{"title":"Heme-Like {CoNO}9, (STTP•-2){CoNO}9, and {CoNO}10 Complexes Supported by 21-Thiaporphyrin Macrocycle.","authors":"Xiao-Rui Ren,Shengfa Ye,Fang Wang,Gao-Xiang Wang,Zi-Bin Zhong,Xuebin Jiang,Wang Chen,Ronghui Cao,Feng Bai,Peng-Cheng Duan","doi":"10.1021/jacs.5c06334","DOIUrl":null,"url":null,"abstract":"Using a weaker ligand field thiaporphyrin macrocycle (STTP) as a heme-like ligand, we succeeded in the isolation of an unprecedented complete series of {CoNO}n (n = 9 and 10 in the Enemark-Feltham notation) and a (STTP•-2){CoNO}9 species. Specifically, electrochemical or chemical reduction of a {CoNO}9 (ST = 1/2) species by potassium graphite (KC8) results in first ligand-based reduction leading to a {CoNO}9 moiety antiferromagnetically coupled to a thiaporphyrin dianionic radical yielding an overall ST = 0 ground state, and subsequent metal-based reduction affording an ST = 1/2 complex comprised of a genuine {CoNO}10 unit ligated by a thiaporphyrin radical. Multiple analytical and spectroscopic measurements using SXRD, IR, NMR, SQUID, and EPR coupled to detailed DFT calculations support the assignment of a high-spin CoII center in {CoNO}9 and (STTP•-2){CoNO}9 and a high spin CoI center in {CoNO}10. Furthermore, the reaction of the {CoNO}9 complex with Ph3CSNO and PhNO was found to furnish cobalt C-diazeniumdiolate heme-like complexes, which provides an alternative route to accessing a hyponitrite-like intermediate in heme models.","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":"15 1","pages":""},"PeriodicalIF":14.4000,"publicationDate":"2025-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/jacs.5c06334","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Using a weaker ligand field thiaporphyrin macrocycle (STTP) as a heme-like ligand, we succeeded in the isolation of an unprecedented complete series of {CoNO}n (n = 9 and 10 in the Enemark-Feltham notation) and a (STTP•-2){CoNO}9 species. Specifically, electrochemical or chemical reduction of a {CoNO}9 (ST = 1/2) species by potassium graphite (KC8) results in first ligand-based reduction leading to a {CoNO}9 moiety antiferromagnetically coupled to a thiaporphyrin dianionic radical yielding an overall ST = 0 ground state, and subsequent metal-based reduction affording an ST = 1/2 complex comprised of a genuine {CoNO}10 unit ligated by a thiaporphyrin radical. Multiple analytical and spectroscopic measurements using SXRD, IR, NMR, SQUID, and EPR coupled to detailed DFT calculations support the assignment of a high-spin CoII center in {CoNO}9 and (STTP•-2){CoNO}9 and a high spin CoI center in {CoNO}10. Furthermore, the reaction of the {CoNO}9 complex with Ph3CSNO and PhNO was found to furnish cobalt C-diazeniumdiolate heme-like complexes, which provides an alternative route to accessing a hyponitrite-like intermediate in heme models.
期刊介绍:
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