First Paramagnetic 4d Transition-Metal Complex with a Redox-Active Tetrathiafulvalene Derivative, [Ru(salen)(PPh3)(TTF-CH=CH-Py)]BF4 [salen2- = N,N'-Ethane-1,2-diylbis(salicylidenamine), PPh3 = Triphenylphosphine, TTF-CH=CH-Py = 4-(2-Tetrathiafulvalenylethenyl)pyridine].
Abstract
The 1st paramagnetic 4d transition-metal complex with a redox-active tetrathiafulvalene ligand was synthesized. The prepn., x-ray structure, electrochem., and ESR measurements of [Ru(salen)(PPh3)(TTF-CH:CH-Py)](BF4) [1(BF4), salenH2 = N,N'-ethane-1,2-diylbis(salicylidenamine), TTF-CH:CH-Py = 4-(2-tetrathiafulvalenylethenyl)pyridine] are reported. The crystal structure reveals that the paramagnetic RuIII (s = 1/2) center is in a tetragonally elongated octahedral geometry and the TTF-CH:CH-Py ligand is coordinated to the axial position of the RuIII ion through the nitrogen atom of the pyridine group. Thus, 1(BF4) is an attractive precursor to study future π-4d interactions in dual-property conducting and magnetic materials.
Keywords
crystal structure ruthenium salen tetrathiafulvalenylethenyl pyridine phosphine complex
electrochem oxidn ruthenium salen tetrathiafulvalenylethenyl pyridine phosphine complex
ESR ruthenium salen tetrathiafulvalenylethenyl pyridine phosphine complex
ethanediylbissalicylidenamine ruthenium tetrathiafulvalenylethenyl pyridine phosphine complex prepn structure electrochem
ruthenium salen tetrathiafulvalenylethenyl pyridine phosphine complex prepn structure electrochem