Heme-Like {CoNO}9, (STTP•-2){CoNO}9, and {CoNO}10 Complexes Supported by 21-Thiaporphyrin Macrocycle.

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Xiao-Rui Ren,Shengfa Ye,Fang Wang,Gao-Xiang Wang,Zi-Bin Zhong,Xuebin Jiang,Wang Chen,Ronghui Cao,Feng Bai,Peng-Cheng Duan
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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.
21-硫卟啉大环支持的血红素类{CoNO}9, (STTP•-2){CoNO}9和{CoNO}10配合物。
利用较弱的配体场thiaporphyrin macrocycle (STTP)作为类红素配体,我们成功地分离出了前所未有的完整的{CoNO}n(在enemmark - feltham标记法中n = 9和10)和(STTP•-2){CoNO}9种。具体来说,石墨钾(KC8)对{CoNO}9 (ST = 1/2)的电化学或化学还原导致第一个配体基还原导致{CoNO}9部分反铁磁偶联到一个硫卟啉二阴离子自由基上,产生一个总的ST = 0基态,随后的金属基还原产生一个由硫卟啉自由基连接的真正的{CoNO}10单元组成的ST = 1/2配合物。使用SXRD, IR, NMR, SQUID和EPR进行的多种分析和光谱测量以及详细的DFT计算支持{CoNO}9和(STTP•-2){CoNO}9的高自旋CoI中心以及{CoNO}10的高自旋CoI中心的分配。此外,{CoNO}9配合物与Ph3CSNO和PhNO的反应被发现提供钴c -重氮二磺酸类血红素配合物,这为在血红素模型中获得亚硝酸盐类中间体提供了另一种途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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