Qing-Qing Wang, Li Sheng, Fei Wang, Jie Xu, Bing Xue
{"title":"介孔富氮氮化碳材料的合成及其作为无金属固体碱在Knoevenagel缩合中的催化应用","authors":"Qing-Qing Wang, Li Sheng, Fei Wang, Jie Xu, Bing Xue","doi":"10.1007/s11164-025-05602-8","DOIUrl":null,"url":null,"abstract":"<div><p>The base-catalyzed organic reactions represented by Knoevenagel condensation are important in the organic synthesis and chemical industry and most reported catalysts are homogeneous organic bases and metal-containing solids which suffer disadvantages in catalyst separation and metal contamination. Therefore, the development of metal-free and efficient heterogeneous base catalysts for the process is highly required. Herein, a series of mesoporous nitrogen-rich carbon nitride (mpg-CN) materials were synthesized using 5-amino-1<i>H</i>-tetrazole as a precursor via a hard-templating method. The synthesized mpg-CN, specially prepared under lower carbonization temperatures had higher nitrogen contents (C<sub>3</sub>N<sub>7</sub>, C<sub>3</sub>N<sub>6</sub>, and C<sub>3</sub>N<sub>5</sub>) than the ordinary carbon nitride (C<sub>3</sub>N<sub>4</sub>). The surface areas and distributions of nitrogen species were dependent on the carbonization temperatures. As metal-free solid bases, mpg-CN exhibited high activity in Knoevenagel condensation reactions. The mpg-C<sub>3</sub>N<sub>6</sub> material showed the highest activity, achieving a benzaldehyde conversion of 80.6% and selectivity to the target product of 99.2%, attributed to its higher fraction of pyrrolic nitrogen species. In addition, the mpg-C<sub>3</sub>N<sub>6</sub> catalyst can be reused five times without significant loss in activity and also demonstrated activity to several substrates.</p></div>","PeriodicalId":753,"journal":{"name":"Research on Chemical Intermediates","volume":"51 6","pages":"3067 - 3089"},"PeriodicalIF":2.8000,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Mesoporous nitrogen-rich carbon nitride materials: synthesis and catalytic application as metal-free solid bases towards Knoevenagel condensation\",\"authors\":\"Qing-Qing Wang, Li Sheng, Fei Wang, Jie Xu, Bing Xue\",\"doi\":\"10.1007/s11164-025-05602-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The base-catalyzed organic reactions represented by Knoevenagel condensation are important in the organic synthesis and chemical industry and most reported catalysts are homogeneous organic bases and metal-containing solids which suffer disadvantages in catalyst separation and metal contamination. Therefore, the development of metal-free and efficient heterogeneous base catalysts for the process is highly required. Herein, a series of mesoporous nitrogen-rich carbon nitride (mpg-CN) materials were synthesized using 5-amino-1<i>H</i>-tetrazole as a precursor via a hard-templating method. The synthesized mpg-CN, specially prepared under lower carbonization temperatures had higher nitrogen contents (C<sub>3</sub>N<sub>7</sub>, C<sub>3</sub>N<sub>6</sub>, and C<sub>3</sub>N<sub>5</sub>) than the ordinary carbon nitride (C<sub>3</sub>N<sub>4</sub>). The surface areas and distributions of nitrogen species were dependent on the carbonization temperatures. As metal-free solid bases, mpg-CN exhibited high activity in Knoevenagel condensation reactions. The mpg-C<sub>3</sub>N<sub>6</sub> material showed the highest activity, achieving a benzaldehyde conversion of 80.6% and selectivity to the target product of 99.2%, attributed to its higher fraction of pyrrolic nitrogen species. In addition, the mpg-C<sub>3</sub>N<sub>6</sub> catalyst can be reused five times without significant loss in activity and also demonstrated activity to several substrates.</p></div>\",\"PeriodicalId\":753,\"journal\":{\"name\":\"Research on Chemical Intermediates\",\"volume\":\"51 6\",\"pages\":\"3067 - 3089\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2025-04-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Research on Chemical Intermediates\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s11164-025-05602-8\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Research on Chemical Intermediates","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11164-025-05602-8","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Mesoporous nitrogen-rich carbon nitride materials: synthesis and catalytic application as metal-free solid bases towards Knoevenagel condensation
The base-catalyzed organic reactions represented by Knoevenagel condensation are important in the organic synthesis and chemical industry and most reported catalysts are homogeneous organic bases and metal-containing solids which suffer disadvantages in catalyst separation and metal contamination. Therefore, the development of metal-free and efficient heterogeneous base catalysts for the process is highly required. Herein, a series of mesoporous nitrogen-rich carbon nitride (mpg-CN) materials were synthesized using 5-amino-1H-tetrazole as a precursor via a hard-templating method. The synthesized mpg-CN, specially prepared under lower carbonization temperatures had higher nitrogen contents (C3N7, C3N6, and C3N5) than the ordinary carbon nitride (C3N4). The surface areas and distributions of nitrogen species were dependent on the carbonization temperatures. As metal-free solid bases, mpg-CN exhibited high activity in Knoevenagel condensation reactions. The mpg-C3N6 material showed the highest activity, achieving a benzaldehyde conversion of 80.6% and selectivity to the target product of 99.2%, attributed to its higher fraction of pyrrolic nitrogen species. In addition, the mpg-C3N6 catalyst can be reused five times without significant loss in activity and also demonstrated activity to several substrates.
期刊介绍:
Research on Chemical Intermediates publishes current research articles and concise dynamic reviews on the properties, structures and reactivities of intermediate species in all the various domains of chemistry.
The journal also contains articles in related disciplines such as spectroscopy, molecular biology and biochemistry, atmospheric and environmental sciences, catalysis, photochemistry and photophysics. In addition, special issues dedicated to specific topics in the field are regularly published.