[{"month":"06","title":"Carbon dot/TiO₂ nanocomposites as photocatalysts for metallaphotocatalytic carbon-heteroatom cross-couplings","article_type":"original","doi":"10.1039/d1gc01284c","year":"2021","author":[{"last_name":"Zhao","first_name":"Zhouxiang","full_name":"Zhao, Zhouxiang"},{"full_name":"Reischauer, Susanne","last_name":"Reischauer","first_name":"Susanne"},{"full_name":"Pieber, Bartholomäus","id":"93e5e5b2-0da6-11ed-8a41-af589a024726","last_name":"Pieber","first_name":"Bartholomäus","orcid":"0000-0001-8689-388X"},{"first_name":"Martina","last_name":"Delbianco","full_name":"Delbianco, Martina"}],"scopus_import":"1","page":"4524-4530","day":"21","quality_controlled":"1","status":"public","oa":1,"type":"journal_article","main_file_link":[{"open_access":"1","url":"https://doi.org/10.1039/D1GC01284C"}],"abstract":[{"text":"Carbon dots have been previosly immobilized on titanium dioxide to generate photocatalysts for pollutant degradation and water splitting. Here we demonstrate that these nanocomposites are valuable photocatalysts for metallaphotocatalytic carbon–heteroatom cross-couplings. These sustainable materials show a large applicability, high photostability, excellent reusability, and broadly absorb across the visible-light spectrum.","lang":"eng"}],"date_created":"2022-08-25T10:25:46Z","article_processing_charge":"No","date_updated":"2024-10-14T12:05:41Z","_id":"11972","issue":"12","language":[{"iso":"eng"}],"extern":"1","citation":{"ieee":"Z. Zhao, S. Reischauer, B. Pieber, and M. Delbianco, “Carbon dot/TiO₂ nanocomposites as photocatalysts for metallaphotocatalytic carbon-heteroatom cross-couplings,” <i>Green Chemistry</i>, vol. 23, no. 12. Royal Society of Chemistry, pp. 4524–4530, 2021.","chicago":"Zhao, Zhouxiang, Susanne Reischauer, Bartholomäus Pieber, and Martina Delbianco. “Carbon Dot/TiO₂ Nanocomposites as Photocatalysts for Metallaphotocatalytic Carbon-Heteroatom Cross-Couplings.” <i>Green Chemistry</i>. Royal Society of Chemistry, 2021. <a href=\"https://doi.org/10.1039/d1gc01284c\">https://doi.org/10.1039/d1gc01284c</a>.","apa":"Zhao, Z., Reischauer, S., Pieber, B., &#38; Delbianco, M. (2021). Carbon dot/TiO₂ nanocomposites as photocatalysts for metallaphotocatalytic carbon-heteroatom cross-couplings. <i>Green Chemistry</i>. Royal Society of Chemistry. <a href=\"https://doi.org/10.1039/d1gc01284c\">https://doi.org/10.1039/d1gc01284c</a>","short":"Z. Zhao, S. Reischauer, B. Pieber, M. Delbianco, Green Chemistry 23 (2021) 4524–4530.","ista":"Zhao Z, Reischauer S, Pieber B, Delbianco M. 2021. Carbon dot/TiO₂ nanocomposites as photocatalysts for metallaphotocatalytic carbon-heteroatom cross-couplings. Green Chemistry. 23(12), 4524–4530.","mla":"Zhao, Zhouxiang, et al. “Carbon Dot/TiO₂ Nanocomposites as Photocatalysts for Metallaphotocatalytic Carbon-Heteroatom Cross-Couplings.” <i>Green Chemistry</i>, vol. 23, no. 12, Royal Society of Chemistry, 2021, pp. 4524–30, doi:<a href=\"https://doi.org/10.1039/d1gc01284c\">10.1039/d1gc01284c</a>.","ama":"Zhao Z, Reischauer S, Pieber B, Delbianco M. Carbon dot/TiO₂ nanocomposites as photocatalysts for metallaphotocatalytic carbon-heteroatom cross-couplings. <i>Green Chemistry</i>. 