Abstract

AbstractA series of banana‐shaped monomers containing naphthalene as central units, azobenzene in side arms with terminal alkenes were synthesized and characterized. Polarizing optical microscopy, DSC and X‐ray diffraction measurements reveal that one compound processes a nematic phase while other four compounds exhibit B6 phase. The absorption spectrum of trans‐azobenzene displays high‐intensity π‐π* transition at 365 and low‐intensity n‐π* transition at 450 nm. These molecules exhibit strong photoisomerisation behaviour in solutions in which trans to cis isomerisation takes 55 seconds whereas reverse process takes about 32 hours. Such a long thermal back relaxation is useful for creation of optical image storage devices.

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