scholarly journals Ring-opening copolymerization of cyclohexene oxide and maleic anhydride catalyzed by mononuclear [Zn(L)(H2O)] or binuclear [Zn2(L)(OAc)2(H2O)] complex based on the Salen-type Schiff-base ligand

2014 ◽  
Vol 32 (6) ◽  
pp. 768-777 ◽  
Author(s):  
Li-ying Wu ◽  
Dai-di Fan ◽  
Xing-qiang Lü ◽  
Rong Lu
Author(s):  
Arron C. Deacy ◽  
Christopher B. Durr ◽  
Ryan W. F. Kerr ◽  
Charlotte K. Williams

A series of heterodinuclear catalysts, coordinated by a Schiff base ligand, for ring opening copolymerisation of phthalic anhydride/cyclohexene oxide, highlight the best metal combinations for fast and selective catalysis.


2011 ◽  
Vol 25 (4) ◽  
pp. 310-316 ◽  
Author(s):  
Lei-Lei Chen ◽  
Li-Qin Ding ◽  
Chu Zeng ◽  
Yong Long ◽  
Xing-Qiang Lü ◽  
...  

2010 ◽  
Vol 8 (6) ◽  
pp. 1305-1310 ◽  
Author(s):  
Elham Aazam ◽  
Martyn Coles

AbstractAluminium and zinc complexes bearing the N,O-chelating Schiff base ligand 4,6-bis-1-(2-(dimethylamino)ethylimino)ethyl)benzene-1,3-diol, (C6H2(OH)2(NCH2CH2NMe2)2) (1a), have been synthesized. Bimetallic aluminium and zinc alkyl complexes (2a–4a) were prepared by treatment of the hexadentate 1a with the appropriate amount of AlMe3, ZnMe2 and ZnEt2, respectively. 2a has been characterized crystallographically, it lies on a crystallographic two-fold rotation axis and each aluminium centre adopts a five coordinate geometry. Complex 2a was tested as a catalyst in the ring-opening polymerisation of ɛ-caprolactone. We describe here the synthesis of two neutral ligands (1a and (C6H2(OH)2(C6H5NH2) (C=O(CH3)) (1b)) and demonstrate their application in the synthesis of molecular aluminium and zinc derivatives.


2014 ◽  
Vol 48 ◽  
pp. 69-72 ◽  
Author(s):  
Xingmei Zhang ◽  
Yaoju Liu ◽  
Yan Chen ◽  
Zhao Zhang ◽  
Daidi Fan ◽  
...  

2015 ◽  
Vol 51 (47) ◽  
pp. 9643-9646 ◽  
Author(s):  
Stephanie M. Quan ◽  
Paula L. Diaconescu

An indium complex supported by a ferrocene-derived Schiff base ligand has unprecedented activity toward ε-caprolactone, δ-valerolactone, and β-butyrolactone ring-opening polymerizations. l-Lactide, d,l-lactide, and trimethylene carbonate polymerizations also showed moderate to high activity.


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