Influence of End Groups on the Stimulus-Responsive Behavior of Poly[oligo(ethylene glycol) methacrylate] in Water

The influence of the chemical structure of both end groups onto the lower critical solution temperature (LCST) of poly[oligo(ethylene glycol) monomethyl ether methacrylate] (POEGMA) in water was systematically investigated. POEGMA of Mn = 3550 g/mol and Mw/Mn = 1.14 prepared by reversible addition-fragmentation chain transfer (RAFT) polymerization was equipped with two different functional end groups in a one-step postpolymerization reaction combining activated esters, functional amines, and functional methane thiosulfonates. As end groups, n-propyl, n-hexadecyl, di(n-octadecyl), poly(ethylene glycol)-550 (PEG), 1H,1H-perfluorononyl, azobenzene, and trimethylethylammonium groups were system…

Preparation of actuating fibres of oriented main-chain liquid crystalline elastomers by a wetspinning process

We present a versatile method to prepare oriented fibres with a defined thickness from main-chain liquid crystalline elastomers. A microfluidic setup is utilized to inject a solution of a photocrosslinkable smectic A main-chain polymer into a co-flowing stream of silicone oil. Diffusion of the solvent into the oil yields solid polymer filaments that are crosslinked in a continuous way by UV-irradiation. The obtained fibres are highly oriented and show a reversible and significant contraction during the liquid crystal's phase transition.

Liquid-Crystalline Elastomer Fibers Prepared in a Microfluidic Device

PNIPAM Copolymers Containing Light-Responsive Chromophores: A Method Toward Molecular Logic Gates

A series of thermo-responsive PNIPAM copolymers containing different amounts of fulgimide moieties has been synthesized via a polymer analogous reaction of poly(pentafluorophenyl acrylate). All copolymers were designed to exhibit a lower critical solution temperature (LCST) in water, which was only weakly dependent on the amount of incorporated chromophoric fulgimide groups. The copolymers showed a photocyclization of the fulgimide side groups upon irradiation with UV-light accompanied with a color change. The closed form of the chromophore had a halftime of 136 min for the visible reisomerization and did not affect the LCST of the polymer. This led to the realization of a logic "NOT A" for…

Microactuators from a main-chain liquid crystalline elastomer via thiol–ene “click” chemistry

Recently it has been described that liquid crystalline elastomer (LCE) particles of the side-chain type can be prepared in microfluidic devices. Here we present the preparation of micrometer-sized LCE particles of the main-chain type by thiol–ene chemistry. The LCE particles are UV-crosslinked via thiol–ene click chemistry of the nematic monomer, carrying terminal thiol and ene groups, and non-mesogenic tetrathiol and tetraene crosslinkers. The preparation of the LCE particles with a microfluidic device by a continuous “on the fly” technique allows their fast processing with an irradiation time of less than 2 seconds. The resulting particles undergo a temperature-driven volume change up to …