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 (US) |
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Pages (from-to) | 3157-3162 |
Number of pages | 6 |
Journal | Synthetic Metals |
Volume | 43 |
Issue number | 1-2 |
DOIs | |
State | Published - Jun 7 1991 |
Funding
ACKNOWLEDGEMENTS This research was supported by the NSF-MRL program through the Materials Research Center of Northwestern University (Grant DMR8821571) and by the Air Force Office of Scientific Research (Contracts 86-0105 and 90-0071).
ASJC Scopus subject areas
- Electronic, Optical and Magnetic Materials
- Condensed Matter Physics
- Mechanics of Materials
- Mechanical Engineering
- Metals and Alloys
- Materials Chemistry