(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>.
Authors
- Prasad V. Bharatam (ORCID: https://orcid.org/0000-0002-7064-8561)
- Astha Gupta (ORCID: https://orcid.org/0000-0003-2623-3665)
- Joy Mukhopadhyay
- S. S. Rana
Institutions
- National Institute of Pharmaceutical Education and Research (IN)
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
Funders
- Department of Biotechnology, Ministry of Science and Technology, India