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通过无卤三阳离子金(III)前体直接形成金(III)乙酰基、烷氧基和炔基官能团。

Direct formation of Au(iii) acetyl, alkoxyl and alkynyl functionalities via halide free tricationic Au(iii) precursors.

作者信息

Corbo Robert, Albayer Mohammad, Hall Neville B, Dutton Jason L

机构信息

Department of Chemistry and Physics, La Trobe Institute for Molecular Sciences, La Trobe University, Melbourne, Victoria, Australia.

出版信息

Dalton Trans. 2018 Mar 28;47(12):4228-4235. doi: 10.1039/c7dt04675h. Epub 2018 Feb 27.

DOI:10.1039/c7dt04675h
PMID:29485647
Abstract

A novel synthetic approach for the synthesis of gold(iii) acetato, alkoxolato and alkynyl complexes was developed via the reactivity of gold(iii) trications containing the N,N-chelating ligand 2,2'-bipyridine and N,N,N-chelating ligand terpyridine through direct reactions with the protic precursors. This protocol avoids the gold(iii) chloride bond activation pathway commonly employed to access these functionalities. For example exposure of [LAu(iii)L']OTf (L = N,N,N-terpyridine, L' = 4-DMAP) to RH (R = OCH, OAc, Ph-[triple bond, length as m-dash]) results in the facile formation of the corresponding functionalised gold(iii) complexes [LAu(iii)R]OTf.

摘要

通过含有N,N-螯合配体2,2'-联吡啶和N,N,N-螯合配体三联吡啶的金(III)三阳离子与质子前体的直接反应,开发了一种合成乙酸金(III)、烷氧基金(III)和炔基金(III)配合物的新型合成方法。该方案避免了通常用于获得这些官能团的氯化金(III)键活化途径。例如,将[LAu(III)L']OTf(L = N,N,N-三联吡啶,L' = 4-DMAP)暴露于RH(R = OCH、OAc、Ph-[三键,长度为m破折号])会导致相应的官能化金(III)配合物[LAu(III)R]OTf的轻松形成。

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