[{"language":[{"iso":"eng"}],"extern":"1","month":"08","status":"public","publisher":"Wiley","date_published":"2021-08-01T00:00:00Z","type":"journal_article","issue":"8","page":"716-720","day":"01","quality_controlled":"1","intvolume":"         5","publication":"ChemPhotoChem","date_updated":"2023-02-21T10:09:37Z","author":[{"first_name":"Susanne","last_name":"Reischauer","full_name":"Reischauer, Susanne"},{"full_name":"Pieber, Bartholomäus","id":"93e5e5b2-0da6-11ed-8a41-af589a024726","orcid":"0000-0001-8689-388X","last_name":"Pieber","first_name":"Bartholomäus"}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","oa":1,"volume":5,"year":"2021","citation":{"short":"S. Reischauer, B. Pieber, ChemPhotoChem 5 (2021) 716–720.","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>","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>.","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.","ista":"Reischauer S, Pieber B. 2021. Recyclable, bifunctional metallaphotocatalysts for C−S cross‐coupling reactions. ChemPhotoChem. 5(8), 716–720.","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>"},"abstract":[{"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 %.","lang":"eng"}],"_id":"11965","date_created":"2022-08-25T08:31:11Z","doi":"10.1002/cptc.202100062","main_file_link":[{"open_access":"1","url":"https://doi.org/10.1002/cptc.202100062"}],"scopus_import":"1","article_type":"letter_note","publication_identifier":{"eissn":["2367-0932"]},"publication_status":"published","title":"Recyclable, bifunctional metallaphotocatalysts for C−S cross‐coupling reactions","oa_version":"Published Version","article_processing_charge":"No"},{"issue":"7","page":"454-454","day":"01","quality_controlled":"1","language":[{"iso":"eng"}],"extern":"1","month":"07","status":"public","publisher":"Wiley","type":"journal_article","date_published":"2020-07-01T00:00:00Z","citation":{"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>","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>.","short":"S. Gisbertz, B. Pieber, ChemPhotoChem 4 (2020) 454–454.","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>","ieee":"S. Gisbertz and B. Pieber, “Heterogeneous photocatalysis in organic synthesis,” <i>ChemPhotoChem</i>, vol. 4, no. 7. Wiley, pp. 454–454, 2020.","ista":"Gisbertz S, Pieber B. 2020. Heterogeneous photocatalysis in organic synthesis. ChemPhotoChem. 4(7), 454–454."},"year":"2020","abstract":[{"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.","lang":"eng"}],"date_created":"2022-08-25T08:33:38Z","_id":"11966","scopus_import":"1","doi":"10.1002/cptc.202000137","publication_identifier":{"eissn":["2367-0932"]},"article_type":"original","publication_status":"published","title":"Heterogeneous photocatalysis in organic synthesis","article_processing_charge":"No","oa_version":"None","intvolume":"         4","date_updated":"2023-02-21T10:09:40Z","publication":"ChemPhotoChem","author":[{"first_name":"Sebastian","last_name":"Gisbertz","full_name":"Gisbertz, Sebastian"},{"full_name":"Pieber, Bartholomäus","orcid":"0000-0001-8689-388X","id":"93e5e5b2-0da6-11ed-8a41-af589a024726","last_name":"Pieber","first_name":"Bartholomäus"}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","volume":4},{"publisher":"Wiley","type":"journal_article","date_published":"2017-05-01T00:00:00Z","extern":"1","keyword":["Organic Chemistry","Physical and Theoretical Chemistry","Analytical Chemistry"],"language":[{"iso":"eng"}],"status":"public","month":"05","day":"01","page":"230-236","quality_controlled":"1","issue":"5","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","author":[{"first_name":"Johannes","last_name":"Ahrens","full_name":"Ahrens, Johannes"},{"full_name":"Bian, Tong","first_name":"Tong","last_name":"Bian"},{"last_name":"Vexler","first_name":"Tom","full_name":"Vexler, Tom"},{"full_name":"Klajn, Rafal","id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b","last_name":"Klajn","first_name":"Rafal"}],"volume":1,"intvolume":"         1","date_updated":"2023-08-07T12:08:05Z","publication":"ChemPhotoChem","publication_identifier":{"eissn":["2367-0932"]},"article_type":"original","scopus_import":"1","doi":"10.1002/cptc.201700009","article_processing_charge":"No","oa_version":"None","publication_status":"published","title":"Irreversible bleaching of donor-acceptor stenhouse adducts on the surfaces of magnetite nanoparticles","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."}],"citation":{"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>.","short":"J. Ahrens, T. Bian, T. Vexler, R. Klajn, ChemPhotoChem 1 (2017) 230–236.","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>","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>.","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.","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."},"year":"2017","date_created":"2023-08-01T09:41:43Z","_id":"13383"}]