Literature DB >> 21789330

Synthesis and coordination chemistry of macrocyclic ligands featuring NHC donor groups.

Peter G Edwards1, F Ekkehardt Hahn.   

Abstract

Poly-NHC (NHC = N-heterocyclic carbene) ligands emerged almost immediately after the first stable NHCs had been described. Macrocyclic ligands, featuring NHC donor groups and their metal complexes, however, remained rare until recently. This perspective highlights modern developments in the fields of synthesis and coordination chemistry of macrocyclic poly-NHC ligands. These include the synthesis of tetracarbene ligands which were obtained from complexes of β-functionalized isocyanides followed by cyclization of the coordinated iscocyanide ligands to NH,NH-functionalized NHCs and the subsequent metal template controlled bridging alkylation of the NH,NH-NHCs to yield the macrocycle. The template synthesis of ligands featuring a mixed NHC/phosphine donor set like [11]ane-P(2)C(NHC) and [16]ane-P(2)C(NHC)(2) by linkage of NH,NH-NHCs to different phosphines is also presented. Finally, methods for the preparation of cyclic polyazolium salts, their deprotonation and metalation and the different modes of coordination of such macrocyclic poly-NHC ligands are discussed.

Entities:  

Year:  2011        PMID: 21789330     DOI: 10.1039/c1dt10864f

Source DB:  PubMed          Journal:  Dalton Trans        ISSN: 1477-9226            Impact factor:   4.390


  2 in total

1.  The palladium-based complexes bearing 1,3-dibenzylbenzimidazolium with morpholine, triphenylphosphine, and pyridine derivate ligands: synthesis, characterization, structure and enzyme inhibitions.

Authors:  Aydın Aktaş; Gül Yakalı; Yeliz Demir; İlhami Gülçin; Muhittin Aygün; Yetkin Gök
Journal:  Heliyon       Date:  2022-09-16

2.  Synthesis and structures of ruthenium-NHC complexes and their catalysis in hydrogen transfer reaction.

Authors:  Chao Chen; Chunxin Lu; Qing Zheng; Shengliang Ni; Min Zhang; Wanzhi Chen
Journal:  Beilstein J Org Chem       Date:  2015-09-30       Impact factor: 2.883

  2 in total

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