Reaction of halfsandwich iridium polychalcogenide complexes with dimethyl acetylenedicarboxylate. Molecular structure of Cp*Ir[S2C2(COOMe)(2)]


Autoria(s): Jin GX; Herberhold M; Reingold AL
Data(s)

1998

Resumo

The pentamethylcyclopentadienyl iridium complexes Cp*Ir(PMe3)(E-n) (E = S, n = 4, 5 or 6; E = Se, n = 2 or 4 E = Te, n = 2) react with dimethyl acetylenedicarboxylate to give Cp*Ir(PMe3)[E2C2(COOMe)(2)] compounds which tend to lose the trimethylphosphine ligand; the molecular structure of the dithiolene derivative, Cp*Ir[S2C2(COOMe)(2)], has been determined.

Identificador

http://202.98.16.49/handle/322003/22647

http://www.irgrid.ac.cn/handle/1471x/156058

Idioma(s)

英语

Fonte

Jin GX;Herberhold M;Reingold AL.Reaction of halfsandwich iridium polychalcogenide complexes with dimethyl acetylenedicarboxylate. Molecular structure of Cp*Ir[S2C2(COOMe)(2)],NEW JOURNAL OF CHEMISTRY,1998,22(10):1035-1036

Palavras-Chave #S2(2-) = 1 #TRANSITION-METAL COMPLEXES #ELEMENTAL SULFUR #LIGANDS #COORDINATION #ADDUCT #2-BENZENEDITHIOLATE(2-)
Tipo

期刊论文