Chromium Amino-bis(phenolate) Complexes as Catalysts for Ring-Opening Polymerization of Cyclohexene Oxide

被引:27
作者
Ambrose, Kenson [1 ]
Murphy, Jennifer N. [1 ]
Kozak, Christopher M. [1 ]
机构
[1] Mem Univ Newfoundland, Dept Chem, St John, NF A1B 3X7, Canada
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会;
关键词
PROPYLENE-OXIDE; CARBON-DIOXIDE; STRUCTURAL-CHARACTERIZATION; COUPLING REACTION; LIGAND SYNTHESIS; METAL-COMPLEXES; COPOLYMERIZATION; EPOXIDES; CO2; REACTIVITY;
D O I
10.1021/acs.macromol.9b01381
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The chromium(III) amino-bis(phenolate) "ate" complex, {Na[CrCl(2)L1]}, 1, where L1 = 6,6'-((1,4-diazepane-1,4-diyl)bis-(methylene))bis(2,4-di-tert-butylphenolato) and its derivatives 2-4 (where the phenolate substituents and the diamino linker were varied) were prepared. Single crystals obtained by recrystallization of 1 were shown by X-ray diffraction to be a related octahedral complex, 1', where one of the O-donors in 1' is protonated, resulting in a monoanionic ligand and affording a neutral Cr(III) dichloride complex. The ligand [L1] chelates in a meridional fashion and anionic chloride donors reside in a trans axial orientation. Cr(III) amino-bis(phenolate) complexes 1-4 showed good activity toward ring-opening polymerization (ROP) of cyclohexene oxide (CHO) without the use of an added cocatalyst, producing high-molecular weight poly(cyclohexene oxide) where 1 was the most active catalyst. Arrhenius data obtained for the ROP of CHO using 1 revealed an activation barrier of 64.0 +/- 9.8 kJ mol(-1) and the nonlinear polymer molecular weight growth versus conversion relationship suggests a step-growth polymerization mechanism.
引用
收藏
页码:7403 / 7412
页数:10
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共 82 条
[1]   Kinetics and mechanism of the electron transfer in [N,N′-bis(salicylidene)-1,2-ethanediamine]chromium(III) complex by N-bromosuccinimide: evidence for the catalytic effect of iron(II) ions [J].
Abdel-Hady, Alaa Eldin Mokhtar .
MONATSHEFTE FUR CHEMIE, 2015, 146 (01) :7-13
[2]   New cobalt, iron and chromium catalysts based on easy-to-handle N4-chelating ligands for the coupling reaction of epoxides with CO2 [J].
Adolph, M. ;
Zevaco, T. A. ;
Altesleben, C. ;
Walter, O. ;
Dinjus, E. .
DALTON TRANSACTIONS, 2014, 43 (08) :3285-3296
[3]   LIVING POLYMERIZATION OF EPOXIDE CATALYZED BY THE PORPHYRIN-ET2ALCL SYSTEM - STRUCTURE OF THE LIVING END [J].
AIDA, T ;
INOUE, S .
MACROMOLECULES, 1981, 14 (05) :1166-1169
[4]   Metalloporphyrins as initiators for living and immortal polymerizations [J].
Aida, T ;
Inoue, S .
ACCOUNTS OF CHEMICAL RESEARCH, 1996, 29 (01) :39-48
[5]   COPOLYMERIZATION OF EPOXIDES BY ALUMINUM PORPHYRIN - REACTIVITY OF (PORPHINATO)ALUMINUM ALKOXIDE AS GROWING SPECIES [J].
AIDA, T ;
WADA, K ;
INOUE, S .
MACROMOLECULES, 1987, 20 (02) :237-241
[6]   Iron amino-bis(phenolate) complexes for the formation of organic carbonates from CO2 and oxiranes [J].
Alhashmialameer, Dalal ;
Collins, Julie ;
Hattenhauer, Karen ;
Kerton, Francesca M. .
CATALYSIS SCIENCE & TECHNOLOGY, 2016, 6 (14) :5364-5373
[7]   Ring-opening polymerization of epoxides and ring-opening copolymerization of CO2 with epoxides by a zinc amino-bis(phenolate) catalyst [J].
Anderson, Timothy S. ;
Kozak, Christopher M. .
EUROPEAN POLYMER JOURNAL, 2019, 120
[8]   Recent Developments in Chain-Growth Polymerizations of Conjugated Polymers [J].
Aplan, Melissa P. ;
Gomez, Enrique D. .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2017, 56 (28) :7888-7901
[9]   New reactivity of the uranyl ion: ring opening polymerisation of epoxides [J].
Baker, Robert J. ;
Walshe, Aurora .
CHEMICAL COMMUNICATIONS, 2012, 48 (07) :985-987
[10]   An efficient method for controlled propylene oxide polymerization: The significance of bimetallic activation in aluminum Lewis acids [J].
Braune, W ;
Okuda, J .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (01) :64-68