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直接获取源自氮杂环卡宾的硫属脲及其配位化学。

Straightforward access to chalcogenoureas derived from N-heterocyclic carbenes and their coordination chemistry.

作者信息

Saab Marina, Nelson David J, Tzouras Nikolaos V, A C A Bayrakdar Tahani, Nolan Steven P, Nahra Fady, Van Hecke Kristof

机构信息

Department of Chemistry, Ghent University, Krijgslaan 281, Building S3, 9000 Ghent, Belgium.

出版信息

Dalton Trans. 2020 Sep 14;49(34):12068-12081. doi: 10.1039/d0dt02558e. Epub 2020 Aug 21.

Abstract

Chalcogen-based urea compounds supported by a wide range of N-heterocyclic carbenes are synthesised and fully characterised. Coordination of selenoureas is further explored with Group 11 transition metals to form new copper, gold and silver complexes. Single crystal X-ray analyses unambiguously establish the solid-state coordination of these complexes and show that the geometry of a complex is highly influenced by a combination of electronic properties - mainly π-accepting ability - and steric hindrance of the ligands, as well as the nature of the metal, affording a variety of coordination behaviours. In this report, we investigate these phenomena using several experimental methods.

摘要

合成并全面表征了由多种氮杂环卡宾支持的基于硫属元素的脲化合物。进一步探索了硒脲与第11族过渡金属的配位作用,以形成新的铜、金和银配合物。单晶X射线分析明确确定了这些配合物的固态配位情况,并表明配合物的几何结构受到电子性质(主要是π接受能力)、配体的空间位阻以及金属性质的综合影响,从而产生了多种配位行为。在本报告中,我们使用几种实验方法研究了这些现象。

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