{"title":"carbene可以用于二氧化碳的无金属还原吗?","authors":"Priyanka Yadav, Pradeep Kumar","doi":"10.1007/s12039-025-02378-7","DOIUrl":null,"url":null,"abstract":"<p>Reduction of <span>\\(\\hbox {CO}_2\\)</span> to <span>\\(\\hbox {CO}_2\\)</span><span>\\(^-\\)</span> is a bottleneck in the conversion of <span>\\(\\hbox {CO}_2\\)</span> into various value-added chemicals. Here, based on quantum chemical calculations, we propose that the complexation of <span>\\(\\hbox {CO}_2\\)</span> with a carbene drastically reduces the electron affinity of <span>\\(\\hbox {CO}_2\\)</span> and thus makes the reduction of <span>\\(\\hbox {CO}_2\\)</span> spontaneous. Using various carbenes of different nucleophilicity, we have shown that the facile reduction of <span>\\(\\hbox {CO}_2\\)</span> in the presence of a carbene can be achieved for a variety of carbenes, and hence, offers an attractive route for converting <span>\\(\\hbox {CO}_2\\)</span> into various useful chemicals.</p><p> the reduction of CO<span>\\(_2\\)</span> to CO<span>\\(_2\\)</span> <span>\\(^-\\)</span> is a bottleneck in the conversion of CO<span>\\(_2\\)</span> into various value-added chemicals. There are two main challenges in converting CO<span>\\(_2\\)</span> to CO<span>\\(_2\\)</span> <span>\\(^-\\)</span>. First, the high energy barrier associated with CO<span>\\(_2\\)</span> to CO<span>\\(_2^-\\)</span> reduction, and a low solubility of CO<span>\\(_2\\)</span> in water. We have shown that by using a carbene-CO<span>\\(_2\\)</span> complex rather a bare CO<span>\\(_2\\)</span>, both of these limitations can be circumvented. </p>","PeriodicalId":616,"journal":{"name":"Journal of Chemical Sciences","volume":"137 3","pages":""},"PeriodicalIF":2.0000,"publicationDate":"2025-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Can carbene be used for a metal free reduction of carbon dioxide?\",\"authors\":\"Priyanka Yadav, Pradeep Kumar\",\"doi\":\"10.1007/s12039-025-02378-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Reduction of <span>\\\\(\\\\hbox {CO}_2\\\\)</span> to <span>\\\\(\\\\hbox {CO}_2\\\\)</span><span>\\\\(^-\\\\)</span> is a bottleneck in the conversion of <span>\\\\(\\\\hbox {CO}_2\\\\)</span> into various value-added chemicals. Here, based on quantum chemical calculations, we propose that the complexation of <span>\\\\(\\\\hbox {CO}_2\\\\)</span> with a carbene drastically reduces the electron affinity of <span>\\\\(\\\\hbox {CO}_2\\\\)</span> and thus makes the reduction of <span>\\\\(\\\\hbox {CO}_2\\\\)</span> spontaneous. Using various carbenes of different nucleophilicity, we have shown that the facile reduction of <span>\\\\(\\\\hbox {CO}_2\\\\)</span> in the presence of a carbene can be achieved for a variety of carbenes, and hence, offers an attractive route for converting <span>\\\\(\\\\hbox {CO}_2\\\\)</span> into various useful chemicals.</p><p> the reduction of CO<span>\\\\(_2\\\\)</span> to CO<span>\\\\(_2\\\\)</span> <span>\\\\(^-\\\\)</span> is a bottleneck in the conversion of CO<span>\\\\(_2\\\\)</span> into various value-added chemicals. There are two main challenges in converting CO<span>\\\\(_2\\\\)</span> to CO<span>\\\\(_2\\\\)</span> <span>\\\\(^-\\\\)</span>. First, the high energy barrier associated with CO<span>\\\\(_2\\\\)</span> to CO<span>\\\\(_2^-\\\\)</span> reduction, and a low solubility of CO<span>\\\\(_2\\\\)</span> in water. We have shown that by using a carbene-CO<span>\\\\(_2\\\\)</span> complex rather a bare CO<span>\\\\(_2\\\\)</span>, both of these limitations can be circumvented. </p>\",\"PeriodicalId\":616,\"journal\":{\"name\":\"Journal of Chemical Sciences\",\"volume\":\"137 3\",\"pages\":\"\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2025-08-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Chemical Sciences\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s12039-025-02378-7\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Sciences","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s12039-025-02378-7","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Can carbene be used for a metal free reduction of carbon dioxide?
Reduction of \(\hbox {CO}_2\) to \(\hbox {CO}_2\)\(^-\) is a bottleneck in the conversion of \(\hbox {CO}_2\) into various value-added chemicals. Here, based on quantum chemical calculations, we propose that the complexation of \(\hbox {CO}_2\) with a carbene drastically reduces the electron affinity of \(\hbox {CO}_2\) and thus makes the reduction of \(\hbox {CO}_2\) spontaneous. Using various carbenes of different nucleophilicity, we have shown that the facile reduction of \(\hbox {CO}_2\) in the presence of a carbene can be achieved for a variety of carbenes, and hence, offers an attractive route for converting \(\hbox {CO}_2\) into various useful chemicals.
the reduction of CO\(_2\) to CO\(_2\)\(^-\) is a bottleneck in the conversion of CO\(_2\) into various value-added chemicals. There are two main challenges in converting CO\(_2\) to CO\(_2\)\(^-\). First, the high energy barrier associated with CO\(_2\) to CO\(_2^-\) reduction, and a low solubility of CO\(_2\) in water. We have shown that by using a carbene-CO\(_2\) complex rather a bare CO\(_2\), both of these limitations can be circumvented.
期刊介绍:
Journal of Chemical Sciences is a monthly journal published by the Indian Academy of Sciences. It formed part of the original Proceedings of the Indian Academy of Sciences – Part A, started by the Nobel Laureate Prof C V Raman in 1934, that was split in 1978 into three separate journals. It was renamed as Journal of Chemical Sciences in 2004. The journal publishes original research articles and rapid communications, covering all areas of chemical sciences. A significant feature of the journal is its special issues, brought out from time to time, devoted to conference symposia/proceedings in frontier areas of the subject, held not only in India but also in other countries.