":"Reisenbauer, Julia","id":"51d862e9-36ee-11f0-86d3-8534c85a5496","last_name":"Reisenbauer","first_name":"Julia"},{"full_name":"Paschke, Ann-Sophie K.","first_name":"Ann-Sophie K.","last_name":"Paschke"},{"full_name":"Scotto, Alessandro","last_name":"Scotto","first_name":"Alessandro"},{"last_name":"Terraneo","first_name":"Luca","full_name":"Terraneo, Luca"},{"first_name":"Niklas","last_name":"Brenner","full_name":"Brenner, Niklas"},{"last_name":"Lefebvre","first_name":"Quentin","full_name":"Lefebvre, Quentin"},{"first_name":"Thomas C.","last_name":"Fessard","full_name":"Fessard, Thomas C."},{"full_name":"Morandi, Bill","last_name":"Morandi","first_name":"Bill"}],"citation":{"ieee":"S. Moon <i>et al.</i>, “Efficient optimization and synthesis of diverse azaarenes via nitrogen atom insertion under continuous flow conditions,” <i>Chemical Communications</i>, vol. 61, no. 87. Royal Society of Chemistry, pp. 16993–16996, 2025.","apa":"Moon, S., Reisenbauer, J., Paschke, A.-S. K., Scotto, A., Terraneo, L., Brenner, N., … Morandi, B. (2025). Efficient optimization and synthesis of diverse azaarenes via nitrogen atom insertion under continuous flow conditions. <i>Chemical Communications</i>. Royal Society of Chemistry. <a href=\"https://doi.org/10.1039/d5cc03194j\">https://doi.org/10.1039/d5cc03194j</a>","mla":"Moon, Sooyeon, et al. “Efficient Optimization and Synthesis of Diverse Azaarenes via Nitrogen Atom Insertion under Continuous Flow Conditions.” <i>Chemical Communications</i>, vol. 61, no. 87, Royal Society of Chemistry, 2025, pp. 16993–96, doi:<a href=\"https://doi.org/10.1039/d5cc03194j\">10.1039/d5cc03194j</a>.","ista":"Moon S, Reisenbauer J, Paschke A-SK, Scotto A, Terraneo L, Brenner N, Lefebvre Q, Fessard TC, Morandi B. 2025. Efficient optimization and synthesis of diverse azaarenes via nitrogen atom insertion under continuous flow conditions. Chemical Communications. 61(87), 16993–16996.","short":"S. Moon, J. Reisenbauer, A.-S.K. Paschke, A. Scotto, L. Terraneo, N. Brenner, Q. Lefebvre, T.C. Fessard, B. Morandi, Chemical Communications 61 (2025) 16993–16996.","chicago":"Moon, Sooyeon, Julia Reisenbauer, Ann-Sophie K. Paschke, Alessandro Scotto, Luca Terraneo, Niklas Brenner, Quentin Lefebvre, Thomas C. Fessard, and Bill Morandi. “Efficient Optimization and Synthesis of Diverse Azaarenes via Nitrogen Atom Insertion under Continuous Flow Conditions.” <i>Chemical Communications</i>. Royal Society of Chemistry, 2025. <a href=\"https://doi.org/10.1039/d5cc03194j\">https://doi.org/10.1039/d5cc03194j</a>.","ama":"Moon S, Reisenbauer J, Paschke A-SK, et al. Efficient optimization and synthesis of diverse azaarenes via nitrogen atom insertion under continuous flow conditions. <i>Chemical Communications</i>. 2025;61(87):16993-16996. doi:<a href=\"https://doi.org/10.1039/d5cc03194j\">10.1039/d5cc03194j</a>"},"main_file_link":[{"url":"https://doi.org/10.1039/D5CC03194J","open_access":"1"}],"date_created":"2025-12-09T14:22:09Z","day":"06","year":"2025","extern":"1","publication":"Chemical Communications","page":"16993-16996","date_published":"2025-10-06T00:00:00Z","month":"10","scopus_import":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87"},{"OA_place":"publisher","oa_version":"Published Version","date_updated":"2025-12-16T11:19:43Z","volume":60,"tmp":{"short":"CC BY-NC (3.0)","legal_code_url":"https://creativecommons.org/licenses/by-nc/3.0/legalcode","name":"Creative Commons Attribution-NonCommercial 3.0 Unported (CC BY-NC 3.0)","image":"/images/cc_by_nc.png"},"status":"public","title":"Versatile dehydrogenation of carbonyls enabled by an iodine(III) reagent","day":"02","date_created":"2025-12-09T14:23:00Z","main_file_link":[{"open_access":"1","url":"https://doi.org/10.1039/D4CC02609H"}],"citation":{"mla":"Botlik, Bence B., et al. “Versatile Dehydrogenation of Carbonyls Enabled by an Iodine(III) Reagent.” <i>Chemical Communications</i>, vol. 60, no. 69, Royal Society of Chemistry, 2024, pp. 9254–57, doi:<a href=\"https://doi.org/10.1039/d4cc02609h\">10.1039/d4cc02609h</a>.","ista":"Botlik BB, Finkelstein P, Paschke A-SK, Reisenbauer J, Morandi B. 2024. Versatile dehydrogenation of carbonyls enabled by an iodine(III) reagent. Chemical Communications. 60(69), 9254–9257.","short":"B.B. Botlik, P. Finkelstein, A.-S.K. Paschke, J. Reisenbauer, B. Morandi, Chemical Communications 60 (2024) 9254–9257.","chicago":"Botlik, Bence B., Patrick Finkelstein, Ann-Sophie K. Paschke, Julia Reisenbauer, and Bill Morandi. “Versatile Dehydrogenation of Carbonyls Enabled by an Iodine(III) Reagent.” <i>Chemical Communications</i>. Royal Society of Chemistry, 2024. <a href=\"https://doi.org/10.1039/d4cc02609h\">https://doi.org/10.1039/d4cc02609h</a>.","ama":"Botlik BB, Finkelstein P, Paschke A-SK, Reisenbauer J, Morandi B. Versatile dehydrogenation of carbonyls enabled by an iodine(III) reagent. <i>Chemical Communications</i>. 