Cyclopentadienylnickel Chelates with Secondary or Tertiary Phosphane Tethers Bearing Imidazol-2-ylidene Ligands

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Original languageEnglish
Pages (from-to)2545-2551
Number of pages8
JournalEuropean Journal of Inorganic Chemistry
Volume2020
Issue number26
Early online date6 May 2020
Publication statusPublished - 8 Jul 2020

Abstract

Treatment of cyclopentadienylnickel chloro or bromo chelates bearing either a tertiary 2-(di-tert-butyl)phosphanylethyl or a secondary 2-(2,4,6-trimethylphenyl)phosphanylethyl tether with imidazolylidene (Arduengo carbene) ligands results in cationic or electroneutral carbene complexes with either a decoordinated or a chelated tether. The outcome depends on the nature of the carbene, the counter anion, and the reactant stoichiometry. The results are the basis of ongoing investigations directed towards a deprotonation of the chelated cationic complexes with a secondary phosphorus atom.

Keywords

    Chelates, Cyclopentadienylalkylphosphane ligands, Imidazolylidene ligands, Nickel, Secondary phosphane ligands

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Cyclopentadienylnickel Chelates with Secondary or Tertiary Phosphane Tethers Bearing Imidazol-2-ylidene Ligands. / Werner, Irina; Kohser, Stefanie; Butenschön, Holger.
In: European Journal of Inorganic Chemistry, Vol. 2020, No. 26, 08.07.2020, p. 2545-2551.

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abstract = "Treatment of cyclopentadienylnickel chloro or bromo chelates bearing either a tertiary 2-(di-tert-butyl)phosphanylethyl or a secondary 2-(2,4,6-trimethylphenyl)phosphanylethyl tether with imidazolylidene (Arduengo carbene) ligands results in cationic or electroneutral carbene complexes with either a decoordinated or a chelated tether. The outcome depends on the nature of the carbene, the counter anion, and the reactant stoichiometry. The results are the basis of ongoing investigations directed towards a deprotonation of the chelated cationic complexes with a secondary phosphorus atom.",
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author = "Irina Werner and Stefanie Kohser and Holger Butensch{\"o}n",
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TY - JOUR

T1 - Cyclopentadienylnickel Chelates with Secondary or Tertiary Phosphane Tethers Bearing Imidazol-2-ylidene Ligands

AU - Werner, Irina

AU - Kohser, Stefanie

AU - Butenschön, Holger

N1 - Funding Information: We thank Dr. Gerald Dräger, Institut für Organische Chemie, Leibniz Universität Hannover, for valuable help with the crystal structure analysis. We thank the Deutsche Forschungsgemeinschaft (DFG) for generous support of this project (DFG BU814 20‐1, 20‐2). Open access funding enabled and organized by Projekt DEAL.

PY - 2020/7/8

Y1 - 2020/7/8

N2 - Treatment of cyclopentadienylnickel chloro or bromo chelates bearing either a tertiary 2-(di-tert-butyl)phosphanylethyl or a secondary 2-(2,4,6-trimethylphenyl)phosphanylethyl tether with imidazolylidene (Arduengo carbene) ligands results in cationic or electroneutral carbene complexes with either a decoordinated or a chelated tether. The outcome depends on the nature of the carbene, the counter anion, and the reactant stoichiometry. The results are the basis of ongoing investigations directed towards a deprotonation of the chelated cationic complexes with a secondary phosphorus atom.

AB - Treatment of cyclopentadienylnickel chloro or bromo chelates bearing either a tertiary 2-(di-tert-butyl)phosphanylethyl or a secondary 2-(2,4,6-trimethylphenyl)phosphanylethyl tether with imidazolylidene (Arduengo carbene) ligands results in cationic or electroneutral carbene complexes with either a decoordinated or a chelated tether. The outcome depends on the nature of the carbene, the counter anion, and the reactant stoichiometry. The results are the basis of ongoing investigations directed towards a deprotonation of the chelated cationic complexes with a secondary phosphorus atom.

KW - Chelates

KW - Cyclopentadienylalkylphosphane ligands

KW - Imidazolylidene ligands

KW - Nickel

KW - Secondary phosphane ligands

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DO - 10.1002/ejic.202000326

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VL - 2020

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EP - 2551

JO - European Journal of Inorganic Chemistry

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