The DOI matches its Crossref record; 63 of the 63 references it cites were found in a registry or an index.
Aggregation‐Induced Emission (AIE): A Historical Perspective
Abstract
Aggregation‐induced emission (AIE) has attracted considerable interest over the last twenty years. In contrast to the large number of available reviews focusing specifically on AIE, this Essay discusses the AIE phenomenon from a broader perspective, with an emphasis on early observations related to AIE made long before the term was coined. Illustrative examples are highlighted from the 20th century where fluorescence enhancement upon rigidification of dyes in viscous or solid environments or J‐aggregate formation was studied. It is shown that these examples already include typical AIE luminogens such as tetraphenylethylene (TPE) as well as stilbenes and oligo‐ or polyphenylenevinylenes and ‐ethynylenes, which became important fluorescent solid‐state materials in OLED research in the 1990s. Further examples include cyanine dyes such as thiazole orange (TO) or its dimers (TOTOs), which have been widely applied as molecular probes in nucleic acid research. The up to 10 000‐fold fluorescence enhancement of such dyes upon intercalation into double‐stranded DNA, attributable to the restricted intramolecular motion (RIM) concept, afforded commercial products for bioimaging and fluorescence sensing applications already in the early 1990s.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“In brief, excitation energy in “floppy” molecules with built-in flexibility or free rotating groups (e.g., rotatable aromatic rings) can be nonradiatively dissipated when their motions are not perturbed (as in the case of solution), resulting in these molecules being nonemissive.”
From The Pursuit of Shortwave Infrared-Emitting Nanoparticles with Bright Fluorescence through Molecular Design and Excited-State Engineering of Molecular Aggregates (2022) · cites this paper as [131]
In the citing paper
“However, when an aggregation occurs or when a molecule is introduced into a rigid microenvironment, the motional freedom becomes restricted, and light emission is turned on or substantially enhanced.”
From The Pursuit of Shortwave Infrared-Emitting Nanoparticles with Bright Fluorescence through Molecular Design and Excited-State Engineering of Molecular Aggregates (2022) · cites this paper as [131]
Citations
Cites
Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole
Luo, J., Xie, Z., Lam, J. W. Y., Cheng, L., Tang, B. Z., Chen, H., Qiu, C., Kwok, H. S., Zhan, X., Liu, Y., et al. (2001) · Chemical Communications · doi:10.1039/b105159h · Cited by 8,358
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
The exciton model in molecular spectroscopy
Kasha, M., Rawls, H. R., & Ashraf El-Bayoumi, M. (1965) · Pure and Applied Chemistry · doi:10.1351/pac196511030371 · Cited by 4,253
Aggregation-induced emission: phenomenon, mechanism and applications
Hong, Y., Lam, J. W. Y., & Tang, B. Z. (2009) · Chemical Communications · doi:10.1039/b904665h · Cited by 4,153
J‐Aggregates: From Serendipitous Discovery to Supramolecular Engineering of Functional Dye Materials
Würthner, F., Kaiser, T. E., & Saha‐Möller, C. R. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201002307 · Cited by 2,597
Self-citationStandards for photoluminescence quantum yield measurements in solution (IUPAC Technical Report)
Brouwer, A. M. (2011) · Pure and Applied Chemistry · doi:10.1351/pac-rep-10-09-31 · Cited by 2,229
Hestand, N. J., & Spano, F. C. (2018) · Chemical Reviews · doi:10.1021/acs.chemrev.7b00581 · Cited by 1,984
Enhanced Emission and Its Switching in Fluorescent Organic Nanoparticles
An, B., Kwon, S., Jung, S.-D., & Park, S. Y. (2002) · Journal of the American Chemical Society · doi:10.1021/ja0269082 · Cited by 1,952
Poly(aryleneethynylene)s: Syntheses, Properties, Structures, and Applications
Bunz, U. H. F. (2000) · Chemical Reviews · doi:10.1021/cr990257j · Cited by 1,661
Aggregation‐Induced Emission: New Vistas at the Aggregate Level
Zhao, Z., Zhang, H., Lam, J. W. Y., & Tang, B. Z. (2020) · Angewandte Chemie International Edition · doi:10.1002/anie.201916729 · Cited by 1,442
Flagged first, then by citations
Research works printed but not linked: 3
- 10.1021/ja005933 · DOI
- Guan J., 2020, Angew. Chem. Int. Ed.
- Scheibe G., 1936, Angew. Chem., 49, 563
Cited by
Sorted by citations
Items 101–200 of 696
Zhang, Y., Fan, M., Xu, Z., Jiang, Y., Ding, H., Li, Z., Shu, K., Zhao, M., Feng, G., Yong, K., et al. (2023) · Journal of Nanobiotechnology · doi:10.1186/s12951-023-01864-9 · Cited by 36
“Therefore, AIEgens have attracted extensive attention among scientists and have been recognized as a better option than conventional organic probes in recent years[5–8].”