2024;60(69):9254-9257. doi:<a href=\"https://doi.org/10.1039/d4cc02609h\">10.1039/d4cc02609h</a>","ieee":"B. B. Botlik, P. Finkelstein, A.-S. K. Paschke, J. Reisenbauer, and B. Morandi, “Versatile dehydrogenation of carbonyls enabled by an iodine(III) reagent,” <i>Chemical Communications</i>, vol. 60, no. 69. Royal Society of Chemistry, pp. 9254–9257, 2024.","apa":"Botlik, B. B., Finkelstein, P., Paschke, A.-S. K., Reisenbauer, J., &#38; Morandi, B. (2024). Versatile dehydrogenation of carbonyls enabled by an iodine(III) reagent. <i>Chemical Communications</i>. Royal Society of Chemistry. <a href=\"https://doi.org/10.1039/d4cc02609h\">https://doi.org/10.1039/d4cc02609h</a>"},"author":[{"full_name":"Botlik, Bence B.","last_name":"Botlik","first_name":"Bence B."},{"last_name":"Finkelstein","first_name":"Patrick","full_name":"Finkelstein, Patrick"},{"first_name":"Ann-Sophie K.","last_name":"Paschke","full_name":"Paschke, Ann-Sophie K."},{"id":"51d862e9-36ee-11f0-86d3-8534c85a5496","full_name":"Reisenbauer, Julia","last_name":"Reisenbauer","first_name":"Julia"},{"full_name":"Morandi, Bill","first_name":"Bill","last_name":"Morandi"}],"publisher":"Royal Society of Chemistry","abstract":[{"text":"We report the utilisation of an iodine(III) reagent to access α,β-unsaturated carbonyls from the corresponding silyl enol ethers and enol phosphates. The transformation can also be carried out in one pot, directly dehydrogenating carbonyls.","lang":"eng"}],"language":[{"iso":"eng"}],"oa":1,"external_id":{"pmid":["39118590"]},"publication":"Chemical Communications","extern":"1","year":"2024","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","scopus_import":"1","date_published":"2024-08-02T00:00:00Z","month":"08","page":"9254-9257","publication_status":"published","type":"journal_article","doi":"10.1039/d4cc02609h","intvolume":"        60","OA_type":"hybrid","license":"https://creativecommons.org/licenses/by-nc/3.0/","_id":"20757","issue":"69","pmid":1,"publication_identifier":{"eissn":["1364-548X"],"issn":["1359-7345"]},"has_accepted_license":"1","quality_controlled":"1","article_processing_charge":"No","article_type":"original","fulldoi":"https://doi.org/10.1039/d4cc02609h"},{"extern":"1","year":"2022","publication":"Chemical Communications","external_id":{"pmid":["35064258"]},"page":"3461-3464","keyword":["Materials Chemistry","Metals and Alloys","Surfaces","Coatings and Films","General Chemistry","Ceramics and Composites","Electronic","Optical and Magnetic Materials","Catalysis"],"scopus_import":"1","date_published":"2022-01-22T00:00:00Z","month":"01","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","title":"Coexistence of 1:1 and 2:1 inclusion complexes of indigo carmine","status":"public","volume":58,"date_updated":"2024-10-14T12:10:24Z","oa_version":"Published Version","oa":1,"abstract":[{"text":"We show that the optical properties of indigo carmine can be modulated by encapsulation within a coordination cage. Depending on the host/guest molar ratio, the cage can predominantly encapsulate either one or two dye molecules. The 1 : 1 complex is fluorescent, unique for an indigo dye in an aqueous solution. We have also found that binding two dye molecules stabilizes a previously unknown conformation of the cage.","lang":"eng"}],"language":[{"iso":"eng"}],"main_file_link":[{"url":"https://doi.org/10.1039/D1CC07081A","open_access":"1"}],"publisher":"Royal Society of Chemistry","author":[{"first_name":"Oksana","last_name":"Yanshyna","full_name":"Yanshyna, Oksana"},{"full_name":"Avram, Liat","last_name":"Avram","first_name":"Liat"},{"full_name":"Shimon, Linda J. W.","last_name":"Shimon","first_name":"Linda J. W."},{"first_name":"Rafal","last_name":"Klajn","id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b","full_name":"Klajn, Rafal"}],"citation":{"ieee":"O. Yanshyna, L. Avram, L. J. W. Shimon, and R. Klajn, “Coexistence of 1:1 and 2:1 inclusion complexes of indigo carmine,” <i>Chemical Communications</i>, vol. 58, no. 21. Royal Society of Chemistry, pp. 3461–3464, 2022.","apa":"Yanshyna, O., Avram, L., Shimon, L. J. W., &#38; Klajn, R. (2022). Coexistence of 1:1 and 2:1 inclusion complexes of indigo carmine. <i>Chemical Communications</i>. Royal Society of Chemistry. <a href=\"https://doi.org/10.1039/d1cc07081a\">https://doi.org/10.1039/d1cc07081a</a>","ista":"Yanshyna O, Avram L, Shimon LJW, Klajn R. 2022. Coexistence of 1:1 and 2:1 inclusion complexes of indigo carmine. Chemical Communications. 