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Our ability to visually perceive our environment is driven by small molecules – retinal – in our eyes. Upon exposure to light retinal undergoes a change in shape which is translated to the very image of this text. Synthetic versions undergoing similar transformations are called photoswitches. These small molecular machines have been used in a range of applications to control by example pharmacological activity, polarity, conductivity and mechanical properties. Over the years several classes of photoswitches have been developed with different photophysical properties. One key design principle which drives photoswitch development is to combine a simple synthetic strategy with visible light response. In 2014 our group has introduced a novel class of photochromic molecules called donor-acceptor Stenhouse adducts (DASA). DASAs combine a number of promising properties such as a straightforward synthesis, visible light response as well as a large molecular shape and polarity change. From 2014 significant effort has been made to understand their switching mechanism and structure-property relationships. Since then their multi-step mechanism has been identified while their donor and acceptor design space has been explored. However, the design space of DASA is limited by the reactivity of both donor and acceptor groups. Furthermore while the multi-step mechanism is understood little efforts have been made to take advantage of the unique and promising characteristics of multiple steps photoswitches.To address some of these problems both the synthetic access to DASA photoswitches as well as the understanding on how structural changes relates to energy landscape have to be improved. If these conditions can be met, DASAs multi-step reaction pathway promises unique photoswitching properties and responses. To widen the synthetic access to DASA we showcase a catalytic method to accelerated the DASA forming reaction and widen the design space of DASA through the use of 1,1,1,3,3,3-hexafluoroisopropanol. By using solvatochromatic shift analysis we were able to link the ground state charge separation of the open form of DASA to the kinetics as well as the effect of concentration and environnment on DASA switching properties. We were able to understand the effect of polarity on the switching pathway and by targeting key barriers in the switching pathway we demonstrate how the same two stimuli can provide a multitude of outcomes in a complex DASA mixture through pathway selectivity. By intercepting intermediates along the reaction pathway we introduced DASA as a negative multi-stage photoswitch. The multi-stage character of the mechanism allows for dual-wavelength control of DASA as well as unique switching properties. To employ the desirable photophysical properties of DASA in applications such as photomechanical work a new chemistry has to developed for main chain incorporation due to DASA susceptibility to nucleophile and radical chemistry. Through Diels–Alder chemistry we demonstrated main chain incorporation of DASA in liquid crystalline networks. Through this work we hope to open the door to widespread use of DASA by realizing the full potential of DASA multi-step switching mechanism in solution as well as in solid materials.

The extracellular matrix (ECM) in which the cells reside provides a dynamic and reversible environment. Spatiotemporal cues are essential when cells are undergoing morphogenesis, repair and differentiation. Emulation of such an intricate system with reversible presentation of nanoscale cues can help us better understand cellular processes and can allow the precise manipulation of cell function in vitro. Herein, we formulated a photoswitchable DNA mechanical nanostructure containing azobenzene moieties and dynamically regulated the spatial distance between adhesion peptides using a photoswitchable DNA polymer with photoirradiation. We found that the DNA polymer reversibly forms two different structures, a relaxed linear and shrunken compact form, observed by AFM. Using the mechanical properties of this DNA polymer, UV and visible light irradiation induced a significant morphology change of the cells between a round shape and spindle shape, thus providing a tool to decipher the language of the ECM better.

Donor–acceptor Stenhouse adducts (DASAs) are visible‐light‐responsive photoswitches with a variety of emerging applications in photoresponsive materials. Their two‐step modular synthesis, centered on the nucleophilic ring opening of an activated furan, makes DASAs readily accessible. However, the use of less reactive donors or acceptors renders the process slow and low yielding, which has limited their development. We demonstrate here that 1,1,1,3,3,3‐hexafluoro‐2‐propanol (HFIP) promotes the ring‐opening reaction and stabilizes the open isomer, allowing greatly reduced reaction times and increased yields for known derivatives. In addition, it provides access to previously unattainable DASA‐based photoswitches and DASA–polymer conjugates. The role of HFIP and the photochromic properties of a set of new DASAs is probed using a combination of 1H NMR and UV/Vis spectroscopy. The use of sterically hindered, electron‐poor amines enabled the dark equilibrium to be decoupled from closed‐isomer half‐lives for the first time., The use of 1,1,1,3,3,3‐hexafluoro‐2‐propanol (HFIP) leads to a streamlined synthetic access to donor–acceptor Stenhouse adduct (DASA) photoswitches through shortened reaction times and increased yields. This approach enables the diversification of DASA structures through the use of previously unreactive donor or acceptor groups, as well as simple access to DASA–polymer conjugates even when using electron‐poor amine donors.

Actin is essential for key processes in all eukaryotic cells. Cellpermeable optojasps provide spatiotemporal control of the actin cytoskeleton, confining toxicity and potentially rendering F‐actin druggable by photopharmacology. Here, we report cryo electron microscopy (cryo‐EM) structures of both isomeric states of one optojasp bound to actin filaments. The high‐resolution structures reveal for the first time the pronounced effects of photoswitching a functionalized azobenzene. By characterizing the optojasp binding site and identifying conformational changes within F‐actin that depend on the optojasp isomeric state, we refine determinants for the design of functional F‐actin photoswitches., Targeting actin requires spatiotemporal control of drug activity. Optojasps are photo‐switchable small molecules, providing direct optical spatiotemporal control of the actin cytoskeleton. We present high‐resolution cryo‐EM structures of both isomeric states of an optojasp bound to F‐actin and describe in detail the binding pocket and conformational changes associated with switching of the azobenzene.

