Abstract

One-electron oxidation of various biphenyl derivatives such as biphenyl (BP), 4-hydroxybiphenyl (HBP), 4,4'-biphenol (DHBP), 4-methoxy-4'-hydroxybiphenyl (MHBP), 4-cyano-4'-hydroxybiphenyl (CNHBP), 4-biphenylmethanol (BPM), and 4-biphenylethanol (BPE) adsorbed on the surface of TiO2 powder slurried in acetonitrile has been investigated by time-resolved diffuse reflectance spectroscopy. From the Langmuir adsorption isotherms for BP and HBP, it is suggested that the OH group plays an important role in adsorbing on the surface ofTiO2. The spectroscopic characteristics of charge transfer complexes of substrates and the TiO2 surface have been studied by steady-state diffuse reflectance spectroscopy. The high efficiency of a one-electron oxidation reaction was observed for hydroxyl-substituted BPs (HBP, DHBP, MHBP, CNHBP), compared with BPM and BPE, indicating that the strength of the electronic coupling element (H(DA)) between the electron acceptor and donor is a key factor in the one-electron oxidation of a substrate adsorbed on the TiO2 powder. The effects of the distance between the electron donor and the acceptor on the electronic coupling element are also discussed.

Keywords

PhotocatalysisBiphenylElectronMaterials scienceChemical engineeringPhotochemistryChemistryCatalysisPhysicsOrganic chemistry

MeSH Terms

Biphenyl CompoundsCatalysisElectronsModelsMolecularMolecular StructureOxidation-ReductionPhotochemistrySurface PropertiesTitanium

Affiliated Institutions

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Publication Info

Year
2004
Type
article
Volume
20
Issue
7
Pages
2753-2759
Citations
60
Access
Closed

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Cite This

Takashi Tachikawa, Sachiko Tojo, Mamoru Fujitsuka et al. (2004). Photocatalytic One-Electron Oxidation of Biphenyl Derivatives Strongly Coupled with the TiO<sub>2</sub> Surface. Langmuir , 20 (7) , 2753-2759. https://doi.org/10.1021/la0361262

Identifiers

DOI
10.1021/la0361262
PMID
15835148

Data Quality

Data completeness: 81%