2021;23(12):4524-4530. doi:<a href=\"https://doi.org/10.1039/d1gc01284c\">10.1039/d1gc01284c</a>"},"publication_identifier":{"eissn":["1463-9270"],"issn":["1463-9262"]},"oa_version":"Published Version","volume":23,"date_published":"2021-06-21T00:00:00Z","publisher":"Royal Society of Chemistry","publication_status":"published","publication":"Green Chemistry","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","intvolume":"        23"},{"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","date_created":"2022-08-25T10:29:21Z","intvolume":"        15","publication":"Green Chemistry","abstract":[{"lang":"eng","text":"The use of high-temperature/pressure gas–liquid continuous flow conditions dramatically enhances the iron-catalyzed aerobic oxidation of 2-benzylpyridines to their corresponding ketones. Pressurized air serves as a readily available oxygen source and propylene carbonate as a green solvent in this radically intensified preparation of synthetically valuable 2-aroylpyridines."}],"type":"journal_article","publisher":"Royal Society of Chemistry","publication_status":"published","volume":15,"date_published":"2013-02-01T00:00:00Z","status":"public","oa_version":"None","quality_controlled":"1","page":"320-324","scopus_import":"1","publication_identifier":{"issn":["1463-9262"],"eissn":["1463-9270"]},"citation":{"ieee":"B. Pieber and C. O. Kappe, “Direct aerobic oxidation of 2-benzylpyridines in a gas-liquid continuous-flow regime using propylene carbonate as a solvent,” <i>Green Chemistry</i>, vol. 15, no. 2. Royal Society of Chemistry, pp. 320–324, 2013.","chicago":"Pieber, Bartholomäus, and C. Oliver Kappe. “Direct Aerobic Oxidation of 2-Benzylpyridines in a Gas-Liquid Continuous-Flow Regime Using Propylene Carbonate as a Solvent.” <i>Green Chemistry</i>. Royal Society of Chemistry, 2013. <a href=\"https://doi.org/10.1039/c2gc36896j\">https://doi.org/10.1039/c2gc36896j</a>.","ista":"Pieber B, Kappe CO. 2013. Direct aerobic oxidation of 2-benzylpyridines in a gas-liquid continuous-flow regime using propylene carbonate as a solvent. Green Chemistry. 15(2), 320–324.","short":"B. Pieber, C.O. Kappe, Green Chemistry 15 (2013) 320–324.","mla":"Pieber, Bartholomäus, and C. Oliver Kappe. “Direct Aerobic Oxidation of 2-Benzylpyridines in a Gas-Liquid Continuous-Flow Regime Using Propylene Carbonate as a Solvent.” <i>Green Chemistry</i>, vol. 15, no. 2, Royal Society of Chemistry, 2013, pp. 320–24, doi:<a href=\"https://doi.org/10.1039/c2gc36896j\">10.1039/c2gc36896j</a>.","ama":"Pieber B, Kappe CO. Direct aerobic oxidation of 2-benzylpyridines in a gas-liquid continuous-flow regime using propylene carbonate as a solvent. <i>Green Chemistry</i>. 2013;15(2):320-324. doi:<a href=\"https://doi.org/10.1039/c2gc36896j\">10.1039/c2gc36896j</a>","apa":"Pieber, B., &#38; Kappe, C. O. (2013). Direct aerobic oxidation of 2-benzylpyridines in a gas-liquid continuous-flow regime using propylene carbonate as a solvent. <i>Green Chemistry</i>. Royal Society of Chemistry. <a href=\"https://doi.org/10.1039/c2gc36896j\">https://doi.org/10.1039/c2gc36896j</a>"},"day":"01","year":"2013","doi":"10.1039/c2gc36896j","author":[{"orcid":"0000-0001-8689-388X","first_name":"Bartholomäus","last_name":"Pieber","id":"93e5e5b2-0da6-11ed-8a41-af589a024726","full_name":"Pieber, Bartholomäus"},{"last_name":"Kappe","first_name":"C. Oliver","full_name":"Kappe, C. Oliver"}],"extern":"1","article_type":"letter_note","language":[{"iso":"eng"}],"issue":"2","title":"Direct aerobic oxidation of 2-benzylpyridines in a gas-liquid continuous-flow regime using propylene carbonate as a solvent","_id":"11973","month":"02","article_processing_charge":"No","date_updated":"2023-02-21T10:09:54Z"}]