Cailing Wu , Shaojie Wu , Qifei Huang , Kai Sun , Xianqiang Huang , Jianji Wang , Bing Yu
{"title":"钾改性氮化碳光催化 N-磺酰基酮亚胺的氨基化反应","authors":"Cailing Wu , Shaojie Wu , Qifei Huang , Kai Sun , Xianqiang Huang , Jianji Wang , Bing Yu","doi":"10.1016/j.cclet.2024.110250","DOIUrl":null,"url":null,"abstract":"<div><div>The development of innovative and sustainable catalytic strategies for organic synthesis is a pivotal aspect of advancing material science and chemical engineering. This research presents a new catalytic method for the aminoacylation of <em>N</em>‑sulfonyl ketimines by utilizing a potassium-doped graphite-like carbon nitride (g-C<sub>3</sub>N<sub>4</sub>) framework. This method not only enhances the catalytic efficiency and broadens the light absorption spectrum of g-C<sub>3</sub>N<sub>4</sub> but also significantly reduces the recombination rate of electron-hole pairs, thereby increasing the reaction yield and selectivity. Importantly, our approach facilitates the synthesis of aminoacylated <em>N</em>-heterocycles, expanding the applicability of potassium-modified g-C<sub>3</sub>N<sub>4</sub> in photocatalytic organic synthesis. A notable accomplishment of this study is the unprecedented generation of carbamoyl radicals <em>via</em> heterogeneous photocatalysis, which can be easily recycled after reaction. This advancement highlights the capability of potassium-doped g-C<sub>3</sub>N<sub>4</sub> (namely <strong>K-CN</strong>) as an advanced heterogeneous photocatalyst for the formation of complex organic compounds.</div></div>","PeriodicalId":10088,"journal":{"name":"Chinese Chemical Letters","volume":"36 2","pages":"Article 110250"},"PeriodicalIF":9.4000,"publicationDate":"2024-07-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Potassium-modified carbon nitride photocatalyzed-aminoacylation of N‑sulfonyl ketimines\",\"authors\":\"Cailing Wu , Shaojie Wu , Qifei Huang , Kai Sun , Xianqiang Huang , Jianji Wang , Bing Yu\",\"doi\":\"10.1016/j.cclet.2024.110250\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The development of innovative and sustainable catalytic strategies for organic synthesis is a pivotal aspect of advancing material science and chemical engineering. This research presents a new catalytic method for the aminoacylation of <em>N</em>‑sulfonyl ketimines by utilizing a potassium-doped graphite-like carbon nitride (g-C<sub>3</sub>N<sub>4</sub>) framework. This method not only enhances the catalytic efficiency and broadens the light absorption spectrum of g-C<sub>3</sub>N<sub>4</sub> but also significantly reduces the recombination rate of electron-hole pairs, thereby increasing the reaction yield and selectivity. Importantly, our approach facilitates the synthesis of aminoacylated <em>N</em>-heterocycles, expanding the applicability of potassium-modified g-C<sub>3</sub>N<sub>4</sub> in photocatalytic organic synthesis. A notable accomplishment of this study is the unprecedented generation of carbamoyl radicals <em>via</em> heterogeneous photocatalysis, which can be easily recycled after reaction. This advancement highlights the capability of potassium-doped g-C<sub>3</sub>N<sub>4</sub> (namely <strong>K-CN</strong>) as an advanced heterogeneous photocatalyst for the formation of complex organic compounds.</div></div>\",\"PeriodicalId\":10088,\"journal\":{\"name\":\"Chinese Chemical Letters\",\"volume\":\"36 2\",\"pages\":\"Article 110250\"},\"PeriodicalIF\":9.4000,\"publicationDate\":\"2024-07-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chinese Chemical Letters\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1001841724007691\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Chemical Letters","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1001841724007691","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Potassium-modified carbon nitride photocatalyzed-aminoacylation of N‑sulfonyl ketimines
The development of innovative and sustainable catalytic strategies for organic synthesis is a pivotal aspect of advancing material science and chemical engineering. This research presents a new catalytic method for the aminoacylation of N‑sulfonyl ketimines by utilizing a potassium-doped graphite-like carbon nitride (g-C3N4) framework. This method not only enhances the catalytic efficiency and broadens the light absorption spectrum of g-C3N4 but also significantly reduces the recombination rate of electron-hole pairs, thereby increasing the reaction yield and selectivity. Importantly, our approach facilitates the synthesis of aminoacylated N-heterocycles, expanding the applicability of potassium-modified g-C3N4 in photocatalytic organic synthesis. A notable accomplishment of this study is the unprecedented generation of carbamoyl radicals via heterogeneous photocatalysis, which can be easily recycled after reaction. This advancement highlights the capability of potassium-doped g-C3N4 (namely K-CN) as an advanced heterogeneous photocatalyst for the formation of complex organic compounds.
期刊介绍:
Chinese Chemical Letters (CCL) (ISSN 1001-8417) was founded in July 1990. The journal publishes preliminary accounts in the whole field of chemistry, including inorganic chemistry, organic chemistry, analytical chemistry, physical chemistry, polymer chemistry, applied chemistry, etc.Chinese Chemical Letters does not accept articles previously published or scheduled to be published. To verify originality, your article may be checked by the originality detection service CrossCheck.