Abstract
A method for preparing organized, highly aligned, multifunctional donor-acceptor covalently bonded self-assemblies on silica surfaces is described. Using the organosilane coupling reagent, I3Si(CH2)2C6H4CH2I (Cp), the high-β chromophore, 4-[N,N-bis(3-hydroxypropyl)amino]styryl-4′-pyridine (Ch) can be easily linked to surfaces via quaternization. Additional chromophore layer can be built up in this manner using chlorosilane/polyvinylalcohol as an intervening structural layer. These multilayer structures have been characterized by FTIR-ATR, UV-vis spectroscopy, advancing contact angle, and second harmonic generation measurements. The studies of NLO properties reveal good structural uniformity and second order susceptibilities χzzz(2) as high as 6 × 10-7 esu for a single CpCh monolayer and 2 × 10-7 esu for multilayer superlattices (λ = 1064 nm).
| Original language | English |
|---|---|
| Pages (from-to) | 3157-3162 |
| Number of pages | 6 |
| Journal | Synthetic Metals |
| Volume | 43 |
| Issue number | 1-2 |
| DOIs | |
| Publication status | Published - 7 Jun 1991 |
| Externally published | Yes |