[{"language":[{"iso":"eng"}],"issue":"8","main_file_link":[{"open_access":"1","url":"https://doi.org/10.1002/cptc.202100062"}],"scopus_import":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","year":"2021","day":"01","doi":"10.1002/cptc.202100062","date_published":"2021-08-01T00:00:00Z","date_updated":"2024-10-14T11:43:32Z","title":"Recyclable, bifunctional metallaphotocatalysts for C−S cross‐coupling reactions","extern":"1","citation":{"apa":"Reischauer, S., &#38; Pieber, B. (2021). Recyclable, bifunctional metallaphotocatalysts for C−S cross‐coupling reactions. <i>ChemPhotoChem</i>. Wiley. <a href=\"https://doi.org/10.1002/cptc.202100062\">https://doi.org/10.1002/cptc.202100062</a>","ieee":"S. Reischauer and B. Pieber, “Recyclable, bifunctional metallaphotocatalysts for C−S cross‐coupling reactions,” <i>ChemPhotoChem</i>, vol. 5, no. 8. Wiley, pp. 716–720, 2021.","ama":"Reischauer S, Pieber B. Recyclable, bifunctional metallaphotocatalysts for C−S cross‐coupling reactions. <i>ChemPhotoChem</i>. 2021;5(8):716-720. doi:<a href=\"https://doi.org/10.1002/cptc.202100062\">10.1002/cptc.202100062</a>","ista":"Reischauer S, Pieber B. 2021. Recyclable, bifunctional metallaphotocatalysts for C−S cross‐coupling reactions. ChemPhotoChem. 5(8), 716–720.","short":"S. Reischauer, B. Pieber, ChemPhotoChem 5 (2021) 716–720.","chicago":"Reischauer, Susanne, and Bartholomäus Pieber. “Recyclable, Bifunctional Metallaphotocatalysts for C−S Cross‐coupling Reactions.” <i>ChemPhotoChem</i>. Wiley, 2021. <a href=\"https://doi.org/10.1002/cptc.202100062\">https://doi.org/10.1002/cptc.202100062</a>.","mla":"Reischauer, Susanne, and Bartholomäus Pieber. “Recyclable, Bifunctional Metallaphotocatalysts for C−S Cross‐coupling Reactions.” <i>ChemPhotoChem</i>, vol. 5, no. 8, Wiley, 2021, pp. 716–20, doi:<a href=\"https://doi.org/10.1002/cptc.202100062\">10.1002/cptc.202100062</a>."},"author":[{"full_name":"Reischauer, Susanne","last_name":"Reischauer","first_name":"Susanne"},{"full_name":"Pieber, Bartholomäus","orcid":"0000-0001-8689-388X","first_name":"Bartholomäus","last_name":"Pieber","id":"93e5e5b2-0da6-11ed-8a41-af589a024726"}],"publication_status":"published","oa_version":"Published Version","type":"journal_article","intvolume":"         5","_id":"11965","publisher":"Wiley","article_type":"letter_note","quality_controlled":"1","oa":1,"date_created":"2022-08-25T08:31:11Z","volume":5,"article_processing_charge":"No","month":"08","status":"public","abstract":[{"lang":"eng","text":"Metallaphotocatalytic cross-coupling reactions are typically carried out by combining homogeneous or heterogeneous photocatalysts with a soluble nickel complex. Previous attempts to realize recyclable catalytic systems use immobilized iridium complexes to harvest light. We present bifunctional materials based on semiconductors for metallaphotocatalytic C−S cross-coupling reactions that can be reused without losing their catalytic activity. Key to the success is the permanent immobilization of a nickel complex on the surface of a heterogeneous semiconductor through phosphonic acid anchors. The optimized catalyst harvests a broad range of the visible light spectrum and requires a nickel loading of only ∼0.1 mol %."}],"page":"716-720","publication":"ChemPhotoChem","publication_identifier":{"eissn":["2367-0932"]}},{"date_updated":"2024-10-14T12:06:48Z","date_published":"2020-07-01T00:00:00Z","doi":"10.1002/cptc.202000137","year":"2020","day":"01","scopus_import":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","issue":"7","language":[{"iso":"eng"}],"_id":"11966","intvolume":"         4","type":"journal_article","oa_version":"None","citation":{"ista":"Gisbertz S, Pieber B. 2020. Heterogeneous photocatalysis in organic synthesis. ChemPhotoChem. 4(7), 454–454.","short":"S. Gisbertz, B. Pieber, ChemPhotoChem 4 (2020) 454–454.","chicago":"Gisbertz, Sebastian, and Bartholomäus Pieber. “Heterogeneous Photocatalysis in Organic Synthesis.” <i>ChemPhotoChem</i>. Wiley, 2020. <a href=\"https://doi.org/10.1002/cptc.202000137\">https://doi.org/10.1002/cptc.202000137</a>.","mla":"Gisbertz, Sebastian, and Bartholomäus Pieber. “Heterogeneous Photocatalysis in Organic Synthesis.” <i>ChemPhotoChem</i>, vol. 4, no. 7, Wiley, 2020, pp. 454–454, doi:<a href=\"https://doi.org/10.1002/cptc.202000137\">10.1002/cptc.202000137</a>.","apa":"Gisbertz, S., &#38; Pieber, B. (2020). Heterogeneous photocatalysis in organic synthesis. <i>ChemPhotoChem</i>. Wiley. <a href=\"https://doi.org/10.1002/cptc.202000137\">https://doi.org/10.1002/cptc.202000137</a>","ieee":"S. Gisbertz and B. Pieber, “Heterogeneous photocatalysis in organic synthesis,” <i>ChemPhotoChem</i>, vol. 4, no. 7. Wiley, pp. 454–454, 2020.","ama":"Gisbertz S, Pieber B. Heterogeneous photocatalysis in organic synthesis. <i>ChemPhotoChem</i>. 