Abstract

The reaction of [Ir(Cl)(cod)]2, P(CH2CH2(CF2)5CF3)3, and CO (1 atm) gives the title compound (2, 97%). Tri(n-octyl)phosphine (3) and rhodium (4) analogues are similarly prepared. Crystal structures of 2 and 4 show anti CCCC conformations in the six perfluoroalkyl groups (average torsion angle 169°), with four chains (two per phosphorus) in parallel coplanar arrays that define ca. 21 × 6 A “rafts”. The other two chains extend on a common side of the raft, which pack back-to-back in stacks, maximizing parallel chains in every dimension. DSC shows one phase transition (melting, 2/4 75/79 °C) prior to thermal decomposition (>200 °C). The IR νCO values (2/3/4 1975/1942/1979 cm-1) show that the CH2CH2 spacers do not completely insulate the metals from the perfluoroalkyl groups. Both 2 and 4 are soluble in CF3C6F11, CF3C6H5, ether, THF, and acetone but insoluble in hexane, toluene, CHCl3, and CH2Cl2 (CF3C6F11/THF partition coefficient >99.7:<0.3). Reactions of 2 with RI, H2, and 3O2 or 1O2 in CF3C6F11 give Ir(CO...

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