PALLADIUM(II) AND PLATINUM(II) COMPLEXES FORMED FROM C6H4-1,3-(CH(2)PCY(2))(2) (CY=CYCLOHEXYL) - CRYSTAL-STRUCTURES AND MOLECULAR-STRUCTURES OF [PDX(C6H3-2,6-(CH(2)PCY(2))(2))], X=CL AND BR
Rj. Cross et al., PALLADIUM(II) AND PLATINUM(II) COMPLEXES FORMED FROM C6H4-1,3-(CH(2)PCY(2))(2) (CY=CYCLOHEXYL) - CRYSTAL-STRUCTURES AND MOLECULAR-STRUCTURES OF [PDX(C6H3-2,6-(CH(2)PCY(2))(2))], X=CL AND BR, Journal of organometallic chemistry, 487(1-2), 1995, pp. 227-233
The reaction of C6H4-1,3-(CH(2)PCy(2))(2) (Cy = cyclohexyl) with [PdCl
2(NCPh)(2)] gave mainly [PdCl2{C6H4-1,3-(CH(2)PCy(2))(2)}]. which was
converted into [PdCl{C6H3-2,6-(CH(2)PCy(2))(2)}] on prolonged reflux,
whereas C6H4-1,3-(CH(2)PCy(2))(2) reacted with [PdBr2(PPh(3))(2)] to g
ive mainly [PdBr{C6H3-2,6-(CH(2)PCy(2))(2)}]. Only [PtCl2{C6H4-1,3-(CH
(2)PCy(2))(2)}](n) was formed in the analogous reaction with [PtCl2(NC
Ph)(2)]. X-ray analysis showed that [PdCl{C6H3-2,6-(CH(2)PCy(2))(2)}]
and [PbBr{C6H3-2,6-(CH(2)Pcy(2))(2)}] are isostructural. Both molecule
s display a conformation of the terdentate PCP ligand that is differen
t-from that recently reported for several related molecules. It is con
cluded that the conformation adopted by C6H3-2,6-(CH(2)PR(2))(2) ligan
ds appears to be dominated by the steric demand of the phosphorus subs
tituents.