Polarized light-induced anisotropy of 4-dimethylamino-4/-nitroazobenzene (D
MANA; NO2-C6H4-N=N-C6H4-N(CH3)(2)) in PMMA is investigated by polarized spe
ctroscopy and compared with the anisotropy of Disperse Orange 3 (DO3; NO2-C
6H4-N=N-C6H4-NH2) studied previously. The orientation factors evaluated fro
m spectroscopic results show that the trans isomers of DMANA isomerize to c
is forms by motion of the p-NO2-C6H4 group easily compared with motion of t
he p-N(CH3)(2)-C6H4 group. This result is different from the result of DO3
in PMMA where the trans forms tend to isomerize to cis forms by motion of t
he amino group side than that of nitro group side. We consider that this di
fference is due to the volume effect of the substituent at the para positio
n of a phenyl group. This study clearly indicates that the motion of push-p
ull ate-dyes in the isomerization processes strongly depends on the relativ
e volume of the p-substituent. (C) 2000 Elsevier Science S.A. All rights re
served.