Twisted intramolecular charge transfer (TICT) and twists beyond TICT: from mechanisms to rational designs of bright and sensitive fluorophores

The M06 suite of density functionals for main group thermochemistry, thermochemical kinetics, noncovalent interactions, excited states, and transition elements: two new functionals and systematic testing of four M06-class functionals and 12 other functionals

Zhao, Y., & Truhlar, D. G. (2008) · Theoretical Chemistry Accounts · doi:10.1007/s00214-007-0310-x · Cited by 30,302

A new hybrid exchange–correlation functional using the Coulomb-attenuating method (CAM-B3LYP)

Yanai, T., Tew, D. P., & Handy, N. C. (2004) · Chemical Physics Letters · doi:10.1016/j.cplett.2004.06.011 · Cited by 14,976

Long-range corrected hybrid density functionals with damped atom–atom dispersion corrections

Chai, J.-D., & Head-Gordon, M. (2008) · Physical Chemistry Chemical Physics · doi:10.1039/b810189b · Cited by 14,648

Aggregation-Induced Emission: Together We Shine, United We Soar!

Mei, J., Leung, N. L. C., Kwok, R. T. K., Lam, J. W. Y., & Tang, B. Z. (2015) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00263 · Cited by 8,270

Aggregation-induced emission

Hong, Y., Lam, J. W. Y., & Tang, B. Z. (2011) · Chemical Society Reviews · doi:10.1039/c1cs15113d · Cited by 6,363

Kinetics of Fluorescence Quenching by Electron and H‐Atom Transfer

Rehm, D., & Weller, A. (1970) · Israel Journal of Chemistry · doi:10.1002/ijch.197000029 · Cited by 3,949

Structural Changes Accompanying Intramolecular Electron Transfer: Focus on Twisted Intramolecular Charge-Transfer States and Structures

Grabowski, Z. R., Rotkiewicz, K., & Rettig, W. (2003) · Chemical Reviews · doi:10.1021/cr940745l · Cited by 3,714

Characterization of electronic transitions in complex molecules

Kasha, M. (1950) · Discussions of the Faraday Society · doi:10.1039/df9500900014 · Cited by 2,903

New Strategies for Fluorescent Probe Design in Medical Diagnostic Imaging

Kobayashi, H., Ogawa, M., Alford, R., Choyke, P. L., & Urano, Y. (2010) · Chemical Reviews · doi:10.1021/cr900263j · Cited by 2,200

Molecular mechanism of Thioflavin-T binding to amyloid fibrils

Biancalana, M., & Koide, S. (2010) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2010.04.001 · Cited by 2,195

Oxidative stress and the amyloid beta peptide in Alzheimer’s disease

Cheignon, C., Tomas, M., Bonnefont-Rousselot, D., Faller, P., Hureau, C., & Collin, F. (2018) · Redox Biology · doi:10.1016/j.redox.2017.10.014 · Cited by 2,185

Amyloid Beta: Structure, Biology and Structure-Based Therapeutic Development

Chen, G.-F., Xu, T.-H., Yan, Y., Zhou, Y.-R., Jiang, Y., Melcher, K., & Xu, H. E. (2017) · Acta Pharmacologica Sinica · doi:10.1038/aps.2017.28 · Cited by 1,965

Triplet photosensitizers: from molecular design to applications

Zhao, J., Wu, W., Sun, J., & Guo, S. (2013) · Chemical Society Reviews · doi:10.1039/c3cs35531d · Cited by 1,579

Cyanines during the 1990s: A Review

Mishra, A., Behera, R. K., Behera, P. K., Mishra, B. K., & Behera, G. B. (2000) · Chemical Reviews · doi:10.1021/cr990402t · Cited by 1,564

Spin—Orbit Coupling and the Radiationless Processes in Nitrogen Heterocyclics

El-Sayed, M. A. (1963) · The Journal of Chemical Physics · doi:10.1063/1.1733610 · Cited by 1,530

A general method to improve fluorophores for live-cell and single-molecule microscopy