58(21), 3461–3464.","mla":"Yanshyna, Oksana, et al. “Coexistence of 1:1 and 2:1 Inclusion Complexes of Indigo Carmine.” <i>Chemical Communications</i>, vol. 58, no. 21, Royal Society of Chemistry, 2022, pp. 3461–64, doi:<a href=\"https://doi.org/10.1039/d1cc07081a\">10.1039/d1cc07081a</a>.","short":"O. Yanshyna, L. Avram, L.J.W. Shimon, R. Klajn, Chemical Communications 58 (2022) 3461–3464.","ama":"Yanshyna O, Avram L, Shimon LJW, Klajn R. Coexistence of 1:1 and 2:1 inclusion complexes of indigo carmine. <i>Chemical Communications</i>. 2022;58(21):3461-3464. doi:<a href=\"https://doi.org/10.1039/d1cc07081a\">10.1039/d1cc07081a</a>","chicago":"Yanshyna, Oksana, Liat Avram, Linda J. W. Shimon, and Rafal Klajn. “Coexistence of 1:1 and 2:1 Inclusion Complexes of Indigo Carmine.” <i>Chemical Communications</i>. Royal Society of Chemistry, 2022. <a href=\"https://doi.org/10.1039/d1cc07081a\">https://doi.org/10.1039/d1cc07081a</a>."},"day":"22","date_created":"2023-08-01T09:32:55Z","article_processing_charge":"No","quality_controlled":"1","article_type":"original","fulldoi":"https://doi.org/10.1039/d1cc07081a","doi":"10.1039/d1cc07081a","type":"journal_article","publication_status":"published","publication_identifier":{"eissn":["1364-548X"],"issn":["1359-7345"]},"pmid":1,"_id":"13353","issue":"21","intvolume":"        58"},{"fulldoi":"https://doi.org/10.1039/d1cc06235b","article_type":"original","article_processing_charge":"No","quality_controlled":"1","publication_identifier":{"issn":["1359-7345"],"eissn":["1364-548X"]},"pmid":1,"issue":"14","_id":"21823","OA_type":"green","intvolume":"        58","doi":"10.1039/d1cc06235b","type":"journal_article","publication_status":"published","page":"2303-2306","date_published":"2022-01-17T00:00:00Z","month":"01","scopus_import":"1","user_id":"ba8df636-2132-11f1-aed0-ed93e2281fdd","year":"2022","extern":"1","publication":"Chemical Communications","external_id":{"pmid":["35075464"]},"oa":1,"language":[{"iso":"eng"}],"abstract":[{"text":"DFT calculations were used to find an optimal substitution site on the triene backbone of a donor–acceptor Stenhouse adduct photoswitch to tune the equillibrium and switching kinetics of DASA without modifying the donor and acceptor groups. Using this approach we demonstrate a new means to tuning DASA based photoswitches by increasing the energy of the closed form relative to the open form. To highlight the potential of this approach a new DASA derivative bearing a methyl substituent on the 5-position of the triene was synthesized and the effect of this substitution was studied using 1H NMR spectroscopy, time-dependent UV-Vis and solvatochromic analysis. The new DASA derivative shows a higher dark equillibrium, favoring the open form, and drastically faster thermal recovery than the unsubstituted derivative with the same donor and acceptor.","lang":"eng"}],"author":[{"full_name":"Peterson, Julie A.","last_name":"Peterson","first_name":"Julie A."},{"last_name":"Stricker","first_name":"Friedrich J","id":"7aca2cfc-46cf-11f0-abd3-8c96b5186745","full_name":"Stricker, Friedrich J"},{"full_name":"Read de Alaniz, Javier","last_name":"Read de Alaniz","first_name":"Javier"}],"citation":{"ama":"Peterson JA, Stricker FJ, Read de Alaniz J. Improving the kinetics and dark equilibrium of donor-acceptor Stenhouse adduct by triene backbone design. <i>Chemical Communications</i>. 2022;58(14):2303-2306. doi:<a href=\"https://doi.org/10.1039/d1cc06235b\">10.1039/d1cc06235b</a>","chicago":"Peterson, Julie A., Friedrich J Stricker, and Javier Read de Alaniz. “Improving the Kinetics and Dark Equilibrium of Donor-Acceptor Stenhouse Adduct by Triene Backbone Design.” <i>Chemical Communications</i>. Royal Society of Chemistry, 2022. <a href=\"https://doi.org/10.1039/d1cc06235b\">https://doi.org/10.1039/d1cc06235b</a>.","short":"J.A. Peterson, F.J. Stricker, J. Read de Alaniz, Chemical Communications 58 (2022) 2303–2306.","mla":"Peterson, Julie A., et al. “Improving the Kinetics and Dark Equilibrium of Donor-Acceptor Stenhouse Adduct by Triene Backbone Design.” <i>Chemical Communications</i>, vol. 58, no. 14, Royal Society of Chemistry, 2022, pp. 2303–06, doi:<a href=\"https://doi.org/10.1039/d1cc06235b\">10.1039/d1cc06235b</a>.","ista":"Peterson JA, Stricker FJ, Read de Alaniz J. 2022. Improving the kinetics and dark equilibrium of donor-acceptor Stenhouse adduct by triene backbone design. Chemical Communications. 