Photomechanical molecular crystals have been investigated as mesoscopic photoactuators. Here, we report how the photomechanical twisting of 1,2-bis(2-methyl-5-phenyl-3-thienyl)perfluorocyclopentene (1a) crystals depends on illumination direction. The ribbon-like crystal of 1a could be successfully prepared by a sublimation method. The ribbon crystal exhibited reversible photomechanical crystal twisting upon alternating irradiation with ultraviolet (UV) and visible light. Moreover, changing the UV illumination direction with respect to the crystal resulted in different twisting modes, ranging from helicoid to cylindrical. Control of photomechanical crystal deformation by illumination direction provides a convenient and useful way to generate a variety of photomechanical motions from a single crystal.

Molecular crystals have shown remarkable adaptability in response to a range of external stimuli. Here, we survey this emerging field and provide a critical overview of the experimental, computational and instrumental tools being used to design and apply such materials.

In order to develop an improved description of the photomechanical response of 9-methylanthracene (9MA) microcrystals, a detailed study of its solid-state photochemical reaction kinetics is performed. The reaction progress is monitored through the decrease in absorption of an optically microcrystalline thin film. The evolution of the time-dependent photoluminescence during the reaction is also measured. Both the photochemical reaction and nonradiative relaxation rates increase as more photoproduct is formed. In order to analyze the data, an extended version of the Finke-Watzky kinetic model for photochemical reactions is derived, denoted the FW-P model. This extended version enables a systematic analysis of photochemical reaction kinetics in solid-state molecular systems at varying levels of approximation. The FW-P model describes the non-exponential decrease in reactant and also correctly predicts the magnitude of the observed decrease in photoluminescence lifetime over the course of the reaction. The lifetime analysis is complicated by the fact that the microcrystalline 9MA sample contains multiple emitting species, and the extended FW-P model fails to capture the exact dependence of the photoluminescence on product formation. Analysis of the 9MA data indicates that both the photodimerization and the nonradiative relaxation rates can be accelerated by a factor of 10 over the course of the reaction. The results in this paper demonstrate that autocatalytic photodimerization kinetics are present in crystalline 9MA and may influence its photomechanical response.

When photochromic molecules are organized in a crystal, the small-scale forces generated by molecular photoisomerization events can combine together to generate work on micro- or macroscopic length scales. In this work, photomechanical nanocrystals themselves are organized on macroscopic length scales using a porous inorganic template. The organic diarylethene component provides the reversible photoresponse, whereas the porous alumina component provides structural support and directionality. This hybrid organic–inorganic photomechanical material acts as a bending actuator. Using ultraviolet and visible photons as power inputs, as little as 0.1 mg of reacted material generates enough force to tilt a 1.28 g mirror and steer a laser beam. The motion can be cycled multiple times in air and under water. Actuator figures-of-merit such as energy-to-work conversion efficiency and stiffness are probably limited by the high elastic modulus of the inorganic template, providing an obvious pathway for optimization.

The isomerization rates of a photochromic donor–acceptor Stenhouse adduct depend on concentration. The net photoisomerization rate decreases with increasing concentration in liquids and polymers.

Four fluorinated derivatives of 9-anthracene carboxylic acid (9AC), a molecule that shows a reversible photomechanical response in its crystal form, have been synthesized and characterized. The spectroscopic properties and crystal structures of 4-fluoro-9-anthracene carboxylic acid (4F-9AC), 2-fluoro-9-anthracene carboxylic acid (2F-9AC), 10-fluoro-9-anthracene carboxylic acid (10F-9AC), and 2,6-difluoro-9-anthracene carboxylic acid (2,6DF-9AC) are all very similar to those of 9AC. However, their photomechanical properties vary widely. 405 nm light was used to induce [4 + 4] photodimerization and a mechanical response in crystalline microneedles and ribbons. Both the photodimer dissociation rate and the mechanical recovery varied by more than an order of magnitude, with 4F-9AC exhibiting the most rapid recovery time, on the order of 30 s. Nanoindentation measurements show that this crystal has a slightly reduced elastic modulus and a significantly reduced hardness, making it less brittle than the 9AC crystal. Large 4F-9AC crystals remain intact after irradiation, without fragmenting, while microneedles can undergo more than 100 mechanical bending cycles. Given the similarity of the crystal packing in all five molecules, the improved photomechanical properties must arise from subtle changes in intermolecular interactions or possibly differences in disorder. These results demonstrate that it is possible to significantly improve the properties of photomechanical materials through small modifications of the molecular structure.

Photoisomerization of cis-dimethyl-2(3-(anthracen-9-yl)allylidene)malonate in a block-shaped microcrystal initiates a phase separation and delamination of the reacted layer from parent crystal.

This paper explores whether the photochromic reaction of a molecule embedded in a polymer film can affect its surface adhesion properties, as measured by shear strength and delamination in water. The adherence of polystyrene (PS) to glass was chosen as a model system. Two commercially available photochromesa spiropyran derivative 1′,3′-dihydro-1′,3′,3′-trimethyl-6-nitrospiro[2H-1-benzopyran-2,2′-(2H)-indole]) (SP) and a diarylethene derivative 1,2-bis(2,4-dimethyl-5-phenyl-3-thienyl)-3,3,4,4,5,5hexafluoro-1-cyclopentene (DAE)are studied in detail. Both photochromic reactions can significantly enhance the adhesion of PS to a glass surface. The most dramatic results were obtained for PS/SP films, whose shear strength increased by a factor of 7 while the delamination rate was suppressed by at least 2 orders of magnitude after exposure to UV light. The enhanced polymer adhesion could only be partially reversed, even after extended exposure to visible light completely regenerated the UV-absorbing isomer. Nanoindentation and heating experiments suggest that the limited reversibility results from changes in polymer internal structure. We hypothesize that the adhesion changes arise from localized polymer and molecular motions that eliminate void spaces and surface gaps at the polymer−glass interface. The results show that adhesive forces between a prototypical polymer and an inorganic substrate can be modulated by photochromic reactions of embedded molecules.