A new Ru(II) complex, [Ru(TTT)2][PF6]2 (TTT = 4′-[(2,2′:5′,2″-terthien-3′-yl)methoxy]-2, 2′:6′,2″-terpyridine) has been synthesized and characterized by 1H NMR and UV-Vis spectroscopy and by cyclic voltammetry. The electrosynthesis of the corresponding conductive polymer, P[Ru(TTT) 2], is reported, as well as its voltammetric and spectroelectrochemical characterization. The comparison between [Ru(TTT) 2][PF6]2 and TTT voltammetric data shows that the presence of the metal ion makes easier the oxidation and the polymerization of the organic framework. On the other hand, UV-Vis data confirm that the presence of the -O-CH2- spacer between coordinating and polymerizing unit (terpyridine and terthiophene, respectively) reduces the electronic delocalization among these moieties, analogously to that observed in the TTT ligand alone. As far as P[Ru(TTT)2] is concerned, the voltammetric characterization evidences the so-called 'charge-trapping' phenomena, already observed also in PTTT, too. Moreover, spectroelectrochemical characterization shows a likely overlapping of the π-πlowast polymer and MLCT complex absorption bands, causing a bathochromic shift with respect to PTTT. © 2012 Elsevier Ltd. All rights reserved.
Homoleptic Ru(II) complex with terpyridine ligands appended with terthiophene moieties. Synthesis, characterization and electropolymerization
ZANARDI, Chiara;
2013-01-01
Abstract
A new Ru(II) complex, [Ru(TTT)2][PF6]2 (TTT = 4′-[(2,2′:5′,2″-terthien-3′-yl)methoxy]-2, 2′:6′,2″-terpyridine) has been synthesized and characterized by 1H NMR and UV-Vis spectroscopy and by cyclic voltammetry. The electrosynthesis of the corresponding conductive polymer, P[Ru(TTT) 2], is reported, as well as its voltammetric and spectroelectrochemical characterization. The comparison between [Ru(TTT) 2][PF6]2 and TTT voltammetric data shows that the presence of the metal ion makes easier the oxidation and the polymerization of the organic framework. On the other hand, UV-Vis data confirm that the presence of the -O-CH2- spacer between coordinating and polymerizing unit (terpyridine and terthiophene, respectively) reduces the electronic delocalization among these moieties, analogously to that observed in the TTT ligand alone. As far as P[Ru(TTT)2] is concerned, the voltammetric characterization evidences the so-called 'charge-trapping' phenomena, already observed also in PTTT, too. Moreover, spectroelectrochemical characterization shows a likely overlapping of the π-πlowast polymer and MLCT complex absorption bands, causing a bathochromic shift with respect to PTTT. © 2012 Elsevier Ltd. All rights reserved.I documenti in ARCA sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.