58(14), 2303–2306.","apa":"Peterson, J. A., Stricker, F. J., &#38; Read de Alaniz, J. (2022). Improving the kinetics and dark equilibrium of donor-acceptor Stenhouse adduct by triene backbone design. <i>Chemical Communications</i>. Royal Society of Chemistry. <a href=\"https://doi.org/10.1039/d1cc06235b\">https://doi.org/10.1039/d1cc06235b</a>","ieee":"J. A. Peterson, F. J. Stricker, and J. Read de Alaniz, “Improving the kinetics and dark equilibrium of donor-acceptor Stenhouse adduct by triene backbone design,” <i>Chemical Communications</i>, vol. 58, no. 14. Royal Society of Chemistry, pp. 2303–2306, 2022."},"publisher":"Royal Society of Chemistry","main_file_link":[{"open_access":"1","url":"https://doi.org/10.1039/D1CC06235B"}],"date_created":"2026-05-06T10:59:03Z","day":"17","title":"Improving the kinetics and dark equilibrium of donor-acceptor Stenhouse adduct by triene backbone design","status":"public","date_updated":"2026-05-18T09:46:30Z","volume":58,"oa_version":"Accepted Version","ddc":["540"]},{"type":"journal_article","doi":"10.1039/d2cc03671a","related_material":{"link":[{"url":"https://doi.org/10.1039/d2cc03671a","relation":"erratum"}]},"publication_status":"published","pmid":1,"publication_identifier":{"issn":["1359-7345"],"eissn":["1364-548X"]},"OA_type":"green","intvolume":"        58","issue":"90","_id":"17869","article_processing_charge":"No","quality_controlled":"1","fulldoi":"https://doi.org/10.1039/d2cc03671a","article_type":"letter_note","volume":58,"date_updated":"2024-12-10T09:27:04Z","title":"Electric-field-induced coupling of aryl iodides with a nickel(0) complex","status":"public","OA_place":"repository","oa_version":"Preprint","language":[{"iso":"eng"}],"abstract":[{"text":"The formation of carbon–carbon bonds with transition metal reagents serves as a cornerstone of organic synthesis. Here, we show that the reactivity of an otherwise kinetically inert transition metal complex can be induced by an external electric field to affect a coupling reaction. These results highlight the importance of electric field effects in reaction chemistry and offers a new strategy to modulate organometallic reactivity.","lang":"eng"}],"oa":1,"date_created":"2024-09-06T13:03:38Z","day":"10","author":[{"full_name":"Orchanian, Nicholas M.","first_name":"Nicholas M.","last_name":"Orchanian"},{"first_name":"Sophia","last_name":"Guizzo","full_name":"Guizzo, Sophia"},{"last_name":"Steigerwald","first_name":"Michael L.","full_name":"Steigerwald, Michael L."},{"full_name":"Nuckolls, Colin","first_name":"Colin","last_name":"Nuckolls"},{"id":"9ebb78a5-cc0d-11ee-8322-fae086a32caf","orcid":"0000-0002-6957-6089","full_name":"Venkataraman, Latha","last_name":"Venkataraman","first_name":"Latha"}],"publisher":"Royal Society of Chemistry","citation":{"ista":"Orchanian NM, Guizzo S, Steigerwald ML, Nuckolls C, Venkataraman L. 2022. Electric-field-induced coupling of aryl iodides with a nickel(0) complex. Chemical Communications. 58(90), 12556–12559.","mla":"Orchanian, Nicholas M., et al. “Electric-Field-Induced Coupling of Aryl Iodides with a Nickel(0) Complex.” <i>Chemical Communications</i>, vol. 58, no. 90, Royal Society of Chemistry, 2022, pp. 12556–59, doi:<a href=\"https://doi.org/10.1039/d2cc03671a\">10.1039/d2cc03671a</a>.","chicago":"Orchanian, Nicholas M., Sophia Guizzo, Michael L. Steigerwald, Colin Nuckolls, and Latha Venkataraman. “Electric-Field-Induced Coupling of Aryl Iodides with a Nickel(0) Complex.” <i>Chemical Communications</i>. Royal Society of Chemistry, 2022. <a href=\"https://doi.org/10.1039/d2cc03671a\">https://doi.org/10.1039/d2cc03671a</a>.","short":"N.M. Orchanian, S. Guizzo, M.L. Steigerwald, C. Nuckolls, L. Venkataraman, Chemical Communications 58 (2022) 12556–12559.","ama":"Orchanian NM, Guizzo S, Steigerwald ML, Nuckolls C, Venkataraman L. Electric-field-induced coupling of aryl iodides with a nickel(0) complex. <i>Chemical Communications</i>. 2022;58(90):12556-12559. doi:<a href=\"https://doi.org/10.1039/d2cc03671a\">10.1039/d2cc03671a</a>","apa":"Orchanian, N. M., Guizzo, S., Steigerwald, M. L., Nuckolls, C., &#38; Venkataraman, L. (2022). Electric-field-induced coupling of aryl iodides with a nickel(0) complex. <i>Chemical Communications</i>. Royal Society of Chemistry. <a href=\"https://doi.org/10.1039/d2cc03671a\">https://doi.org/10.1039/d2cc03671a</a>","ieee":"N. M. Orchanian, S. Guizzo, M. L. Steigerwald, C. Nuckolls, and L. Venkataraman, “Electric-field-induced coupling of aryl iodides with a nickel(0) complex,” <i>Chemical Communications</i>, vol. 58, no. 90. Royal Society of Chemistry, pp. 12556–12559, 2022."