Distinction of trans–cis photoisomers with comparable optical properties in multiple-state photochromic systems – examining a molecule with three azobenzenes via in situ irradiation NMR spectroscopy. Issue 84 (5th October 2016)

• Record Type: Journal Article
• Authors: Kind, Jonas; Kaltschnee, Lukas; Leyendecker, Martin; Thiele, Christina M.
• Is Part Of: Chemical communications. Volume 52:Issue 84(2016)
• Page Start: 12506
• Page End: 12509
• Publication Date: 2016-10-05
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1039/c6cc06771a
• Languages: English
• ISSNs: 1359-7345

Abstract

Abstract : In situ irradiation NMR spectroscopy allows for the distinction and quantification of different photoisomers. Abstract : Photochromic compounds like azobenzenes are widely used for the production of stimuli responsive materials. To analyse cascaded azobenzene switching inside a benzene-tricarboxamide (BTA) with three azobenzene moieties in a site-specific fashion, we used in situ irradiation NMR spectroscopy. Four photoisomers can be distinguished by their chemical shifts. Analysis of 1 H, 13 C and 15 N shifts reveals that the configuration of one sidechain has an influence on the chemical shifts of both the other sidechains. Interconversion kinetics upon irradiation with ultraviolet (UV) light as well as molar fractions in photostationary states (PSS) were examined. Analysis of thermal fading of the different photoisomers into the ground state shows that thermal relaxation rates of all three azobenzene moieties behave as if they were independent of each other.