| Literature DB >> 30793824 |
Alexander Schlimm1, Roland Löw2, Talina Rusch3, Fynn Röhricht2, Thomas Strunskus4, Tobias Tellkamp2, Frank Sönnichsen2, Uwe Manthe5, Olaf Magnussen3, Felix Tuczek1, Rainer Herges2.
Abstract
We report on a very unusual case of surface catalysis involving azobenzenes in contact with a Au(111) surface. A rate acceleration of the cis-trans isomerization on gold up to a factor of 1300 compared to solution is observed. By using carefully designed molecular frameworks, the electronic coupling to the surface can be systematically tuned. The isomerization kinetics of molecules with very weak coupling to the metal is similar to that found in solution. For their counterparts with strong coupling, the relaxation rate is shown to depend on the spin-density distribution in the triplet states of the molecules. This suggests that an intersystem crossing is involved in the relaxation process. Aside from their impact on catalytic processes, these effects could be used to trigger reactions over long distances.Entities:
Keywords: azobenzene; catalysis; self-assembled monolayers; surface spectroscopy; vibrational spectroscopy
Year: 2019 PMID: 30793824 DOI: 10.1002/anie.201814342
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336