Visible‐ and Near‐Infrared Light‐Driven Molecular Photoswitches for Biological Applications

Diarylethenes for Memories and Switches

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Photothermal therapy and photoacoustic imaging via nanotheranostics in fighting cancer

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Photochromism of Diarylethene Molecules and Crystals: Memories, Switches, and Actuators

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Spiropyran-based dynamic materials

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Azobenzene photoswitches for biomolecules

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Recent Strategies to Develop Innovative Photosensitizers for Enhanced Photodynamic Therapy

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Smart micro/nanoparticles in stimulus-responsive drug/gene delivery systems

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Reversible Photocontrol of Biological Systems by the Incorporation of Molecular Photoswitches

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Linear and Nonlinear Optical Properties of Photochromic Molecules and Materials

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Light‐Controlled Tools

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In Vivo Photopharmacology

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Light-Driven Liquid Crystalline Materials: From Photo-Induced Phase Transitions and Property Modulations to Applications

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Fulgides for Memories and Switches

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Liquid Crystals: Versatile Self-Organized Smart Soft Materials

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The evolution of spiropyran: fundamentals and progress of an extraordinarily versatile photochrome

Kortekaas, L., & Browne, W. R. (2019) · Chemical Society Reviews · doi:10.1039/c9cs00203k · Cited by 782

NIR‐Triggered Anticancer Drug Delivery by Upconverting Nanoparticles with Integrated Azobenzene‐Modified Mesoporous Silica

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A Roadmap to Success in Photopharmacology

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Azobenzene Photoswitching without Ultraviolet Light

Beharry, A. A., Sadovski, O., & Woolley, G. A. (2011) · Journal of the American Chemical Society · doi:10.1021/ja209239m · Cited by 720

Emerging combination strategies with phototherapy in cancer nanomedicine

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Emerging Targets in Photopharmacology

Lerch, M. M., Hansen, M. J., van Dam, G. M., Szymański, W., & Feringa, B. L. (2016) · Angewandte Chemie International Edition · doi:10.1002/anie.201601931 · Cited by 674

Visible-to-NIR-Light Activated Release: From Small Molecules to Nanomaterials

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Heteroaryl azo dyes as molecular photoswitches

Crespi, S., Simeth, N. A., & König, B. (2019) · Nature Reviews Chemistry · doi:10.1038/s41570-019-0074-6 · Cited by 650

Current developments in fluorescent PET (photoinduced electron transfer) sensors and switches

Daly, B., Ling, J., & de Silva, A. P. (2015) · Chemical Society Reviews · doi:10.1039/c4cs00334a · Cited by 633

Three-dimensional control of the helical axis of a chiral nematic liquid crystal by light

Zheng, Z., Li, Y., Bisoyi, H. K., Wang, L., Bunning, T. J., & Li, Q. (2016) · Nature · doi:10.1038/nature17141 · Cited by 569

Photoswitching Using Visible Light: A New Class of Organic Photochromic Molecules

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LAF1 ubiquitination by COP1 controls photomorphogenesis and is stimulated by SPA1

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Tunable Heptamethine–Azo Dye Conjugate as an NIR Fluorescent Probe for the Selective Detection of Mitochondrial Glutathione over Cysteine and Homocysteine

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Molecular photoswitches in aqueous environments

Volarić, J., Szymański, W., Simeth, N. A., & Feringa, B. L. (2021) · Chemical Society Reviews · doi:10.1039/d0cs00547a · Cited by 452

Light-Directing Chiral Liquid Crystal Nanostructures: From 1D to 3D

Bisoyi, H. K., & Li, Q. (2014) · Accounts of Chemical Research · doi:10.1021/ar500249k · Cited by 445

Photoswitchable Inhibitors of Microtubule Dynamics Optically Control Mitosis and Cell Death

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Photochromism into nanosystems: towards lighting up the future nanoworld.

Wang, L., & Li, Q. (2018) · Chemical Society Reviews · doi:10.1039/c7cs00630f · Cited by 407

Development of fluorescent probes based on protection–deprotection of the key functional groups for biological imaging

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Retinal isomerization in bacteriorhodopsin captured by a femtosecond x-ray laser

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Photochromic and Luminescence Switching Properties of a Versatile Diarylethene-Containing 1,10-Phenanthroline Ligand and Its Rhenium(I) Complex

Yam, V. W., Ko, C., & Zhu, N. (2004) · Journal of the American Chemical Society · doi:10.1021/ja047446q · Cited by 363

On the Promise of Photopharmacology Using Photoswitches: A Medicinal Chemist’s Perspective

Fuchter, M. J. (2020) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.0c00629 · Cited by 353

Photo-triggered full-color circularly polarized luminescence based on photonic capsules for multilevel information encryption

Lin, S., Tang, Y., Kang, W., Bisoyi, H. K., Guo, J., & Li, Q. (2023) · Nature Communications · doi:10.1038/s41467-023-38801-1 · Cited by 349

PHOTACs enable optical control of protein degradation

Reynders, M., Matsuura, B. S., Bérouti, M., Simoneschi, D., Marzio, A., Pagano, M., & Trauner, D. H. (2020) · Science Advances · doi:10.1126/sciadv.aay5064 · Cited by 344

Recent developments in reversible photoregulation of oligonucleotide structure and function

Lubbe, A. S., Szymański, W., & Feringa, B. L. (2017) · Chemical Society Reviews · doi:10.1039/c6cs00461j · Cited by 337

Recent Implementations of Molecular Photoswitches into Smart Materials and Biological Systems

Pianowski, Z. (2019) · Chemistry - A European Journal · doi:10.1002/chem.201805814 · Cited by 336

Recent progress in the development of organic dye based near-infrared fluorescence probes for metal ions

Wu, D., Chen, L., Lee, W., Ko, G., Yin, J., & Yoon, J. (2017) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2017.06.011 · Cited by 335

Indigoid Photoswitches: Visible Light Responsive Molecular Tools

Petermayer, C., & Dube, H. (2018) · Accounts of Chemical Research · doi:10.1021/acs.accounts.7b00638 · Cited by 331

Two-Way Photoswitching Using One Type of Near-Infrared Light, Upconverting Nanoparticles, and Changing Only the Light Intensity

Boyer, J., Carling, C., Gates, B. D., & Branda, N. R. (2010) · Journal of the American Chemical Society · doi:10.1021/ja107184z · Cited by 329

Long-Lived Photoacid Based upon a Photochromic Reaction

Shi, Z., Peng, P., Strohecker, D., & Liao, Y. (2011) · Journal of the American Chemical Society · doi:10.1021/ja203851c · Cited by 327

Photocontrol of Antibacterial Activity: Shifting from UV to Red Light Activation

Wegener, M., Hansen, M. J., Driessen, A. J. M., Szymański, W., & Feringa, B. L. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.7b09281 · Cited by 325

Reversible Spatiotemporal Control of Induced Protein Degradation by Bistable PhotoPROTACs

Pfaff, P., Samarasinghe, K. T. G., Crews, C. M., & Carreira, E. M. (2019) · ACS Central Science · doi:10.1021/acscentsci.9b00713 · Cited by 320

The (photo)chemistry of Stenhouse photoswitches: guiding principles and system design

Lerch, M. M., Szymański, W., & Feringa, B. L. (2018) · Chemical Society Reviews · doi:10.1039/c7cs00772h · Cited by 316

Near Infrared (NIR) absorbing dyes as promising photosensitizer for photo dynamic therapy

Chinna Ayya Swamy, P., Sivaraman, G., Priyanka, R. N., Raja, S. O., Ponnuvel, K., Shanmugpriya, J., & Gulyani, A. (2020) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2020.213233 · Cited by 311

Acylhydrazones as Widely Tunable Photoswitches

van Dijken, D. J., Kovaříček, P., Ihrig, S. P., et al. (2015) · Journal of the American Chemical Society · doi:10.1021/jacs.5b09519 · Cited by 296

Development of Azo‐Based Fluorescent Probes to Detect Different Levels of Hypoxia

Piao, W., Tsuda, S., Tanaka, Y., Maeda, S., Liu, F., Takahashi, S., Kushida, Y., Komatsu, T., Ueno, T., Terai, T., et al. (2013) · Angewandte Chemie International Edition · doi:10.1002/anie.201305784 · Cited by 294

Design and Synthesis of Donor–Acceptor Stenhouse Adducts: A Visible Light Photoswitch Derived from Furfural

Helmy, S., Oh, S., Leibfarth, F. A., Hawker, C. J., & de Alaniz, J. R. (2014) · The Journal of Organic Chemistry · doi:10.1021/jo502206g · Cited by 290

Advances in Application of Azobenzene as a Trigger in Biomedicine: Molecular Design and Spontaneous Assembly

Cheng, H., Zhang, S., Qi, J., Liang, X., & Yoon, J. (2021) · Advanced Materials · doi:10.1002/adma.202007290 · Cited by 286

Tunable Visible and Near Infrared Photoswitches

Hemmer, J. R., Poelma, S. O., Treat, N. J., Page, Z. A., Dolinski, N. D., Diaz, Y. J., Tomlinson, W., Clark, K. D., Hooper, J. P., Hawker, C. J., et al. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.6b07434 · Cited by 281

Rational Design in Photopharmacology with Molecular Photoswitches

Kobauri, P., Dekker, F. J., Szymański, W., & Feringa, B. L. (2023) · Angewandte Chemie International Edition · doi:10.1002/anie.202300681 · Cited by 276

Photoresponsive molecular tools for emerging applications of light in medicine

Welleman, I. M., Hoorens, M. W. H., Feringa, B. L., Boersma, H. H., & Szymański, W. (2020) · Chemical Science · doi:10.1039/d0sc04187d · Cited by 274

Design of Bis-spiropyran Ligands as Dipolar Molecule Receptors and Application to in Vivo Glutathione Fluorescent Probes

Shao, N., Jin, J., Wang, H., et al. (2009) · Journal of the American Chemical Society · doi:10.1021/ja908215t · Cited by 268

Oxygen-Dependent Regulation of Excited-State Deactivation Process of Rational Photosensitizer for Smart Phototherapy

Zhao, X., Long, S., Li, M., Cao, J., Li, Y., Guo, L., Sun, W. C., Du, J., Fan, J., & Peng, X. (2019) · Journal of the American Chemical Society · doi:10.1021/jacs.9b11800 · Cited by 266

Visible Light Switching of a BF 2 -Coordinated Azo Compound

Yang, Y., Hughes, R. P., & Aprahamian, I. (2012) · Journal of the American Chemical Society · doi:10.1021/ja306030d · Cited by 255

Recent advances in diarylethene-based multi-responsive molecular switches

Pu, S., Sun, Q., Fan, C., et al. (2016) · Journal of Materials Chemistry C · doi:10.1039/c6tc00110f · Cited by 249

Fluorescent Photochromic α‐Cyanodiarylethene Molecular Switches: An Emerging and Promising Class of Functional Diarylethene

Lin, S., Gutierrez‐Cuevas, K. G., Zhang, X., Guo, J., & Li, Q. (2020) · Advanced Functional Materials · doi:10.1002/adfm.202007957 · Cited by 249

The Endeavor of Diarylethenes: New Structures, High Performance, and Bright Future

Zhang, J., & Tian, H. (2018) · Advanced Optical Materials · doi:10.1002/adom.201701278 · Cited by 246

Optically Rewritable Transparent Liquid Crystal Displays Enabled by Light‐Driven Chiral Fluorescent Molecular Switches

Li, J., Bisoyi, H. K., Tian, J., Guo, J., & Li, Q. (2019) · Advanced Materials · doi:10.1002/adma.201807751 · Cited by 245

Light controlled protein release from a supramolecular hydrogel

Peng, K., Tomatsu, I., & Kros, A. (2010) · Chemical Communications · doi:10.1039/c002565h · Cited by 244

Hemithioindigo—an emerging photoswitch

Wiedbrauk, S., & Dube, H. (2015) · Tetrahedron Letters · doi:10.1016/j.tetlet.2015.05.022 · Cited by 236

Tumor microenvironment responsive drug delivery systems

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New molecular switch architectures

Harris, J. D., Moran, M. J., & Aprahamian, I. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1714499115 · Cited by 220

Disequilibrating azobenzenes by visible-light sensitization under confinement

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Optical lock-in detection imaging microscopy for contrast-enhanced imaging in living cells

