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Updated: Jun 2, 2026

The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes
Published on: April 10, 2015
Synthesis, functionalization, characterization, and photophysical study of carbonyl-containing isocyano rhenium(I)
Apple Wai-Yi Cheung1, Larry Tso-Lun Lo, Chi-Chiu Ko
1Department of Biology and Chemistry, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong, China.
Abstract:
New classes of tunable rhenium(I) diimine luminophores with formula of [Re(CO)(CNR)(3)(N-N)]PF(6) and [Re(CO)(L(x))(CNC(6)H(4)Cl-4)(2)(1,10-phenanthroline)]PF(6), (R = C(6)H(5), 4-BrC(6)H(4), 4-ClC(6)H(4), 4-MeOC(6)H(4), 2,6-(i)Pr(2)C(6)H(3); N-N = 1,10-phenanthroline, 5,6-dibromo-1,10-phenanthroline, 4,4'-di-tert-butyl-2,2'-bipyridine; L(x) = MeCN, pyridine and PPh(3)) have been synthesized. Different synthetic routes including photo-ligand substitution and thermal carbonyl ligand substitution through the oxidative decarbonylation with trimethyl amine N-oxide, for the facial and meridional isomeric forms of [Re(CO)(CNR)(3)(N-N)]PF(6) were investigated. On the basis of these synthetic strategies, different ligand modification and functionalization of the rhenium(I) diimine luminophores with tailored excited state properties could be readily achieved. The structures of both facial and meridional conformations of [Re(CO)(CNR)(3)(N-N)]PF(6) and the complex precursors fac-[Re(CO)(3)(CNC(6)H(3)(i)Pr-2,6)(3)]OTf were determined by X-ray crystallography. These complexes display an orange to red (3)MLLCT [dπ(Re) → π*(N-N)] phosphorescence at room temperature. Detailed photophysical investigations revealed that the physical, photophysical, electrochemical, and excited state properties can be fine-tuned and tailored through the modifications of the substituents on isocyanide or diimine ligands.
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