Grimm, J. B., English, B. P., Chen, J., Slaughter, J. P., Zhang, Z., Revyakin, A., Patel, R., Macklin, J. J., Normanno, D., Singer, R. H., et al. (2015) · Nature Methods · doi:10.1038/nmeth.3256 · Cited by 1,501

An Increased Percentage of Long Amyloid β Protein Secreted by Familial Amyloid β Protein Precursor (βApp 717 ) Mutants

Suzuki, N., Cheung, T. T., Cai, X.-D., Odaka, A., Otvos, L., Eckman, C., Golde, T. E., & Younkin, S. G. (1994) · Science · doi:10.1126/science.8191290 · Cited by 1,471

Cleavage of Amyloid β Peptide During Constitutive Processing of Its Precursor

Esch, F. S., Keim, P. S., Beattie, E. C., Blacher, R. W., Culwell, A. R., Oltersdorf, T., McClure, D., & Ward, P. J. (1990) · Science · doi:10.1126/science.2111583 · Cited by 1,410

RNA Mimics of Green Fluorescent Protein

Paige, J. S., Wu, K. Y., & Jaffrey, S. R. (2011) · Science · doi:10.1126/science.1207339 · Cited by 1,350

Charge Separation in Excited States of Decoupled Systems—TICT Compounds and Implications Regarding the Development of New Laser Dyes and the Primary Process of Vision and Photosynthesis

Rettig, W. (1986) · Angewandte Chemie International Edition in English · doi:10.1002/anie.198609711 · Cited by 1,324

Fluorescent probes for super-resolution imaging in living cells

Fernández-Suárez, M., & Ting, A. Y. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2531 · Cited by 1,306

Recent advances in twisted intramolecular charge transfer (TICT) fluorescence and related phenomena in materials chemistry

Sasaki, S., Drummen, G. P. C., & Konishi, G.-I. (2016) · Journal of Materials Chemistry C · doi:10.1039/c5tc03933a · Cited by 1,189

Solvent effects on emission yield and lifetime for coumarin laser dyes. Requirements for a rotatory decay mechanism

Jones, G., Jackson, W. R., Choi, C. Y., & Bergmark, W. R. (1985) · The Journal of Physical Chemistry · doi:10.1021/j100248a024 · Cited by 1,174

Breaking the Diffraction Barrier: Super-Resolution Imaging of Cells

Huang, B., Babcock, H., & Zhuang, X. (2010) · Cell · doi:10.1016/j.cell.2010.12.002 · Cited by 1,156

Twisted Intramolecular Charge Transfer and Aggregation-Induced Emission of BODIPY Derivatives

Hu, R., Lager, E., Aguilar-Aguilar, A., Liu, J., Lam, J. W. Y., Sung, H. H. Y., Williams, I. D., Zhong, Y., Wong, K. S., Peña-Cabrera, E., et al. (2009) · The Journal of Physical Chemistry C · doi:10.1021/jp902962h · Cited by 1,023

Photoinduced Electron Transfer Reactions for Macromolecular Syntheses

Dadashi-Silab, S., Doran, S., & Yagci, Y. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00586 · Cited by 846

Reinterpretation of the anomalous fluorescense of -n,n-dimethylamino-benzonitrile

Rotkiewicz, K., Grellmann, K. H., & Grabowski, Z. R. (1973) · Chemical Physics Letters · doi:10.1016/0009-2614(73)80367-7 · Cited by 792

Evolution of Fluorescein as a Platform for Finely Tunable Fluorescence Probes

Urano, Y., Kamiya, M., Kanda, K., Ueno, T., Hirose, K., & Nagano, T. (2005) · Journal of the American Chemical Society · doi:10.1021/ja043919h · Cited by 683

Rhodamine B and rhodamine 101 as reference substances for fluorescence quantum yield measurements

Karstens, T., & Kobs, K. (1980) · The Journal of Physical Chemistry · doi:10.1021/j100451a030 · Cited by 678

A general method to fine-tune fluorophores for live-cell and in vivo imaging

Grimm, J. B., Muthusamy, A. K., Liang, Y., Brown, T. A., Lemon, W. C., Patel, R., Lu, R., Macklin, J. J., Keller, P. J., Ji, N., et al. (2017) · Nature Methods · doi:10.1038/nmeth.4403 · Cited by 665

Temperature Measurement in Microfluidic Systems Using a Temperature-Dependent Fluorescent Dye

Ross, D., Gaitan, M., & Locascio, L. E. (2001) · Analytical Chemistry · doi:10.1021/ac010370l · Cited by 631

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 627

Efficient and long-lived room-temperature organic phosphorescence: theoretical descriptors for molecular designs

Ma, H., Peng, Q., An, Z., Huang, W., & Shuai, Z. (2019) · Journal of the American Chemical Society · doi:10.1021/jacs.8b11224 · Cited by 613

Formation and relaxation of excited states in solution: A new time dependent polarizable continuum model based on time dependent density functional theory

Caricato, M., Mennucci, B., Tomasi, J., Ingrosso, F., Cammi, R., Corni, S., & Scalmani, G. (2006) · The Journal of Chemical Physics · doi:10.1063/1.2183309 · Cited by 606

Die Viskositätsabhängigkeit der Fluoreszenzquantenausbeuten einiger Farbstoffsysteme

Förster, T., & Hoffmann, G. (1971) · Zeitschrift für Physikalische Chemie · doi:10.1524/zpch.1971.75.1_2.063 · Cited by 573

Intermolecular and supramolecular photoinduced electron transfer processes of fullerene–porphyrin/phthalocyanine systems

El-Khouly, M. E., Ito, O., Smith, P. M., & D’Souza, F. (2004) · Journal of Photochemistry and Photobiology C: Photochemistry Reviews · doi:10.1016/j.jphotochemrev.2004.01.003 · Cited by 568

Umwandlung von Elektronenanregungsenergie

Lippert, E., Lüder, W., Moll, F., Nägele, W., Boos, H., Prigge, H., & Seibold‐Blankenstein, I. (1961) · Angewandte Chemie · doi:10.1002/ange.19610732103 · Cited by 506

Uncharged thioflavin-T derivatives bind to amyloid-beta protein with high affinity and readily enter the brain

Klunk, W. E., Wang, Y., Huang, G.-F., Debnath, M. L., Holt, D. P., & Mathis, C. A. (2001) · Life Sciences · doi:10.1016/s0024-3205(01)01232-2 · Cited by 457

Photobiocatalysis: Activating Redox Enzymes by Direct or Indirect Transfer of Photoinduced Electrons

Lee, S. H., Choi, D. S., Kuk, S. K., & Park, C. B. (2018) · Angewandte Chemie International Edition · doi:10.1002/anie.201710070 · Cited by 422

Development of a Highly Sensitive Fluorescence Probe for Hydrogen Peroxide

Abo, M., Urano, Y., Hanaoka, K., Terai, T., Komatsu, T., & Nagano, T. (2011) · Journal of the American Chemical Society · doi:10.1021/ja203521e · Cited by 394

A G-quadruplex–containing RNA activates fluorescence in a GFP-like fluorophore

Huang, H., Suslov, N. B., Li, N.-S., Shelke, S. A., Evans, M. E., Koldobskaya, Y., Rice, P. A., & Piccirilli, J. A. (2014) · Nature Chemical Biology · doi:10.1038/nchembio.1561 · Cited by 349

Mechanism-Based Molecular Design of Highly Selective Fluorescence Probes for Nitrative Stress

Ueno, T., Urano, Y., Kojima, H., & Nagano, T. (2006) · Journal of the American Chemical Society · doi:10.1021/ja061972v · Cited by 348

Generation of Triplet Excited States via Photoinduced Electron Transfer in meso-anthra-BODIPY: Fluorogenic Response toward Singlet Oxygen in Solution and in Vitro

Filatov, M. A., Karuthedath, S., Polestshuk, P. M., Savoie, H., Flanagan, K. J., Sy, C., Sitte, E., Telitchko, M., Laquai, F., Boyle, R. W., et al. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.7b00551 · Cited by 345

Aziridinyl Fluorophores Demonstrate Bright Fluorescence and Superior Photostability by Effectively Inhibiting Twisted Intramolecular Charge Transfer

