Reversible photoisomerization of an azobenzene-functionalized self-assembled monolayer probed by sum-frequency generation vibrational spectroscopy

Literature Information

Publication Date 2009-05-20
DOI 10.1039/B823330F
Impact Factor 3.676
Authors

Steffen Wagner, Felix Leyssner, Christian Kördel, Sebastian Zarwell, Roland Schmidt, Karola Rück-Braun, Petra Tegeder


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Abstract

Sum-frequency generation (SFG) vibrational spectroscopy is employed to investigate the reversible, photoinduced trans/cis isomerization of an azobenzene-functionalized self-assembled monolayer (SAM) on a gold substrate. A CN marker group at the outer phenyl ring is used as a direct measure of the switching state. The azobenzene unit is connected to the surface by a tripodal linker system with an adamantane core, which results in both a sufficient decoupling of the functional azobenzene unit from the metallic substrate and a free volume to prevent steric hindrance, thus allowing the isomerization process. Optical excitation at 405 nm induces the trans→cis isomerization, whereas light exposure at 470 nm leads to the back reaction. The effective cross sections for the reactions are σeff(cis) = 4 ± 1 × 10−18 cm2 at 405 nm (trans→cis) and σeff(trans) = 2.5 ± 0.9 × 10−19 cm2 at 470 nm (cis→trans). We propose that the photoisomerization is driven by a direct (intramolecular) electronic excitation of the azobenzene conjugate, analogous to the free molecules in solution.

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Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
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