},"main_file_link":[{"url":"https://doi.org/10.26434/chemrxiv-2022-lfnw1","open_access":"1"}],"year":"2022","extern":"1","external_id":{"pmid":["36245392"]},"publication":"Chemical Communications","month":"10","date_published":"2022-10-10T00:00:00Z","scopus_import":"1","page":"12556-12559","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87"},{"pmid":1,"publication_identifier":{"issn":["1359-7345"],"eissn":["1364-548X"]},"OA_type":"closed access","intvolume":"        57","issue":"46","_id":"21082","type":"journal_article","doi":"10.1039/d1cc01452h","publication_status":"published","fulldoi":"https://doi.org/10.1039/d1cc01452h","article_type":"original","article_processing_charge":"No","quality_controlled":"1","has_accepted_license":"1","language":[{"iso":"eng"}],"abstract":[{"text":"A novel chiral aromatic δ-amino acid building block was shown to fully induce handedness in quinoline oligoamide foldamers with the possibility of further increasing the bias by combining multiples of these units in the same sequence. Through its incorporation within the helix, both N- and C-termini are still accessible for further functionalisation.","lang":"eng"}],"date_created":"2026-01-29T15:18:02Z","day":"29","publisher":"Royal Society of Chemistry","author":[{"last_name":"Bindl","first_name":"Daniel","full_name":"Bindl, Daniel"},{"full_name":"Heinemann, Elisabeth","first_name":"Elisabeth","last_name":"Heinemann"},{"orcid":"0000-0001-5996-956X","id":"6a3def15-d4b4-11ef-9fa9-a24c1f545ec3","full_name":"Mandal, Pradeep K","first_name":"Pradeep K","last_name":"Mandal"},{"first_name":"Ivan","last_name":"Huc","full_name":"Huc, Ivan"}],"citation":{"ieee":"D. Bindl, E. Heinemann, P. K. Mandal, and I. Huc, “Quantitative helix handedness bias through a single H vs. CH3 stereochemical differentiation,” <i>Chemical Communications</i>, vol. 57, no. 46. Royal Society of Chemistry, pp. 5662–5665, 2021.","apa":"Bindl, D., Heinemann, E., Mandal, P. K., &#38; Huc, I. (2021). Quantitative helix handedness bias through a single H vs. CH3 stereochemical differentiation. <i>Chemical Communications</i>. Royal Society of Chemistry. <a href=\"https://doi.org/10.1039/d1cc01452h\">https://doi.org/10.1039/d1cc01452h</a>","ista":"Bindl D, Heinemann E, Mandal PK, Huc I. 2021. Quantitative helix handedness bias through a single H vs. CH3 stereochemical differentiation. Chemical Communications. 57(46), 5662–5665.","mla":"Bindl, Daniel, et al. “Quantitative Helix Handedness Bias through a Single H vs. CH3 Stereochemical Differentiation.” <i>Chemical Communications</i>, vol. 57, no. 46, Royal Society of Chemistry, 2021, pp. 5662–65, doi:<a href=\"https://doi.org/10.1039/d1cc01452h\">10.1039/d1cc01452h</a>.","short":"D. Bindl, E. Heinemann, P.K. Mandal, I. Huc, Chemical Communications 57 (2021) 5662–5665.","ama":"Bindl D, Heinemann E, Mandal PK, Huc I. Quantitative helix handedness bias through a single H vs. CH3 stereochemical differentiation. <i>Chemical Communications</i>. 2021;57(46):5662-5665. doi:<a href=\"https://doi.org/10.1039/d1cc01452h\">10.1039/d1cc01452h</a>","chicago":"Bindl, Daniel, Elisabeth Heinemann, Pradeep K Mandal, and Ivan Huc. “Quantitative Helix Handedness Bias through a Single H vs. CH3 Stereochemical Differentiation.” <i>Chemical Communications</i>. Royal Society of Chemistry, 2021. <a href=\"https://doi.org/10.1039/d1cc01452h\">https://doi.org/10.1039/d1cc01452h</a>."},"volume":57,"date_updated":"2026-02-20T07:01:01Z","status":"public","title":"Quantitative helix handedness bias through a single H vs. CH3 stereochemical differentiation","oa_version":"None","date_published":"2021-04-29T00:00:00Z","month":"04","page":"5662-5665","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","year":"2021","extern":"1","external_id":{"pmid":["33972976 "]},"publication":"Chemical Communications"},{"page":"3909-3912","scopus_import":"1","date_published":"2021-03-15T00:00:00Z","month":"03","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","extern":"1","year":"2021","publication":"Chemical Communications","external_id":{"pmid":["33871510"]},"oa":1,"abstract":[{"text":"<p>A cascade Suzuki–Miyaura cross-coupling between two non-symmetrical coupling partners gave rise to 9,10-dihydrophenanthrenes with full site-selectivity. The choice of base was critical to facilitate the challenging coupling of the secondary boronate group.