{"title":"外电场对N \\(_2\\)与N-杂环碳反应制氨的催化作用","authors":"Priyanka Yadav, Pradeep Kumar","doi":"10.1007/s12039-023-02162-5","DOIUrl":null,"url":null,"abstract":"<div><p>Based on quantum chemical calculations, we have investigated an external electric field (EEF) as a potential catalyst for ammonia formation from the reaction of N<span>\\(_2\\)</span> with 3,5-di-tert-butyl-2-oxopiperidine-1-carbonitrile carbene. It is shown that by choosing the EEF at suitable direction and strength, the barrier for the reaction can be reduced from <span>\\(\\sim\\)</span> 17.10 kcal mol<span>\\(^{-1}\\)</span> to <span>\\(\\sim\\)</span> 0.97 kcal mol<span>\\(^{-1}\\)</span>. It was also shown by computing the reaction rate that in the presence of EEF, the rate of title reaction can be increased by trillionfold. Therefore, N<span>\\(_2\\)</span> with N-heterocyclic carbene (NHC) in the presence of an external electric field gives the possibility of a very efficient way of making ammonia from nitrogen.</p><h3>Graphical abstract</h3><p>In the present work, we have shown that without any catalyst, the reaction of N<sub>2</sub> with N-heterocyclic carbene is a high barrier reaction, but by choosing an external electric field at a\nsuitable direction and strength, the rate of N<sub>2</sub> with NHC can be increased by a trillionfold.\nTherefore, N<sub>2</sub> with NHC in the presence of an external electric field gives the possibility of\na very efficient way of making ammonia from nitrogen.</p><figure><div><div><div><picture><source><img></source></picture></div></div></div></figure></div>","PeriodicalId":50242,"journal":{"name":"Journal of Chemical Sciences","volume":"135 2","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2023-05-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"External electric field as a catalyst for ammonia formation via reaction of N\\\\(_2\\\\) and N-heterocyclic carbene\",\"authors\":\"Priyanka Yadav, Pradeep Kumar\",\"doi\":\"10.1007/s12039-023-02162-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Based on quantum chemical calculations, we have investigated an external electric field (EEF) as a potential catalyst for ammonia formation from the reaction of N<span>\\\\(_2\\\\)</span> with 3,5-di-tert-butyl-2-oxopiperidine-1-carbonitrile carbene. It is shown that by choosing the EEF at suitable direction and strength, the barrier for the reaction can be reduced from <span>\\\\(\\\\sim\\\\)</span> 17.10 kcal mol<span>\\\\(^{-1}\\\\)</span> to <span>\\\\(\\\\sim\\\\)</span> 0.97 kcal mol<span>\\\\(^{-1}\\\\)</span>. It was also shown by computing the reaction rate that in the presence of EEF, the rate of title reaction can be increased by trillionfold. Therefore, N<span>\\\\(_2\\\\)</span> with N-heterocyclic carbene (NHC) in the presence of an external electric field gives the possibility of a very efficient way of making ammonia from nitrogen.</p><h3>Graphical abstract</h3><p>In the present work, we have shown that without any catalyst, the reaction of N<sub>2</sub> with N-heterocyclic carbene is a high barrier reaction, but by choosing an external electric field at a\\nsuitable direction and strength, the rate of N<sub>2</sub> with NHC can be increased by a trillionfold.\\nTherefore, N<sub>2</sub> with NHC in the presence of an external electric field gives the possibility of\\na very efficient way of making ammonia from nitrogen.</p><figure><div><div><div><picture><source><img></source></picture></div></div></div></figure></div>\",\"PeriodicalId\":50242,\"journal\":{\"name\":\"Journal of Chemical Sciences\",\"volume\":\"135 2\",\"pages\":\"\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2023-05-10\",\"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/s12039-023-02162-5\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Chemistry\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Sciences","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s12039-023-02162-5","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Chemistry","Score":null,"Total":0}
External electric field as a catalyst for ammonia formation via reaction of N\(_2\) and N-heterocyclic carbene
Based on quantum chemical calculations, we have investigated an external electric field (EEF) as a potential catalyst for ammonia formation from the reaction of N\(_2\) with 3,5-di-tert-butyl-2-oxopiperidine-1-carbonitrile carbene. It is shown that by choosing the EEF at suitable direction and strength, the barrier for the reaction can be reduced from \(\sim\) 17.10 kcal mol\(^{-1}\) to \(\sim\) 0.97 kcal mol\(^{-1}\). It was also shown by computing the reaction rate that in the presence of EEF, the rate of title reaction can be increased by trillionfold. Therefore, N\(_2\) with N-heterocyclic carbene (NHC) in the presence of an external electric field gives the possibility of a very efficient way of making ammonia from nitrogen.
Graphical abstract
In the present work, we have shown that without any catalyst, the reaction of N2 with N-heterocyclic carbene is a high barrier reaction, but by choosing an external electric field at a
suitable direction and strength, the rate of N2 with NHC can be increased by a trillionfold.
Therefore, N2 with NHC in the presence of an external electric field gives the possibility of
a very efficient way of making ammonia from nitrogen.
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.