Photoswitchable (pre)catalysts, N,N'-bis-azobenzene-based (NHC)gold(I) and N,N'-bis-azobenzene-derived (NHC)copper(I) complexes are reported. Trans to cis isomerization of the attached photoswitchable moieties in the Au(I) complex enables four-fold decrement in the rate of oxazoline formation reaction. Whereas the progress of the copper(I) catalyzed, azide-alkyne cycloaddition reaction gets reduced by at least threefold.
View Article and Find Full Text PDFAzobenzene-based protonated N-heterocyclic carbenes (NHCs), N,N'-bis(azobenzene)imidazolium chlorides (IAz-X⋅HCl; X=OMe, Br, H) were successfully synthesized and switching abilities of the attached azobenzene units along with the concomitant photoinduced generation of geometric isomers were studied. Upon irradiation with 365 nm UV light, a p-methoxy-azobenzene derivative get transformed from all-trans isomer to nearly all-cis isomer at the photostationary state. The extent of photomodulation of electronic properties in the NHC ring of the p-methoxy-azobenzene derivative is determined through the Tolman Electronic Parameter (TEP).
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