Abstract
N-Heterocyclic carbene complexes of platinum(II) have been synthesized, notably monocarbene complexes cis-[(IPr)Pt(dmso)(Cl)2], 6, cis-[(IMes)Pt(dmso)(Cl)2], 7, cis-[(SIPr)Pt(dmso)(Cl)2], 8, cis-[(SIMes)Pt(dmso)(Cl)2], 9, and cis-[(TTP)Pt(dmso)(Cl) 2], 10. All complexes have been fully characterized by multinuclear NMR spectroscopy. Complex 7, 9, and 10 have been characterized by X-ray crystallography. The data obtained have allowed for the differentiation between electronic contributions (σ and π) present in the Pt-NHC bond. Supported by computational analyses, the percentage of π back-donation from the metal to the NHC is found to be on the order of 10%. More interestingly, we find that saturated NHC (SIPr and SIMes) are more efficient π back-acceptors than their unsaturated NHC congeners (IPr and IMes). The synergistic effect between π back-donation and σ donation present in the saturated NHC systems results in increased electron density at the platinum center compared to the bonding situation in the unsaturated NHC examples.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 5880-5889 |
| Number of pages | 10 |
| Journal | Organometallics |
| Volume | 26 |
| Issue number | 24 |
| DOIs | |
| State | Published - Nov 19 2007 |
| Externally published | Yes |
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry