| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5384404 | Chemical Physics Letters | 2011 | 5 Pages |
Abstract
⺠Choice of aromatic bridge coupled with the substitution pattern on the ring allows targeting specific spectral features (absorption or transparency windows). ⺠Asymmetric bridges (e.g., azulene) produce large hyperpolarizabilities. ⺠Zwitter-ionic mesomers rationalize hyperpolarizability and spectral trends.
Related Topics
Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
B. Christopher Rinderspacher, Jan W. Andzelm, Adam M. Rawlett, Joseph M. Dougherty, MyVan Baranoski, Matthew C. Davis,