Alternating ring-opening copolymerization of cyclohexene oxide with phthalic anhydride catalyzed by iron(III) salen complexes

2015 ◽  
Vol 23 (2) ◽  
pp. 161-166 ◽  
Author(s):  
Robert Mundil ◽  
Zdeněk Hošt’álek ◽  
Ivana Šeděnková ◽  
Jan Merna
Polymers ◽  
2021 ◽  
Vol 13 (10) ◽  
pp. 1651
Author(s):  
Felipe de la Cruz-Martínez ◽  
Marc Martínez de Sarasa Buchaca ◽  
Almudena del Campo-Balguerías ◽  
Juan Fernández-Baeza ◽  
Luis F. Sánchez-Barba ◽  
...  

The catalytic activity and high selectivity reported by bimetallic heteroscorpionate acetate zinc complexes in ring-opening copolymerization (ROCOP) reactions involving CO2 as substrate encouraged us to expand their use as catalysts for ROCOP of cyclohexene oxide (CHO) and cyclic anhydrides. Among the catalysts tested for the ROCOP of CHO and phthalic anhydride at different reaction conditions, the most active catalytic system was the combination of complex 3 with bis(triphenylphosphine)iminium as cocatalyst in toluene at 80 °C. Once the optimal catalytic system was determined, the scope in terms of other cyclic anhydrides was broadened. The catalytic system was capable of copolymerizing selectively and efficiently CHO with phthalic, maleic, succinic and naphthalic anhydrides to afford the corresponding polyester materials. The polyesters obtained were characterized by spectroscopic, spectrometric, and calorimetric techniques. Finally, the reaction mechanism of the catalytic system was proposed based on stoichiometric reactions.


2014 ◽  
Vol 5 (20) ◽  
pp. 6068-6075 ◽  
Author(s):  
Prabhjot K. Saini ◽  
Charles Romain ◽  
Yunqing Zhu ◽  
Charlotte K. Williams

Di-zinc and di-magnesium catalysts for the ring-opening copolymerization of phthalic anhydride and cyclohexene oxide are presented. They are applied in terpolymerizations to prepare block copoly(ester-carbonates).


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.


2005 ◽  
Vol 70 (2) ◽  
pp. 470-476 ◽  
Author(s):  
Ben W. Greatrex ◽  
Dennis K. Taylor
Keyword(s):  

2000 ◽  
Vol 12 (1) ◽  
pp. 177-184 ◽  
Author(s):  
Satoshi Akimoto ◽  
Mitsutoshi Jikei ◽  
Masa-aki Kakimoto

A novel photosensitive polyimide based on a polyimide containing the hydroxytriphenylamine structure (HTA-PI) and 2, 3, 4-tris[1-oxo-2-diazonaphthoquinone-4-sulfonyloxy] benzophenone (D4SB) as a photoreactive compound has been developed. The HTAPI was prepared by the ring-opening polyaddition of 4, 4′-hexafluoroisopropylidenebis(phthalic anhydride) (6FDA) and 4,4′-diamino-4″-hydroxytriphenylamine (DHTA), followed by thermal cyclization in refluxing N-methyl-2-pyrrolidone (NMP). The resulting polyimide film showed excellent transparency to 436 nm light. Photosensitive polyimide containing 30 wt% of D4SB showed a sensitivity of 800 mJ cm−2 and a contrast of 0.8 when it was exposed to 436 nm light followed by development with 5% tetramethylammonium hydroxide (TMAH) aqueous solution at 45°C.


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