Mesoionic and N-Heterocyclic Carbenes Coordinated N+ Center: Experimental and Computational Analysis

N-Heterocyclic carbenes, carbocyclic carbenes, remote N-heterocyclic carbenes and N-heterocyclic silylenes are known to form L -> N+ coordination bonds. However, mesoionic carbenes (MICs) are not reported to form coordination bonds with cationic nitrogen. Herein, synthesis and quantum chemical studies were performed on 1,2,3-triazol-5-ylidene stabilized N+ center. Six compounds with MIC -> N+<- NHC were synthesized. Density functional theory calculations and energy decomposition analysis were carried out to explore the bonding situation between MIC and N+ center. The C -> N+ bond lengths were in the range of 1.295-1.342 angstrom and bond dissociation energies were <400 kcal/mol. Natural bond orbital analysis supported the presence of excess electron density (>3 electrons) at the N+ center. The computational and X-ray diffraction analysis results confirmed the presence of divalent N-I character of center nitrogen and MIC -> N+<- NHC coordination interactions.

Automated summary

Six compounds with MIC -> N+<- NHC coordination interactions were synthesized and studied. Computational and analysis results suggest the formation of coordination bonds with specific bond lengths and bond dissociation energies between MIC and N+ center.