Oligooxyethylene liquid phthalocyanines
β Scribed by Arthur W. Snow; James S. Shirk; Richard G. S. Pong
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 109 KB
- Volume
- 04
- Category
- Article
- ISSN
- 1088-4246
No coin nor oath required. For personal study only.
β¦ Synopsis
A series of methyl-terminated oligooxyethylene ( CH ~3~( OCH ~2~ CH ~2~)~n~ O , n = 8.8)-substituted phthalocyanines with peripheral substitution at four Ξ² positions, at four Ξ± positions and at the eight Ξ± positions was synthesized and structurally characterized. These compounds are isotropic liquids above 10 Β°C. Non-linear optical properties of the tetra-Ξ±- and tetra-Ξ²-substituted compounds were examined. Both are reverse saturable absorbers in the visible region of the spectrum, but the tetra-Ξ±-substituted compound has the larger non-linear absorption coefficient and can be a useful optical limiter in cases where a non-volatile liquid is desirable.
π SIMILAR VOLUMES
on temperature, concentration, and, mainly, the structure of This work describes the synthesis of new branched, nonionic Vthe molecules. The influence of the molecular structure on surfactants, with the general formula C k C n GE 8 M, where C k and the shape of the micelles in the absence of micella
## Abstract In this investigation, liquid chromatography using Cuβphthalocyanine stationary phases were examined for polycyclic aromatic hydrocarbon (PAH) analyses. The results have indicated that Cuβphthalocyanine phases can be useful for PAH separations by their planarity recognition capabilities