Abstract: | The first acyclic diene metathesis (ADMET) polymerization of unsaturated ketone containing monomers using the molybdenum catalyst, Mo(CHCMe2Ph)(N-2,6-C6H3-i-Pr2)[OCCH3(CF3)2]2 is reported. 6,6,8,8-Tetramethyl-1,12-tridecadiene-7-one undergoes homopolymerization; copoly-merizations are carried out with 1,9-decadiene and 2,12-dimethyl-2,12-dipentenylcyclododecan-1-one, 2,12-diallylcyclododecan-1-one, and trans-2,12-diallyl-2,12-dimethylcyclododecan-1-one These polymerizations are initiated under bulk conditions and are continued in solution. No evidence of Wittig chemistry is observed between the carbonyl functional group and the catalyst when a high degree of steric hindrance exists around the carbonyl moiety. Polymer structures were characterized by IR, 1H NMR, and 13C NMR spectroscopy. Molecular weights were determined by endgroup analysis and gel permeation chromatography. |