Relationship between solid state charge transfer behavior and molecular structure in a series of 1-(p-substituted phenylazo)-2-naphthols
- 1 October 1974
- journal article
- research article
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 61 (7) , 2740-2746
- https://doi.org/10.1063/1.1682408
Abstract
Charge transfer properties of a series of substituted arylazonapthols are shown to correlate with the Hammett's substituent constant σ. For both contact charge exchange of the dyes to metal and field assisted, photostimulated charge transfer from the dyes into nonpolar fluids, the amount of charge transferred is found to increase with increasing σ. However, the efficiency of charge transfer into fluids does not change with σ. In addition the energies of the highest filled and lowest unoccupied molecular levels are shown (by measurement of the oxidation and reduction potentials) to decrease as σ increases. The correlations establish a relationship between charge exchange phenomena and the energy levels of the dyes.Keywords
This publication has 17 references indexed in Scilit:
- PHOTOSENSITIZATION OF CONDUCTION IN MOLECULAR SOLIDS*Photochemistry and Photobiology, 2008
- Photoconductivity and semiconductivity in organic crystalsDiscussions of the Faraday Society, 1971
- Imaging Method Based on Photoelectrophoresis*Journal of the Optical Society of America, 1969
- Electrical and Photoelectric Properties of Organic Polymeric SemiconductorsRussian Chemical Reviews, 1968
- Organic Dyes as Photoelectric SemiconductorsAngewandte Chemie International Edition in English, 1965
- Organic semiconductors: Effect of substituents and metal ions on electrical conductivity of Schiff basesAustralian Journal of Chemistry, 1965
- An Examination of Structure‐Reactivity RelationshipsPublished by Wiley ,1964
- Polarographic Oxidation Potentials of Aromatic CompoundsJournal of the American Chemical Society, 1963
- Free Radicals from the Heterogeneous Decomposition of Butane1Journal of the American Chemical Society, 1957
- 794. The direct introduction of the diazonium group into aromatic nuclei. Part I. The basic reaction, yielding diazonium salts from polyalkylbenzenes, phenol ethers, phenols, and aromatic tertiary aminesJournal of the Chemical Society, 1957