(Pyrazolylethyl-amine)zinc(II) carboxylate complexes as catalysts for the copolymerization of CO2 and cyclohexene oxide

dc.contributor.authorMatiwane, A.
dc.contributor.authorObuah, C.
dc.contributor.authorDarkwa, J.
dc.date.accessioned2022-06-02T11:01:08Z
dc.date.available2022-06-02T11:01:08Z
dc.date.issued2022
dc.descriptionResearch Articleen_US
dc.description.abstractPyrazolyl compounds 2-(3,5-di-tert-butyl-1H-pyrazol-1-yl)ethyl-amine) (L1), 2-(3,5-diphenyl-1H-pyrazol- 1-yl)ethyl-amine (L2), and 2-(3-phenyl-5-(trifluoromethyl)-1H-pyrazol-1-yl)ethyl-amine (L3) were reacted with a mixture of zinc(II) acetate and 3,5-dinitrobenzoic acid to form the bidentate complexes [(2-(3,5-di-tert-butyl-1H-pyrazol-1-yl)-ethyl-amine)-Zn(C6H5COO(NO2)2] (1), [(2-(3,5-diphenyl-1Hpyrazol- 1-yl)ethyl-amine)Zn(C6H5COO(NO2)2] (2), and [(2-(5-phenyl-3-(trifluoro-methyl)-1H-pyrazol- 1-yl)ethyl-amine)Zn(C6H5COO(NO2)2] (3) respectively. All three zinc complexes were tested as catalysts for the copolymerization of CO2 and cyclohexene oxide (CHO) and found active to form poly(cyclohexene carbonate) (PCHC) and cyclohexene carbonate (CCHC) at CO2 pressures as low as 1.5 MPa and under solvent- free conditions in the absence of a co-catalyst. Increase in CO2 pressure resulted in activity and showed selectivity up to 99% selectivity for the formation of the copolymer PCHC. Optimum temperature for the polymerization was 100 C and even at this temperature selectivity towards formation of PCHC was found to be 99%. The copolymers obtained have moderate molecular weights (3860–11,500 g/mol) and polydispersity indices varying from 2.73 to 4.93.en_US
dc.identifier.otherhttps://doi.org/10.1016/j.poly.2020.114767.
dc.identifier.urihttp://ugspace.ug.edu.gh/handle/123456789/38117
dc.language.isoenen_US
dc.publisherPolyhedronen_US
dc.subjectZinc(II) complexen_US
dc.subjectPyrazoleen_US
dc.subjectPoly(cyclohexene carbonate)en_US
dc.subjectCyclohexene carbonateen_US
dc.subjectCarbon dioxideen_US
dc.title(Pyrazolylethyl-amine)zinc(II) carboxylate complexes as catalysts for the copolymerization of CO2 and cyclohexene oxideen_US
dc.typeArticleen_US
dcterms.bibliographicCitationVol.190,No.114767

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