Abstract
A systematic study of the reaction of 1-chloromethyl-4-(2-trichlorosilylethyl)-benzene (coupling agent) with the surface SiOH groups of glass for times from 15 min to 48 h, followed by stilbazole chromophore precursor deposition/quaternization, is reported. Second harmonic generation characteristics of these thin film materials indicate that a 15 min coupling agent reaction attains approximately 65% of full surface coverage (based on χzzz(2)) of benzylic chloride moieties, but that 24 h is the optimal time for maximum coverage. The surface-anchored chromophoric chloride salts in such materials undergo facile ion exchange with iodide, p-aminobenzenesulphonate, and ethyl orange, leading to enhancements in χzzz(2) of up to 50%.
Original language | English |
---|---|
Pages (from-to) | 142-145 |
Number of pages | 4 |
Journal | Thin Solid Films |
Volume | 242 |
Issue number | 1-2 |
DOIs | |
State | Published - 15 Apr 1994 |
Externally published | Yes |
Bibliographical note
Funding Information:This research was supported by the NSF-MRL program through the Materials Research Center of North-western University (Grant DMR9120521) and by the Air Force Office of Scientific Research (Contract 90-0071). A.K.K. thanks NSERC of Canada for a postdoctoral fellowship.