Phase Transfer Activation of Fluorous Analogs of Grubbs’ Second-Generation Catalyst: Ring-Opening Metathesis Polymerization

Grubbs’ second-generation alkene metathesis catalyst and the fluorous analog (H₂IMes)­((R_f8(CH₂)₂)₃P)­(Cl)₂Ru­(CHPh) (<b>1</b>; H₂IMes/R_f8 = 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene/(CF₂)₇CF₃) catalyze ring-opening metathesis polymerizations of norbornene at essentially identical rates (CDCl₃, RT). However, dramatic accelerations can be observed with <b>1</b> in the presence of the fluorous solvent perfluoro­(methylcyclohexane) (PFMC). The fluorous phosphine (R_f8(CH₂)₂)₃P must first dissociate from <b>1</b> to generate the 14-valence-electron intermediate that begins the catalytic cycle and should be scavenged by the PFMC phase (PFMC/toluene partition coefficient >99.7:<0.3). This would allow alkenes to more effectively compete for active catalyst. However, faster rates are seen only when <b>1</b> (partition coefficient 39.6:60.4) is added as a PFMC solution or a PFMC/CDCl₃ biphase mixture, as opposed to CDCl₃ solution, and possible additional contributing factors are analyzed. Analogous effects are observed with a 7-oxanorbornene-based <i>N</i>-butylsuccinimide. The molecular weights, polydispersities, glass transition temperatures, and cis/trans CC linkage ratios of the polynorbornene produced under monophasic and biphasic conditions are compared and are usually similar