The binuclear complex trichlorobis(4-methyl- 1,8-naphthyridine)dicopper has been prepared and characterized by x-ray diffraction and ESR spectroscopy. The emerald green crystals conform to monoclinic space group P21/c with a = 11.795 (5), b = 14.850 (5), c = 11.320 (5) A, /3 = 99.20 (9)O, Z = 4. The structure. refined to a final conventional R value of 0.05 1 on 281 5 counter data, consists of dimeric molecules containing two equivalent copper atoms in pseudotetrahedral environments, bridged by one chlorine atom and by two 4-methyl-1 $-naphthyridine ligands, which act as bidentate bimetallic ligands. The equivalence of the two copper atoms is substantiated by the ESR spectra. The electronic structure of the complex is also discussed.

Synthesis and characterization of the mixed-valence copper complex trichlorobis(4-methyl-1,8-naphthyridine)dicopper / D. Gatteschi;C. Mealli;L. Sacconi. - In: INORGANIC CHEMISTRY. - ISSN 0020-1669. - STAMPA. - 15:(1976), pp. 2774-2778. [10.1021/ic50165a041]

Synthesis and characterization of the mixed-valence copper complex trichlorobis(4-methyl-1,8-naphthyridine)dicopper

GATTESCHI, DANTE;SACCONI, LUIGI
1976

Abstract

The binuclear complex trichlorobis(4-methyl- 1,8-naphthyridine)dicopper has been prepared and characterized by x-ray diffraction and ESR spectroscopy. The emerald green crystals conform to monoclinic space group P21/c with a = 11.795 (5), b = 14.850 (5), c = 11.320 (5) A, /3 = 99.20 (9)O, Z = 4. The structure. refined to a final conventional R value of 0.05 1 on 281 5 counter data, consists of dimeric molecules containing two equivalent copper atoms in pseudotetrahedral environments, bridged by one chlorine atom and by two 4-methyl-1 $-naphthyridine ligands, which act as bidentate bimetallic ligands. The equivalence of the two copper atoms is substantiated by the ESR spectra. The electronic structure of the complex is also discussed.
1976
15
2774
2778
D. Gatteschi;C. Mealli;L. Sacconi
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/653276
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