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首页> 外文期刊>Inorganic Chemistry Communications >Ring-opening copolymerization of CHO and MA catalyzed by the asymmetrical Cr(III)-bis-Schiff-base complex
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Ring-opening copolymerization of CHO and MA catalyzed by the asymmetrical Cr(III)-bis-Schiff-base complex

机译:由不对称Cr(III)-BIS-Schiff-Base络合物催化的CHO和MA的开环共聚合

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摘要

Using an asymmetrical Cr(III)-bis-Schiff-base complex [Cr(L)Cl] (1; H2L obtained from condensation of 5-bromo-salicylaldehyde and HL0 ((Z)-4-((2-aminophenylimino)(phenyl)methyl)-3-methyl-1H-pyrazol-5(4H)-one) as the catalyst, bulk solvent-free ring-opening copolymerization of CHO (cyclohexene oxide) and MA (maleic anhydride) in the presence of cocatalyst DMAP (4-(dimethylamino)-pyridine) was effectively realized, in which, on the condition of low 1/DMAP concentration for a controllable polymerization, perfectly alternating polyester while not poly(ester-co-ether) could be obtained. (C) 2017 Elsevier B.V. All rights reserved.
机译:使用不对称Cr(III)-BIS-Shiff-基络合物[Cr(L)Cl](1;从5-溴 - 水杨醛和HL O-((Z)-4 - ((2-氨基烯基氨基)((2-氨基烯基氨基)获得( 苯基)甲基)-3-甲基-1H-吡唑-5(4h) - 酮类为催化剂,在助催化剂DMAP存在下,CHO(环己烯)和MA(马来酸酐)的本体无溶剂环开环共聚 (4-(二甲基氨基) - 吡啶)有效地实现,其中,在可控聚合的低1 / DMAP浓度的条件下,可以获得完全交替的聚酯,而不是聚(酯 - 共醚)。(c) 2017年Elsevier BV保留所有权利。

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