Zinc complexes chelated by bifunctional ketiminate ligands: Structure, reactivity and possible applications in initiation of ROP and copolymerization of epoxides with carbon dioxide

被引:13
|
作者
Olejnik, Roman [1 ]
Bilek, Michal [1 ]
Ruzickova, Zdenka [1 ]
Hostalek, Zdenek [2 ]
Merna, Jan [2 ]
Ruzicka, Ales [1 ]
机构
[1] Univ Pardubice, Fac Chem Technol, Dept Gen & Inorgan Chem, CZ-53210 Pardubice, Czech Republic
[2] Inst Chem Technol, Fac Chem Technol, Dept Polymers, CZ-16628 Prague 6, Czech Republic
关键词
Ketiminate; Zinc complexes; NMR; XRD; ROP; RING-OPENING POLYMERIZATION; L-LACTIDE; EPSILON-CAPROLACTONE; ALUMINUM COMPLEXES; EFFICIENT INITIATORS; MAGNESIUM COMPLEXES; BETA-BUTYROLACTONE; CRYSTAL-STRUCTURES; CYCLIC MONOMERS; METAL-COMPLEXES;
D O I
10.1016/j.jorganchem.2015.07.001
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Bifunctional ketiminate zinc complexes were synthesized via alkyl or LiCl elimination route from appropriate zinc species (ZnCl2 or ZnEt2) and methoxyaryl substituted monoanionic ketimine {[2- or 3- or 4-(MeO)C6FH4]}N(H)C(Me)=CHC(Me)=O. Homo- or heteroleptic complexes were prepared and characterized by the help of multinuclear NMR spectroscopy techniques. One of the heteroleptic ethyl substituted zinc complexes - {kappa(2)-N,O-[(2-MeO)C6H4N=C(Me)-CH=C(Me)-O]ZnEt}(2) was selected for further reactivity experiments with alcohols and amines. Molecular structures of some products were determined by X-Ray diffraction methods showing di- or trinuclear arrangement in solid state caused by the presence of intramolecular zinc oxygen or zinc nitrogen bridges. {kappa(2)-N,O-[(2-MeO)C6H4N=C(Me)-CH=C(Me)-O]ZnEt}(2) was also screened for of its catalytic activity in co/polymerization reactions (ROP: trimethylene carbonate, c-caprolactone, L-lactide; copolymerization of epoxides with CO2). (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:237 / 246
页数:10
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