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Effect of functional ionic group of viologen derivative on the visible-light driven CO2 reduction to formic acid with the system consisting of water-soluble zinc porphyrin and formate dehydrogenase

Abstract

Effect of the functional ionic group of 4,4’-bipyridinium salt derivatives (4,4’-BPs) as the electron carrier on the visible-light driven conversion of CO2 to formic acid with the system consisting of water-soluble zinc tetraphneylporphyrin tetrasulfonate (ZnTPPS) and formate dehydrogenase (FDH) in the presence of triethanolamine (TEOA) as an electron donor was investigated. 1,1’-Diaminoethyl- (DAV), 1-aminoethyl-1’-methyl- (AMV), 1-carboxymethyl-1’-methyl- (CMV) and 1,1’-dicarboxymethyl-4,4’-bipyridinium salt (DCV) were prepared as the 4,4’-BPs with the functional ionic group. Irradiation of a CO2 saturated buffer solution containing TEOA, ZnTPPS, 4,4’-BP and FDH with visible light irradiation resulted in the production of formic acid. By using 4,4’-BPs with cationic aminoethyl-group, DAV or AMV as an electron carrier, the effective visible-light driven formic acid production based on the CO2 reduction was observed compared with the 4,4’-BPs with anionic carboxymethyl-group, CMV or DCV. The formic acid production rate with DAV approximately was 3.2 times larger than that of the system with DCV.

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Publication details

The article was received on 30 Jul 2017, accepted on 13 Nov 2017 and first published on 14 Nov 2017


Article type: Paper
DOI: 10.1039/C7PP00277G
Citation: Photochem. Photobiol. Sci., 2017, Accepted Manuscript
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    Effect of functional ionic group of viologen derivative on the visible-light driven CO2 reduction to formic acid with the system consisting of water-soluble zinc porphyrin and formate dehydrogenase

    S. Ikeyama and Y. Amao, Photochem. Photobiol. Sci., 2017, Accepted Manuscript , DOI: 10.1039/C7PP00277G

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