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디하이드로트리사이클로펜타디엔-에틸렌 공중합체의 제조

Copolymerization of Dihydrotricyclopentadiene and Ethylene

초록/요약

Regioselective partial hydrogenation of tricyclopentadiene (TCPD) was achieved with a high turnover number of 10000 by catalysis with a N-heterocyclic carbene palladium complex. Copolymerization of ethylene and the partially hydrogenated product, dihydrotricyclopentadiene (HTCPD), was realized using a catalytic system of [8-(??5-C5Me4)-2-Me(C9H8N)-??N]TiMe2 (C9H10NH = 1,2,3,4-tetrahydroquinoline) activated with (Ph3C)+[B(C6F5)4]-. The copolymer was unambiguously characterized through the analysis of one- and two-dimensional NMR spectra. The monomer reactivity ratios, rethylene and rHTCPD, determined through the Fineman-Ross plot, were 2.8 and 0.025, respectively, indicating negligible successive insertion of two HTCPD. A nearly alternating copolymer with a HTCPD content of 45 mol% was obtained with a satisfactory activity (4.7 ?~106 g/molTi⋅h), of which Tg was 177oC, significantly higher than that of norbornene/ethylene copolymer at the same cycloolefin content. Tensile stress-strain curves indicated that the brittleness observed for a high Tg norbornene/ethylene copolymer was relieved to show some ductile property for the HTCPD/ethylene copolymer of the same level of high Tg.

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목차

1. Introduction
2. Result and Discussion
2.1 Preparation of HTCPD monomer
2.2 Copolymerization reactions
2.3 Tensile properties
2.4 Summary and Conclusion
3. Experiment Section
4. Reference
5. Supporting Information

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