Liu, X., Qiao, Q., Tian, W., Liu, W., Chen, J., Lang, M. J., & Xu, Z. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.6b03924 · Cited by 334

Molecular design of highly efficient heavy-atom-free triplet BODIPY derivatives for photodynamic therapy and bioimaging

Nguyen, V., Yim, Y., Kim, S., Ryu, B., Swamy, K. M. K., Kim, G., Kwon, N., Kim, C., Park, S., & Yoon, J. (2020) · Angewandte Chemie International Edition · doi:10.1002/anie.202002843 · Cited by 326

Intersystem Crossing Mediated by Photoinduced Intramolecular Charge Transfer: Julolidine−Anthracene Molecules with Perpendicular π Systems

Dance, Z. E. X., Mickley, S. M., Wilson, T. M., Ricks, A. B., Scott, A. M., Ratner, M. A., & Wasielewski, M. R. (2008) · The Journal of Physical Chemistry A · doi:10.1021/jp800561g · Cited by 315

Photoinduced Electron Transfer at Molecule−Metal Interfaces

Lindstrom, C. D., & Zhu, X.-Y. (2006) · Chemical Reviews · doi:10.1021/cr0501689 · Cited by 280

Molecular Design of UV–vis Absorption and Emission Properties in Organic Fluorophores: Toward Larger Bathochromic Shifts, Enhanced Molar Extinction Coefficients, and Greater Stokes Shifts

Liu, X., Xu, Z., & Cole, J. M. (2013) · The Journal of Physical Chemistry C · doi:10.1021/jp404170w · Cited by 278

Advances in the chemistry of small molecule fluorescent probes

Wysocki, L. M., & Lavis, L. D. (2011) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2011.10.013 · Cited by 263

Plug-and-Play Fluorophores Extend the Spectral Properties of Spinach

Song, W., Strack, R. L., Svensen, N., & Jaffrey, S. R. (2014) · Journal of the American Chemical Society · doi:10.1021/ja410819x · Cited by 257

Photoinduced Intramolecular Charge Transfer in 4-(Dimethyl)aminobenzonitrile − A Theoretical Perspective

Rappoport, D., & Furche, F. (2004) · Journal of the American Chemical Society · doi:10.1021/ja037806u · Cited by 253

Quantitative Design of Bright Fluorophores and AIEgens by the Accurate Prediction of Twisted Intramolecular Charge Transfer (TICT)

Wang, C., Qiao, Q., Chi, W., Chen, J., Liu, W., Tan, D., McKechnie, S., Lyu, D., Jiang, X., Zhou, W., et al. (2020) · Angewandte Chemie International Edition · doi:10.1002/anie.201916357 · Cited by 249

FLUORESZENZSPEKTRUM UND FRANCK-CONDON-PRINZIP IN LÖSUNGEN AROMATISCHER VERBINDUNGEN

LIPPERT, E., LÜDER, W., & BOOS, H. (1962) · Advances in Molecular Spectroscopy · doi:10.1016/b978-1-4832-1332-3.50070-6 · Cited by 244

A General Descriptor Δ E Enables the Quantitative Development of Luminescent Materials Based on Photoinduced Electron Transfer

Chi, W., Chen, J., Liu, W., Wang, C., Qi, Q., Qiao, Q., Tan, T. M., Xiong, K., Liu, X., Kang, K., et al. (2020) · Journal of the American Chemical Society · doi:10.1021/jacs.0c01473 · Cited by 230

Motion-induced change in emission (MICE) for developing fluorescent probes

Su, D., Teoh, C. L., Wang, L., Liu, X., & Chang, Y.-T. (2017) · Chemical Society Reviews · doi:10.1039/c7cs00018a · Cited by 223

A General Strategy to Control Viscosity Sensitivity of Molecular Rotor‐Based Fluorophores

Ye, S., Zhang, H., Fei, J., Wolstenholme, C. H., & Zhang, X. (2021) · Angewandte Chemie International Edition · doi:10.1002/anie.202011108 · Cited by 207

Quaternary Piperazine-Substituted Rhodamines with Enhanced Brightness for Super-Resolution Imaging