Azobenzene and its derivatives are one of the most widespread molecular scaffolds used in a range of modern applications, as well as in fundamental research. After photoexcitation, azo‐based photoswitches revert back to the most stable isomer on a timescale (t1/2 ) that determines the range of potential applications. Attempts to bring t1/2 to extreme values prompted the development of azobenzene and azoheteroarene derivatives that either rebalance the E‐ and Z‐isomer stabilities, or exploit unconventional thermal isomerization mechanisms. In the former case, one successful strategy has been the creation of macrocycle strain, which tends to impact the E/Z stability asymmetrically, and thus significantly modifyt1/2 . On the bright side, bridged derivatives have shown an improved optical switching owing to the higher quantum yields and absence of degradation. However, in most (if not all) cases, bridged derivatives display a reversed thermal stability (more stable Z‐isomer), and smaller t1/2 than the acyclic counterparts, which restricts their potential interest to applications requiring a fast forward and backwards switch. In this paper, the impact of alkyl bridges on the thermal stability of phenyl‐azoheteroarenes is investigated by using computational methods, and it is revealed that it is indeed possible to combine such improved photoswitching characteristics while preserving the regular thermal stability (more stable E‐isomer), and increased t1/2 values under the appropriate connectivity and bridge length., Taking the strain: The thermal relaxation and photoisomerization of bridged azoheteroarenes based on 3‐pyrazole and 2‐imidazole have been investigated computationally, revealing the impact of the bridge length on the thermal stability, half‐life time, kinetics, and the preferred pathway for this class of molecules.

Developing a novel strategy to synthesize photoresponsive polymers is of significance owing to their potential applications. We report a photoinduced strain‐assisted synthesis of main‐chain stiff‐stilbene polymers by using ring‐opening metathesis polymerization (ROMP), activating a macrocyclic π‐bond connected to a stiff‐stilbene photoswitch through a linker. Since the linker acts as an external constraint, the photoisomerization to the E‐form leads to the stiff‐stilbene being strained and thus reactive to ROMP. The photoisomerization of Z‐form to E‐form was investigated using time‐dependent NMR studies and UV/Vis spectroscopy. The DFT calculation showed that the E‐form was less stable due to a lack of planarity. By the internal strain developed due to the linker constraint through photoisomerization, the E‐form underwent ROMP by a second generation Grubbs catalyst. In contrast, Z‐form did not undergo polymerization under similar conditions. The MALDI‐TOF spectrum of E‐form after polymerization showed the presence of oligomers of >5.2 kDa., A polymer with several photoresponsive units is reported, which is of a great significance owing to the excellent stimuli‐response behavior. A photoinduced strain‐assisted ROMP of a macrocyclic π‐bond connected to a stiff‐stilbene through a linker is described. As the linker acts as an external constraint, photoisomerization to the E‐form causes stiff‐stilbene to be strained and thus to be reactive toward ROMP, resulting in a polymer with multiple stiff‐stilbene units.

A series of substituted azothiophenes was prepared and investigated toward their isomerization behavior. Compared to azobenzene (AB), the presented compounds showed red‐shifted absorption and almost quantitative photoisomerization to their (Z) states. Furthermore, it was found that electron‐withdrawing substitution on the phenyl moiety increases, while electron‐donating substitution decreases the thermal half‐lives of the (Z)‐isomers due to higher or lower stabilization by a lone pair–π interaction. Additionally, computational analysis of the isomerization revealed that a pure singlet state transition state is unlikely in azothiophenes. A pathway via intersystem crossing to a triplet energy surface of lower energy than the singlet surface provided a better fit with experimental data of the (Z)→(E) isomerization. The insights gained in this study provide the necessary guidelines to design effective thiophenylazo‐photoswitches for applications in photopharmacology, material sciences, or solar energy harvesting applications., Switch it up! A series of substituted thiophenylazobenzenes was synthesized. The thermal (Z)→(E) isomerization rates can be tuned by attractive lone pair⋅⋅⋅π interactions, which stabilize the (Z) isomer: Lowering the electron density at the phenyl or increasing the electron density at the thiophenyl moieties increases the half‐lives up to two orders of magnitude. Computations support involvement of a triplet TS in the thermal (E)→(Z) isomerization process.

Arylazopyrazoles are an emerging class of photoswitches with redshifted switching wavelength, high photostationary states, long thermal half‐lives and facile synthetic access. Understanding pathways for a simple modulation of the thermal half‐lives, while keeping other parameters of interest constant, is an important aspect for out‐of‐equilibrium systems design and applications. Here, it is demonstrated that the thermal half‐life of a water‐soluble PEG‐tethered arylazo‐bis(o‐methylated)pyrazole (AAP) can be tuned by more than five orders of magnitude using simple pH adjustment, which is beyond the tunability of azobenzenes. The mechanism of thermal relaxation is investigated by thorough spectroscopic analyses and density functional theory (DFT) calculations. Finally, the concepts of a tunable half‐life are transferred from the molecular scale to the material scale. Based on the photochromic characteristics of E‐ and Z‐AAP, transient information storage is showcased in form of light‐written patterns inside films cast from different pH, which in turn leads to different times of storage. With respect to prospective precisely tunable materials and time‐programmed out‐of‐equilibrium systems, an externally tunable half‐life is likely advantageous over changing the entire system by the replacement of the photoswitch., Arylazopyrazoles are an emerging class of photoswitches with redshifted switching wavelength, high photostationary states, long thermal half‐lives and facile synthetic access. Understanding pathways for a simple modulation of the thermal half‐lives, while keeping other parameters of interest constant, is an important aspect for out‐of‐equilibrium systems design and applications. Here, it is demonstrated that the thermal half‐life of a water‐soluble PEG‐tethered arylazo‐bis(o‐methylated)pyrazole (AAP) can be tuned by more than five orders of magnitude using simple pH adjustment, which is beyond the tunability of azobenzenes.

