Buried Liquid Interfaces as a Form of Chemistry in Confinement: The Case of 4-Dimethylaminobenzonitrile at the Silica-Aqueous Interface.

Abstract

Time-resolved fluorescence emission and resonance-enhanced second harmonic generation (SHG) spectra were collected from 4-dimethylaminobenzonitrile (DMABN) adsorbed to the aqueous-silica interface in order to identify how strongly associating solvent-substrate interactions change DMABN's photoisomerization properties. In bulk polar solution, DMABN forms an excited twisted intramolecular charge-transfer (TICT) state that emits with a distinctive, solvatochromic fluorescent signature. At the silica-aqueous interface, the TICT fluorescence disappears, similar to DMABN's behavior in nonpolar environments. SHG spectra confirm that the interface is, in fact, polar, and DMABN's unusual fluorescence emission acquired from the interface is attributed to strong hydrogen bonding associations between the water molecules and the silica surface that prevent adsorbate isomerization. Additionally, SHG spectra show a strong resonance at long wavelengths that is unexpected based on bulk absorbance spectra and selection rules for nonlinear hyperpolarizabilities. Using both Zerner's INDO semiempirical and TD-DFT calculations, this spectroscopic behavior is attributed to a combination of strong electric fields present at the aqueous-silica interface and surface-induced changes to DMABN's ground-state molecular structure.