J
José Vidal-Gancedo
Researcher at Institute of Cost and Management Accountants of Bangladesh
Publications - 127
Citations - 3964
José Vidal-Gancedo is an academic researcher from Institute of Cost and Management Accountants of Bangladesh. The author has contributed to research in topics: Electron paramagnetic resonance & Tetrathiafulvalene. The author has an hindex of 35, co-authored 123 publications receiving 3753 citations. Previous affiliations of José Vidal-Gancedo include University of Valencia & Catalan Institution for Research and Advanced Studies.
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A new multifunctional ferrocenyl-substituted ferrocenophane derivative: optical and electronic properties and selective recognition of Mg2+ ions.
Juan Luis Lopez,Alberto Tárraga,Arturo Espinosa,M. Desamparados Velasco,Pedro Molina,Vega Lloveras,José Vidal-Gancedo,Concepció Rovira,Jaume Veciana,David J. Evans,Klaus Wurst +10 more
TL;DR: The synthesis, characterisation, and X-ray structure of a new strained asymmetric diferrocene derivative (2) is reported, which acts as a highly specific electrochemical and optical Mg(2+) ion sensor, as revealed by spectroscopic and electrochemical techniques.
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Ferromagnetic interactions in organic/molecular materials†
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Synthesis and doping of a multifunctional tetrathiafulvalene-substituted poly(isocyanide)
Elba Gomar-Nadal,Laurent Mugica,José Vidal-Gancedo,Juan Casado,Juan T. López Navarrete,Jaume Veciana,Concepció Rovira,David B. Amabilino +7 more
TL;DR: In this article, a poly(isocyanide) containing tetrathiafulvalene (TTF) moieties in the side chains has been synthesized and characterized in its neutral state and has been oxidized to generate mixed valence states which display charge mobility in solution.
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Multistability in a BEDT-TTF based molecular conductor.
Elena Laukhina,José Vidal-Gancedo,Vladimir Laukhin,Jaume Veciana,Igor Chuev,V. Tkacheva,Klaus Wurst,Concepció Rovira +7 more
TL;DR: It is suggested that dipole-dipole interactions can play a key role in the rich polymorphism of this molecular solid.
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Induced Self-Assembly of a Tetrathiafulvalene-Based Open-Shell Dyad through Intramolecular Electron Transfer
Judith Guasch,Luca Grisanti,Vega Lloveras,José Vidal-Gancedo,Manuel Souto,Dayana C. Morales,Marta Vilaseca,Cristina Sissa,Anna Painelli,Imma Ratera,Concepció Rovira,Jaume Veciana +11 more
TL;DR: An organic switch: An open-shell dyad, consisting of an electron acceptor perchlorotriphenylmethyl radical unit linked to an electron π-donor tetrathiafulvalene unit through a vinyleneπ-bridge was synthesized and the self-assembly of the dyad in solution induced by its intramolecular electron transfer was studied.