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含氧和含硫氮杂环卡宾形成的易化和 σ 键强度影响因素的定量分析。

A Quantitative Analysis of Factors Influencing Ease of Formation and σ-Bonding Strength of Oxa- and Thia-N-Heterocyclic Carbenes.

机构信息

School of Chemical and Physical Sciences, Lennard-Jones Laboratories, Keele University , Staffordshire ST5 5BG, United Kingdom.

Laboratory of Molecular Modelling, National Medicines Institute , 30/34 Chełmska Street, 00-725 Warsaw, Poland.

出版信息

J Org Chem. 2017 Dec 1;82(23):12485-12491. doi: 10.1021/acs.joc.7b02283. Epub 2017 Oct 30.

Abstract

The index described previously (carbene relative energy of formation) has been extended to oxygen and sulfur heterocycles. This provides a quantitative overview of factors determining ease of formation of (i) neutral N-heterocyclic carbenes (NHCs) by deprotonation of heterocyclic salts and (ii) anionic NHCs by deprotonation of heterocyclic mesomeric betaines. The influence of the nature and ring position of oxygen and sulfur is discussed for a range of known and unknown systems. Attention is directed to unexplored systems of potential interest.

摘要

前文所描述的指数(卡宾相对形成能)已扩展到氧杂环和硫杂环。这为确定(i)通过杂环盐的去质子化形成中性 N-杂环卡宾(NHC)的难易程度以及(ii)通过杂环离域两性离子的去质子化形成阴离子 NHC 的因素提供了定量概述。讨论了氧和硫的性质和环位置对一系列已知和未知体系的影响。还关注了潜在有价值的未被探索的体系。

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