The influence of surface proximity on photoswitching activity of stilbene-functionalized N-heterocyclic carbene monolayers. Issue 51 (7th June 2021)

• Record Type: Journal Article
• Authors: Dery, Shahar; Alshanski, Israel; Mervinetsky, Evgeniy; Feferman, Daniel; Yitzchaik, Shlomo; Hurevich, Mattan; Gross, Elad
• Is Part Of: Chemical communications. Volume 57:Issue 51(2021)
• Page Start: 6233
• Page End: 6236
• Publication Date: 2021-06-07
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1039/d1cc02491d
• Languages: English
• ISSNs: 1359-7345

Abstract

Abstract : Stilbene-functionalized NHC accumulated vertical adsorption geometry on Au film, enabling reversible changes in surface potential following photoisomerization. Stronger interaction with Pt film quenched stilbene-NHC influence on surface potential. Abstract : Self-assembly of photo-responsive molecules is a robust technology for reversibly tuning the properties of functional materials. Herein, we probed the crucial role of surface–adsorbate interactions on the adsorption geometry of stilbene-functionalized N-heterocyclic carbenes (stilbene-NHCs) monolayers and its impact on surface potential. Stilbene-NHCs on Au film accumulated in a vertical orientation that enabled high photoisomerization efficiency and reversible changes in surface potential. Strong metal–adsorbate interactions led to flat-lying adsorption geometry of stilbene-NHCs on Pt film, which quenched the photo-isomerization influence on surface potential. It is identified that photo-induced response can be optimized by positioning the photo-active group in proximity to weakly-interacting surfaces.