Literature DB >> 24849867

Bis-NHC chelate complexes of nickel(0) and platinum(0).

Matthias Brendel1, Carolin Braun, Frank Rominger, Peter Hofmann.   

Abstract

For a long time d(10)-ML2 fragments have been known for their potential to activate unreactive bonds by oxidative addition. In the development of more active species, two approaches have proven successful: the use of strong σ-donating ligands leading to electron-rich metal centers and the employment of chelating ligands resulting in a bent coordination geometry. Combining these two strategies, we synthesized bis-NHC chelate complexes of nickel(0) and platinum(0). Bis(1,5-cyclooctadiene)nickel(0) and -platinum(0) react with bisimidazolium salts, deprotonated in situ at room temperature, to yield tetrahedral or trigonal-planar bis-NHC chelate olefin complexes. The synthesis and characterization of these complexes as well as a first example of C-C bond activation with these systems are reported. Due to the enforced cis arrangement of two NHCs, these compounds should open interesting perspectives for bond-activation chemistry and catalysis.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  carbene ligands; chelates; nickel; platinum

Year:  2014        PMID: 24849867     DOI: 10.1002/anie.201401024

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

1.  Bite-angle bending as a key for understanding group-10 metal reactivity of d10-[M(NHC)2] complexes with sterically modest NHC ligands.

Authors:  Florian Hering; Jörn Nitsch; Ursula Paul; Andreas Steffen; F Matthias Bickelhaupt; Udo Radius
Journal:  Chem Sci       Date:  2014-12-03       Impact factor: 9.825

2.  Crystal structure of (η4-cyclo-octa-diene)(3,3'-dimesityl-1,1'-methyl-enediimidazoline-2,2'-diyl-idene)nickel(0) tetra-hydro-furan monosolvate.

Authors:  Carlos D Yamamoto; Zijie Zhang; Sabine Chantal E Stieber
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2018-09-07
  2 in total

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