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Dynamic photopolymer networks that take advantage of the thermodynamically controlled reversibility of thiol–succinic anhydride adducts were synthesized from commercial substrates and investigated as a new class of covalent adaptable networks (CANs). Through systematic studies of the catalyst and stoichiometry effects on the exchange dynamics two distinctive exchange mechanisms were found, and then demonstrated to contribute to the overall dynamic characteristics. By varying the catalyst activity, i.e. basicity and/or nucleophilicity, control over the dynamic responsiveness through changes in the type of dynamic covalent chemistry mode (reversible addition vs. reversible exchange) was achieved in otherwise compositionally analogous materials. More specifically, the participation of the associative mechanism (thiol–thioester exchange) in the otherwise dissociative networks, and its relevance on materials properties was demonstrated by dielectric analysis (DEA) and dynamic mechanical analysis (DMA). The activation energies ( E a ) for viscous flow obtained from DMA stress relaxation experiments and from dielectric modulus and loss crossover points were shown to match well between the two techniques. The E a in stoichiometric systems was found to be 110–120 kJ mol −1 , whereas 50% excess thiol systems were characterized by E a ranging 95–105 kJ mol −1 . The thermodynamic equilibrium conversion, estimated in the temperature controlled FTIR, for a stoichiometric 3-mercaptopropionate-succinic anhydride combination was determined at 92 ± 1% at ambient temperature, and decreased to 67 ± 1% at 120 °C within one hour of equilibration time (Δ H ° = −46 ± 5 kJ mol −1 ). Such high potential for reversibility of the thioester anhydride linkages resembles maleimide-furan Diels–Alder networks but has many other attributes that make these CANs of unprecedented value in fundamental research on dynamic materials. 

Abstract An athermal approach to mRNA enrichment from total RNA using a self‐immolative thioester linked nucleic acids (TENA) is described. Oligo(thymine) (oT) TENA has a six‐atom spacing between bases which allowed TENA to selectively base‐pair with polyadenine RNA. As a result of the neutral backbone of TENA and the hydrophobicity of the octanethiol end group, oT TENA is water insoluble and efficiently pulled down 93±2 % of EGFP mRNA at a concentration of 10 ng μL⁻¹. Self‐immolative degradation of TENA upon ambient temperature exposure to nucleophilic buffer components (Tris, DTT) allowed recovery of 55±27 ng of mRNA from 3.1 μg of total RNA, which was not statistically different from the amount recovered using Dynabeads® mRNA DIRECT Kit (89±24 ng). Gene expression as measured by RT‐qPCR was comparable for both enrichment methods, suggesting that the mild conditions required for enrichment of mRNA using oT TENA are compatible with RT‐qPCR and other downstream molecular biology applications. 

Abstract Diarylethene‐functionalized liquid‐crystalline elastomers (DAE‐LCEs) containing thiol‐anhydride bonds were prepared and shown to undergo reversible, reprogrammable photoinduced actuation. Upon exposure to UV light, a monodomain DAE‐LCE generated 5.5 % strain. This photogenerated strain was demonstrated to be optically reversible over five cycles of alternating UV/Visible light exposure with minimal photochrome fatigue. The incorporation of thiol‐anhydride dynamic bonds allowed for retention of actuated states. Further, re‐programming of the nematic director was achieved by heating above the temperature for bond exchange to occur (70 °C) yet below the nematic‐to‐isotropic transition temperature (100 °C) such that order was maintained between mesogens. The observed thermal stability of each of the diarylethene isomers of over 72 h allowed for decoupling of photo‐induced processes and polymer network effects, showing that both polymer relaxation and back‐isomerization of the diarylethene contributed to LCE relaxation over a period of 12 hours after actuation unless bond exchange occurred.