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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Synthesis and characterization of the titanium complexes bearing two β-enaminoketonato ligands with electron withdrawing groups/modified phenyls and their behaviors for ethylene (co-)polymerization
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Synthesis and characterization of the titanium complexes bearing two β-enaminoketonato ligands with electron withdrawing groups/modified phenyls and their behaviors for ethylene (co-)polymerization

机译:带有两个具有吸电子基团/修饰苯基的β-烯酮酮配体的钛配合物的合成,表征及其在乙烯(共)聚合反应中的行为

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摘要

A series of new titanium complexes with two asymmetric bidentate β-enaminoketonato [N,O] ligands (2b-t), [PhNC(CF_3)CHC(Ar)O] _2TiCl_2 (2b, Ar = -C_6H_4F(o); 2c, Ar = -C_6H_4F(m); 2d, Ar = -C_6H_4F(p); 2e, Ar = -C_6H_4Cl(p); 2f, Ar = -C_6H _4OMe(p); 2g, Ar = -C_6H_4CF_3(p); 2h, Ar = -C_6H_4CF_3(m); 2i, Ar = -C_6H _4CF_3(o); 2j, Ar = -C_6H_4Cl(o); 2k, Ar = -C_6H_4Br(o); 2l, Ar = -C_6H_4I(o); 2m, Ar = -C_6H_3F_2(2,4); 2n, Ar = -C _6H_3F_2(2,6); 2o, Ar = -C_6H _3F_2(3,4); 2p, Ar = -C_6H_3F _2(3,5); 2q, Ar = -C_6F_5; 2r, Ar = C _6F_4OMe; 2s, Ar = -C_6H_3Cl _2(2,6); 2t, Ar = -C_6H_3Cl_2(2,5)), have been synthesized based on substituted acetophenones. X-Ray analyses reveal that complexes 2h, 2k, 2m, and 2n adopt distorted octahedral geometry around the titanium center, in which the two chloride ligands are situated in the cis-orientation. 2s also adopts distorted octahedral geometry, but the two chloride ligands in it are situated in the trans-orientation due to the increase of the steric effect of the phenyl derived from the acetophenone. The influence of the substituent effects on catalyst performance, including catalytic activities and the molecular weight distribution of the polymers obtained, was investigated in detail. With modified methylaluminoxane (MMAO) as a cocatalyst, complexes 2b-r and 2t are active catalysts for ethylene polymerization at room temperature, and produce high molecular weight polymers. It is observed that the catalytic activities are significantly enhanced by introducing some electron-withdrawing groups, such as -F, -Cl and -CF_3, into the suitable positions of the phenyl ring close to the oxygen donor. It should be noted that complexes 2c-i, 2p, 2n and 2t are also capable of promoting the living copolymerization of ethylene with norbornene at room temperature, yielding high molecular weight copolymers with narrow molecular weight distributions (PDI = 1.05-1.30).
机译:一系列具有两个不对称双齿β-烯胺酮[N,O]配体(2b-t)[PhNC(CF_3)CHC(Ar)O] _2TiCl_2(2b,Ar = -C_6H_4F(o); 2c, Ar = -C_6H_4F(m); 2d,Ar = -C_6H_4F(p); 2e,Ar = -C_6H_4Cl(p); 2f,Ar = -C_6H _4OMe(p); 2g,Ar = -C_6H_4CFe(3); 2h ,Ar = -C_6H_4CF_3(m); 2i,Ar = -C_6H _4CF_3(o); 2j,Ar = -C_6H_4Cl(o); 2k,Ar = -C_6H_4Br(o); 2l,Ar = -C_6H_4I(o); 2m,Ar = -C_6H_3F_2(2,4); 2n,Ar = -C _6H_3F_2(2,6); 2o,Ar = -C_6H _3F_2(3,4); 2p,Ar = -C_6H_3F _2(3,5) ; 2q,Ar = -C_6F_5; 2r,Ar = C _6F_4OMe; 2s,Ar = -C_6H_3Cl _2(2,6); 2t,Ar = -C_6H_3Cl_2(2,5)),是基于取代的苯乙酮合成的。 X射线分析表明,络合物2h,2k,2m和2n在钛中心周围采用扭曲的八面体几何形状,其中两个氯化物配体位于顺式方向。 2s也采用扭曲的八面体几何形状,但是由于衍生自苯乙酮的苯基的空间效应增加,其中的两个氯化物配体位于反方向。详细研究了取代基对催化剂性能的影响,包括催化活性和所得聚合物的分子量分布。用改性的甲基铝氧烷(MMAO)作为助催化剂,络合物2b-r和2t是室温下乙烯聚合的活性催化剂,可生产高分子量的聚合物。观察到,通过将一些吸电子基团,例如-F,-Cl和-CF_3引入到靠近氧供体的苯环的合适位置,可以显着提高催化活性。应当指出,络合物2c-1、2p,2n和2t还能够在室温下促进乙烯与降冰片烯的活性共聚,从而产生具有窄分子量分布的高分子量共聚物(PDI = 1.05-1.30)。

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