The
photoisomerization
characteristic parameters [photostationary states (PSSs), cross section
σ, and quantum yield η] of indolyl fulgimide compounds
dispersed in solution are quantitatively compared to those of the
same compounds covalently immobilized as a monolayer on functionalized
Si(111) surfaces (see Adv. Mater.
2013,
25, 416). The photoisomerization kinetics of fulgimide
compounds in solution is monitored using UV–vis spectroscopy
and that of monolayers is monitored by in situ calibrated Fourier
transform infrared spectroscopy. Although the isomeric composition
at PSSs is very similar in solution and at surfaces, a strong influence
of the incident light polarization is found on photoisomerization
cross section σ (σs ≪ σp < σsol). Accounting for the local excitation
electromagnetic field indicates that the fulgimide groups adopt a
preferential tilt angle with respect to the surface normal and their
transition dipole is almost parallel to the surface plane for either
C or E/Z isomers. Density functional theory indicates that this orientation
corresponds to photochromic groups that are lying in contact with
the underlying monolayer. This interaction plausibly explains why
the quantum yield of photoisomerization is found nearly twice lower
at the surface than in the solution.