A novel rosin-based photoresponsive
anionic amphiphile, sodium N-azophenyl maleopimaric
acid imide carboxylate (AzoMPCOONa),
has been successfully synthesized. Its molecular structure was characterized
by 1H and 13C NMR and mass spectrometry (MS).
The photoisomerization of AzoMPCOONa was evaluated by ultraviolet
(UV)–visible spectrometry and 1H NMR. The structure
of AzoMPCOONa could be converted between the trans and cis isomers
by irradiation with UV/visible light. Importantly, a fascinating photoresponsive
viscoelastic solution was prepared by mixing AzoMPCOONa and cetyltrimethylammonium
bromide (CTAB). The properties of the photoresponsive viscoelastic
solution were further investigated by rheology, circular dichroism
(CD), and cryogenic transmission electron microscopy (cryo-TEM). Initially,
the AzoMPCOONa/CTAB system was a gel-like solution composed of entangled
wormlike micelles possessing the right-handed chiral structure. After
UV irradiation for 10 min, the gel-like solution transformed into
a slightly viscous solution, its zero-shear viscosity dramatically
reduced by 2 orders of magnitude, and the aggregates were converted
into rod-like micelles and spherical micelles. In addition, the right-handed
chiral structure of the aggregates disappeared. These dramatic changes
in the viscosity and the aggregate structure can be attributed to
the photoisomerization of the azobenzene group in AzoMPCOONa, which
led to changes in the molecular geometry and the packing parameter
of the AzoMPCOONa/CTAB system. Interestingly, the right-handed chiral
structure of wormlike micelles also is photoresponsive. The results
reveal the superiority of forest resources for preparing viscoelastic
solutions.