Ye, Z., Yang, W., Wang, C., Zheng, Y., Chi, W., Liu, X., Huang, Z., Li, X., & Xiao, Y. (2019) · Journal of the American Chemical Society · doi:10.1021/jacs.9b04893 · Cited by 204

Bodipy–Anthracene Dyads as Triplet Photosensitizers: Effect of Chromophore Orientation on Triplet-State Formation Efficiency and Application in Triplet–Triplet Annihilation Upconversion

Wang, Z., & Zhao, J. (2017) · Organic Letters · doi:10.1021/acs.orglett.7b02047 · Cited by 203

Self-Assembly Solid-State Enhanced Red Emission of Quinolinemalononitrile: Optical Waveguides and Stimuli Response

Shi, C., Guo, Z., Yan, Y., Zhu, S., Xie, Y., Zhao, Y. S., Zhu, W., & Tian, H. (2013) · ACS Applied Materials & Interfaces · doi:10.1021/am302466m · Cited by 201

Single Molecules, Cells, and Super‐Resolution Optics (Nobel Lecture)

Betzig, E. (2015) · Angewandte Chemie International Edition · doi:10.1002/anie.201501003 · Cited by 193

Structural relaxation of rhodamine dyes with different N-substitution patterns: A study of fluorescence decay times and quantum yields

Vogel, M., Rettig, W., Sens, R., & Drexhage, K. H. (1988) · Chemical Physics Letters · doi:10.1016/0009-2614(88)85007-3 · Cited by 177

Consideration of Molecular Structure in the Excited State to Design New Luminogens with Aggregation‐Induced Emission

Kokado, K., & Sada, K. (2019) · Angewandte Chemie International Edition · doi:10.1002/anie.201814462 · Cited by 171

A structural remedy toward bright dipolar fluorophores in aqueous media

Singha, S., Kim, D., Roy, B., Sambasivan, S., Moon, H., Rao, A. S., Kim, J. Y., Joo, T., Park, J. W., Rhee, Y. M., et al. (2015) · Chemical Science · doi:10.1039/c5sc01076d · Cited by 170

Cyanine Conformational Restraint in the Far-Red Range

Michie, M. S., Götz, R., Franke, C., Bowler, M., Kumari, N., Magidson, V., Levitus, M., Loncarek, J., Sauer, M., & Schnermann, M. J. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.7b07272 · Cited by 170

Spin-Allowed Transitions Control the Formation of Triplet Excited States in Orthogonal Donor-Acceptor Dyads

Buck, J. T., Boudreau, A. M., DeCarmine, A., Wilson, R. W., Hampsey, J., & Mani, T. (2019) · Chem · doi:10.1016/j.chempr.2018.10.001 · Cited by 170

Time-Dependent Density Functional Theory (TDDFT) Study of the Excited Charge-Transfer State Formation of a Series of Aromatic Donor−Acceptor Systems

Jamorski Jödicke, C., & Lüthi, H. P. (2003) · Journal of the American Chemical Society · doi:10.1021/ja020361+ · Cited by 168

Spin–Orbit Charge-Transfer Intersystem Crossing (SOCT-ISC) in Bodipy-Phenoxazine Dyads: Effect of Chromophore Orientation and Conformation Restriction on the Photophysical Properties

Dong, Y., Sukhanov, A. A., Zhao, J., Elmali, A., Li, X., Dick, B., Karatay, A., & Voronkova, V. K. (2019) · The Journal of Physical Chemistry C · doi:10.1021/acs.jpcc.9b06170 · Cited by 159

Branching in Amyloid Fibril Growth

Andersen, C. B., Yagi, H., Manno, M., Martorana, V., Ban, T., Christiansen, G., Otzen, D. E., Goto, Y., & Rischel, C. (2009) · Biophysical Journal · doi:10.1016/j.bpj.2008.11.024 · Cited by 158

Quantitatively Mapping Cellular Viscosity with Detailed Organelle Information via a Designed PET Fluorescent Probe

Liu, T., Liu, X., Spring, D. R., Qian, X. H., Cui, J., & Xu, Z. (2014) · Scientific Reports · doi:10.1038/srep05418 · Cited by 155

