Photoisomerization Reaction of Unsymmetrical Azobenzene Disulfide Self-Assembled Monolayers: Modification of Azobenzene Dyes to Improve Thermal Endurance for Photoreaction
journal contributionposted on 2003-02-05, 00:00 authored by Kaoru Tamada, Haruhisa Akiyama, Tian-Xin Wei, Seung-Ae Kim
Recently we have developed an unsymmetrical azobenzene disulfide with a short alkyl side chain, 4-hexyl-4‘-(12-(dodecyldithio)-dodecyloxy)azobenzene (C6AzSSC12), aiming of a high efficiency in photoisomerization in SAMs on planar gold surfaces (Tamada, K.; et al. Langmuir 2002, 18, 5239). In this paper, we introduce an additional modification on the molecule to improve the thermal endurance for the photoreaction by attachment of a methyl group to the azobenzene ring, thus avoiding dye aggregation sterically. A “methyl-derivatized” azobenzenethiol (C6Az(Me)SH) SAM revealed a significant improvement in their photoreactivity compared with an unmodified azobenzenethiol (C6AzSH) SAM due to the steric effect of the methyl group. A “methyl-derivatized” unsymmetrical azobenzene disulfide (C6Az(Me)SSC12) SAM exhibited quite a similar photoresponse to that of C6AzSSC12 SAM before heat treatment owing to the free volume given by the unsymmetrical structure; however, only the C6Az(Me)SSC12 SAM could retain high photoreactivity in phase-segregated domains formed by annealing, unlike the C6AzSSC12 SAM. The C6Az(Me)SH and C6Az(Me)SSC12 SAMs exhibited a reaction kinetics different from that of C6AzSSC12 SAM due to a different quantum yield and the molecular tilt angle of the azobenzene unit. The C6Az(Me)SH SAM exhibited a typical character of “congested surface”, where the reaction rate from cis to trans was faster, while that from trans to cis was slower compared with those of C6Az(Me)SSC12 SAM.