Reversibly Softening and Stiffening Organogels Using a Wavelength-Controlled Disulfide-Diselenide Exchange.

Wavelength-dependent light-responsive seleno-sulfide dynamic covalent bonds were used to prepare organogels with reversible changes in stiffness. The disulfide cross-link organogels prepared from norbornene-terminated poly(ethylene glycol) (PEG-diNB) and poly(2-hydroxypropyl methacrylate-stat-mercaptoethyl acrylate) (PEG-diNB-poly(HPMA-stat-MEMA)) polymers underwent exchange reactions with 5,5'-diselenide-bis(2-aminobenzoic acid) upon irradiation with UV light. Following irradiation with visible light, the seleno-sulfide bonds were cleaved, reforming disulfide cross-links and the 5,5'-diselenide-bis(2-aminobenzoic acid). Reduction in G' with disulfide-diselenide exchange was consistent with that observed following a thiol-disulfide exchange reaction. Recovery of G' upon disulfide bond formation was 85-95% of the initial value in the as-prepared gel over five cycles of bond cleaving and reformation. This initial study shows the potential of the wavelength-controlled disulfide-diselenide chemistry to develop light-responsive reversible organogels. These organogels have the potential to be used in functional materials such as polymeric actuators or biomimetic soft robotics.