2020;4(7):454-454. doi:<a href=\"https://doi.org/10.1002/cptc.202000137\">10.1002/cptc.202000137</a>"},"author":[{"full_name":"Gisbertz, Sebastian","last_name":"Gisbertz","first_name":"Sebastian"},{"orcid":"0000-0001-8689-388X","full_name":"Pieber, Bartholomäus","id":"93e5e5b2-0da6-11ed-8a41-af589a024726","last_name":"Pieber","first_name":"Bartholomäus"}],"publication_status":"published","title":"Heterogeneous photocatalysis in organic synthesis","extern":"1","page":"454-454","status":"public","abstract":[{"lang":"eng","text":"The front cover artwork is provided by the group of Dr. Bartholomäus Pieber at the Max Planck Institute of Colloids and Interfaces (Germany). The image symbolizes the activation of a heterogeneous photocatalyst by visible light and its application for organic synthesis. Read the full text of the Review at 10.1002/cptc.202000014."}],"month":"07","article_processing_charge":"No","volume":4,"quality_controlled":"1","date_created":"2022-08-25T08:33:38Z","publisher":"Wiley","article_type":"original","publication_identifier":{"eissn":["2367-0932"]},"publication":"ChemPhotoChem"},{"issue":"5","language":[{"iso":"eng"}],"keyword":["Organic Chemistry","Physical and Theoretical Chemistry","Analytical Chemistry"],"scopus_import":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","doi":"10.1002/cptc.201700009","year":"2017","day":"01","date_published":"2017-05-01T00:00:00Z","date_updated":"2024-10-14T12:15:59Z","publication_status":"published","citation":{"ama":"Ahrens J, Bian T, Vexler T, Klajn R. Irreversible bleaching of donor-acceptor stenhouse adducts on the surfaces of magnetite nanoparticles. <i>ChemPhotoChem</i>. 2017;1(5):230-236. doi:<a href=\"https://doi.org/10.1002/cptc.201700009\">10.1002/cptc.201700009</a>","ieee":"J. Ahrens, T. Bian, T. Vexler, and R. Klajn, “Irreversible bleaching of donor-acceptor stenhouse adducts on the surfaces of magnetite nanoparticles,” <i>ChemPhotoChem</i>, vol. 1, no. 5. Wiley, pp. 230–236, 2017.","apa":"Ahrens, J., Bian, T., Vexler, T., &#38; Klajn, R. (2017). Irreversible bleaching of donor-acceptor stenhouse adducts on the surfaces of magnetite nanoparticles. <i>ChemPhotoChem</i>. Wiley. <a href=\"https://doi.org/10.1002/cptc.201700009\">https://doi.org/10.1002/cptc.201700009</a>","short":"J. Ahrens, T. Bian, T. Vexler, R. Klajn, ChemPhotoChem 1 (2017) 230–236.","chicago":"Ahrens, Johannes, Tong Bian, Tom Vexler, and Rafal Klajn. “Irreversible Bleaching of Donor-Acceptor Stenhouse Adducts on the Surfaces of Magnetite Nanoparticles.” <i>ChemPhotoChem</i>. Wiley, 2017. <a href=\"https://doi.org/10.1002/cptc.201700009\">https://doi.org/10.1002/cptc.201700009</a>.","ista":"Ahrens J, Bian T, Vexler T, Klajn R. 2017. Irreversible bleaching of donor-acceptor stenhouse adducts on the surfaces of magnetite nanoparticles. ChemPhotoChem. 1(5), 230–236.","mla":"Ahrens, Johannes, et al. “Irreversible Bleaching of Donor-Acceptor Stenhouse Adducts on the Surfaces of Magnetite Nanoparticles.” <i>ChemPhotoChem</i>, vol. 1, no. 5, Wiley, 2017, pp. 230–36, doi:<a href=\"https://doi.org/10.1002/cptc.201700009\">10.1002/cptc.201700009</a>."},"author":[{"full_name":"Ahrens, Johannes","first_name":"Johannes","last_name":"Ahrens"},{"first_name":"Tong","last_name":"Bian","full_name":"Bian, Tong"},{"full_name":"Vexler, Tom","last_name":"Vexler","first_name":"Tom"},{"full_name":"Klajn, Rafal","first_name":"Rafal","id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b","last_name":"Klajn"}],"title":"Irreversible bleaching of donor-acceptor stenhouse adducts on the surfaces of magnetite nanoparticles","extern":"1","type":"journal_article","oa_version":"None","_id":"13383","intvolume":"         1","publisher":"Wiley","article_type":"original","article_processing_charge":"No","volume":1,"quality_controlled":"1","date_created":"2023-08-01T09:41:43Z","status":"public","abstract":[{"lang":"eng","text":"Two novel donor–acceptor Stenhouse adducts (DASAs) featuring the catechol moiety were synthesized and characterized. Both compounds bind strongly to the surfaces of magnetite nanoparticles. An adrenaline-derived DASA renders the particles insoluble in all common solvents, likely because of poor solvation of the zwitterionic isomer generated on the nanoparticle surfaces. Well-soluble nanoparticles were successfully obtained using dopamine-derived DASA equipped with a long alkyl chain. Upon its attachment to nanoparticles, this DASA undergoes an irreversible decoloration reaction owing to the formation of the zwitterionic form. The reaction follows first-order kinetics and proceeds more rapidly on large nanoparticles. Interestingly, decoloration can be suppressed in the presence of free DASA molecules in solution or at high nanoparticle concentrations."}],"month":"05","page":"230-236","publication":"ChemPhotoChem","publication_identifier":{"eissn":["2367-0932"]}}]