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Amphiphilic Diarylethene as a Photoswitchable Probe for Imaging Living Cells

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Pyroptosis‐Mediated Synergistic Photodynamic and Photothermal Immunotherapy Enabled by a Tumor‐Membrane‐Targeted Photosensitive Dimer

Tang, Y., Bisoyi, H. K., Chen, X., Liu, Z., Chen, X., Zhang, S., & Li, Q. (2023) · Advanced Materials · doi:10.1002/adma.202300232 · Cited by 214

Photoswitchable Molecules in Long-Wavelength Light-Responsive Drug Delivery: From Molecular Design to Applications

Jia, S., Fong, W., Graham, B., & Boyd, B. J. (2018) · Chemistry of Materials · doi:10.1021/acs.chemmater.8b00357 · Cited by 203

Future‐Oriented Advanced Diarylethene Photoswitches: From Molecular Design to Spontaneous Assembly Systems

Cheng, H., Zhang, S., Bai, E.-Y., Cao, X., Wang, J., Qi, J., Liu, J., Zhao, J., Zhang, L., & Yoon, J. (2021) · Advanced Materials · doi:10.1002/adma.202108289 · Cited by 203

Stepping Out of the Blue: From Visible to Near‐IR Triggered Photoswitches

Zhang, Z., Wang, W., O’Hagan, M., Dai, J., Zhang, J., & Tian, H. (2022) · Angewandte Chemie International Edition · doi:10.1002/anie.202205758 · Cited by 203

Microtubule nucleation: beyond the template

Roostalu, J., & Surrey, T. (2017) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2017.75 · Cited by 197

Triplet Pathways in Diarylethene Photochromism: Photophysical and Computational Study of Dyads Containing Ruthenium(II) Polypyridine and 1,2-Bis(2-methylbenzothiophene-3-yl)maleimide Units

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How to switch a fluorophore: from undesired blinking to controlled photoswitching

van de Linde, S., & Sauer, M. (2013) · Chemical Society Reviews · doi:10.1039/c3cs60195a · Cited by 191

Electron-Accepting Micelles Deplete Reduced Nicotinamide Adenine Dinucleotide Phosphate and Impair Two Antioxidant Cascades for Ferroptosis-Induced Tumor Eradication

Guo, X., Liu, F., Deng, J., Dai, P., Qin, Y., Li, Z., Wang, B., Fan, A., Wang, Z., & Zhao, Y. (2020) · ACS Nano · doi:10.1021/acsnano.0c00764 · Cited by 190

Ion Exchange Membranes: Constructing and Tuning Ion Transport Channels

Zuo, P., Xu, Z., Zhu, Q., Ran, J., Ge, L., Ge, X., Wu, L., Yang, Z., & Xu, T. (2022) · Advanced Functional Materials · doi:10.1002/adfm.202207366 · Cited by 188

Switching Diarylethenes Reliably in Both Directions with Visible Light

Fredrich, S., Göstl, R., Herder, M., et al. (2015) · Angewandte Chemie International Edition · doi:10.1002/anie.201509875 · Cited by 186

Let spiropyran help polymers feel force!

Li, M., Zhang, Q., Zhou, Y., et al. (2017) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2017.11.001 · Cited by 185

Supramolecularly Engineered NIR‐II and Upconversion Nanoparticles In Vivo Assembly and Disassembly to Improve Bioimaging

Zhao, M., Li, B., Wang, P., Lu, L., Zhang, Z., Liu, L., Wang, S., Li, D., Wang, R., & Zhang, F. (2018) · Advanced Materials · doi:10.1002/adma.201804982 · Cited by 183

Nitrogen Bridged Diazocines: Photochromes Switching within the Near-Infrared Region with High Quantum Yields in Organic Solvents and in Water

Lentes, P., Stadler, E., Röhricht, F., et al. (2019) · Journal of the American Chemical Society · doi:10.1021/jacs.9b06104 · Cited by 181

Reversible Two-Photon Photoswitching and Two-Photon Imaging of Immunofunctionalized Nanoparticles Targeted to Cancer Cells

Zhu, M., Zhang, G., Li, C., Aldred, M. P., Chang, E., Drezek, R. A., & Li, A. D. Q. (2010) · Journal of the American Chemical Society · doi:10.1021/ja106895k · Cited by 180

Colorimetric and NIR Fluorescence Probe with Multiple Binding Sites for Distinguishing Detection of Cys/Hcy and GSH in Vivo

Xiong, K., Huo, F., Chao, J., Zhang, Y., & Yin, C. (2018) · Analytical Chemistry · doi:10.1021/acs.analchem.8b04485 · Cited by 176

Controlling Dark Equilibria and Enhancing Donor–Acceptor Stenhouse Adduct Photoswitching Properties through Carbon Acid Design

Hemmer, J. R., Page, Z. A., Clark, K. D., et al. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b06067 · Cited by 175

An Efficient Near‐Infrared Emissive Artificial Supramolecular Light‐Harvesting System for Imaging in the Golgi Apparatus

Chen, X., Cao, Q. C., Bisoyi, H. K., et al. (2020) · Angewandte Chemie International Edition · doi:10.1002/anie.202003427 · Cited by 173

Bidirectional Photocontrol of Peptide Conformation with a Bridged Azobenzene Derivative

Samanta, S., Qin, C., Lough, A. J., & Woolley, G. A. (2012) · Angewandte Chemie International Edition · doi:10.1002/anie.201202383 · Cited by 169

Structure Property Analysis of the Solution and Solid-State Properties of Bistable Photochromic Hydrazones

Shao, B., Qian, H., Li, Q., & Aprahamian, I. (2019) · Journal of the American Chemical Society · doi:10.1021/jacs.9b03932 · Cited by 165

Conjugated Polymer Nanoparticles with Appended Photo‐Responsive Units for Controlled Drug Delivery, Release, and Imaging

Senthilkumar, T., Zhou, L., Gu, Q., et al. (2018) · Angewandte Chemie International Edition · doi:10.1002/anie.201807158 · Cited by 161

Photoswitching-Enabled Novel Optical Imaging: Innovative Solutions for Real-World Challenges in Fluorescence Detections

Tian, Z., & Li, A. D. Q. (2012) · Accounts of Chemical Research · doi:10.1021/ar300108d · Cited by 158