Chiral supramolecular assemblies are abundant in nature, but controlling the chirality of artificial systems still remains a challenge. In this work, we developed a system where supramolecular chirality can be controlled between chiral and achiral states, namely a chiral “1/0” switch using a flower-like azobenzene compound with a binaphthol core. Upon photoisomerization by ultraviolet irradiation, the terminal alkyl tails envelop the chiral “centre” with a reduction in the dihedral angle of the binaphthol moiety from 76.1° to 61.4°, like “closing petals”. In the doped liquid crystal E7 matrix, this hierarchical conformational transition prevents the transfer of chirality to the host liquid crystal, resulting in a degradation from cholesteric phase (HTP value: 13.84 μm−1) to an achiral nematic phase.

Azobenzenes are photoswitchable molecules capable of generating significant structural changes upon E-to-Z photoisomerization in peptides or small molecules, thereby controlling geometry and functionality. E-to-Z photoisomerization usually is achieved upon irradiation at 350 nm (π–π* transition), while the Z-to-E isomerization proceeds photochemically upon irradiation at >400 nm (n–π* transition) or thermally. Photoswitchable compounds have frequently been employed as modules, e.g., to control protein–DNA interactions. However, their use in conjunction with minor groove-binding imidazole/pyrrole (Im/Py) polyamides is yet unprecedented. Dervan-type Im/Py polyamides were equipped with an azobenzene unit, i.e., 3-(3-(aminomethyl)phenyl)azophenylacetic acid, as the linker between two Im/Py polyamide strands. Only the (Z)-azobenzene-containing polyamides bound to the minor groove of double-stranded DNA hairpins. Photoisomerization was exemplarily evaluated by 1H NMR experiments, while minor groove binding of the (Z)-azobenzene derivatives was proven by CD titration experiments. The resulting induced circular dichroism (ICD) bands of the bound ligands, together with the photometric determination of the dsDNA melting temperature, revealed a significant stabilization of the DNA upon association with the ligand. The (Z)-azobenzene acted as a building block inducing a reverse turn, which favored hydrogen bonds between the pyrrole/imidazole amide and the DNA bases. In contrast, the E-configured polyamides did not induce any ICD characteristic for minor groove binding. The incorporation of the photoswitchable azobenzene unit is a promising strategy to obtain photoswitchable Im/Py hairpin polyamides capable of interacting with the dsDNA minor groove only in the Z-configuration.

Stimuli-responsive mechanical deformations widely occur in biological systems but the design of biomimetic shape-changing materials, especially those based on noncovalent interactions, remains highly challenging. Here, hydrogen-bonded supramolecular microfibers are reported, which can perform light-driven spiral deformation by switching an intrinsic azobenzene unit without monomer dissociation. The key design feature rests on rationally spaced multiple hydrogen bonds, which inhibits the disassembly pathway upon irradiation, allowing partial photomechanical actuation of the azobenzene cores in the confined environment of the assemblies. The light-controlled deformation process of the supramolecular microfibers can be switched in a fully reversible manner. This combination of confinement-inhibited disassembly and photoswitching to induce assembly deformation and actuation along length scales supports a distinctive strategy to design supramolecular materials with photomechanical motion.

Glycerolipids, Sphingolipids, and Sterols are the three major classes of membrane lipids. Both glycerolipids and sphingolipids are comprised of combinations of polar headgroups and fatty acid tails. The fatty acid tail can be chemically modified with an azobenzene photoswitch giving rise to photoswitchable lipids. This approach has yielded a number of photopharmacological tools that allow to control various aspects of lipid assembly, metabolism, and physiology with light.

The photoisomerization behavior of styryl 9M, a common dye used in material sciences, is investigated using tandem ion mobility spectrometry (IMS) coupled with laser spectroscopy. Styryl 9M has two alkene linkages, potentially allowing for four geometric isomers. IMS measurements demonstrate that at least three geometric isomers are generated using electrospray ionization with the most abundant forms assigned to a combination of EE (major) and ZE (minor) geometric isomers, which are difficult to distinguish using IMS as they have similar collision cross sections. Two additional but minor isomers are generated by collisional excitation of the electrosprayed styryl 9M ions and are assigned to the EZ and ZZ geometric isomers, with the latter predicted to have a p-stacked configuration. The isomer assignments are supported through calculations of equilibrium structures, collision cross sections, and statistical isomerization rates. Photoexcitation of selected isomers using an IMS-photo-IMS strategy shows that each geometric isomer photoisomerizes following absorption of near-infrared and visible light, with the EE isomer possessing a S-1

