1055422-07-5Relevant academic research and scientific papers
Ultrafast Light-Driven Substrate Expulsion from the Active Site of a Photoswitchable Catalyst
Pescher, Manuel D.,van Wilderen, Luuk J. G. W.,Grützner, Susanne,Slavov, Chavdar,Wachtveitl, Josef,Hecht, Stefan,Bredenbeck, Jens
, p. 12092 - 12096 (2017)
The photoswitchable piperidine general base catalyst is a prototype structure for light control of catalysis. Its azobenzene moiety moves sterically shielding groups to either protect or expose the active site, thereby changing the basicity and hydrogen-bonding affinity of the compound. The reversible switching dynamics of the catalyst is probed in the infrared spectral range by monitoring hydrogen bond (HB) formation between its active site and methanol (MeOH) as HB donor. Steady-state infrared (IR) and ultrafast IR and UV/Vis spectroscopies are used to uncover ultrafast expulsion of MeOH from the active site within a few picoseconds. Thus, the force generated by the azobenzene moiety even in the final phase of its isomerization is sufficient to break a strong HB within 3 ps and to shut down access to the active site.
Photoswitchable catalysts: Correlating structure and conformational dynamics with reactivity by a combined Experimental and computational approach
Stoll, Ragnar S.,Peters, Maike V.,Kuhn, Andreas,Hecht, Stefan,Heiles, Sven,Thiele, Christina M.,Goddard, Richard,Buehl, Michael
supporting information; experimental part, p. 357 - 367 (2009/06/18)
Photocontrol of a piperidine's Bronsted basicity was achieved by incorporation of a bulky azobenzene group and could be translated into pronounced reactivity differences between ON- and OFF- states in general base catalysis. This enabled successful photomodulation of the catalyst's activity in the nitroaldol reaction (Henry reaction). A modular synthetic route to the photoswitchable catalysts was developed and allowed for preparation and characterization of three azobenzene-derived bases as well as one stilbene-derived base. Solid-state structures obtained by X-ray crystal structure analysis confirmed efficient blocking of the active site in the E isomer representing the OFF-states, whereas a freely accessible active site was revealed for a representative Z isomer in the crystal. To correlate structure with reactivity of the catalysts, conformational dynamics were thoroughly studied in solution by NMR spectroscopy, taking advantage of residual dipolar couplings (RDCs), in combination with comprehensive DFT computational investigations of conformations and proton affinities.
Photoswitching of basicity
Peters, Maike V.,Stoll, Ragnar S.,Kuehn, Andreas,Hecht, Stefan
supporting information; experimental part, p. 5968 - 5972 (2009/03/11)
(Figure Presented) Smart bases: By using a photochromic azobenzene-derived blocking group, a piperidine base can be switched between a sterically shielded, inactive form and an accessible, reactive form (see picture; C dark gray, H light gray, O red, N blue). Thus, light can be used for the reversible external modulation of ground-state basicity and hence activity in general base catalysis.
