Please use this identifier to cite or link to this item: https://cris.library.msu.ac.zw//handle/11408/5289
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dc.contributor.authorNonkululeko Miyaen_US
dc.contributor.authorNyasha Makuveen_US
dc.contributor.authorEdward Ocanseyen_US
dc.contributor.authorGift Mehlanaen_US
dc.contributor.authorJames Darkwaen_US
dc.contributor.authorBanothile C.E. Makhubelaen_US
dc.date.accessioned2022-12-16T09:41:33Z-
dc.date.available2022-12-16T09:41:33Z-
dc.date.issued2022-09-19-
dc.identifier.urihttps://cris.library.msu.ac.zw//handle/11408/5289-
dc.description.abstractWidespread consumption of fossil resources yielding waste CO2 has reached an all-time high and this poses an environmental threat that is contributing to global warming and climate change. Using CO2 as a C1 source may serve as an avenue to convert waste to valuable platform chemicals such as formates. In this contribution, we report on the design and synthesis of new pincer Pd(II) N^C^N and N^N^N complexes. Herein, we investigate the role of an N^C^N or N^N^N ligand backbone in Pd(II) pre-catalysts and the corresponding catalytic activity in CO2 hydrogenation. Catalytic activity and selectivity with TON (turnover number) up to 537, in a THF/H2O biphasic (affording catalyst separation) system, was achieved. The CO2-to-CH3OH conversion sequence in the presence of an amine using these Pd pincer catalysts is also investigated.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofInorganica Chimica Actaen_US
dc.subjectImineen_US
dc.subjectPd pincer complexesen_US
dc.subjectCO2 hydrogenationen_US
dc.subjectHomogenous catalysisen_US
dc.titlePalladium complexes bearing bis-aldimine N^C^N and N^N^N pincer ligands; A study of homogeneous/heterogeneous catalyzed CO2 hydrogenationen_US
dc.typeresearch articleen_US
dc.identifier.doihttps://doi.org/10.1016/j.ica.2022.121207-
dc.contributor.affiliationResearch Centre for Synthesis and Catalysis, Department of Chemical Sciences, University of Johannesburgen_US
dc.contributor.affiliationSynthesis and Catalysis, Department of Chemical Sciences, University of Johannesburgen_US
dc.contributor.affiliationSynthesis and Catalysis, Department of Chemical Sciences, University of Johannesburgen_US
dc.contributor.affiliationDepartment of Chemical Technology, Faculty of Science and Technology, Midlands State University,en_US
dc.contributor.affiliationResearch Centre for Synthesis and Catalysis, Department of Chemical Sciences, University of Johannesburg; Department of Natural Resources and Materials, Botswana Institute of Technology Research and Innovation,en_US
dc.contributor.affiliationResearch Centre for Synthesis and Catalysis, Department of Chemical Sciences, University of Johannesburg; Department of Natural Resources and Materials, Botswana Institute of Technology Research and Innovation,en_US
dc.relation.issn0020-1693en_US
dc.description.volume545 (2023)en_US
dc.description.startpage1en_US
dc.description.endpage11en_US
item.fulltextWith Fulltext-
item.openairetyperesearch article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.grantfulltextopen-
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