Abstract
The terminal carbide ligands in [(Cy3P)2X2Ru≡C] complexes (X=halide or pseudohalide) coordinate molecular iodine, affording charge-transfer complexes rather than oxidation products. Crystallographic and vibrational spectroscopic data show the perturbations of iodine to vary with the auxiliary ligand sphere on ruthenium, demonstrating the σ-donor properties of carbide complexes to be tunable.
Originalsprog | Engelsk |
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Tidsskrift | Angewandte Chemie |
Vol/bind | 55 |
Udgave nummer | 40 |
Sider (fra-til) | 12484-12487 |
Antal sider | 4 |
ISSN | 0044-8249 |
DOI | |
Status | Udgivet - 26 sep. 2016 |