Abstract
The melting points of several fluorescent chromophores, such as anthracene, several p-oligophenylenes, and BBD, have been dramatically reduced by the addition of alkyl or vinyl substituents. In the case of anthracene and p-terphenyl, the melting points of a number of derivatives are below room temperature. Some of the desirable characteristics that accompany these structural modifications are a dramatic increase in solubility in aromatic solvents and a greater immunity to self-quenching and quenching by high Z atoms. In all cases, the substituents have been so positioned that the favorable fluorescence characteristics of the parent chromophore have not been impaired.
| Original language | English |
|---|---|
| Pages (from-to) | 517-520 |
| Number of pages | 4 |
| Journal | Journal of Physical Chemistry |
| Volume | 84 |
| Issue number | 5 |
| DOIs | |
| State | Published - 1980 |
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