Transition metal complexes with thiosemicarbazide-based ligands. part 37. Synthesis and study of the first thiosemi-carbazide-derived copper(I) complexes: Crystal structure of [2-(diphenylphosphino)benzaldehyde thiosemicarbazonato(-l)] copper(I)nitrate-methanol solvate

Citation
C. Argay et al., Transition metal complexes with thiosemicarbazide-based ligands. part 37. Synthesis and study of the first thiosemi-carbazide-derived copper(I) complexes: Crystal structure of [2-(diphenylphosphino)benzaldehyde thiosemicarbazonato(-l)] copper(I)nitrate-methanol solvate, J COORD CH, 51(1), 2000, pp. 9-19
Citations number
36
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
JOURNAL OF COORDINATION CHEMISTRY
ISSN journal
00958972 → ACNP
Volume
51
Issue
1
Year of publication
2000
Pages
9 - 19
Database
ISI
SICI code
0095-8972(2000)51:1<9:TMCWTL>2.0.ZU;2-W
Abstract
The preparation and physical characterization of two copper(I) complexes Cu (HL)NO3 and [Cu(HL)(2)]NO3 . MeOH formed with a newly synthesized tridentat e [S,N,P] HL = 2-(diphenylphosphino)benzaldehyde thiosemicarbazone ligand a nd the crystal structure analysis of the latter have been carried out. An X -ray study of [Cu(HL)(2)]NO3 . MeOH revealed a copper(I) ion coordinated te trahedrally to S,N,P,P atoms donated by two HL ligands. One is tridentate [ S,N,P], whereas the second HL ligand is monodentate, ligating only its phos phorus atom to the copper. The geometry around the four-coordinate Cu(I) is comparable with Cu{N,S,P,X} tetrahedra (X = N, P, or S) retrieved from the Cambridge Structural Database. In addition, with a restriction to Cu{N,P,X ,X} (X = C, N, P) tetrahedra - S is excluded - ca. 60 structures against th ree or four cases were found to be maintained by Cu(I) ions substantiating the principal role of the phosphorus ligands in the reduction of Cu(II) to Cu(I).