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对映体纯的N,N,O-蝎形锌酰胺和氯化物配合物作为环酯杂选择性开环聚合的高效引发剂。

Enantiopure N,N,O-scorpionate zinc amide and chloride complexes as efficient initiators for the heteroselective ROP of cyclic esters.

作者信息

Honrado Manuel, Otero Antonio, Fernández-Baeza Juan, Sánchez-Barba Luis F, Garcés Andrés, Lara-Sánchez Agustín, Rodríguez Ana M

机构信息

Departamento de Química Inorgánica, Orgánica y Bioquímica-Centro de Innovación en Química Avanzada (ORFEO-CINQA), Universidad de Castilla-La Mancha, Campus Universitario, 13071-Ciudad Real, Spain.

出版信息

Dalton Trans. 2014 Dec 7;43(45):17090-100. doi: 10.1039/c4dt02178a.

Abstract

The reaction of bpzbeH, bpzteH (racemic mixture) or (R,R)-bpzmmH (enantiopure) with the amide complexes Zn{N(SiMe3)2}2 or Zn{N(SiHMe2)2}2 in 1 : 1 molar ratio in toluene afforded the mononuclear amide zinc complexes [Zn(NR2)(κ(3)-NNO)] (1-6) [κ(3)-NNO = bpzbe, R = SiMe3 1, SiHMe2 2; bpzte, R = SiMe3 3, SiHMe2 4; (R,R)-bpzmm, SiMe3 5, SiHMe2 6]. These complexes were employed in a protonolysis reaction with HCl-Et2O in 2 : 1 molar ratio to yield the dinuclear amide/chloride zinc complexes [Zn(κ(2)-NN-μ-O)2{ZnCl(NR2)}] (7-12) [κ(2)-NN-μ-O = bpzbe, R = SiMe3 7, SiHMe2 8; bpzte, R = SiMe3 9, SiHMe2 10; (R,R)-bpzmm, SiMe3 11, SiHMe2 12]. The mononuclear complexes 5 and 6 and dinuclear complexes 11 and 12 are the first enantiopure-scorpionate zinc amide complexes to be synthesized. The single-crystal X-ray structure analysis of derivatives 1 and 3 confirmed a monomeric 4-coordinative structure in which the heteroscorpionate ligands are in a κ(3) coordination mode, while 8 had a dimeric molecular disposition with two μ-bridging alkoxides of the heteroscorpionate ligands between the two six- and four-coordinate Zn(II) centers. Interestingly, the chiral amide-containing zinc complexes 1-5 and 11 can act as single-component initiators for the ring-opening polymerization of ε-caprolactone and lactides under mild conditions, affording, in a few hours, medium/low molecular weight polymers with low polydispersity indices. MALDI-ToF mass spectra confirmed that the initiation occurred through a nucleophilic attack by the amide on the lactide monomer, and inspection of the kinetic parameters showed that propagations present the usual pseudo-first order dependence on monomer and catalyst concentrations. In addition, microstructural analysis of poly(rac-lactide)s revealed that the myrtenal substituent on the alkoxide fragment has a significant influence on the degree of stereoselectivity, producing enriched-heterotactic PLAs with a P(s) value of up to 0.79 under mild conditions.

摘要

将bpzbeH、bpzteH(外消旋混合物)或(R,R)-bpzmmH(对映体纯)与酰胺配合物Zn{N(SiMe3)2}2或Zn{N(SiHMe2)2}2以1:1的摩尔比在甲苯中反应,得到单核酰胺锌配合物[Zn(NR2)(κ(3)-NNO)](1 - 6)[κ(3)-NNO = bpzbe,R = SiMe3 1,SiHMe2 2;bpzte,R = SiMe3 3,SiHMe2 4;(R,R)-bpzmm,SiMe3 5,SiHMe2 6]。这些配合物用于与HCl-Et2O以2:1的摩尔比进行质子olysis反应,生成双核酰胺/氯化锌配合物[Zn(κ(2)-NN-μ-O)2{ZnCl(NR2)}](7 - 12)[κ(2)-NN-μ-O = bpzbe,R = SiMe3 7,SiHMe2 8;bpzte,R = SiMe3 9,SiHMe2 10;(R,R)-bpzmm,SiMe3 11,SiHMe2 12]。单核配合物5和6以及双核配合物11和12是首批合成的对映体纯的螯合锌酰胺配合物。衍生物1和3的单晶X射线结构分析证实了单体的4配位结构,其中杂螯合配体处于κ(3)配位模式,而8具有二聚体分子排列,在两个六配位和四配位的Zn(II)中心之间有两个杂螯合配体的μ-桥连醇盐。有趣的是,含手性酰胺的锌配合物1 - 5和11在温和条件下可作为ε-己内酯和丙交酯开环聚合的单组分引发剂,在几小时内得到低多分散指数的中/低分子量聚合物。基质辅助激光解吸电离飞行时间质谱(MALDI-ToF)证实引发是通过酰胺对丙交酯单体的亲核攻击发生的,动力学参数检查表明链增长对单体和催化剂浓度呈现通常的准一级依赖性。此外,聚(外消旋丙交酯)的微观结构分析表明,醇盐片段上的桃金娘烯基取代基对立体选择性程度有显著影响,在温和条件下可产生P(s)值高达0.79的富杂规聚丙交酯。

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