钴
环氧丙烷
铵
配体(生物化学)
化学
高分子化学
氧化物
环氧化物
第四纪
无机化学
共聚物
有机化学
催化作用
环氧乙烷
聚合物
受体
古生物学
生物
生物化学
作者
Jong Geun Seong,Sunghun Na,Anish Cyriac,Byung-Woo Kim,Wing Bun Lee
出处
期刊:Macromolecules
[American Chemical Society]
日期:2010-01-26
卷期号:43 (2): 903-908
被引量:127
摘要
Terpolymerizations of CO2/propylene oxide (PO)/cyclohexene oxide (CHO), CO2/PO/1-hexene oxide (HO), and CO2/PO/1-butene oxide (BO) were carried out without the formation of cyclic carbonates and ether linkages with a cobalt(III) complex of a Salen-type ligand tethered by four quaternary ammonium salts (1). The activities were excellent, in the range of (0.62−1.6) × 106 g/mol-Co (TOF, 4400−14 000 h−1). In all three of terpolymerizations, the data for the PO mole fractions in the feed (fPO) and the polymers (FPO) fit the Fineman−Ross plot well to determine the monomer reactivity ratios. The linear dependencies of the Tg’s of the polymers on the mole fractions of the third monomers (FCHO, FHO, and FBO) were observed with the relationships of “Tg (°C) = 81 × FCHO + 40”, “Tg (°C) = −62 × FHO + 38”, and “Tg (°C) = −27 × FBO + 38”, respectively. The decomposition temperature of the resin increased when the third monomer was employed. The GPC data indicated that the polymer chains grew in an immortal passion from...
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