Zala Stopar, Evelin Gruden, Melita Tramšek, Gašper Tavčar
{"title":"ⅵ基团羰基NHC配位化合物的一锅合成及表征。","authors":"Zala Stopar, Evelin Gruden, Melita Tramšek, Gašper Tavčar","doi":"10.3390/molecules30112433","DOIUrl":null,"url":null,"abstract":"<p><p>The reactions of <i>N</i>-heterocyclic carbenes (IMesNHC and IPrNHC) with transition metal carbonyls of group VI (Cr(CO)<sub>6</sub>, Mo(CO)<sub>6</sub>, and W(CO)<sub>6</sub>) were carried out in acetonitrile in simple one-pot syntheses and led to the formation of the coordination compounds IMesNHC-Cr(CO)<sub>5</sub> (<b>1a</b>), IMesNHC-Mo(CO)<sub>5</sub> (<b>2a</b>), IMesNHC-W(CO)<sub>5</sub> (<b>3a</b>), IPrNHC-Cr(CO)<sub>5</sub> (<b>1b</b>), IPrNHC-Mo(CO)<sub>5</sub> (<b>2b</b>), and IPrNHC-W(CO)<sub>5</sub> (<b>3b</b>). With the exception of <b>1b</b>, the coordination compounds were formed selectively and in high yields. The method represents an effective and easy-to-perform alternative to the previously described methods for NHC-M(CO)<sub>5</sub> (M = Cr, Mo, W). All prepared compounds were characterized by NMR and Raman spectroscopy. Compounds <b>1a</b>, <b>2a</b>, <b>3a</b>, and <b>2b</b> were also crystallized and structurally characterized by X-ray structure analysis. Finally, the structural features of all compounds were compared with DFT calculations of structurally optimized coordination compounds.</p>","PeriodicalId":19041,"journal":{"name":"Molecules","volume":"30 11","pages":""},"PeriodicalIF":4.2000,"publicationDate":"2025-06-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12155831/pdf/","citationCount":"0","resultStr":"{\"title\":\"One-Pot Syntheses and Characterization of Group VI Carbonyl NHC Coordination Compounds.\",\"authors\":\"Zala Stopar, Evelin Gruden, Melita Tramšek, Gašper Tavčar\",\"doi\":\"10.3390/molecules30112433\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The reactions of <i>N</i>-heterocyclic carbenes (IMesNHC and IPrNHC) with transition metal carbonyls of group VI (Cr(CO)<sub>6</sub>, Mo(CO)<sub>6</sub>, and W(CO)<sub>6</sub>) were carried out in acetonitrile in simple one-pot syntheses and led to the formation of the coordination compounds IMesNHC-Cr(CO)<sub>5</sub> (<b>1a</b>), IMesNHC-Mo(CO)<sub>5</sub> (<b>2a</b>), IMesNHC-W(CO)<sub>5</sub> (<b>3a</b>), IPrNHC-Cr(CO)<sub>5</sub> (<b>1b</b>), IPrNHC-Mo(CO)<sub>5</sub> (<b>2b</b>), and IPrNHC-W(CO)<sub>5</sub> (<b>3b</b>). With the exception of <b>1b</b>, the coordination compounds were formed selectively and in high yields. The method represents an effective and easy-to-perform alternative to the previously described methods for NHC-M(CO)<sub>5</sub> (M = Cr, Mo, W). All prepared compounds were characterized by NMR and Raman spectroscopy. Compounds <b>1a</b>, <b>2a</b>, <b>3a</b>, and <b>2b</b> were also crystallized and structurally characterized by X-ray structure analysis. Finally, the structural features of all compounds were compared with DFT calculations of structurally optimized coordination compounds.</p>\",\"PeriodicalId\":19041,\"journal\":{\"name\":\"Molecules\",\"volume\":\"30 11\",\"pages\":\"\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-06-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12155831/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecules\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.3390/molecules30112433\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecules","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.3390/molecules30112433","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
One-Pot Syntheses and Characterization of Group VI Carbonyl NHC Coordination Compounds.
The reactions of N-heterocyclic carbenes (IMesNHC and IPrNHC) with transition metal carbonyls of group VI (Cr(CO)6, Mo(CO)6, and W(CO)6) were carried out in acetonitrile in simple one-pot syntheses and led to the formation of the coordination compounds IMesNHC-Cr(CO)5 (1a), IMesNHC-Mo(CO)5 (2a), IMesNHC-W(CO)5 (3a), IPrNHC-Cr(CO)5 (1b), IPrNHC-Mo(CO)5 (2b), and IPrNHC-W(CO)5 (3b). With the exception of 1b, the coordination compounds were formed selectively and in high yields. The method represents an effective and easy-to-perform alternative to the previously described methods for NHC-M(CO)5 (M = Cr, Mo, W). All prepared compounds were characterized by NMR and Raman spectroscopy. Compounds 1a, 2a, 3a, and 2b were also crystallized and structurally characterized by X-ray structure analysis. Finally, the structural features of all compounds were compared with DFT calculations of structurally optimized coordination compounds.
期刊介绍:
Molecules (ISSN 1420-3049, CODEN: MOLEFW) is an open access journal of synthetic organic chemistry and natural product chemistry. All articles are peer-reviewed and published continously upon acceptance. Molecules is published by MDPI, Basel, Switzerland. Our aim is to encourage chemists to publish as much as possible their experimental detail, particularly synthetic procedures and characterization information. There is no restriction on the length of the experimental section. In addition, availability of compound samples is published and considered as important information. Authors are encouraged to register or deposit their chemical samples through the non-profit international organization Molecular Diversity Preservation International (MDPI). Molecules has been launched in 1996 to preserve and exploit molecular diversity of both, chemical information and chemical substances.