Dual fluorescence of donor-acceptor molecules and the Twisted Intramolecular Charge Transfer (TICT) states

Grabowski, Z. R., Rotkiewicz, K., & Siemiarczuk, A. (1979) · Journal of Luminescence · doi:10.1016/0022-2313(79)90153-4 · Cited by 154

Cy3B™: Improving the Performance of Cyanine Dyes

Cooper, M. E., Ebner, A., Briggs, M., Burrows, M., Gardner, N., Richardson, R., & West, R. (2004) · Journal of Fluorescence · doi:10.1023/b:jofl.0000016286.62641.59 · Cited by 153

Design and Synthesis of Highly Sensitive Fluorogenic Substrates for Glutathione S-Transferase and Application for Activity Imaging in Living Cells

Fujikawa, Y., Urano, Y., Komatsu, T., Hanaoka, K., Kojima, H., Terai, T., Inoue, H., & Nagano, T. (2008) · Journal of the American Chemical Society · doi:10.1021/ja802423n · Cited by 146

One Stone, Three Birds: pH Triggered Transformation of Aminopyronine and Iminopyronine Based Lysosome Targeting Viscosity Probe for Cancer Visualization

Song, Y. Y., Zhang, H., Wang, X., Geng, X., Sun, Y., Liu, J., & Li, Z. (2020) · Analytical Chemistry · doi:10.1021/acs.analchem.0c04644 · Cited by 145

The role of amyloid-beta in the regulation of memory

Morley, J. E., & Farr, S. A. (2014) · Biochemical Pharmacology · doi:10.1016/j.bcp.2013.12.018 · Cited by 141

Development of a Series of Near-Infrared Dark Quenchers Based on Si-rhodamines and Their Application to Fluorescent Probes

Myochin, T., Hanaoka, K., Iwaki, S., Ueno, T., Komatsu, T., Terai, T., Nagano, T., & Urano, Y. (2015) · Journal of the American Chemical Society · doi:10.1021/jacs.5b00246 · Cited by 136

A new synthesis of symmetric boraindacene (BODIPY) dyes

Wu, L., & Burgess, K. (2008) · Chemical Communications · doi:10.1039/b810503k · Cited by 133

Consideration of Molecular Structure in the Excited State to Design New Luminogens with Aggregation‐Induced Emission

Kokado, K., & Sada, K. (2019) · Angewandte Chemie · doi:10.1002/ange.201814462 · Cited by 121

A New “Turn-on” Naphthalenedimide-Based Chemosensor for Mercury Ions with High Selectivity: Successful Utilization of the Mechanism of Twisted Intramolecular Charge Transfer, Near-IR Fluorescence, and Cell Images

Li, Q., Ming, P., Li, H., Zhong, C., Zhang, L., Cheng, X., Peng, X., Wang, Q., Qin, J., & Li, Z. (2012) · Organic Letters · doi:10.1021/ol300607m · Cited by 118

A Photoexcitation‐Induced Twisted Intramolecular Charge Shuttle

Chi, W., Qiao, Q., Lee, R., Liu, W., Teo, Y. S., Gu, D., Lang, M. J., Chang, Y., Xu, Z., & Liu, X. (2019) · Angewandte Chemie International Edition · doi:10.1002/anie.201902766 · Cited by 118

Improving the quantum yields of fluorophores by inhibiting twisted intramolecular charge transfer using electron-withdrawing group-functionalized piperidine auxochromes

Lv, X., Gao, C., Han, T., Shi, H., & Guo, W. (2019) · Chemical Communications · doi:10.1039/c9cc09138f · Cited by 116

Pseudo-Jahn–Teller and TICT-models: a photophysical comparison of meta- and para-DMABN derivatives

Rettig, W., Bliss, B., & Dirnberger, K. (1999) · Chemical Physics Letters · doi:10.1016/s0009-2614(99)00316-4 · Cited by 101

A Unified Push–Pull Model for Understanding the Ring-Opening Mechanism of Rhodamine Dyes

Chi, W., Qi, Q., Lee, R., Xu, Z., & Liu, X. (2020) · The Journal of Physical Chemistry C · doi:10.1021/acs.jpcc.9b11673 · Cited by 101

