Synthesis, Optical, Electrochemical, and Theoretical Studies of Dipolar Ruthenium Alkynyl Complexes with Oligo(phenylenevinylene) Bridges.

The syntheses of oligo(p-phenylenevinylene)s (OPVs) end-functionalized with a ligated ruthenium alkynyl unit as a donor and a nitro as acceptor, namely trans-[Ru{C≡C-1-C ₆ H ₄ -4-(E)-CH=CH-1-C ₆ H ₂ -2,5-Et ₂ -4-(E)-CH=CH-1-C ₆ H ₂ -2,5-Et ₂ -4-(E)-CH=CH-1-C ₆ H ₄ -4-NO ₂ }Cl(dppe) ₂ ] (Ru4), trans-[Ru{C≡C-1-C ₆ H ₄ -4-(E)-CH=CH-1-C ₆ H ₂ -2,5-Et ₂ -4-(E)-CH=CH-1-C ₆ H ₂ -2,5-Et ₂ -4-(E)-CH=CH-1-C ₆ H ₂ -2,5-(n-hexyl) ₂ -4-(E)-CH=CH-1-C ₆ H ₂ -2,5-(n-hexyl) ₂ -4-(E)-CH=CH-1-C ₆ H ₄ -4-NO ₂ }Cl(dppe) ₂ ] (Ru6), and trans-[Ru{C≡C-1-C ₆ H ₄ -4-(E)-CH=CH-1-C ₆ H ₂ -2,5-Et ₂ -4-(E)-CH=CH-1-C ₆ H ₂ -2,5-Et ₂ -4-(E)-CH=CH-1-C ₆ H ₂ -2,5-(n-hexyl) ₂ -4-(E)-CH=CH-1-C ₆ H ₂ -2,5-(n-hexyl) ₂ -4-(E)-CH=CH-1-C ₆ H ₂ -2,5-(2-ethyl-n-hexyl) ₂ -4-(E)-CH=CH-1-C ₆ H ₂ -2,5-(2-ethyl-n-hexyl) ₂ -4-(E)-CH=CH-1-C ₆ H ₄ -4-NO ₂ }Cl(dppe) ₂ ] (Ru8), are reported, together with those of precursor alkynes. Their electrochemical properties were assessed by cyclic voltammetry (CV), their linear optical and quadratic nonlinear optical (NLO) properties assayed by UV/Vis-NIR spectroscopy and hyper-Rayleigh scattering studies at 1064 nm, respectively, and their linear optical properties in the formally Ru ^III state examined by UV/Vis-NIR spectroelectrochemistry. Computational studies employing time-dependent density functional theory were undertaken on model complexes to rationalize the optical observations.
(© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)