Palladium complexes bearing bis-aldimine N^C^N and N^N^N pincer ligands; A study of homogeneous/heterogeneous catalyzed CO2 hydrogenation

Widespread 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 forma...

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Main Authors: Nonkululeko Miya, Nyasha Makuve, Edward Ocansey, Gift Mehlana, James Darkwa, Banothile C.E. Makhubela
Other Authors: Research Centre for Synthesis and Catalysis, Department of Chemical Sciences, University of Johannesburg
Format: research article
Language:English
Published: Elsevier 2022
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Online Access:https://cris.library.msu.ac.zw//handle/11408/5289
https://doi.org/10.1016/j.ica.2022.121207
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author Nonkululeko Miya
Nyasha Makuve
Edward Ocansey
Gift Mehlana
James Darkwa
Banothile C.E. Makhubela
author2 Research Centre for Synthesis and Catalysis, Department of Chemical Sciences, University of Johannesburg
author_facet Research Centre for Synthesis and Catalysis, Department of Chemical Sciences, University of Johannesburg
Nonkululeko Miya
Nyasha Makuve
Edward Ocansey
Gift Mehlana
James Darkwa
Banothile C.E. Makhubela
author_sort Nonkululeko Miya
collection DSpace
description Widespread 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.
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spelling ir-11408-52892022-12-16T09:41:33Z Palladium complexes bearing bis-aldimine N^C^N and N^N^N pincer ligands; A study of homogeneous/heterogeneous catalyzed CO2 hydrogenation Nonkululeko Miya Nyasha Makuve Edward Ocansey Gift Mehlana James Darkwa Banothile C.E. Makhubela Research Centre for Synthesis and Catalysis, Department of Chemical Sciences, University of Johannesburg Synthesis and Catalysis, Department of Chemical Sciences, University of Johannesburg Synthesis and Catalysis, Department of Chemical Sciences, University of Johannesburg Department of Chemical Technology, Faculty of Science and Technology, Midlands State University, Research 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, Research 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, Imine Pd pincer complexes CO2 hydrogenation Homogenous catalysis Widespread 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. 545 (2023) 1 11 2022-12-16T09:41:33Z 2022-12-16T09:41:33Z 2022-09-19 research article https://cris.library.msu.ac.zw//handle/11408/5289 https://doi.org/10.1016/j.ica.2022.121207 en Inorganica Chimica Acta 0020-1693 open Elsevier
spellingShingle Imine
Pd pincer complexes
CO2 hydrogenation
Homogenous catalysis
Nonkululeko Miya
Nyasha Makuve
Edward Ocansey
Gift Mehlana
James Darkwa
Banothile C.E. Makhubela
Palladium complexes bearing bis-aldimine N^C^N and N^N^N pincer ligands; A study of homogeneous/heterogeneous catalyzed CO2 hydrogenation
title Palladium complexes bearing bis-aldimine N^C^N and N^N^N pincer ligands; A study of homogeneous/heterogeneous catalyzed CO2 hydrogenation
title_full Palladium complexes bearing bis-aldimine N^C^N and N^N^N pincer ligands; A study of homogeneous/heterogeneous catalyzed CO2 hydrogenation
title_fullStr Palladium complexes bearing bis-aldimine N^C^N and N^N^N pincer ligands; A study of homogeneous/heterogeneous catalyzed CO2 hydrogenation
title_full_unstemmed Palladium complexes bearing bis-aldimine N^C^N and N^N^N pincer ligands; A study of homogeneous/heterogeneous catalyzed CO2 hydrogenation
title_short Palladium complexes bearing bis-aldimine N^C^N and N^N^N pincer ligands; A study of homogeneous/heterogeneous catalyzed CO2 hydrogenation
title_sort palladium complexes bearing bis-aldimine n^c^n and n^n^n pincer ligands; a study of homogeneous/heterogeneous catalyzed co2 hydrogenation
topic Imine
Pd pincer complexes
CO2 hydrogenation
Homogenous catalysis
url https://cris.library.msu.ac.zw//handle/11408/5289
https://doi.org/10.1016/j.ica.2022.121207
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