Direct formation of Au(iii) acetyl, alkoxyl and alkynyl functionalities via halide free tricationic Au(iii) precursors
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 precur...
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Published in | Dalton transactions : an international journal of inorganic chemistry Vol. 47; no. 12; pp. 4228 - 4235 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
Royal Society of Chemistry
28.03.2018
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Subjects | |
Online Access | Get full text |
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Summary: | 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
. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/c7dt04675h |