(Carbene) → SO <sub>2</sub> complexes: ligand-stabilised carbocyclic carbenes ( <i>ls</i> CCCs) are better than N-heterocyclic carbenes

Cyclic carbenes can form coordination complexes with sulfur dioxide (SO<sub>2</sub>). Two N-heterocyclic carbene (NHC) → SO<sub>2</sub> coordination complexes were reported along with their crystal structures. However, computational analyses of the nature and strength of coordination bonds provided conflicting indications. Thus, it was essential to identify the properties that enhance the bond strength of carbene → SO<sub>2</sub>. In this work, density functional theory (DFT) studies were carried out to estimate the electronic, geometric and energetic parameters of several (NHC) → SO<sub>2</sub> complexes. This study was extended to include carbocyclic carbene (CCC) → SO<sub>2</sub>, remote N-heterocyclic carbene (<i>r</i>NHC) → SO<sub>2</sub>, abnormal N-heterocyclic carbene (<i>a</i>NHC) → SO<sub>2</sub>, cyclic alkyl amino carbene (CAAC) → SO<sub>2</sub>, and amido carbene (<i>am</i>NHC) → SO<sub>2</sub> complexes. Results revealed a set of ligand-stabilised carbocyclic carbenes (<i>ls</i>CCCs), which could stabilise the donor → acceptor bonds between cyclic carbenes and SO<sub>2</sub>.

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Publication Details

Journal
Dalton Transactions
Published
2025-01-01
DOI
https://doi.org/10.1039/d5dt00602c
Primary Topic
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

(Carbene) → SO 2 complexes: ligand-stabilised carbocyclic carbenes ( ls CCCs) are better than N-heterocyclic carbenes

Prasad V. Bharatam, Astha Gupta, Joy Mukhopadhyay, S. S. Rana
Dalton Transactions
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
article

(Carbene) → SO 2 complexes: ligand-stabilised carbocyclic carbenes ( ls CCCs) are better than N-heterocyclic carbenes

Prasad V. Bharatam, Astha Gupta, Joy Mukhopadhyay, S. S. Rana
article en

Abstract

Cyclic carbenes can form coordination complexes with sulfur dioxide (SO<sub>2</sub>). Two N-heterocyclic carbene (NHC) → SO<sub>2</sub> coordination complexes were reported along with their crystal structures. However, computational analyses of the nature and strength of coordination bonds provided conflicting indications. Thus, it was essential to identify the properties that enhance the bond strength of carbene → SO<sub>2</sub>. In this work, density functional theory (DFT) studies were carried out to estimate the electronic, geometric and energetic parameters of several (NHC) → SO<sub>2</sub> complexes. This study was extended to include carbocyclic carbene (CCC) → SO<sub>2</sub>, remote N-heterocyclic carbene (<i>r</i>NHC) → SO<sub>2</sub>, abnormal N-heterocyclic carbene (<i>a</i>NHC) → SO<sub>2</sub>, cyclic alkyl amino carbene (CAAC) → SO<sub>2</sub>, and amido carbene (<i>am</i>NHC) → SO<sub>2</sub> complexes. Results revealed a set of ligand-stabilised carbocyclic carbenes (<i>ls</i>CCCs), which could stabilise the donor → acceptor bonds between cyclic carbenes and SO<sub>2</sub>.

Dalton TransactionsVol. 54(24)
National Institute of Pharmaceutical Education and Research (IN)
Department of Biotechnology, Ministry of Science and Technology, India
Openalex Percentile: Top 92%
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
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