</p>","lang":"eng"}],"language":[{"iso":"eng"}],"main_file_link":[{"open_access":"1","url":"DOI\thttps://doi.org/10.1039/D1CC00648G"}],"author":[{"last_name":"Willems","first_name":"Suzanne","full_name":"Willems, Suzanne"},{"full_name":"Toupalas, Georgios","first_name":"Georgios","last_name":"Toupalas"},{"first_name":"Julia","last_name":"Reisenbauer","full_name":"Reisenbauer, Julia","id":"51d862e9-36ee-11f0-86d3-8534c85a5496"},{"first_name":"Bill","last_name":"Morandi","full_name":"Morandi, Bill"}],"citation":{"apa":"Willems, S., Toupalas, G., Reisenbauer, J., &#38; Morandi, B. (2021). A site-selective and stereospecific cascade Suzuki–Miyaura annulation of alkyl 1,2-bisboronic esters and 2,2′-dihalo 1,1′-biaryls. <i>Chemical Communications</i>. Royal Society of Chemistry. <a href=\"https://doi.org/10.1039/d1cc00648g\">https://doi.org/10.1039/d1cc00648g</a>","ieee":"S. Willems, G. Toupalas, J. Reisenbauer, and B. Morandi, “A site-selective and stereospecific cascade Suzuki–Miyaura annulation of alkyl 1,2-bisboronic esters and 2,2′-dihalo 1,1′-biaryls,” <i>Chemical Communications</i>, vol. 57, no. 32. Royal Society of Chemistry, pp. 3909–3912, 2021.","chicago":"Willems, Suzanne, Georgios Toupalas, Julia Reisenbauer, and Bill Morandi. “A Site-Selective and Stereospecific Cascade Suzuki–Miyaura Annulation of Alkyl 1,2-Bisboronic Esters and 2,2′-Dihalo 1,1′-Biaryls.” <i>Chemical Communications</i>. Royal Society of Chemistry, 2021. <a href=\"https://doi.org/10.1039/d1cc00648g\">https://doi.org/10.1039/d1cc00648g</a>.","short":"S. Willems, G. Toupalas, J. Reisenbauer, B. Morandi, Chemical Communications 57 (2021) 3909–3912.","ama":"Willems S, Toupalas G, Reisenbauer J, Morandi B. A site-selective and stereospecific cascade Suzuki–Miyaura annulation of alkyl 1,2-bisboronic esters and 2,2′-dihalo 1,1′-biaryls. <i>Chemical Communications</i>. 2021;57(32):3909-3912. doi:<a href=\"https://doi.org/10.1039/d1cc00648g\">10.1039/d1cc00648g</a>","mla":"Willems, Suzanne, et al. “A Site-Selective and Stereospecific Cascade Suzuki–Miyaura Annulation of Alkyl 1,2-Bisboronic Esters and 2,2′-Dihalo 1,1′-Biaryls.” <i>Chemical Communications</i>, vol. 57, no. 32, Royal Society of Chemistry, 2021, pp. 3909–12, doi:<a href=\"https://doi.org/10.1039/d1cc00648g\">10.1039/d1cc00648g</a>.","ista":"Willems S, Toupalas G, Reisenbauer J, Morandi B. 2021. A site-selective and stereospecific cascade Suzuki–Miyaura annulation of alkyl 1,2-bisboronic esters and 2,2′-dihalo 1,1′-biaryls. Chemical Communications. 57(32), 3909–3912."},"publisher":"Royal Society of Chemistry","day":"15","date_created":"2025-12-09T14:25:17Z","tmp":{"short":"CC BY (3.0)","legal_code_url":"https://creativecommons.org/licenses/by/3.0/legalcode","image":"/images/cc_by.png","name":"Creative Commons Attribution 3.0 Unported (CC BY 3.0)"},"title":"A site-selective and stereospecific cascade Suzuki–Miyaura annulation of alkyl 1,2-bisboronic esters and 2,2′-dihalo 1,1′-biaryls","status":"public","volume":57,"date_updated":"2025-12-16T12:06:53Z","oa_version":"Published Version","OA_place":"publisher","ddc":["540"],"article_type":"original","fulldoi":"https://doi.org/10.1039/d1cc00648g","article_processing_charge":"No","has_accepted_license":"1","quality_controlled":"1","publication_identifier":{"eissn":["1364-548X"],"issn":["1359-7345"]},"pmid":1,"license":"https://creativecommons.org/licenses/by/3.0/","_id":"20765","issue":"32","intvolume":"        57","OA_type":"hybrid","doi":"10.1039/d1cc00648g","type":"journal_article","publication_status":"published"},{"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","page":"591-594","scopus_import":"1","month":"05","date_published":"2021-05-01T00:00:00Z","publication":"Chemical Communications","external_id":{"pmid":["33325935"]},"extern":"1","year":"2021","publisher":"Royal Society of Chemistry","author":[{"last_name":"Medina Rivero","first_name":"Samara","full_name":"Medina Rivero, Samara"},{"full_name":"García Arroyo, Paloma","first_name":"Paloma","last_name":"García Arroyo"},{"last_name":"Li","first_name":"Liang","full_name":"Li, Liang"},{"last_name":"Gunasekaran","first_name":"Suman","full_name":"Gunasekaran, Suman"},{"first_name":"Thijs","last_name":"Stuyver","full_name":"Stuyver, Thijs"},{"last_name":"Mancheño","first_name":"María José","full_name":"Mancheño, María José"},{"full_name":"Alonso, Mercedes","last_name":"Alonso","first_name":"Mercedes"},{"first_name":"Latha","last_name":"Venkataraman","full_name":"Venkataraman, Latha","id":"9ebb78a5-cc0d-11ee-8322-fae086a32caf","orcid":"0000-0002-6957-6089"},{"last_name":"Segura","first_name":"José L.","full_name":"Segura, José L."