Dinuclear iron(iii) complexes bearing phenylene-bridged bis(amino triphenolate) ligands as catalysts for the copolymerization of cyclohexene oxide with carbon dioxide or phthalic anhydride

2018 ◽  
Vol 9 (38) ◽  
pp. 4733-4743 ◽  
Author(s):  
Zhan Shi ◽  
Qingzhe Jiang ◽  
Zhaozheng Song ◽  
Zhihui Wang ◽  
Canglong Gao
Keyword(s):  
Carbon Dioxide ◽  
Phthalic Anhydride ◽  
Cyclohexene Oxide ◽  
Dinuclear Iron

Dinuclear iron(iii) complexes bearing rigid ortho-, meta-, and para-phenylene bridges as effective catalysts for CHO/CO2 and CHO/PA copolymerizations.

Cationic Co–Salphen Complexes Bisligated by DMAP as Catalysts for the Copolymerization of Cyclohexene Oxide with Phthalic Anhydride or Carbon Dioxide

2017 ◽  
Vol 50 (20) ◽  
pp. 7895-7900 ◽  
Author(s):  
Masahiro Hatazawa ◽  
Rei Takahashi ◽  
Jingyuan Deng ◽  
Hirohiko Houjou ◽  
Kyoko Nozaki
Keyword(s):  
Carbon Dioxide ◽  
Phthalic Anhydride ◽  
Cyclohexene Oxide

Bimetallic bis(benzotriazole iminophenolate) cobalt, nickel and zinc complexes as versatile catalysts for coupling of carbon dioxide with epoxides and copolymerization of phthalic anhydride with cyclohexene oxide

2016 ◽  
Vol 6 (6) ◽  
pp. 1779-1791 ◽  
Author(s):  
Chun-Yue Yu ◽  
Hui-Ju Chuang ◽  
Bao-Tsan Ko
Keyword(s):  
Carbon Dioxide ◽  
Phthalic Anhydride ◽  
Nickel Catalysts ◽  
Zinc Complexes ◽  
Cyclohexene Oxide ◽  
Cobalt Nickel ◽  
Cobalt And Nickel

New bimetallic bis(benzotriazole iminophenolate) cobalt and nickel catalysts were developed for versatile catalysis of CO2/epoxide coupling and PA/CHO copolymerization.

scholarly journals Ring-Opening Copolymerization of Cyclohexene Oxide and Cyclic Anhydrides Catalyzed by Bimetallic Scorpionate Zinc Catalysts

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 ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Reaction Mechanism ◽  
Catalytic System ◽  
Phthalic Anhydride ◽  
Ring Opening ◽  
High Selectivity ◽  
Zinc Complexes ◽  
Cyclohexene Oxide ◽  
Reaction Conditions ◽  
Cyclic Anhydrides

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.

Alternating Copolymerization of Carbon Dioxide with Cyclohexene Oxide Catalyzed by a Novel Catalyst

2012 ◽  
Vol 549 ◽  
pp. 445-448
Author(s):  
Li Dan Fan ◽  
Gang Qin ◽  
Xin Xin Cao ◽  
Shao Kui Cao
Keyword(s):  
Carbon Dioxide ◽  
Catalytic Activity ◽  
Reaction Time ◽  
Zinc Complex ◽  
Cyclohexene Oxide ◽  
Novel Catalyst ◽  
Alternating Copolymerization

A novel catalyst for the copolymerization of CO2 and cyclohexene oxide(CHO) was prepared by using BTE and ZnCl2. The zinc complex showed catalytic activity for the copolymerization. The obtained copolymer was characterized by IR and NMR. Effect of reaction time on copolymerization was investigated.

scholarly journals Study on Thermal Decomposition Behaviors of Terpolymers of Carbon Dioxide, Propylene Oxide, and Cyclohexene Oxide

2018 ◽  
Vol 19 (12) ◽  
pp. 3723 ◽  
Author(s):  
Shaoyun Chen ◽  
Min Xiao ◽  
Luyi Sun ◽  
Yuezhong Meng
Keyword(s):  
Carbon Dioxide ◽  
Thermal Stability ◽  
Thermal Decomposition ◽  
Thermogravimetric Analysis ◽  
Propylene Carbonate ◽  
Cyclohexene Oxide ◽  
Block Polymers ◽  
Rate Method ◽  
Poly Propylene ◽  
Thermal Stability Of

The terpolymerization of carbon dioxide (CO2), propylene oxide (PO), and cyclohexene oxide (CHO) were performed by both random polymerization and block polymerization to synthesize the random poly (propylene cyclohexene carbonate) (PPCHC), di-block polymers of poly (propylene carbonate–cyclohexyl carbonate) (PPC-PCHC), and tri-block polymers of poly (cyclohexyl carbonate–propylene carbonate–cyclohexyl carbonate) (PCHC-PPC-PCHC). The kinetics of the thermal degradation of the terpolymers was investigated by the multiple heating rate method (Kissinger-Akahira-Sunose (KAS) method), the single heating rate method (Coats-Redfern method), and the Isoconversional kinetic analysis method proposed by Vyazovkin with the data from thermogravimetric analysis under dynamic conditions. The values of ln k vs. T−1 for the thermal decomposition of four polymers demonstrate the thermal stability of PPC and PPC-PCHC are poorer than PPCHC and PCHC-PPC-PCHC. In addition, for PPCHC and PCHC-PPC-PCHC, there is an intersection between the two rate constant lines, which means that, for thermal stability of PPCHC, it is more stable than PCHC-PPC-PCHC at the temperature less than 309 °C and less stable when the decomposed temperature is more than 309 °C. Pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) and thermogravimetric analysis/infrared spectrometry (TG/FTIR) techniques were applied to investigate the thermal degradation behavior of the polymers. The results showed that unzipping was the main degradation mechanism of all polymers so the final pyrolysates were cyclic propylene carbonate and cyclic cyclohexene carbonate. For the block copolymers, the main chain scission reaction first occurs at PC-PC linkages initiating an unzipping reaction of PPC chain and then, at CHC–CHC linkages, initiating an unzipping reaction of the PCHC chain. That is why the T−5% of di-block and tri-block polymers were not much higher than that of PPC while two maximum decomposition temperatures were observed for both the block copolymer and the second one were much higher than that of PPC. For PPCHC, the random arranged bulky cyclohexane groups in the polymer chain can effectively suppress the backbiting process and retard the unzipping reaction. Thus, it exhibited much higher T−5% than that of PPC and block copolymers.

Kinetics of Ternary Copolymerization of Carbon Dioxide with Propylene Oxide, Butene Oxide, and Cyclohexene Oxide

2019 ◽  
Vol 61 (4) ◽  
pp. 395-403 ◽  
Author(s):  
O. M. Chukanova ◽  
K. O. Korenkov ◽  
E. O. Perepelitsina ◽  
N. O. Garifullin ◽  
I. V. Sedov
Keyword(s):  
Carbon Dioxide ◽  
Propylene Oxide ◽  
Cyclohexene Oxide ◽  
Kinetics Of
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