Engineering the Charge‐Transfer State to Facilitate Spin–Orbit Charge Transfer Intersystem Crossing in Spirobis[anthracene]diones

Lv, M., Yu, Y., Sandoval‐Salinas, M. E., Xu, J., Lei, Z., Casanova, D., Yang, Y., & Chen, J. (2020) · Angewandte Chemie International Edition · doi:10.1002/anie.202009439 · Cited by 101

7-Azabicyclo[2.2.1]heptane as a Unique and Effective Dialkylamino Auxochrome Moiety: Demonstration in a Fluorescent Rhodamine Dye

Song, X., Johnson, A., & Foley, J. (2008) · Journal of the American Chemical Society · doi:10.1021/ja8075617 · Cited by 96

Tracking RNA with light: selection, structure, and design of fluorescence turn-on RNA aptamers

Trachman, R. J., & Ferré-D’Amaré, A. R. (2019) · Quarterly Reviews of Biophysics · doi:10.1017/s0033583519000064 · Cited by 82

ThX – a next-generation probe for the early detection of amyloid aggregates

Needham, L.-M., Weber, J., Varela, J. A., Fyfe, J. W. B., Do, D. T., Xu, C. K., Tutton, L., Cliffe, R., Keenlyside, B., Klenerman, D., et al. (2020) · Chemical Science · doi:10.1039/c9sc04730a · Cited by 82

Photoinduced Electron Transfer in Organic Solar Cells

Song, P., Li, Y., Ma, F., Pullerits, T., & Sun, M. (2016) · The Chemical Record · doi:10.1002/tcr.201500244 · Cited by 81

A TICT based two-photon fluorescent probe for bisulfite anion and its application in living cells

Yu, S., Yang, X., Shao, Z., Feng, Y., Xi, X., Shao, R., Guo, Q., & Meng, X. (2016) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2016.05.099 · Cited by 64

A General Strategy to Enhance Donor‐Acceptor Molecules Using Solvent‐Excluding Substituents

Hoelzel, C. A., Hu, H., Wolstenholme, C. H., Karim, B. A., Munson, K. T., Jung, K. H., Zhang, H., Liu, Y., Yennawar, H. P., Asbury, J. B., et al. (2020) · Angewandte Chemie International Edition · doi:10.1002/anie.201915744 · Cited by 64

Quantitative assessment of rhodamine spectra

Zhou, W., Fang, X., Qiao, Q., Jiang, W., Zhang, Y., & Xu, Z. (2021) · Chinese Chemical Letters · doi:10.1016/j.cclet.2021.02.003 · Cited by 59

Azetidine-Containing Heterospirocycles Enhance the Performance of Fluorophores

Zhou, J., Lin, X., Ji, X., Xu, S., Liu, C., Dong, X., & Zhao, W. (2020) · Organic Letters · doi:10.1021/acs.orglett.0c01414 · Cited by 53

Engineering the Charge‐Transfer State to Facilitate Spin–Orbit Charge Transfer Intersystem Crossing in Spirobis[anthracene]diones

Lv, M., Yu, Y., Sandoval‐Salinas, M. E., Xu, J., Lei, Z., Casanova, D., Yang, Y., & Chen, J. (2020) · Angewandte Chemie · doi:10.1002/ange.202009439 · Cited by 32

Solvent effects on intramolecular charge separation

Köhler, G., Wolschann, P., & Rotkiewicz, K. (1992) · Journal of Chemical Sciences · doi:10.1007/bf02863364 · Cited by 15

Near-infrared (NIR) fluorescence-emitting small organic molecules for cancer imaging and therapy

Li, H., Kim, Y., Jung, H., Hyun, J. Y., & Shin, I. (2022) · Chemical Society Reviews · doi:10.1039/d2cs00722c · Cited by 356

Design strategies and applications of cyanine dyes in phototherapy

Yuan, J., Yang, H., Huang, W., Liu, S., Zhang, H., Zhang, X., & Peng, X. (2025) · Chemical Society Reviews · doi:10.1039/d3cs00585b · Cited by 143

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