Molecular materials based upon organic π-donors and magnetic anions

Autor: Eugenio Coronado, F. Bérézovsky, Carlos J. Gómez-García, Smail Triki, J. Sala Pala
Přispěvatelé: Chimie, Electrochimie Moléculaires et Chimie Analytique (CEMCA), Institut Brestois Santé Agro Matière (IBSAM), Université de Brest (UBO)-Université de Brest (UBO)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC), RENARD, NICOLAS
Jazyk: angličtina
Rok vydání: 2000
Předmět:
Zdroj: Journal de Physique IV Proceedings
Journal de Physique IV Proceedings, EDP Sciences, 2000, 10, pp.Pr3--35-Pr3-40
Scopus-Elsevier
ISSN: 1155-4339
1764-7177
Popis: Electrochemical combination of the magnetic dinuclear anion [MM'(C 2 O 4 )(NCS) 8 ] 4- (MM' = CrCr, CrFe) or paramagnetic mononuclear anion [Cr(NCS) 6 ] 3- with the ET organic π-donor (ET = BEDT-TTF = bis(ethylenedithio)tetrathiafulvalene) gives rise to two new series of molecular hybrid salts formulated (ET) 5 [MM'(C 2 O 4 )(NCS) 8 (MM' = CrCr (1), CrFe (2)), (ET) 8 [MM'(C 2 O 4 )(NCS) 8 ] (3), (ET) 5.5 f Cr(NCS) 6 ] (4) and (ET) 5 [(C 2 H 5 ) 4 N] [Cr(NCS) 6 ](THF) (5) (THF = tetrahydrofuran). The crystal structures consist of alternating organic and inorganic layers. The organic part does not produce any detectable effect on the magnetic properties coming from the inorganic sublattice. They indicate the presence of antiferromagnetic coupling in the homometallic dimers (1 and 3), while the coupling is ferromagnetic in the heterometallic one (2). Conductivity measurements reveal a metallic state for compounds 3 and 5.
Databáze: OpenAIRE