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.
2013
49
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10278/3753459
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