Azoheteroarene photoswitches have attracted attention due to their unique properties. We present the stationary photochromism and ultrafast photoisomerization mechanism of thiophenylazobenzene (TphAB). It demonstrates impressive fatigue resistance and photoisomerization efficiency, and shows favorably separated (E)‐ and (Z)‐isomer absorption bands, allowing for highly selective photoconversion. The (Z)‐isomer of TphAB adopts an unusual orthogonal geometry where the thiophenyl group is perfectly perpendicular to the phenyl group. This geometry is stabilized by a rare lone‐pair⋅⋅⋅π interaction between the S atom and the phenyl group. The photoisomerization of TphAB occurs on the sub‐ps to ps timescale and is governed by this interaction. Therefore, the adoption and disruption of the orthogonal geometry requires significant movement along the inversion reaction coordinates (CNN and NNC angles). Our results establish TphAB as an excellent photoswitch with versatile properties that expand the application possibilities of AB derivatives., My own way: Thiophenylazobenzene is a sulfur‐based azoheteroarene photoswitch with impressive fatigue resistance, photoisomerization efficiency, and highly selective photoconversion. Its (Z)‐isomer adopts an unusual orthogonal geometry stabilized by an intramolecular lone‐pair⋅⋅⋅π interaction governing the ultrafast photoisomerization, which requires a mechanism involving significant movement along the inversion reaction coordinate.

Azoarenes remain privileged photoswitches – molecules that can be interconverted between two states using light – enabling a huge range of light addressable multifunctional systems and materials. Two key innovations to improve the addressability and Z-isomer stability of the azoarenes have been ortho-substitution of the benzene ring(s) or replacement of one of the benzenes for a pyrazole (to give arylazopyrazole switches). Here we study the combination of such high-performance features within a single switch architecture. Through computational analysis and experimental measurements of representative examples, we demonstrate that ortho-benzene substitution of the arylazopyrazoles drastically increases the Z-isomer stability and allows further tuning of their addressability. This includes the discovery of new azopyrazoles with a Z-isomer thermal half-life of ≈46 years. Such results therefore define improved designs for high performance azo switches, which will allow for high precision optically addressable applications using such components.

A new series of [Pd2(L)4] cages based on photochromic dithienylethene (DTE) ligands allowed us to gain insight into the successive photoswitching of multiple DTE moieties in a confined metallo‐supramolecular assembly. Three new X‐ray structures of [Pd2(o‐L4)4], [Pd2(o‐L1)2(c‐L1)2] and [Pd2(c‐L1)4] (o‐L and c‐L = open and closed forms of DTE ligands, respectively) were obtained. The structures deliver snapshots of three different combinations of DTE photoisomeric states within the cage, facilitating a comparison of the all‐open with the all‐closed, and most notably, an intermediate form where open and closed switches co‐exist in the same cage. Moreover, a series of spherical anionic borate clusters was introduced in order to study their roles in the light‐controllable host–guest chemistry. The binding guests show higher affinities with the flexible open cage [Pd2(o‐L1)4] than with the rigid closed cage [Pd2(c‐L1)4]. For the [B12F12]2− guest, thermodynamic data obtained from NMR experiments was compared to results from isothermal titration calorimetry (ITC).

Some molecular photoisomers can be isomerized to a metastable high-energy state by exposure to light. These molecules can then be thermally or catalytically converted back to their initial state, releasing heat in the process. Such a reversible photochemical process has been considered for developing molecular solar thermal (MOST) systems. In this review, we introduce the concept, criteria, and state-of-the-art of MOST systems, with an emphasis on the three most promising molecular systems: norbornadiene/quadricyclane, E/Z-azobenzene, and dihydroazulene/vinylheptafulvene. After discussing the fundamental working principles, we focus on molecular design strategies for improving solar energy storage performance, remaining challenges, and potential focus areas. Finally, we summarize the current molecular incorporation into functional devices and conclude with a perspective on challenges and future directions., Z.W. and K.M.-P. would like to thank the financial support from K. & A. Wallenberg foundation, the Swedish Foundation for Strategic Research, the Swedish research foundation FORMAS, and the European Union’s Horizon 2020 research and innovation program under grant agreement No. 951801. K.M.-P. acknowledges support from the Catalan Institution for Research and Advanced Studies. P.E. thanks the K. & A. Wallenberg foundation (2014.0226) and the Swedish Research Council (2020-04935). T.L. and Z.-Y.Z. thank the financial support from National Key Research and Development Program of China (2017YFA0207500), National Natural Science Foundation of China (22022507, 51973111), and Beijing National Laboratory for Molecular Sciences (BNLMS202004). D.S. thanks the financial support from MINECO/FEDER (CTQ2017-87372-P). O.B., J.L., and H.A.W. thank the Deutsche Forschungsgemeinschaft (DFG, project 392607742, 62201757). Additional support by the DFG is acknowledged through the Research Unit FOR 1878 “funCOS – Functional Molecular Structures on Complex Oxide Surfaces.” J.L. and O.B. acknowledge the cooperation with the groups of Julien Bachmann, Christian Papp, Andreas Hirsch, Andreas Görling, and Hans-Peter Steinrück in the framework of the studies described in this review. M.B.N. thanks the University of Copenhagen for financial support., With funding from the Spanish government through the ‘Severo Ochoa Centre of Excellence’ accreditation (CEX2019-000917-S).

