LIVING RING-OPENING METATHESIS POLYMERIZATION OF AMINO ESTER FUNCTIONALIZED NORBORNENES

The living ring-opening metathesis polymerisation of norbornene monome rs bearing amino ester residues, using the molybdenum initiators Mo(=C HCMe2Ph)(=N-2,6-i-Pr2C6H3)(OR)(2), (R = CMe3, I-A, CMe2CF3, I-B, CMe(C F3)(2), I-C), is reported. The monomers are derived from reactions of exo-and endo-himic anhydrides with the amino ester hydrochlorides of g lycine (1), alanine (2) and isoleucine (3). The optically pure monomer s derived from 2 and 3 afford optically active polymers whose optical activities are independent of cis content and molecular weight, indica ting the absence of a cooperative effect between chiral centres along the chain. The polymers derived from the exo monomers show a cis-trans vinylene dependence upon the ancillary alkoxide ligands of the initia tor with I-A giving high trans contents and I-C giving high cis. The c is/trans content for the endo polymers show relatively little or no de pendence upon the initiator. Poly(exo-l) is exceptional in its ability to incorporate various hydrocarbons in the solid state, including hex ane and methane. (C) 1997 Elsevier Science Ltd. All rights reserved.