Abstract
Acyclic diene metathesis (ADMET) polymerization of an α,ω-diene monomer of bis(undec-10-enoate) with isosorbide (M1) using a RuCl(2)(IMesH(2))(CH-2-O (i) Pr-C(6)H(4)) (HG2, IMesH(2) = 1,3-bis(2,4,6-trimethylphenyl)imidazolin-2-ylidene) catalyst and conducted at 50 °C (in vacuo) in ionic liquids (ILs) afforded higher-molecular-weight polymers (P1, M (n) = 32 200-39 200) than those reported previously (M (n) = 5600-14700). 1-n-Butyl-3-methyl imidazolium hexafluorophosphate ([Bmim]PF(6)) and 1-n-hexyl-3-methyl imidazolium bis(trifluoromethanesulfonyl)imide ([Hmim]TFSI) were suitable as effective solvents among a series of imidazolium salts and the pyridinium salts. The polymerization of α,ω-diene monomers of bis(undec-10-enoate) with isomannide (M2), 1,4-cyclohexanedimethanol (M3), and 1,4-butanediol (M4) in [Bmim]PF(6) and [Hmim]TFSI also afforded the higher-molecular-weight polymers. The M (n) values in the resultant polymers did not decrease even under the scale-up conditions (300 mg to 1.0 g scale, M1, M2, and M4) in the polymerizations in [Hmim]TFSI; the subsequent reaction of P1 with ethylene (0.8 MPa, 50 °C, and 5 h) gave oligomers (proceeded via depolymerization). Tandem hydrogenation of the resultant unsaturated polymers (P1) in a [Bmim]PF(6)-toluene biphasic system upon the addition of Al(2)O(3) (1.0 MPa H(2) at 50 °C) gave the corresponding saturated polymers (HP1), which waswere isolated by a phase separation in the toluene layer. The [Bmim]PF(6) layer containing the ruthenium catalyst could be recycled without a decrease in the activity/selectivity of the olefin hydrogenation at least eight times.