This comparative analysis reveals red-shifted absorption bands in bis(protic-NHC) complexes, highlighting distinct electronic behaviors.
This report concludes our efforts on the synthesis of a series of Ru(II)-CNC pincer complexes with stepwise replacement of classical-NHCs by protic-NHCs. Building upon our work on Ru(II)-CNC pincer complexes with classical-NHCs (1a-d) and mixed protic- & classical-NHCs (2a-d), a new set of air- and moisture- stable ruthenium(II)-CNC pincer complexes (3a-d), bearing two protic-NHC ligands, has been synthesized via high-temperature reactions of bis(imidazolyl)-and bis(benzimidazolyl)pyridine ligands with Ru(III)-NHC precursors. All new complexes have been characterized by multinuclear NMR spectroscopy, HRMS, and the molecular structure of 3a has been determined by single-crystal X-ray diffraction. Comparative UV-Vis and electrochemical analyses indicate that bis(protic-NHC) complexes display red-shifted absorption bands and lower oxidation potentials relative to their mono-protic- and classical-NHC counterparts, despite possessing less electron-rich metal centres. DFT calculations attribute this trend to greater solvation stabilization of the oxidized bis(protic-NHC) species. This study presents a direct comparison between mixed and bis(protic-NHC) Ru pincer complexes, providing valuable insights into the electronic structure and redox behaviour upon stepwise replacement of classical-NHC with protic-NHC.
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Saha et al. (2025) studied this question.
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