Effects of Clay Nanosheets on the Photostability of Cationic Porphyrin

Author:

Tahara Yoshinori1,Hirade Yugo2,Arakawa Kyosuke3,Shimada Tetsuya1,Ishida Tamao14,Tachibana Hiroshi1,Takagi Shinsuke14ORCID

Affiliation:

1. Department of Applied Chemistry, Faculty of Urban Environmental Sciences, Tokyo Metropolitan University, Hachiohji, Tokyo 192-0397, Japan

2. Advanced Collaborative Research Organization for Smart Society (ACROSS), Waseda University, Shinjuku-ku, Tokyo 169-8555, Japan

3. Department of Applied and Pure Chemistry, Faculty of Science and Technology, Tokyo University of Science, Noda-City 278-8510, Chiba, Japan

4. Research Center for Hydrogen Energy-Based Society (ReHES), Tokyo Metropolitan University, Hachiohji, Tokyo 192-0397, Japan

Abstract

The photodecomposition behavior of cationic porphyrin ZnTMAP4+ (zinc tetrakis-(N,N,N-trimethylanilinium-4-yl) porphyrin) in water and complexed with clay nanosheets was investigated by light irradiation to the Soret band of ZnTMAP4+. The decomposition of ZnTMAP4+ was observed by UV–visible absorption spectroscopy. While the decomposition quantum yield (ϕdec) was 3.4 × 10−4 in water, that was 9.4 × 10−7 on the exfoliated clay nanosheets. It was revealed that the photostability of ZnTMAP4+ was stabilized by the complex formation with clay. When ZnTMAP4+ was intercalated between the stacked clay nanosheets, ϕdec was further decreased to 4.9 × 10−7. The photostability increased by 361 times and 693 times for the exfoliated and stacked state, respectively. These results indicate that the flat clay surface has the potential to control intra- and intermolecular photochemical reactions.

Funder

JSPS KAKENHI

Publisher

MDPI AG

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