},{"first_name":"Juan","last_name":"Casado","full_name":"Casado, Juan"}],"citation":{"chicago":"Medina Rivero, Samara, Paloma García Arroyo, Liang Li, Suman Gunasekaran, Thijs Stuyver, María José Mancheño, Mercedes Alonso, Latha Venkataraman, José L. Segura, and Juan Casado. “Single-Molecule Conductance in a Unique Cross-Conjugated Tetra(Aminoaryl)Ethene.” <i>Chemical Communications</i>. Royal Society of Chemistry, 2021. <a href=\"https://doi.org/10.1039/d0cc07124b\">https://doi.org/10.1039/d0cc07124b</a>.","short":"S. Medina Rivero, P. García Arroyo, L. Li, S. Gunasekaran, T. Stuyver, M.J. Mancheño, M. Alonso, L. Venkataraman, J.L. Segura, J. Casado, Chemical Communications 57 (2021) 591–594.","ama":"Medina Rivero S, García Arroyo P, Li L, et al. Single-molecule conductance in a unique cross-conjugated tetra(aminoaryl)ethene. <i>Chemical Communications</i>. 2021;57(5):591-594. doi:<a href=\"https://doi.org/10.1039/d0cc07124b\">10.1039/d0cc07124b</a>","ista":"Medina Rivero S, García Arroyo P, Li L, Gunasekaran S, Stuyver T, Mancheño MJ, Alonso M, Venkataraman L, Segura JL, Casado J. 2021. Single-molecule conductance in a unique cross-conjugated tetra(aminoaryl)ethene. Chemical Communications. 57(5), 591–594.","mla":"Medina Rivero, Samara, et al. “Single-Molecule Conductance in a Unique Cross-Conjugated Tetra(Aminoaryl)Ethene.” <i>Chemical Communications</i>, vol. 57, no. 5, Royal Society of Chemistry, 2021, pp. 591–94, doi:<a href=\"https://doi.org/10.1039/d0cc07124b\">10.1039/d0cc07124b</a>.","ieee":"S. Medina Rivero <i>et al.</i>, “Single-molecule conductance in a unique cross-conjugated tetra(aminoaryl)ethene,” <i>Chemical Communications</i>, vol. 57, no. 5. Royal Society of Chemistry, pp. 591–594, 2021.","apa":"Medina Rivero, S., García Arroyo, P., Li, L., Gunasekaran, S., Stuyver, T., Mancheño, M. J., … Casado, J. (2021). Single-molecule conductance in a unique cross-conjugated tetra(aminoaryl)ethene. <i>Chemical Communications</i>. Royal Society of Chemistry. <a href=\"https://doi.org/10.1039/d0cc07124b\">https://doi.org/10.1039/d0cc07124b</a>"},"day":"01","date_created":"2024-09-09T06:44:58Z","abstract":[{"text":"A 1,1,2,2-tetrakis(4-aminophenyl)ethene with three paths of π-conjugation, linear-cis, linear-trans and a cross-conjugation, has been prepared. The molecule is able to bind to gold electrodes forming molecular junctions for single-molecule conductance measurements. Only two regimes of conduction are found experimentally. The modelling of the conductance allows to assign them to through-bond transmission in the linear case, while the cross-conjugated channel is further assisted by through-space transmission, partially alleviating the destructive quantum interference.","lang":"eng"}],"language":[{"iso":"eng"}],"oa_version":"None","title":"Single-molecule conductance in a unique cross-conjugated tetra(aminoaryl)ethene","status":"public","date_updated":"2024-12-10T10:23:49Z","volume":57,"article_type":"original","fulldoi":"https://doi.org/10.1039/d0cc07124b","quality_controlled":"1","article_processing_charge":"No","_id":"17901","issue":"5","intvolume":"        57","OA_type":"closed access","publication_identifier":{"issn":["1359-7345"],"eissn":["1364-548X"]},"pmid":1,"publication_status":"published","doi":"10.1039/d0cc07124b","type":"journal_article"},{"doi":"10.1039/c6cc04466b","type":"journal_article","publication_status":"published","publication_identifier":{"issn":["1359-7345"],"eissn":["1364-548X"]},"issue":"60","_id":"21100","OA_type":"closed access","intvolume":"        52","article_processing_charge":"No","quality_controlled":"1","has_accepted_license":"1","fulldoi":"https://doi.org/10.1039/c6cc04466b","article_type":"original","status":"public","title":"Crystal structure of a complex between β-glucopyranose and a macrocyclic receptor with dendritic multicharged water solubilizing chains","volume":52,"date_updated":"2026-02-23T09:18:46Z","oa_version":"None","language":[{"iso":"eng"}],"abstract":[{"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.","lang":"eng"}],"publisher":"Royal Society of Chemistry","author":[{"last_name":"Mandal","first_name":"Pradeep K","orcid":"0000-0001-5996-956X","id":"6a3def15-d4b4-11ef-9fa9-a24c1f545ec3","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","last_name":"Ferrand","first_name":"Yann"},{"full_name":"Davis, Anthony P.","last_name":"Davis","first_name":"Anthony P."},{"first_name":"Ivan","last_name":"Huc","full_name":"Huc, Ivan"}],"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,” <i>Chemical Communications</i>, 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., &#38; Huc, I. (2016). Crystal structure of a complex between β-glucopyranose and a macrocyclic receptor with dendritic multicharged water solubilizing chains. <i>Chemical Communications</i>. Royal Society of Chemistry. <a href=\"https://doi.org/10.1039/c6cc04466b\">https://doi.org/10.1039/c6cc04466b</a>","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.” <i>Chemical Communications</i>. Royal Society of Chemistry, 2016. <a href=\"https://doi.org/10.1039/c6cc04466b\">https://doi.org/10.1039/c6cc04466b</a>.","short":"P.K. Mandal, B. Kauffmann, H. Destecroix, Y. Ferrand, A.P. Davis, I. Huc, Chemical Communications 52 (2016) 9355–9358.","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. <i>Chemical Communications</i>. 