| Literature DB >> 26134857 |
N R Krekiehn1, M Müller1, U Jung1, S Ulrich2, R Herges2, O M Magnussen1.
Abstract
Direct comparative studies of the photoisomerization of azobenzene derivatives in self-assembled adlayers on Au and as free molecules in dichloromethane solution were performed using UV/vis spectroscopy. For all studied systems a highly reversible trans-cis isomerization in the adlayer is observed. Quantitative studies of the absorbance changes and photoisomerization kinetics reveal that in azobenzenes mounted as freestanding vertical groups on the surface via triazatriangulene-based molecular platforms photoswitching is nearly uninhibited by the local environment in the adlayer. The blue-shift of the π-π* transition in adlayers of these molecules is in good agreement with theoretical studies of the effect of excitonic coupling between the molecules. In contrast, in azobenzene-containing thiol self-assembled monolayers the fraction of photoswitching molecules and the photoisomerization kinetics are significantly reduced compared to free molecules in solution.Entities:
Year: 2015 PMID: 26134857 DOI: 10.1021/acs.langmuir.5b01645
Source DB: PubMed Journal: Langmuir ISSN: 0743-7463 Impact factor: 3.882