Stimuli‐responsive photonic actuators for integrated biomimetic and intelligent systems

Gao, J., Tang, Y., Martella, D., Guo, J., Wiersma, D. S., & Li, Q. (2023) · Responsive materials · doi:10.1002/rpm.20230008 · Cited by 158

Visible light-responsive materials: the (photo)chemistry and applications of donor–acceptor Stenhouse adducts in polymer science

Clerc, M., Sandlass, S., Rifaie‐Graham, O., et al. (2023) · Chemical Society Reviews · doi:10.1039/d3cs00508a · Cited by 157

Coupling Probiotics with 2D CoCuMo‐LDH Nanosheets as a Tumor‐Microenvironment‐Responsive Platform for Precise NIR‐II Photodynamic Therapy

Yang, Y.-S., Hu, T., Bian, Y., Meng, F., Yu, S., Li, H., Zhang, Q., Gu, L., Weng, X., Tan, C., et al. (2023) · Advanced Materials · doi:10.1002/adma.202211205 · Cited by 156

Hemiindigo: Highly Bistable Photoswitching at the Biooptical Window

Petermayer, C., Thumser, S., Kink, F., et al. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.7b07531 · Cited by 155

N , N ′-Disubstituted Indigos as Readily Available Red-Light Photoswitches with Tunable Thermal Half-Lives

Huang, C.-Y. D., Bonasera, A., Hristov, L. V., et al. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.7b08726 · Cited by 155

Photoswitchable diarylethenes: From molecular structures to biological applications

Li, Z., Zeng, X., Gao, C., Song, J., He, F., Tian, H., Guo, H., & Yin, J. (2023) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2023.215451 · Cited by 155

Unraveling Dual Aggregation‐Induced Emission Behavior in Steric‐Hindrance Photochromic System for Super Resolution Imaging

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1,2‐Dithienyldicyanoethene‐Based, Visible‐Light‐Driven, Chiral Fluorescent Molecular Switch: Rewritable Multimodal Photonic Devices

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All-Visible-Light-Activated Dithienylethenes Induced by Intramolecular Proton Transfer

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Red-Light-Responsive Supramolecular Valves for Photocontrolled Drug Release from Mesoporous Nanoparticles

Wang, D., & Wu, S. (2015) · Langmuir · doi:10.1021/acs.langmuir.5b04399 · Cited by 147

Chemo- and biosensing applications of spiropyran and its derivatives - A review

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In vivo metallophilic self-assembly of a light-activated anticancer drug

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Covalent labeling of nucleic acids

Klöcker, N., Weissenboeck, F. P., & Rentmeister, A. (2020) · Chemical Society Reviews · doi:10.1039/d0cs00600a · Cited by 145

Photoresponsive Drug/Gene Delivery Systems

Zhou, Y., Ye, H., Chen, Y., Zhu, R., & Yin, L. (2018) · Biomacromolecules · doi:10.1021/acs.biomac.8b00422 · Cited by 142

Controlled drug release to cancer cells from modular one-photon visible light-responsive micellar system

Poelma, S. O., Oh, S. S., Helmy, S., Knight, A., Burnett, G. L., Soh, H. T., Hawker, C. J., & de Alaniz, J. R. (2016) · Chemical Communications · doi:10.1039/c6cc04127b · Cited by 140

Ultra‐Small Nano‐Assemblies as Tumor‐Targeted and Renal Clearable Theranostic Agent for Photodynamic Therapy

Zhang, D., Teng, K., Zhao, L., Niu, L., & Yang, Q. (2023) · Advanced Materials · doi:10.1002/adma.202209789 · Cited by 140

Isomer-Specific Hydrogen Bonding as a Design Principle for Bidirectionally Quantitative and Redshifted Hemithioindigo Photoswitches

Zweig, J. E., & Newhouse, T. R. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.7b04448 · Cited by 139

A Photo‐ and Thermo‐Driven Azoarene‐Based Circularly Polarized Luminescence Molecular Switch in a Liquid Crystal Host

Kang, W., Tang, Y., Meng, X., et al. (2023) · Angewandte Chemie International Edition · doi:10.1002/anie.202311486 · Cited by 139

Two-Photon Neuronal and Astrocytic Stimulation with Azobenzene-Based Photoswitches

Izquierdo-Serra, M., Gascón-Moya, M., Hirtz, J. J., Pittolo, S., Poskanzer, K. E., Ferrer, È., Alibés, R., Busquè, F., Yuste, R., Hernando, J. C., et al. (2014) · Journal of the American Chemical Society · doi:10.1021/ja5026326 · Cited by 138

Multiaddressable Photochromic Architectures: From Molecules to Materials

Nie, H. F., Self, J. L., Kuenstler, A. S., et al. (2019) · Advanced Optical Materials · doi:10.1002/adom.201900224 · Cited by 137

Optical control of insulin release using a photoswitchable sulfonylurea

Broichhagen, J., Schönberger, M., Cork, S. C., Frank, J. A., Marchetti, P., Bugliani, M., Shapiro, A. M. J., Trapp, S., Rutter, G. A., Hodson, D. J., et al. (2014) · Nature Communications · doi:10.1038/ncomms6116 · Cited by 136

Irradiation‐Wavelength Directing Circularly Polarized Luminescence in Self‐Organized Helical Superstructures Enabled by Hydrogen‐Bonded Chiral Fluorescent Molecular Switches

He, Y.-R., Zhang, S., Bisoyi, H. K., et al. (2021) · Angewandte Chemie International Edition · doi:10.1002/anie.202111344 · Cited by 136

Large, Tunable, and Reversible pH Changes by Merocyanine Photoacids

Wimberger, L., Prasad, S. K. K., Peeks, M. D., Andréasson, J., Schmidt, T. W., & Beves, J. E. (2021) · Journal of the American Chemical Society · doi:10.1021/jacs.1c08810 · Cited by 136

Triggered azobenzene-based prodrugs and drug delivery systems

Zhu, J., Guo, T., Wang, Z., & Zhao, Y. (2022) · Journal of Controlled Release · doi:10.1016/j.jconrel.2022.03.041 · Cited by 136

Visible Light‐Driven Molecular Switches and Motors: Recent Developments and Applications

Wang, H., Bisoyi, H. K., Zhang, X., et al. (2021) · Chemistry - A European Journal · doi:10.1002/chem.202103906 · Cited by 128

