Abstract
AbstractCofacial dinuclear metalloporphyrins exhibited a catalytic activity for the electrochemical reduction of carbon dioxide. The cofacial dinuclear porphyrin was automatically generated by mixing a cationic cobalt porphyrin (CoTMPyP) and an anionic metalloporphyrin (MTPPS) in solution. The redox system of this complex was examined by electrochemical methods. According to the cyclic voltammogram, the catalytic active species was generated at −1.8V vs. Ag/Ag+, which was considered to be a monovalent cobalt porphyrin, Co(I)TMPyP. The catalytic activity of the dinuclear complex was two times greater than that of the mononuclear one because the anionic porphyrin acted as an electron mediator.
Dates
Type | When |
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Created | 21 years, 8 months ago (Dec. 11, 2003, 6 a.m.) |
Deposited | 1 year, 11 months ago (Sept. 13, 2023, 10:28 a.m.) |
Indexed | 11 months, 3 weeks ago (Sept. 9, 2024, 11:17 a.m.) |
Issued | 21 years, 10 months ago (Nov. 1, 2003) |
Published | 21 years, 10 months ago (Nov. 1, 2003) |
Published Online | 21 years, 8 months ago (Dec. 9, 2003) |
Published Print | 21 years, 10 months ago (Nov. 1, 2003) |
@article{Enoki_2003, title={Electrochemical reduction of carbon dioxide catalyzed by cofacial dinuclear metalloporphyrin}, volume={204}, ISSN={1521-3900}, url={http://dx.doi.org/10.1002/masy.200351413}, DOI={10.1002/masy.200351413}, number={1}, journal={Macromolecular Symposia}, publisher={Wiley}, author={Enoki, Osamu and Imaoka, Takane and Yamamoto, Kimihisa}, year={2003}, month=nov, pages={151–158} }