A Single Small-Scale Plutonium Redox Reaction System Yields Three Crystallographically-Characterizable Organoplutonium Complexes

An approach to obtaining substantial amounts of data from a hazardous starting material that can only be obtained and handled in small quantities is demonstrated by the investigation of a single small-scale reaction of cyclooctatetraene, C8H8, with a solution obtained from the reduction of Cp ' Pu-3 (Cp ' = C5H4SiMe3) with potassium graphite. This one reaction coupled with oxidation of a product has provided single-crystal X-ray structural data on three organoplutonium compounds as well as information on redox chemistry thereby demonstrating an efficient route to new reactivity and structural information on this highly radioactive element. The crystal structures were obtained from the reduction of C8H8 by a putative Pu(II) complex, (Cp ' Pu-3(II))(1-), generated in situ, to form the Pu(III) cyclooctatetraenide complex, [K(crypt)][(C8H8)(2)Pu-III], 1-Pu, and the tetra(cyclopentadienyl) Pu(III) complex, [K(crypt)][Cp ' Pu-4(III)], 2-Pu. Oxidation of the sample of 1-Pu with Ag(I) afforded a third organoplutonium complex that has been structurally characterized for the first time, (C8H8)(2)Pu-IV, 3-Pu. Complexes 1-Pu and 3-Pu contain Pu sandwiched between parallel (C8H8)(2-) rings. The (Cp'Pu-4(III))(-) anion in 2-Pu features three eta(5)-Cp' rings and one eta(1)-Cp ' ring, which is a rare example of a formal Pu-C eta(1)-bond. In addition, this study addresses the challenge of small-scale synthesis imparted by radiological and material availability of transuranium isotopes, in particular that of pure metal samples. A route to an anhydrous Pu(III) starting material from the more readily available (PuO2)-O-IV was developed to facilitate reproducible syntheses and allow complete spectroscopic analysis of 1-Pu and 2-Pu. (PuO2)-O-IV was converted to (PuBr3)-Br-III(DME)(2) (DME = CH3OCH2CH2OCH3) and subsequently (PuBr3)-Br-III(THF)(x), which was used to independently synthesize 1-Pu, 2-Pu, and 3-Pu.