Refereed/Peer-reviewed Local activation of an anti-cancer drug when and where needed can improve selectivity and reduce undesirable side effects. Photoswitchable drugs can be selectively switched between active and inactive states by illumination with light; however, the clinical development of these drugs has been restricted by the difficulty in delivering light deep into tissue where needed. Optical fibres have great potential for light delivery in vivo, but their use in facilitating photoswitching in anti-cancer compounds has not yet been explored. In this paper, a photoswitchable chemotherapeutic is switched using an optical fibre, and the cytotoxicity of each state is measured against HCT-116 colorectal cancer cells. The performance of optical-fibre-enabled photoswitching is characterised through its dose response. The UV–Vis spectra confirm light delivered by an optical fibre effectively enables photoswitching. The activated drug is shown to be twice as effective as the inactive drug incausing cancer cell death, characterised using an MTT assay and fluorescent microscopy. This is the first study in which a photoswitchable anti-cancer compound is switched using an optical fibre and demonstrates the feasibility of using optical fibres to activate photoswitchable drugs for potential future clinical applications.

International audience; The design of photoswitchable transition metal complexes with tailored properties is one of the most important challenges in chemistry.S tudies explaining the underlying mechanismsa re, however,s carce. Herein, the early relaxation dynamics towards NO photoisomerization in trans-[RuCl(NO)(py) 4 ] 2 + is elucidated by meanso fn on-adiabatic dynamics, which provided time-resolved information and branching ratios. Three deactivation mechanisms(I, II, III) in the ratio 3:2:4w ere identified. Pathways Ia nd III involve ul-trafast intersystem crossinga nd internal conversion, whereas pathway II involves only internal conversion.

The photophysical and photochemical properties of sulfoxide and sulfone derivatives of hemithioindigo photoswitches are scrutinized and compared to the unoxidized parent chromophores. Oxidation results in significantly blue‐shifted absorptions and mostly reduction of photochromism while thermal stabilities of individual isomers remain largely unaltered. Effective photoswitching takes place at shorter wavelengths compared to parent hemithioindigos and high isomeric yields can be obtained reversibly in the respective photostationary states. Reversible solid‐state photoswitching is observed for a twisted sulfone derivative accompanied by visible color changes. These results establish oxidized hemithioindigo photoswitches as promising and versatile tools for robust light‐control of molecular behavior for a wide range of applications., Light up your chemistry! A series of sulfur‐oxidized hemithioindigo chromophores are introduced as versatile photoswitch motives for light‐controlled molecular behavior (see figure).

Because isoenzymes of the experimentally and therapeutically extremely relevant sirtuin family show high similarity, addressing the unique selectivity pocket of sirtuin 2 is a promising strategy towards selective inhibitors. An unrelated approach towards selective inhibition of isoenzymes with varied tissue distribution is targeted drug delivery or spatiotemporal activation by photochemical activation. Azologization of two nicotinamide‐mimicking lead structures was undertaken to combine both approaches and yielded a set of 33 azobenzenes and azopyridines that have been evaluated for their photochemical behaviour and bioactivity. For some compounds, inhibitory activity reached the sub‐micromolar range in their thermodynamically favoured E form and could be decreased by photoisomerization to the metastable Z form. Besides, derivatization with long‐chain fatty acids yielded potent sirtuin 2 inhibitors, featuring another intriguing aspect of azo‐based photoswitches. In these compounds, switching to the Z isomer increased aqueous solubility and thereby enhanced biological activity by up to a factor of 21. The biological activity of two compounds was confirmed by hyperacetylation of sirtuin specific histone proteins in a cell‐based activity assay., Switched into action: Besides fine‐tuning molecular geometry for enzyme inhibition, photoinduced isomerization of azopyridine‐based nicotinamide mimics results in improved aqueous solubility, enforcing the effect on target protein sirtuin 2. The resulting Sirt2 inhibitor could be used to study binding events in cellular systems with spatiotemporal control by two independent molecular and supramolecular effects.

Proton‐responsive photochromic molecules are attractive for their ability to react on non‐invasive rapid optical stimuli and the importance of protonation/deprotonation processes in various fields. Conventionally, their acidic/basic sites are on hetero‐atoms, which are orthogonal to the photo‐active π‐center. Here, we incorporate azulene, an acid‐sensitive pure hydrocarbon, into the skeleton of a diarylethene‐type photoswitch. The latter exhibits a novel proton‐gated negative photochromic ring‐closure and its optical response upon protonation in both open and closed forms is much more pronounced than those of diarylethene photoswitches with hetero‐atom based acidic/basic moieties. The unique behavior of the new photoswitch can be attributed to direct protonation on its π‐system, supported by 1H NMR and theoretical calculations. Our results demonstrate the great potential of integrating non‐alternant hydrocarbons into photochromic systems for the development of multi‐responsive molecular switches., Incorporation of an azulene moiety into a diarylethene photoswitch gives rise to unprecedented acid‐dependent negative photochromism. The unusual photochromic behavior can be understood by direct protonation on the photoactive π‐system due to the unique electronic structure of azulene.

It was demonstrated that styrylquinolizinium derivatives may be applied as photoswitchable DNA ligands. At lower ligand:DNA ratios (≤1.5), these compounds bind to duplex DNA by intercalation, with binding constants ranging from Kb = 4.1 × 104 M to 2.6 × 105 M (four examples), as shown by photometric and fluorimetric titrations as well as by CD and LD spectroscopic analyses. Upon irradiation at 450 nm, the methoxy-substituted styrylquinolizinium derivatives form the corresponding syn head-to-tail cyclobutanes in a selective [2 + 2] photocycloaddition, as revealed by X-ray diffraction analysis of the reaction products. These photodimers bind to DNA only weakly by outside-edge association, but they release the intercalating monomers upon irradiation at 315 nm in the presence of DNA. As a result, it is possible to switch between these two ligands and likewise between two different binding modes by irradiation with different excitation wavelengths.

A multiphotochromic hybrid system is presented in which a light-driven overcrowded alkene-based molecular rotary motor is connected to a dithienylethene photoswitch. Ring closing of the dithienylethene moiety, using an irradiation wavelength different from the wavelength applied to operate the molecular motor, results in inhibition of the rotary motion as is demonstrated by detailed 1H-NMR and UV/Vis experiments. For the first time, a light-gated molecular motor is thus obtained. Furthermore, the excitation wavelength of the molecular motor is red-shifted from the UV into the visible-light region upon attachment of the dithienylethene switch.

Donor–acceptor Stenhouse adducts (DASAs) are negative photochromes that switch with visible light and are highly promising for applications ranging from smart materials to biological systems. However, the strong solvent dependence of the photoswitching kinetics limits their application. The nature of the photoswitching mechanism in different solvents is key for addressing the solvatochromism of DASAs, but as yet has remained elusive. Here, we employ spectroscopic analyses and TD‐DFT calculations to reveal changing solvatochromic shifts and energies of the species involved in DASA photoswitching. Time‐resolved visible pump‐probe spectroscopy suggests that the primary photochemical step remains the same, irrespective of the polarity and protic nature of the solvent. Disentangling the different factors determining the solvent‐dependence of DASA photoswitching, presented here, is crucial for the rational development of applications in a wide range of different media.

The spatiotemporal dynamics of proteins and organelles play an important role in controlling diverse cellular processes. Optogenetic tools using photosensitive proteins and chemically induced dimerization (CID), which allow control of protein dimerization, have been used to elucidate the dynamics of biological systems and to dissect the complicated biological regulatory networks. However, the inherent limitations of current optogenetic and CID systems remain a significant challenge for the fine‐tuning of cellular activity at precise times and locations. Herein, we present a novel chemo‐optogenetic approach, photoswitchable chemically induced dimerization (psCID), for controlling cellular function by using blue light in a rapid and reversible manner. Moreover, psCID is tunable; that is, the dimerization and dedimerization degrees can be fine‐tuned by applying different doses of illumination. Using this approach, we control the localization of proteins and positioning of organelles in live cells with high spatial (μm) and temporal (ms) precision.

We report the first cellular application of the emerging near‐quantitative photoswitch pyrrole hemithioindigo, by rationally designing photopharmaceutical PHTub inhibitors of the cytoskeletal protein tubulin. PHTubs allow simultaneous visible‐light imaging and photoswitching in live cells, delivering cell‐precise photomodulation of microtubule dynamics, and photocontrol over cell cycle progression and cell death. This is the first acute use of a hemithioindigo photopharmaceutical for high‐spatiotemporal‐resolution biological control in live cells. It additionally demonstrates the utility of near‐quantitative photoswitches, by enabling a dark‐active design to overcome residual background activity during cellular photopatterning. This work opens up new horizons for high‐precision microtubule research using PHTubs and shows the cellular applicability of pyrrole hemithioindigo as a valuable scaffold for photocontrol of a range of other biological targets., Pyrrole hemithioindigos can be near‐quantitatively photoisomerised by the laser wavelengths available on confocal microscopes. The first pyrrole hemithioindigo‐based photopharmaceuticals, PHTubs, which are photoswitchable tubulin inhibitors, have been developed. PHTubs optically inhibit microtubule dynamics in live cells with single‐cell, second‐scale spatiotemporal precision, with both lit‐active and dark‐active compounds demonstrated in action.

Donor-acceptor Stenhouse adducts (DASAs) are negative photochromes that hold great promise for a variety of applications. Key to optimizing their switching properties is a detailed understanding of the photoswitching mechanism, which, as yet, is absent. Here we characterize the actinic step of DASA-photoswitching and its key intermediate, which was studied using a combination of ultrafast visible and IR pump-probe spectroscopies and TD-DFT calculations. Comparison of the time-resolved IR spectra with DFT computations allowed to unambiguously identify the structure of the intermediate, confirming that light absorption induces a sequential reaction path in which a Z-E photoisomerization of C2-C3 is followed by a rotation around C3-C4 and a subsequent thermal cyclization step. First and second-generation DASAs share a common photoisomerization mechanism in chlorinated solvents with notable differences in kinetics and lifetimes of the excited states. The photogenerated intermediate of the second-generation DASA was photo-accumulated at low temperature and probed with time-resolved spectroscopy, demonstrating the photoreversibility of the isomerization process. Taken together, these results provide a detailed picture of the DASA isomerization pathway on a molecular level.

[Image: see text] Switches that can be actively steered by external stimuli along multiple pathways at the molecular level are the basis for next-generation responsive material systems. The operation of commonly employed molecular photoswitches revolves around one key structural coordinate. Photoswitches with functionalities that depend on and can be addressed along multiple coordinates would offer novel means to tailor and control their behavior and performance. The recently developed donor–acceptor Stenhouse adducts (DASAs) are versatile switches suitable for such applications. Their photochemistry is well understood, but is only responsible for part of their overall photoswitching mechanism. The remaining thermal switching pathways are to date unknown. Here, rapid-scan infrared absorption spectroscopy is used to obtain transient fingerprints of reactions occurring on the ground state potential energy surface after reaching structures generated through light absorption. The spectroscopic data are interpreted in terms of structural transformations using kinetic modeling and quantum chemical calculations. Through this combined experimental–theoretical approach, we are able to unravel the complexity of the multidimensional ground-state potential energy surface explored by the photoswitch and use this knowledge to predict, and subsequently confirm, how DASA switches can be guided along this potential energy surface. These results break new ground for developing user-geared DASA switches but also shed light on the development of novel photoswitches in general.

Arylazopyrazoles show significant potential as next‐generation photoswitches, in particular because of the high thermal stability of their Z‐isomers. Herein we investigate the potential to perform Z−E isomer chemical switching of arylazopyrazoles using acid. We show that acid‐accelerated isomerisation allows for robust Z−E switching using mild acids and opens up the possibility to use light‐acid cycles to near quantitatively and reversibly switch the arylazopyrazoles at room temperature. We attribute the chemical switching to azonium formation, facilitated by mesomeric stabilisation by the pyrazole ring. Coupled with their exceptionally long Z‐isomer half‐lives, we believe our study may open up a wider array of functional opportunities for the arylazopyrazoles.

The aromatic core of an overcrowded alkene-based molecular motor is extended with the goal of inducing isomerization with visible light instead of harmful UV light. In our design, the common naphthalene moiety in the upper half of the motor is changed to pyrene. The photochemical and thermal isomerization processes are studied in detail using DFT calculations as well as NMR and UV/VIS spectroscopy. Our studies confirm that extension of the pi-system of the upper half successfully leads to a shift of the excitation wavelength into the visible region, while retaining proper rotary function.

In the last decade, innovative therapeutic strategies against inherited retinal degenerations (IRDs) have emerged. In particular, chemical- and opto-genetics approaches or a combination of them have been identified for modulating neuronal/optical activity in order to restore vision in blinding diseases. The ‘chemical-genetics approach’ (optopharmacology) uses small molecules (exogenous photoswitches) for restoring light sensitivity by activating ion channels. The ‘opto-genetics approach’ employs light-activated photosensitive proteins (exogenous opsins), introduced by viral vectors in injured tissues, to restore light response. These approaches offer control of neuronal activities with spatial precision and limited invasiveness, although with some drawbacks. Currently, a combined therapeutic strategy (optogenetic pharmacology) is emerging. This review describes the state of the art and provides an overview of the future perspectives in vision restoration.

Switching systems operating in a cooperative manner capable of converting light energy into mechanical motion are of great interest for optical devices, data storage, nanoscale energy converters and molecular sensing. Herein, photoswitchable monolayers were formed at the air-water interface from either a pure bis(thiaxanthylidene)-based photoswitchable amphiphile or from a mixture of the photoswitchable amphiphile with a conventional lipid dipalmitoyl-phosphatidylcholine (DPPC). Efficient photoisomerization of the anti-folded to syn-folded geometry of the amphiphile's central core induces changes in the surface pressure in either direction, depending on the initial molecular density. Additionally, the switching behavior can be regulated in the presence of DPPC, which influences the packing of the molecules, thereby controlling the transformation upon irradiation. Bis(thiaxanthylidene)-based photoswitchable monolayers provide a promising system to explore cooperativity and amplification of motion.

A straightforward synthesis of azobenzenes with bathochromically-shifted absorption bands is presented. It employs an ortho-lithiation of aromatic substrates, followed by a coupling reaction with aryldiazonium salts. The products are obtained with good to excellent yields after simple purification. Moreover, with the presented methodology, a structurally diverse panel of different azobenzenes, including unsymmetric tetra-ortho-substituted ones, can be readily obtained, which paves the way for future development of red-light-addressable azobenzene derivatives for in vivo application.

Electronic structure calculations and nonadiabatic dynamics simulations (more than 2000 trajectories) are used to explore the Z–E photoisomerization mechanism and excited‐state decay dynamics of two arylazopyrazole photoswitches. Two chiral S1/S0 conical intersections with associated enantiomeric S1 relaxation paths that are barrierless and efficient (timescale of ca. 50 fs) were found. For the parent arylazopyrazole (Z8) both paths contribute evenly to the S1 excited‐state decay, whereas for the dimethyl derivative (Z11) each of the two chiral cis minima decays almost exclusively through one specific enantiomeric S1 relaxation path. To our knowledge, the Z11 arylazopyrazole is thus the first example for nearly stereospecific unidirectional excited‐state relaxation.

Control over main-chain motion of chiral π-conjugated polymers can lead to unexpected new functionalities. Here, it is shown that by combining photoswitchable azobenzene units in conjugation with chiral fluorene comonomers and appropriate plasticizers, the polymer organization and chiroptical properties of these alternating copolymers steered by light and its state of polarization can be dynamically controlled. The configuration of the stereogenic centers in the side chains of the fluorene units determines the handedness of the cholesteric organization in thermally annealed films, indicating cooperative behavior. The polymer alignment and helicity of the supramolecular arrangement can be switched by irradiating with linearly and circularly polarized light, respectively. Intriguingly, when switching the handedness of thermally induced cholesteric organizations by illuminating with circularly polarized light that is opposite to the handedness of the cholesteric phases, a nematic-like intermediate state is observed during helix interconversion. By the sequence of irradiation with left and right circularly polarized light followed by thermal annealing, an asymmetric motion, reminiscent of that seen in molecular motors is observed. These findings suggest that functional conjugated polymers can exhibit emergent properties at mesoscopic scale.