Visible-Light-Activated Heteroaryl Azoswitches: Toward a More Colorful Future

Dang, T., Zhang, Z., & Li, T. (2024) · Journal of the American Chemical Society · doi:10.1021/jacs.4c03135 · Cited by 127

In Situ Formation of an Azo Bridge on Proteins Controllable by Visible Light

Hoppmann, C., Maslennikov, I., Choe, S., & Wang, L. (2015) · Journal of the American Chemical Society · doi:10.1021/jacs.5b06234 · Cited by 125

Photoresponsive self-healing supramolecular hydrogels for light-induced release of DNA and doxorubicin

Pianowski, Z., Karcher, J., & Schneider, K. (2016) · Chemical Communications · doi:10.1039/c5cc09633b · Cited by 122

Metal–Photoswitch Friendship: From Photochromic Complexes to Functional Materials

Thaggard, G. C., Haimerl, J., Park, K. C., Lim, J., Fischer, R. A., Kankanamalage, B. K. P. M., Yarbrough, B. J., Wilson, G. R., & Shustova, N. B. (2022) · Journal of the American Chemical Society · doi:10.1021/jacs.2c09879 · Cited by 122

Inorganic photochromic materials: Recent advances, mechanism, and emerging applications

Du, J., Yang, Z., Lin, H., et al. (2024) · Responsive materials · doi:10.1002/rpm.20240004 · Cited by 121

Recent advances in photo‐responsive carbon dots for tumor therapy

Zhang, H., Liu, Y., & Qu, S. (2024) · Responsive Materials · doi:10.1002/rpm.20240012 · Cited by 121

Derivatized Benzothiazoles as Two-Photon-Absorbing Organic Photosensitizers Active under Near Infrared Light Irradiation

Kundu, B. K., Han, G., & Sun, Y. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.2c12244 · Cited by 119

A Visible‐ and NIR‐Light Responsive Photothermal Therapy Agent by Chirality‐Dependent MoO 3− x Nanoparticles

Li, Y., Miao, Z., Shang, Z., et al. (2019) · Advanced Functional Materials · doi:10.1002/adfm.201906311 · Cited by 117

Thermodynamics and kinetics of protonated merocyanine photoacids in water

Berton, C., Busiello, D. M., Zamuner, S., et al. (2020) · Chemical Science · doi:10.1039/d0sc03152f · Cited by 116

Reversible photo-control over transmembrane anion transport using visible-light responsive supramolecular carriers

Kerckhoffs, A., & Langton, M. J. (2020) · Chemical Science · doi:10.1039/d0sc02745f · Cited by 113

A Modern Look at Spiropyrans: From Single Molecules to Smart Materials

Kozlenko, A. S., Ожогин, И. В., Пугачев, А. Д., Lukyanova, M. B., El‐Sewify, I. M., & Lukyanov, B. S. (2023) · Topics in Current Chemistry · doi:10.1007/s41061-022-00417-2 · Cited by 113

Photoswitchable Nanoparticles Enable High-Resolution Cell Imaging: PULSAR Microscopy

Hu, D., Tian, Z., Wu, W., et al. (2008) · Journal of the American Chemical Society · doi:10.1021/ja805948u · Cited by 112

Two-photon brightness of azobenzene photoswitches designed for glutamate receptor optogenetics

Carroll, E. C., Berlin, S., Levitz, J., Kienzler, M. A., Yuan, Z., Madsen, D., Larsen, D. S., & Isacoff, E. Y. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1416942112 · Cited by 111

Multimodal Magnetic‐Resonance/Optical‐Imaging Contrast Agent Sensitive to NADH

Tu, C., Nagao, R. J., & Louie, A. Y. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200900984 · Cited by 111

Taking Photochromism beyond Visible: Direct One‐Photon NIR Photoswitches Operating in the Biological Window

Klaue, K., Garmshausen, Y., & Hecht, S. (2017) · Angewandte Chemie International Edition · doi:10.1002/anie.201709554 · Cited by 108

Recent advances in the use of photochromic dyes for photocontrol in biomedicine

Cheng, H., Yoon, J., & Tian, H. (2018) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2018.06.003 · Cited by 106

Supercharged Proteins and Polypeptides

Ma, C., Malessa, A., Boersma, A. J., Liu, K., & Herrmann, A. (2020) · Advanced Materials · doi:10.1002/adma.201905309 · Cited by 106

NIR-II phototherapy agents with aggregation-induced emission characteristics for tumor imaging and therapy

Shi, T., Huang, C., Li, Y., Huang, F., & Yin, S. (2022) · Biomaterials · doi:10.1016/j.biomaterials.2022.121535 · Cited by 106

Nanocomposites of Spiropyran-Functionalized Polymers and Upconversion Nanoparticles for Controlled Release Stimulated by Near-Infrared Light and pH

Chen, S., Gao, Y., Cao, Z., et al. (2016) · Macromolecules · doi:10.1021/acs.macromol.6b01760 · Cited by 105

Visible-Light-Driven Photoswitching of Aggregated-Induced Emission-Active Diarylethenes for Super-Resolution Imaging

Li, C., Xiong, K., Chen, Y., Fan, C., Wang, Y., Ye, H., & Zhu, M. (2020) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.0c03122 · Cited by 104

Visible‐Light‐Driven Halogen Bond Donor Based Molecular Switches: From Reversible Unwinding to Handedness Inversion in Self‐Organized Soft Helical Superstructures

Wang, H., Bisoyi, H. K., Li, B., et al. (2019) · Angewandte Chemie International Edition · doi:10.1002/anie.201913977 · Cited by 104

Photomodulation of ionic current through hemithioindigo-modified gramicidin channels

Lougheed, T., Borisenko, V., Hennig, T., et al. (2004) · Organic & Biomolecular Chemistry · doi:10.1039/b408485c · Cited by 103

Dihydroazulene: from controlling photochromism to molecular electronics devices

Broman, S. L., & Nielsen, M. B. (2014) · Physical Chemistry Chemical Physics · doi:10.1039/c4cp02442g · Cited by 102

Hole Catalysis as a General Mechanism for Efficient and Wavelength-Independent Z → E Azobenzene Isomerization

Goulet‐Hanssens, A., Rietze, C., Titov, E., et al. (2018) · Chem · doi:10.1016/j.chempr.2018.06.002 · Cited by 102

Near-Infrared Fluorescent Probes for Hypoxia Detection via Joint Regulated Enzymes: Design, Synthesis, and Application in Living Cells and Mice

Tian, X., Li, Z., Sun, Y. L., Wang, P., & Ma, H. (2018) · Analytical Chemistry · doi:10.1021/acs.analchem.8b04249 · Cited by 100

Spiropyran–Merocyanine Based Photochromic Fluorescent Probes: Design, Synthesis, and Applications

Mandal, M., Banik, D., Karak, A., Manna, S. K., & Mahapatra, A. K. (2022) · ACS Omega · doi:10.1021/acsomega.2c04969 · Cited by 100

Light-controlled modulation of gene expression by chemical optoepigenetic probes

Reis, S. A., Ghosh, B., Hendricks, J. A., Szantai‐Kis, D. M., Toerk, L., Ross, K. N., Lamb, J., Read-Button, W., Zheng, B., Wang, H., et al. (2016) · Nature Chemical Biology · doi:10.1038/nchembio.2042 · Cited by 98

Taming the Complexity of Donor–Acceptor Stenhouse Adducts: Infrared Motion Pictures of the Complete Switching Pathway

Zulfikri, H., Koenis, M. A. J., Lerch, M. M., et al. (2019) · Journal of the American Chemical Society · doi:10.1021/jacs.9b00341 · Cited by 97

Light-fueled transient supramolecular assemblies in water as fluorescence modulators

Chen, X., Hou, X., Bisoyi, H. K., Feng, W., Cao, Q. C., Huang, S., Yang, H., Chen, D., & Li, Q. (2021) · Nature Communications · doi:10.1038/s41467-021-25299-8 · Cited by 96

Sensitized Two‐NIR‐Photon Z→E Isomerization of a Visible‐Light‐Addressable Bistable Azobenzene Derivative

Moreno, J., Gerecke, M., Grubert, L., et al. (2015) · Angewandte Chemie International Edition · doi:10.1002/anie.201509111 · Cited by 93

Photoswitchable paclitaxel-based microtubule stabilisers allow optical control over the microtubule cytoskeleton

Müller‐Deku, A., Meiring, J. C. M., Loy, K., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-18389-6 · Cited by 93

In-Situ Imaging of Azoreductase Activity in the Acute and Chronic Ulcerative Colitis Mice by a Near-Infrared Fluorescent Probe

Tian, Y., Li, Y., Jiang, W., Zhou, D.-Y., Fei, J., & Li, C. (2019) · Analytical Chemistry · doi:10.1021/acs.analchem.9b02857 · Cited by 91

A Reversible Photoacid Functioning in PBS Buffer under Visible Light

Abeyrathna, N., & Liao, Y. (2015) · Journal of the American Chemical Society · doi:10.1021/jacs.5b06218 · Cited by 89

Precisely Traceable Drug Delivery of Azoreductase-Responsive Prodrug for Colon Targeting via Multimodal Imaging

Zhao, X.-B., Ha, W., Gao, K., et al. (2020) · Analytical Chemistry · doi:10.1021/acs.analchem.0c01220 · Cited by 89

How Azobenzene Photoswitches Restore Visual Responses to the Blind Retina

Tochitsky, I., Helft, Z., Meseguer, V., Fletcher, R. B., Vessey, K. A., Telias, M., Denlinger, B. L., Malis, J. G., Fletcher, E. L., & Krämer, R. (2016) · Neuron · doi:10.1016/j.neuron.2016.08.038 · Cited by 87

Reversible Handedness Inversion and Circularly Polarized Light Reflection Tuning in Self‐Organized Helical Superstructures Using Visible‐Light‐Driven Macrocyclic Chiral Switches

Wang, H., Tang, Y., Bisoyi, H. K., et al. (2022) · Angewandte Chemie International Edition · doi:10.1002/anie.202216600 · Cited by 87

Dual optical control and mechanistic insights into photoswitchable group II and III metabotropic glutamate receptors

Levitz, J., Broichhagen, J., Leippe, P., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1619652114 · Cited by 86

Hypoxia‐Responsive Photosensitizer Targeting Dual Organelles for Photodynamic Therapy of Tumors

Tang, Y., Wang, X., Zhu, G., Liu, Z., Chen, X., Bisoyi, H. K., Chen, X., Chen, X., Xu, Y., Li, J., et al. (2022) · Small · doi:10.1002/smll.202205440 · Cited by 86

Direct Photocontrol of Peptidomimetics: An Alternative to Oxygen‐Dependent Photodynamic Cancer Therapy

Babii, O., Afonin, S., Garmanchuk, L., Nikulina, V. V., Nikolaienko, T. V., Storozhuk, O. V., Шелест, Д. В., Dasyukevich, O. I., Остапченко, Л. І., Iurchenko, V., et al. (2016) · Angewandte Chemie International Edition · doi:10.1002/anie.201600506 · Cited by 85

Light-activated photodeformable supramolecular dissipative self-assemblies

Chen, X., Feng, W., Bisoyi, H. K., Zhang, S., Chen, X., Yang, H., & Li, Q. (2022) · Nature Communications · doi:10.1038/s41467-022-30969-2 · Cited by 85

Tumor microenvironment-induced structure changing drug/gene delivery system for overcoming delivery-associated challenges

Zhang, M., Guo, X., Wang, M., & Liu, K. (2020) · Journal of Controlled Release · doi:10.1016/j.jconrel.2020.04.026 · Cited by 84

Donor–Acceptor Dihydropyrenes Switchable with Near-Infrared Light

Klaue, K., Han, W., Liesfeld, P., et al. (2020) · Journal of the American Chemical Society · doi:10.1021/jacs.0c04219 · Cited by 84

Spiropyran-Based Drug Delivery Systems

Fagan, A., Bartkowski, M., & Giordani, S. (2021) · Frontiers in Chemistry · doi:10.3389/fchem.2021.720087 · Cited by 84

Branched Photoswitchable Tethered Ligands Enable Ultra-efficient Optical Control and Detection of G Protein-Coupled Receptors In Vivo

Acosta-Ruiz, A., Gutzeit, V. A., Skelly, M. J., Meadows, S. M., Lee, J., Parekh, P. K., Orr, A. G., Liston, C. M., Pleil, K. E., Broichhagen, J., et al. (2019) · Neuron · doi:10.1016/j.neuron.2019.10.036 · Cited by 83

Optical control of NMDA receptors with a diffusible photoswitch

Laprell, L., Repak, E., Franckevicius, V., Hartrampf, F. W. W., Terhag, J., Hollmann, M., Sumser, M., Rebola, N., DiGregorio, D. A., & Trauner, D. H. (2015) · Nature Communications · doi:10.1038/ncomms9076 · Cited by 82

2-Azo-, 2-diazocine-thiazols and 2-azo-imidazoles as photoswitchable kinase inhibitors: limitations and pitfalls of the photoswitchable inhibitor approach

Schehr, M., Lanes, C., Weisner, J., Heintze, L., Müller, M. P., Pichlo, C., Charl, J., Brunstein, E., Ewert, J., Lehr, M., et al. (2019) · Photochemical & Photobiological Sciences · doi:10.1039/c9pp00010k · Cited by 82

Azoreductase-Responsive Nanoprobe for Hypoxia-Induced Mitophagy Imaging

Ma, D., Huang, C., Zheng, J., Zhou, W., Tang, J., Chen, W., Li, J., & Yang, R. (2018) · Analytical Chemistry · doi:10.1021/acs.analchem.8b03492 · Cited by 80

DNA gated photochromism and fluorescent switch in a thiazole orange modified diarylethene

Liu, K., Wen, Y., Shi, T., et al. (2014) · Chemical Communications · doi:10.1039/c4cc02783c · Cited by 79

Visible-Light-Dependent Photocyclization: Design, Synthesis, and Properties of a Cyanine-Based Dithienylethene

Hu, F., Cao, M., Ma, X., et al. (2015) · The Journal of Organic Chemistry · doi:10.1021/acs.joc.5b01466 · Cited by 78

A Robust, GFP-Orthogonal Photoswitchable Inhibitor Scaffold Extends Optical Control over the Microtubule Cytoskeleton

Gao, L., Meiring, J. C. M., Kraus, Y., Wranik, M., Weinert, T., Pritzl, S. D., Bingham, R., Ntouliou, E., Jansen, K. I., Olieric, N., et al. (2020) · Cell chemical biology · doi:10.1016/j.chembiol.2020.11.007 · Cited by 78

Visible and near-infrared light activated azo dyes

Chen, H., Chen, W., Lin, Y., et al. (2021) · Chinese Chemical Letters · doi:10.1016/j.cclet.2021.03.020 · Cited by 78

Photoactivated theranostic nanomaterials based on aggregation‐induced emission luminogens for cancer photoimmunotherapy

Tang, Y., Wang, X., Chen, S., & Li, Q. (2024) · Responsive materials · doi:10.1002/rpm.20240003 · Cited by 77

Synthesis and Characterization of Photoswitchable Lipids Containing Hemithioindigo Chromophores

Eggers, K., Fyles, T. M., & Montoya‐Pelaez, P. J. (2001) · The Journal of Organic Chemistry · doi:10.1021/jo0056848 · Cited by 76

Hemithioindigos for Cellular Photopharmacology: Desymmetrised Molecular Switch Scaffolds Enabling Design Control over the Isomer‐Dependency of Potent Antimitotic Bioactivity

Sailer, A., Ermer, F., Kraus, Y., et al. (2019) · ChemBioChem · doi:10.1002/cbic.201800752 · Cited by 76

A Visible and Near-Infrared Light Activatable Diazocoumarin Probe for Fluorogenic Protein Labeling in Living Cells

Dai, S., & Yang, D. (2020) · Journal of the American Chemical Society · doi:10.1021/jacs.0c08068 · Cited by 76

Light‐Activated Nanoprobes for Biosensing and Imaging

Li, M., Zhao, J., Chu, H., Mi, Y., Zhou, Z., Di, Z., Zhao, M., & Li, L. (2018) · Advanced Materials · doi:10.1002/adma.201804745 · Cited by 74

Expanding excitation wavelengths for azobenzene photoswitching into the near-infrared range via endothermic triplet energy transfer

Isokuortti, J., Kuntze, K., Virkki, M., Ahmed, Z., Vuorimaa, E., Filatov, M. A., Turshatov, A. A., Laaksonen, T., Priimägi, A., & Durandin, N. A. (2021) · Chemical Science · doi:10.1039/d1sc01717a · Cited by 74

Small-molecule photoswitches for fluorescence bioimaging: engineering and applications

Olesińska, M., & Deo, C. (2023) · Chemical Communications · doi:10.1039/d2cc05870g · Cited by 74

Pyrrole Hemithioindigo Antimitotics with Near‐Quantitative Bidirectional Photoswitching that Photocontrol Cellular Microtubule Dynamics with Single‐Cell Precision**

Sailer, A., Meiring, J. C. M., Heise, C., et al. (2021) · Angewandte Chemie International Edition · doi:10.1002/anie.202104794 · Cited by 73

Stimuli‐responsive fluorescent hydrogels: Strategies and applications

Lei, M., Wang, Q., Gu, R., & Qu, D. (2024) · Responsive materials · doi:10.1002/rpm.20230027 · Cited by 73

Optimized Photoactivatable Lipid Nanoparticles Enable Red Light Triggered Drug Release

Chander, N., Morstein, J., Bolten, J. S., Shemet, A., Cullis, P. R., Trauner, D. H., & Witzigmann, D. (2021) · Small · doi:10.1002/smll.202008198 · Cited by 71

Light‐Driven Reversible Transformation between Self‐Organized Simple Cubic Lattice and Helical Superstructure Enabled by a Molecular Switch Functionalized Nanocage

Zhou, K., Bisoyi, H. K., Jin, J., et al. (2018) · Advanced Materials · doi:10.1002/adma.201800237 · Cited by 69

Combining hydrophilic and hydrophobic environment sensitive dyes to detect a wide range of cellular polarity

Park, S. J., Juvekar, V., Jo, J. H., et al. (2019) · Chemical Science · doi:10.1039/c9sc04859f · Cited by 69

Photochromic Carbon Nanomaterials: An Emerging Class of Light‐Driven Hybrid Functional Materials

Hassan, F. M., Tang, Y., Bisoyi, H. K., & Li, Q. (2024) · Advanced Materials · doi:10.1002/adma.202401912 · Cited by 69

Photomodulation of Fluorescent Upconverting Nanoparticle Markers in Live Organisms by Using Molecular Switches

Boyer, J., Carling, C., Chua, S. Y., et al. (2012) · Chemistry - A European Journal · doi:10.1002/chem.201103767 · Cited by 68

Photochemical switching of luminescence and singlet oxygen generation by chemical signal communication

Silvi, S., Constable, E. C., Housecroft, C. E., et al. (2009) · Chemical Communications · doi:10.1039/b900712a · Cited by 67

A red-shifted photochromic sulfonylurea for the remote control of pancreatic beta cell function

Broichhagen, J., Frank, J. A., Johnston, N. R., Mitchell, R. K., Šmid, K., Marchetti, P., Bugliani, M., Rutter, G. A., Trauner, D. H., & Hodson, D. J. (2015) · Chemical Communications · doi:10.1039/c5cc01224d · Cited by 67

Diarylethene based fluorescent switchable probes for the detection of amyloid-β pathology in Alzheimer's disease

Lv, G., Cui, B., Lan, H., et al. (2014) · Chemical Communications · doi:10.1039/c4cc07656g · Cited by 66

A highly efficient supramolecular photoswitch for singlet oxygen generation in water

Liu, G., Xu, X., Chen, Y., et al. (2016) · Chemical Communications · doi:10.1039/c6cc02996e · Cited by 66

Photoactivation of an Inhibitor of the 12/15‐Lipoxygenase Pathway

Herre, S., Schadendorf, T., Ivanov, I., et al. (2006) · ChemBioChem · doi:10.1002/cbic.200600082 · Cited by 65

A switchable peptide sensor for real-time lysosomal tracking

Chen, L., Wu, J., Schmuck, C., & Tian, H. (2014) · Chemical Communications · doi:10.1039/c4cc00670d · Cited by 64

A photochromic upconversion nanoarchitecture: towards activatable bioimaging and dual NIR light-programmed singlet oxygen generation

Mi, Y., Cheng, H.-B., Chu, H., Zhao, J., Yu, M., Gu, Z., Zhao, Y., & Li, L. (2019) · Chemical Science · doi:10.1039/c9sc03524a · Cited by 64

Diarylethenes with a Narrow Singlet–Triplet Energy Gap Sensitizer: a Simple Strategy for Efficient Visible‐Light Photochromism

Zhang, Z., Zhang, J., Wu, B., Li, X., Chen, Y., Huang, J., Zhu, L., & Tian, H. (2018) · Advanced Optical Materials · doi:10.1002/adom.201700847 · Cited by 63

Cucurbituril-activated photoreaction of dithienylethene for controllable targeted lysosomal imaging and anti-counterfeiting

Liu, G., Xu, X., Dai, X., et al. (2021) · Materials Horizons · doi:10.1039/d1mh00811k · Cited by 63

Transforming a Sword into a Knife: Persistent Phototoxicity Inhibition and Alternative Therapeutical Activation of Highly-Photosensitive Phytochlorin

Yu, N., Qiu, P., Ren, Q., Wen, M., Geng, P., Macharia, D. K., Zhu, M., & Chen, Z. (2021) · ACS Nano · doi:10.1021/acsnano.1c07241 · Cited by 63

Heterocyclic Hemithioindigos: Highly Advantageous Properties as Molecular Photoswitches**

Josef, V., Hampel, F., & Dube, H. (2022) · Angewandte Chemie International Edition · doi:10.1002/anie.202210855 · Cited by 63

Photoswitchable Spiropyran Dyads for Biological Imaging

Xiong, Y., Rivera‐Fuentes, P., Sezgin, E., et al. (2016) · Organic Letters · doi:10.1021/acs.orglett.6b01717 · Cited by 62

Photopharmacological control of bipolar cells restores visual function in blind mice

Laprell, L., Tochitsky, I., Kaur, K., Manookin, M. B., Stein, M., Barber, D. M., Schön, C., Michalakis, S., Biel, M., Krämer, R., et al. (2017) · Journal of Clinical Investigation · doi:10.1172/jci92156 · Cited by 62

Reversible modulation of circadian time with chronophotopharmacology

Kolarski, D., Miró‐Vinyals, C., Sugiyama, A., Srivastava, A., Ono, D., Nagai, Y., Iida, M., Itami, K., Tama, F., Szymański, W., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-23301-x · Cited by 62

Reversible and Tunable Photoswitching of Protein Function through Genetic Encoding of Azobenzene Amino Acids in Mammalian Cells

Luo, J., Samanta, S., Convertino, M., Dokholyan, N. V., & Deiters, A. (2018) · ChemBioChem · doi:10.1002/cbic.201800226 · Cited by 60

Efficient green light-excited switches based on dithienylethenes with BF 2 -doped π-conjugated systems

Li, Z., Dai, Y., Lu, Z., et al. (2019) · Chemical Communications · doi:10.1039/c9cc06838d · Cited by 59

A spiropyran–coumarin platform: an environment sensitive photoresponsive drug delivery system for efficient cancer therapy

Barman, S., Das, J., Biswas, S., et al. (2017) · Journal of Materials Chemistry B · doi:10.1039/c7tb00379j · Cited by 57

Photoresponsive azo-combretastatin A-4 analogues

Rastogi, S. K., Zhao, Z., Barrett, S. L., et al. (2017) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2017.11.012 · Cited by 57

Visible Light Mediated Bidirectional Control over Carbonic Anhydrase Activity in Cells and in Vivo Using Azobenzenesulfonamides

Aggarwal, K., Kuka, T. P., Banik, M., et al. (2020) · Journal of the American Chemical Society · doi:10.1021/jacs.0c05383 · Cited by 55

A far-red emitting probe for unambiguous detection of mobile zinc in acidic vesicles and deep tissue

Rivera‐Fuentes, P., Wrobel, A. T., Zastrow, M. L., et al. (2015) · Chemical Science · doi:10.1039/c4sc03388d · Cited by 54

Bright Ion Channels and Lipid Bilayers

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Second Near‐Infrared Window Fluorescence Materials for In Vivo Dynamic Multiplexed Imaging

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