448 - Integrated stacking motifs of TTF-like donors and cyclic trinuclear acceptor complexes of monovalent coinage metals: Supramolecular structures, magento-opto-electronic properties, and potential apps Mukunda M. Ghimire1, mukundaghimire@my.unt.edu, Oumarou C. Simon3, Vladimir N. Nesterov4, Alceo Macchioni2, Cristiano Zuccaccia2, Rossana Galassi3, Mohammad A. Omary1. (1) Department of Chemistry, University of North Texas, Denton, Texas, United States (2) University of Perugia, Perugia, Italy (3) Chemistry Division, School of Science and Technology, Camerino, Italy (4) University of North Texas, Denton, Texas, United States A series of new charge transfer compounds [M(3,5-(CF3)2pz)]3@D (where M = Cu, Ag, or Au; D = DBTTF, TTF, or BEDT-TTF) and [Ag(3,5-(NO2)2pz)]3@D (where D = DBTTF or TTF) have been synthesized and characterized by elemental analysis, IR, ESI-MS, 1H NMR, and single crystal X-ray diffraction analyses. This series of compounds have been found to exhibit remarkable supramolecular structures in both the solid state and solution, whereby they exhibit supramolecular stacked chains and oligomers, respectively. The supramolecular donor-acceptor solid and solution adducts also exhibit indefinite stability, even in the presence of air, and remarkable magento-opto-electronic properties, as highlighted by 1H and 19F NMR, UV/visible spectroscopy, magnetic susceptibility, and FT-IR investigations. The potential applications of this new class of supramolecular binary donor-acceptor adducts in molecular electronics, including solar cells, (super)conductors, magnetic switching devices, and field effect transistors (FETs) will be overviewed.

Integrated stacking motifs of TTF-like donors and cyclic trinuclear acceptor complexes of monovalent coinage metals: Supramolecular structures, magneto-opto-electronic properties and potential apps.

Rossana Galassi;
2016-01-01

Abstract

448 - Integrated stacking motifs of TTF-like donors and cyclic trinuclear acceptor complexes of monovalent coinage metals: Supramolecular structures, magento-opto-electronic properties, and potential apps Mukunda M. Ghimire1, mukundaghimire@my.unt.edu, Oumarou C. Simon3, Vladimir N. Nesterov4, Alceo Macchioni2, Cristiano Zuccaccia2, Rossana Galassi3, Mohammad A. Omary1. (1) Department of Chemistry, University of North Texas, Denton, Texas, United States (2) University of Perugia, Perugia, Italy (3) Chemistry Division, School of Science and Technology, Camerino, Italy (4) University of North Texas, Denton, Texas, United States A series of new charge transfer compounds [M(3,5-(CF3)2pz)]3@D (where M = Cu, Ag, or Au; D = DBTTF, TTF, or BEDT-TTF) and [Ag(3,5-(NO2)2pz)]3@D (where D = DBTTF or TTF) have been synthesized and characterized by elemental analysis, IR, ESI-MS, 1H NMR, and single crystal X-ray diffraction analyses. This series of compounds have been found to exhibit remarkable supramolecular structures in both the solid state and solution, whereby they exhibit supramolecular stacked chains and oligomers, respectively. The supramolecular donor-acceptor solid and solution adducts also exhibit indefinite stability, even in the presence of air, and remarkable magento-opto-electronic properties, as highlighted by 1H and 19F NMR, UV/visible spectroscopy, magnetic susceptibility, and FT-IR investigations. The potential applications of this new class of supramolecular binary donor-acceptor adducts in molecular electronics, including solar cells, (super)conductors, magnetic switching devices, and field effect transistors (FETs) will be overviewed.
2016
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11581/407538
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo

Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact