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捕获稀有且难以捉摸的膦烯类硫属化物。

Trapping Rare and Elusive Phosphinidene Chalcogenides.

机构信息

Department of Chemistry and the Centre for Advanced Materials and Biomaterials Research, Western University, 1151 Richmond St., London, Ontario, N6A 5B7, Canada.

Department of Chemistry, NanoScience Center, University of Jyväskylä, P.O. Box 35, 40014, University of Jyväskylä, Finland.

出版信息

Angew Chem Int Ed Engl. 2017 May 22;56(22):6236-6240. doi: 10.1002/anie.201611196. Epub 2017 Jan 10.

Abstract

Four-membered rings with a P Ch core (Ch=S, Se) and phosphorus in the +3 oxidation state have been synthesized. The utility of these rings as a source of monomeric phosphinidene chalcogenides was probed by the addition of an N-heterocyclic carbene, resulting in a base-stabilized phosphinidene sulfide. Similarly, persistence of the phosphinidene selenide in solution was shown through cycloaddition chemistry with 2,3-dimethylbutadiene at elevated temperatures. The observed reactivity was explained by detailed computational work that established the conditions upon which the P Ch rings can liberate phosphinidene chalcogenides.

摘要

已合成具有 P Ch 核(Ch=S、Se)和磷处于+3 氧化态的四元环。通过添加 N-杂环卡宾,研究了这些环作为单价膦化物的来源的用途,得到了碱稳定的膦化物硫。同样,通过在高温下与 2,3-二甲基丁二烯进行环加成反应,证明了在溶液中磷硒化物的稳定性。通过详细的计算工作解释了观察到的反应性,该计算工作确定了 P Ch 环可以释放磷化物的条件。

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