Development of powerful fluorescence imaging probes and techniques sets the basis for the spatiotemporal tracking of cells at different physiological and pathological stages. While current imaging approaches rely on passive probe–analyte interactions, here we develop photochromic fluorescent glycoprobes capable of remote light-controlled intracellular target recognition. Conjugation between a fluorophore and spiropyran produces the photochromic probe, which is subsequently equipped with a glycoligand “antenna” to actively localize a target cell expressing a selective receptor. We demonstrate that the amphiphilic glycoprobes that form micelles in water can selectively enter the target cell to operate photochromic cycling as controlled by alternate UV/Vis irradiations. We further show that remote light conversion of the photochromic probe from one isomeric state to the other activates its reactivity toward a target intracellular analyte, producing locked fluorescence that is no longer photoisomerizable. We envision that this research may spur the use of photochromism for the development of bioimaging probes., Fluorescence sensing in biological environments is prone to background signal interference. Here the authors design a photochromic fluorescent glycoprobe for light-controlled photo-switchable cell imaging and photo-activated target recognition, resulting in an increased sensing precision.

International audience; Vinylidene-naphthofurans are a new class of photochromic molecules, easily synthetized, with a unique structure combining an allene group linked to a dihydrofuran ring. These uncoloured molecules show acidochromism in solution and photochromic properties when adsorbed in silica gel or dissolved in acidified alcoholic solutions but not in common solvents or in the solid state. A mechanism for their thermally reversible photochromic behaviour is proposed based on NMR analysis of UV-irradiated CH3OD + THF-d8 acidified solutions: the UV light promotes the addition of methanol to the naphthofuran affording a set of non-coloured photoproducts which evolve towards a non-coloured compound P2. In the presence of acid, the later is quickly converted into a cationic violet dye that returns thermally to the initial closed naphthofuran in the dark. This photochromic system switches between the uncoloured and violet state after UV or sunlight exposure (15 s) and returns thermally to the initial uncoloured state in 2–8 min, in the dark, at room temperature.

Two amidine-substituted spiropyran derivatives have been characterized with respect to the DNA-binding properties over a broad pH interval. The two derivatives differ in the number of positive charges. By varying the pH, the protonation state of the derivatives is also changed, allowing for additional variations in the charge distribution. We show that the closed spiro isomer does not bind for either of the two derivatives, whereas the open merocyanine forms bind both in the protonated and in the nonprotonated state, but with dramatically different binding constants. Flow-oriented linear dichroism (LD) measurements also show that there are differences in the binding modes between the various forms. We rationalize these differences in terms of structure and charge distribution.

Azobenzenes have been used as photoresponsive units for the control of numerous biological processes. Primary prerequisites for such applications are site-selective incorporation of photoswitchable units into biomolecules and the possibility of using non-destructive and deep-tissue-penetrating visible light for the photoisomerization. Here we report a push-pull azobenzene that readily undergoes a Staudinger-Bertozzi ligation with azide groups, that can be addressed with visible light (>440nm) and exhibits the solvato- and acidochromism typical for push-pull systems. The thermal relaxation in aqueous environment proceeds on the low-millisecond timescale, thus enabling control over biological processes on similar timescales. The approach is demonstrated in the modification of a quartz surface and in the incorporation of an azobenzene unit into a functional peptide, the third zinc finger in the mammalian factor Sp1.

2,2'-Dihydroxyazobenzene (DAB), 2,2'-azotoluene (AT) and azobenzene (AB) were isolated in argon and xenon matrices and their molecular structures and photochemical transformations were characterized by infrared spectroscopy and theoretical calculations. All these compounds can adopt the E and Z isomeric forms around the central CNNC moiety, which can be enriched by several conformational and tautomeric modifications for DAB and AT. A number of DAB and AT isomeric forms were identified for the first time. For DAB, the E azo-enol isomer with two intramolecular six-membered quasi-rings formed via OH . . . N hydrogen bonds was found after deposition. Irradiation with UV light generated a different E azo-enol form with two intramolecular H-bonded five- membered quasi-rings. Phototransformation was shown to be reversible and the forms could be interconverted by irradiation at different wavelengths. The isomerization between these two forms constitutes a direct experimental observation of an E -> E isomerization in azobenzene-type molecules. Further irradiation generated a form(s) bearing both OH and NH groups. For AT, two E isomers with the CH3 groups forming five- membered and five/ six-membered quasi-rings with the azo group were observed in the as-deposited matrices. Irradiation of AT with UV light generated a Z form that can be converted back to the E form at different irradiation wavelengths. E-AB was deposited in a xenon matrix and both E -> Z and Z -> E phototransformations were observed (contrary to what was previously reported in an argon matrix where only the Z -> E conversion occurred). AB photoisomerization becomes more pronounced at elevated temperatures, thus indicating that the matrix effects responsible for hindering the AB photoisomerization are essentially due to steric restrictions. The different photoisomerization channels observed for these compounds are discussed in terms of a small-amplitude pedal motion.

International audience; In neurons, ligand-gated ion channels decode the chemical signal of neurotransmitters into an electric response, resulting in a transient excitation or inhibition. Neurotransmitters act on multiple receptor types and subtypes, with spatially and temporally precise patterns. Hence, understanding the neural function of a given receptor requires methods for its targeted, rapid activation/inactivation in defined brain regions. To address this, we have developed a versatile optochemical genetic strategy, which allows the reversible control of defined receptor subtypes in designated cell types, with millisecond and micrometer precision. In this chapter, we describe the engineering of light-activated and -inhibited neuronal nicotinic acetylcholine receptors, as well as their characterization and use in cultured cells.