Synthesis of cis- and trans-ReOMe2(bipy)Cl and related cationic oxorhenium(V) complexes

The purpose of this study was to prepare high oxidation-state rhenium oxome thyl complexes, including cationic compounds, and test selected examples fo r olefin polymerization activity. Reaction of ReOMe2(PMe3)(2)Cl with pyridi ne N-oxide and 2,2'-bipyridine (bipy) gave cis-ReOMe2(bipy)Cl. Conversely, treatment of ReO(bipy)Cl-3 with AlMe3 gave trans-ReOMe2(bipy)Cl. The compou nd cis-ReOMe2(bipy)Cl isomerized quantitatively to trans-ReOMe2(bipy)Cl upo n heating in benzene (Delta H double dagger=29(3) kcal mol(-1), Delta S dou ble dagger=6(9) e.u.; at 79 degrees C, k(obs)=1.34(9)x10(-2) min(-1) and t( 1/2)=52 min). Reaction of cis-ReOMe2(bipy)Cl with AgX (X-=PF6-, BF4-, or BP h4-) in acetonitrile gave the cationic acetonitrile adducts [ReOMe2(bipy)(C H3CN)]X. Treatment of the PF6- salt with PR3 (PR3=PMe3, P(OMe)(3), PMe2Ph, P(n-Bu)(3), and PMePh2) yielded the cationic PR3 adducts cis-[ReOMe2(bipy)( PR3)][PF6]. The BF4- salt of the PMe3 adduct, cis-[ReOMe2(bipy)(PMe3)][BF4] , was prepared by the reaction of ReOMe2(PMe3)(2)Cl with [Ag(CH3CN)(2)][BF4 ] in acetonitrile followed by treatment with bipy in CH2Cl2. Single crystal X-ray crystallographic analyses of cis-ReOMe2(bipy)Cl, trans-ReOMe2(bipy)C l, and cis-[ReOMe2(bipy)(PMe3)][BF4] revealed that they have distorted octa hedral structures. Analogs of cis-ReOMe2(bipy)Cl, trans-ReOMe2(bipy)Cl, and cis-[ReOMe2(bipy)(PMe3)][BF4] were also prepared in which the bipy ligand was replaced with 1,10-phenanthroline (phen). An additional analog of cis-[ ReOMe2(bipy)(PMe3)][BF4] was prepared in which the bipy ligand was replaced by 4,4'-dimethyl-2,2'-bipyridine. In preliminary experiments, ethylene was polymerized using both cis-ReOMe2(bipy)Cl and trans-ReOMe2(bipy)Cl as cata lyst precursors.