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作 者:Jing-Xuan Zhang Fu Kit Sheong Zhengyu Lu Hong Zhang Zhenyang Lin
机构地区:[1]Department of Chemistry,The Hong Kong University of Science and Technology,Clear Water Bay,Hong Kong,China [2]Institute for Advanced Study,The Hong Kong University of Science and Technology,Clear Water Bay,Hong Kong,China [3]College of Chemistry and Chemical Engineering,Xiamen University,Xiamen,Fujian 361005,China
出 处:《Chinese Journal of Chemistry》2020年第12期1565-1570,共6页中国化学(英文版)
基 金:We thank the Research Grants Council of Hong Kong(N_HKUST603/15);the NSFC(No.21561162001)for supporting this research.
摘 要:of main obsevation and conclusion 1,3-Dipolar aycloaddition reaction between organic azide and metal carbyne is a useful strategy to con-struct metallacycles.However,the electronic behavior of organic azide in 1,3-dipolar aycloaddition reactions is less explored.Tthis work revealed theunexpected role of organic azide as electrophiles in its cycloaditions with various metal carbynes.The feasility and regioselectivity of a Fischer-typeosmiun carbyne in its reaction with an organic azide are explained by the increased nucleophilicity of carbyne carbon upon bending.
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