New route to unsymmetrical phthalocyanine analogs by the use of structurally distorted subphthalocyanines
In addition to traditional uses as dyes and in photocopying devices, phthalocyanines (Pcs) are now rapidly growing in importance in many fields such as chemical sensors, electrochromism, batteries, photodynamic cancer therapy, molecular metals, photochemical hole burning, and liquid crystals. In thi...
Saved in:
Published in | Journal of the American Chemical Society Vol. 112; no. 26; pp. 9640 - 9641 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
WASHINGTON
American Chemical Society
01.12.1990
Amer Chemical Soc |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | In addition to traditional uses as dyes and in photocopying devices, phthalocyanines (Pcs) are now rapidly growing in importance in many fields such as chemical sensors, electrochromism, batteries, photodynamic cancer therapy, molecular metals, photochemical hole burning, and liquid crystals. In this communication, the authors present a completely new method for the preparation of monosubstituted type unsymmetrical Pcs and Pc analogues, which utilizes the so-called subphthalocyanines (SubPcs). |
---|---|
Bibliography: | istex:8FE6E78CEA5DF477BEFF447DFBDCA5AD098C3C26 ark:/67375/TPS-V4TX32SH-R |
ISSN: | 0002-7863 1520-5126 |
DOI: | 10.1021/ja00182a034 |