Abstract
One of the novel multidimensional charge-transfer (CT) chromophores, 2-[4-(4,5-di(4-nitrophenyl)imidazolyl)phenyl]-4,5-di(4-aminophenyl)imidazole (DNPIPDAPI), was designed and synthesized; the polyimide was formed with it and 2,5-bis(4-aminophenyl)-3,4-diphenylthiophene (TPTDA) (BMI). The thermal and temporal stability of the poling-induced orientation were evaluated. The temporal orientation of the poled polyimide film with DNPIPDAPI was over 1000 h at 150°C, retaining 85% of the initial d33 value. Comparing with 1-D chromophores, the synthetic multiple CT chromophore possesses a better property in controlling the decay of the SHG activity.
Original language | English |
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Pages (from-to) | 4314-4316 |
Number of pages | 3 |
Journal | Macromolecules |
Volume | 35 |
Issue number | 11 |
DOIs | |
State | Published - 21 May 2002 |
Externally published | Yes |