2016;52(60):9355-9358. doi:<a href=\"https://doi.org/10.1039/c6cc04466b\">10.1039/c6cc04466b</a>","mla":"Mandal, Pradeep K., et al. “Crystal Structure of a Complex between β-Glucopyranose and a Macrocyclic Receptor with Dendritic Multicharged Water Solubilizing Chains.” <i>Chemical Communications</i>, vol. 52, no. 60, Royal Society of Chemistry, 2016, pp. 9355–58, doi:<a href=\"https://doi.org/10.1039/c6cc04466b\">10.1039/c6cc04466b</a>.","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."},"date_created":"2026-01-29T21:42:03Z","day":"28","year":"2016","extern":"1","publication":"Chemical Communications","page":"9355-9358","date_published":"2016-06-28T00:00:00Z","month":"06","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87"},{"main_file_link":[{"open_access":"1","url":"https://doi.org/10.1039/C4CC08541H"}],"publisher":"Royal Society of Chemistry","author":[{"full_name":"Lee, Ji-Woong","last_name":"Lee","first_name":"Ji-Woong"},{"last_name":"Klajn","first_name":"Rafal","id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b","full_name":"Klajn, Rafal"}],"citation":{"mla":"Lee, Ji-Woong, and Rafal Klajn. “Dual-Responsive Nanoparticles That Aggregate under the Simultaneous Action of Light and CO2.” <i>Chemical Communications</i>, vol. 51, no. 11, Royal Society of Chemistry, 2015, pp. 2036–39, doi:<a href=\"https://doi.org/10.1039/c4cc08541h\">10.1039/c4cc08541h</a>.","ista":"Lee J-W, Klajn R. 2015. Dual-responsive nanoparticles that aggregate under the simultaneous action of light and CO2. Chemical Communications. 51(11), 2036–2039.","chicago":"Lee, Ji-Woong, and Rafal Klajn. “Dual-Responsive Nanoparticles That Aggregate under the Simultaneous Action of Light and CO2.” <i>Chemical Communications</i>. Royal Society of Chemistry, 2015. <a href=\"https://doi.org/10.1039/c4cc08541h\">https://doi.org/10.1039/c4cc08541h</a>.","ama":"Lee J-W, Klajn R. Dual-responsive nanoparticles that aggregate under the simultaneous action of light and CO2. <i>Chemical Communications</i>. 2015;51(11):2036-2039. doi:<a href=\"https://doi.org/10.1039/c4cc08541h\">10.1039/c4cc08541h</a>","short":"J.-W. Lee, R. Klajn, Chemical Communications 51 (2015) 2036–2039.","ieee":"J.-W. Lee and R. Klajn, “Dual-responsive nanoparticles that aggregate under the simultaneous action of light and CO2,” <i>Chemical Communications</i>, vol. 51, no. 11. Royal Society of Chemistry, pp. 2036–2039, 2015.","apa":"Lee, J.-W., &#38; Klajn, R. (2015). Dual-responsive nanoparticles that aggregate under the simultaneous action of light and CO2. <i>Chemical Communications</i>. Royal Society of Chemistry. <a href=\"https://doi.org/10.1039/c4cc08541h\">https://doi.org/10.1039/c4cc08541h</a>"},"day":"18","date_created":"2023-08-01T09:44:48Z","oa":1,"abstract":[{"lang":"eng","text":"Metallic nanoparticles co-functionalised with monolayers of UV- and CO2-sensitive ligands were prepared and shown to respond to these two types of stimuli reversibly and in an orthogonal fashion. The composition of the coating could be tailored to yield nanoparticles capable of aggregating exclusively when both UV and CO2 were applied at the same time, analogously to the behaviour of an AND logic gate."}],"language":[{"iso":"eng"}],"oa_version":"Published Version","title":"Dual-responsive nanoparticles that aggregate under the simultaneous action of light and CO2","status":"public","volume":51,"date_updated":"2024-10-14T12:17:58Z","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","page":"2036-2039","scopus_import":"1","keyword":["Materials Chemistry","Metals and Alloys","Surfaces","Coatings and Films","General Chemistry","Ceramics and Composites","Electronic","Optical and Magnetic Materials","Catalysis"],"date_published":"2015-11-18T00:00:00Z","month":"11","publication":"Chemical Communications","external_id":{"pmid":["25417754"]},"extern":"1","year":"2015","_id":"13395","issue":"11","intvolume":"        51","publication_identifier":{"issn":["1359-7345"],"eissn":["1364-548X"]},"pmid":1,"publication_status":"published","doi":"10.1039/c4cc08541h","type":"journal_article","article_type":"original","fulldoi":"https://doi.org/10.1039/c4cc08541h","quality_controlled":"1","article_processing_charge":"No"}]