碳二亚胺
活动站点
催化作用
化学
反应性(心理学)
硝基苯
星团(航天器)
立体化学
高分子化学
有机化学
计算机科学
医学
病理
程序设计语言
替代医学
作者
Jonathan A. Kephart,Benjamin S. Mitchell,Werner Kaminsky,Alexandra Velian
标识
DOI:10.26434/chemrxiv-2022-zkfsp
摘要
This study provides detailed insights into the interconnected reactivity of the three catalytically active sites of an atomically precise nanocluster Cr3(py)3Co6Se8L6 (Cr3(py)3, L = Ph2PNTol–, Ph = phenyl, Tol = 4-tolyl). Catalytic and stoichiometric studies into tosyl azide activation and carbodiimide formation enabled the isolation and crystallographic characterization of key metal-nitrenoid catalytic intermediates, including the tris(nitrenoid) cluster Cr3(NTs)3, the catalytic resting state Cr3(NTs)3(CNtBu)3, and the mono(nitrenoid) cluster Cr3(NTs)(CNtBu)2. Nitrene transfer proceeds via a stepwise mechanism, with the three active sites engaging sequentially to produce carbodiimide. Comparative structural analysis and CNtBu bind-ing studies reveal that the chemical state of neighboring active sites regulates the affinity for substrates of an individual Cr-nitrenoid edge site, intertwining their reactivity through the inorganic support.
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