首页> 外文期刊>European journal of inorganic chemistry >Benzotriazole Phenoxide Hafnium Complexes as Efficient Catalysts for the Ring-Opening Polymerization of Lactide: Synthesis, Characterization, and Kinetics of Polymerization Catalysis
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Benzotriazole Phenoxide Hafnium Complexes as Efficient Catalysts for the Ring-Opening Polymerization of Lactide: Synthesis, Characterization, and Kinetics of Polymerization Catalysis

机译:苯并三唑酚盐Ha配合物作为丙交酯开环聚合的高效催化剂:聚合反应的合成,表征和动力学

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摘要

Hafnium complexes bearing bis- or tetra-BTP ligands (BTP = N,O-bidentate benzotriazole phenoxide) have been synthesized and structurally characterized. The reactions of [Hf(OiPr)_4(iPrOH)] with 2-(2H-benzotriazol-2-yl)-4,6-bis(1- methyl-1-phenylethyl)phenol (~(CMe2Ph)BTP-H), 2-(2H-benzotriazol- 2-yl)-4,6-di-tert-butylphenol (~(tBu)BTP-H), and 2-tertbutyl- 6-(5-chloro-2H-benzotriazol-2-yl)-4-methylphenol (~(TMCl)BTP-H) (2.0 mol-equiv.) in hexane at 30 ℃ afforded the monomeric hafnium complexes [(~(CMe2Ph)BTP)_2Hf(OiPr)_2] (1), [(~(tBu)BTP)_2Hf(OiPr)_2] (2), and [(~(TM)ClBTP)_2Hf(OiPr)_2] (3). The bis-adduct hafnium analogue [(C8BTP)_2Hf(OiPr)_2] (4) was obtained by similar treatment of the sterically less bulky 2-(2Hbenzotriazol- 2-yl)-4-(2,4,4-trimethylpentan-2-yl)phenol (~(C8)BTP-H) as ligand at 0 ℃ and with a ligand/metal precursor ratio of 2:1, and treatment of [Hf(OiPr)_4(iPrOH)] with ~(C8)BTP-H (4.0 molequiv.) at 30 ℃ gave the hafnium tetra-adduct [(~(C8)BTP)_4Hf] (5). Single-site hafnium 4 proved to be an active catalyst in the polymerization of lactide (LA) in solution with "living" and "immortal" characteristics, producing polymers with the expected molecular weights and narrow molecular weight distributions (PDI ≤ 1.30). BTP-containing Hf complex 5 efficiently catalyzed the polymerization in a controlled fashion even though 160 equiv. of IPA was added to the Hf catalyst present at a low concentration. Kinetic tests for the polymerization of LA were conducted to compare the activities of hafnium alkoxides 1-4; a kinetic study of 4 revealed the polymerizations to be first order in both complex 4 and L-LA concentrations.
机译:带有双或四-BTP配体(BTP = N,O-二齿苯并三唑酚盐)的配合物已经合成并进行了结构表征。 [Hf(OiPr)_4(iPrOH)]与2-(2H-苯并三唑-2-基)-4,6-双(1-甲基-1-苯基乙基)苯酚(〜(CMe2Ph)BTP-H)的反应,2-(2H-苯并三唑-2-基)-4,6-二叔丁基苯酚(〜(tBu)BTP-H)和2-叔丁基-6-(5-氯-2H-苯并三唑-2-于30℃的己烷中的yl)-4-甲基苯酚(〜(TMCl)BTP-H)(2.0摩尔当量)提供单体ha络合物[(〜(CMe2Ph)BTP)_2Hf(OiPr)_2](1) [(〜(tBu)BTP)_2Hf(OiPr)_2](2)和[[〜(TM)ClBTP)_2Hf(OiPr)_2](3)。双加合物treatment类似物[(C8BTP)_2Hf(OiPr)_2](4)是通过对体积较小的2-(2H苯并三唑-2-基)-4-(2,4,4-三甲基戊烷-在0℃下以2-基)苯酚(〜(C8)BTP-H)作为配体/配体/金属前体比率为2:1,并用〜(C8)处理[Hf(OiPr)_4(iPrOH)] BTP-H(4.0摩尔当量)在30℃下得到tetra四加合物[(〜(C8)BTP)_4Hf](5)。单中心ha 4被证明是具有“活性”和“永生”特性的丙交酯(LA)在溶液中聚合的活性催化剂,可生产具有预期分子量和窄分子量分布(PDI≤1.30)的聚合物。含BTP的Hf络合物5即使控制量为160当量也有效地催化了聚合反应。向低浓度的Hf催化剂中加入50%的IPA。进行了LA聚合反应的动力学测试,以比较醇盐1-4的活性。 4的动力学研究表明,在络合物4和L-LA浓度下,聚合反应都是一级反应。

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