| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 178216 | Dyes and Pigments | 2008 | 5 Pages |
Abstract
3,6-Disubstituted carbazole chromophores containing thiazole and benzothiazole units were synthesized and characterized by NMR, IR, and UV. The first-order hyperpolarizabilities (β) were calculated via solvatochromic method. Our experiments suggest that the incorporation of thiazole and benzothiazole into carbazole-based chromophores can allow for significant enhancement of molecular hyperpolarizabilities. Nonlinear optical properties of AπDπA carbazole chromophores are superior to those of the corresponding DπA aryl compounds.
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Chemical Engineering (General)
Authors
Ying Qian,