| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5381710 | Chemical Physics Letters | 2013 | 6 Pages |
Abstract
- Choice of bridge/substitution pattern allows targeting specific spectral features.
- Fulvalenoid bridges (e.g., [5.6.5]-fulvalene) produce large hyperpolarizabilities.
- Hyperpolarizability trends follow either polarizability or dipole, but not both.
- Zwitter-ionic mesomers rationalize results.
Related Topics
Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
B. Christopher Rinderspacher,