N-Heterocyclic Carbene (NHC) Ligand Exchange of Bis(NHC)–Pd(II) Complexes

N-heterocyclic carbene (NHC)-Pd(II) bonds are recognized as rather robust bonds to equip palladium(II) centers with decent stability and stereoelectronic tunability. In this report, the authentic carbene-Pd(II) bonds in <i>N</i>-ammonium- and sulfonate-functionalized NHC complexes were activated, and NHC ligand exchange was triggered to afford four well-defined, sulfobetaine-type, zwitterionic heterobiscarbene complexes. Combined experimental studies and density functional theory calculations indicated that electrostatic interactions play a minimal role in the energy of this reaction; instead, the exchange appears to be driven primarily by the precipitation of the resulting zwitterionic complexes.

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Publication Details

Journal
Inorganic Chemistry
Published
2024-11-07
DOI
https://doi.org/10.1021/acs.inorgchem.4c03652
Citations
3
Primary Topic
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
Type
article
Field-Weighted Citation Impact
0.75

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article

N-Heterocyclic Carbene (NHC) Ligand Exchange of Bis(NHC)–Pd(II) Complexes

Qi Meng, Hao Jin, Qiaoqiao Teng, Gilles Frison et al.
3 citations
Inorganic Chemistry
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
0.75
article

N-Heterocyclic Carbene (NHC) Ligand Exchange of Bis(NHC)–Pd(II) Complexes

Qi Meng, Hao Jin, Qiaoqiao Teng, Gilles Frison, Yaru Zhao, Lina Zhang, Wei Liu
article en
3 citations

Abstract

N-heterocyclic carbene (NHC)-Pd(II) bonds are recognized as rather robust bonds to equip palladium(II) centers with decent stability and stereoelectronic tunability. In this report, the authentic carbene-Pd(II) bonds in <i>N</i>-ammonium- and sulfonate-functionalized NHC complexes were activated, and NHC ligand exchange was triggered to afford four well-defined, sulfobetaine-type, zwitterionic heterobiscarbene complexes. Combined experimental studies and density functional theory calculations indicated that electrostatic interactions play a minimal role in the energy of this reaction; instead, the exchange appears to be driven primarily by the precipitation of the resulting zwitterionic complexes.

Inorganic ChemistryVol. 63(46)
Centre National de la Recherche Scientifique (FR), Sorbonne Université (FR), Laboratoire de Chimie Théorique (FR), Changzhou University (CN)
National Natural Science Foundation of China, Centre National de la Recherche Scientifique, Changzhou University, Sorbonne Université, Natural Environment Research Council
Clean water and sanitation
Openalex Percentile: Top 31%
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
0.75
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