The 'transHcis' reversible photoisomerization process tends to align azobenzene derivatives perpendicular to the polarization direction of the pumping beam. It is shown that in the trans-rcis optical transition the cis state is aligned perpendicular to the pumping light polarization. This is shown f
Langmuir-blodgett films of photochromic polyglutamates, 7. The photomechanical effect in monolayers of polyglutamates with azobenzene moieties in the side chains
✍ Scribed by Henning Menzel
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 700 KB
- Volume
- 195
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
Monolayers of the photochromic hairy‐rod type polymers poly(5‐[2‐[4‐(4‐hexylphenylazo)‐phenoxy]ethyl]‐L‐glutamate) (1) and poly(5‐(2‐[4‐(4‐decyloxyphenylazo)phenoxy]ethyl)‐L‐glutamate) (2) were investigated at the air/water interface. At constant surface pressure the monolayers of the polymers exhibit a reversible expansion upon irradiation with ultraviolet (UV)‐light, due to the photoinduced E‐Z‐isomerization of the azobenzene chromophore and a concomitant restructuring of the monolayer. The area increase is lower than expected from the isotherms of monolayers spread from irradiated and non‐irradiated solutions. This can be attributed to a hindrance of photoisomerization, as proved by UV/Vis spectroscopic investigations. The hindrance of photoisomerization, and the photomechanical effect depend on temperature, surface pressure and the nature of the polymer, which all influence the flexibility of the monolayer. From a comparison of the isomerization rate and the rate of the photomechanical effect a two‐step mechanism for the monolayer restructuring is deduced.
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## Abstract The phase behavior of so called “hairy rod”‐like polymers with mesogenic elements in the side chains was investigated by means of differential scanning calorimetry and X‐ray diffraction and correlated with the properties of their monolayers at the air/water interface. The side chains of