Synthesis and Characterization of Cyclotetraphosphato Complexes of Rh(I), Ir(I), Ru(II), and Pd(II)

• Published in: Inorganic chemistry Vol. 43; no. 2; pp. 399 - 401
• Main Authors: Kamimura, Sou, Kuwata, Shigeki, Iwasaki, Masakazu, Ishii, Youichi
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 26.01.2004
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/ic0350382

The cyclotetraphosphate ion (P4O12 4-) as a PPN (PPN = (PPh3)2N+) salt reacts with [MCl(cod)]2 (M = Rh, Ir; cod = 1,5-cyclooctadiene) to give the dinuclear complexes (PPN)2[{M(cod)}2(P4O12)], in which the two metal moieties are situated trans to each other with respect to the P4O4 ring in the solid state. In solution, however, these complexes exist as mixtures of trans and cis isomers. On the other hand, the P4O12 4- ion reacts with 4 equiv of [Rh(cod)(MeCN) x ]+ cation to give the tetranuclear complex [{Rh(cod)}4(P4O12)], where the four Rh(cod) fragments are bound to the P4O12 platform alternately on both sides of the P4O4 ring. Dinuclear P4O12 complexes of ruthenium and palladium are also synthesized.