BackgroundTang, L., Wu, Z., Zhang, Q., Hu, Q., Dang, X., Cui, F., Tang, L., & Xiao, T. (2024) · Chemical Communications · doi:10.1039/d4cc00616j · Cited by 36
Choi, S.-K., Rho, J., Yoon, S. E., Seok, J., Kim, H., Min, J., Yoon, W., Lee, S., Yun, H., Kwon, O., et al. (2020) · Bioconjugate Chemistry · doi:10.1021/acs.bioconjchem.0c00467 · Cited by 35
Rouillon, J., Monnereau, C., & Andraud, C. (2021) · Chemistry - A European Journal · doi:10.1002/chem.202100926 · Cited by 36
Fluorescent supramolecular polymers of barbiturate dyes with thiophene-cored twisted π-systems
Kawaura, M., Aizawa, T., Takahashi, S., Miyasaka, H., Sotome, H., & Yagai, S. (2021) · Chemical Science · doi:10.1039/d1sc06246h · Cited by 35
Xiao, F., Li, Y., Li, J., Lei, D., Wang, G., Zhang, T., Hu, X., & Dou, X. (2022) · Aggregate · doi:10.1002/agt2.260 · Cited by 36
Helmers, I., Hossain, M. S., Bäumer, N., Wesarg, P., Soberats, B., Shimizu, L. S., & Fernández, G. (2022) · Angewandte Chemie International Edition · doi:10.1002/anie.202200390 · Cited by 34
He, S., Yu, S., Wei, J., Ding, L., Yang, X., & Wu, Y. (2022) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2022.114043 · Cited by 34
Organosilicon Fluorescent Materials
Chen, Z., Feng, S., & Wang, D. (2023) · Polymers · doi:10.3390/polym15020332 · Cited by 33
Engineering the solid-state luminescence of organic crystals and cocrystals
Dar, A. A., Lone, S. H., Ahmad, I., Ahangar, A. A., Ganie, A. A., & Femina, C. (2023) · Materials Advances · doi:10.1039/d3ma00853c · Cited by 33
Misra, S., Singh, P., Das, A., Brandão, P., Sahoo, P., Sepay, N., Bhattacharjee, G., Datta, P., Mahapatra, A. K., Satpati, B., et al. (2020) · Materials Advances · doi:10.1039/d0ma00584c · Cited by 33
Long, R., Tang, C., Wei, Q., Tong, C., Tong, X., Shi, S., Guo, Y., & Yang, Y. (2021) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2021.130666 · Cited by 33
Aggregation‐Dependent Thermally Activated Delayed Fluorescence Emitters: AIE or ACQ?
Wu, Y., Ni, F., Chen, Z., Yang, W., Xiang, Y., Gong, S., Cao, X., & Yang, C. (2023) · Advanced Optical Materials · doi:10.1002/adom.202300186 · Cited by 33
Lee, J. J., Kang, J., & Kim, C. (2023) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2023.133168 · Cited by 33
Xiao, T., Chen, D., Qian, H., Shen, Y., Zhang, L., Li, Z., & Sun, X. (2022) · Dyes and Pigments · doi:10.1016/j.dyepig.2022.110958 · Cited by 32
Ni, Y., Yang, L., Kong, L., Wang, C., Zhang, Q., & Yang, J. (2022) · Materials Chemistry Frontiers · doi:10.1039/d2qm00937d · Cited by 32
Application of Nanomaterials in the Production of Biomolecules in Microalgae: A Review
Yuan, X.-L., Gao, X., Liu, C., Liang, W., Xue, H., Li, Z., & Jin, H. (2023) · Marine Drugs · doi:10.3390/md21110594 · Cited by 31
Budziak-Wieczorek, I., Ślusarczyk, L., Myśliwa‐Kurdziel, B., Kurdziel, M., Srebro‐Hooper, M., Korona‐Głowniak, I., Gagoś, M., Gładyszewski, G., Stepulak, A., Kluczyk, D., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-26690-1 · Cited by 31
Zhang, Q., Cui, F., Dang, X., Wang, Q., Li, Z., Sun, X., & Xiao, T. (2024) · Chemistry - A European Journal · doi:10.1002/chem.202401426 · Cited by 30
Asthana, S., Mouli, M. S. S. V., Tamrakar, A., Wani, M. A., Mishra, A. K., Pandey, R., & Pandey, M. D. (2024) · Analytical Methods · doi:10.1039/d4ay00618f · Cited by 30
Bhaumik, S. K., & Banerjee, S. (2022) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.2c07836 · Cited by 30
Boron difluoride hydrazone (BODIHY) complexes: A new class of fluorescent molecular rotors
Bismillah, A. N., & Aprahamian, I. (2023) · Journal of Physical Organic Chemistry · doi:10.1002/poc.4485 · Cited by 30
A salicylaldoximate-based AIE probe for the detection of the nerve agent simulant DCP
Li, D., Zong, L., Li, D., Sui, S., Xiao, Y., Zhuang, B. A., Shen, Y., Huang, Z., & Wu, W. (2023) · Journal of Materials Chemistry C · doi:10.1039/d2tc05201f · Cited by 29
Yi, S., Liu, H., Chen, Z., Fan, C., Liu, G., & Pu, S. (2023) · Dyes and Pigments · doi:10.1016/j.dyepig.2023.111211 · Cited by 29
A tetrazine-fused aggregation induced emission luminogen for bioorthogonal fluorogenic bioprobe
Choi, S.-K., Lee, Y., Yoon, S. E., Choi, H., Kim, J., Kim, J. H., Lee, S., Kim, W., & Kim, E. (2021) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2021.129966 · Cited by 28
Stereodefined tetraarylethylenes: Synthesis and applications
Zhang, M., & Zhao, W. (2021) · Aggregate · doi:10.1002/agt2.60 · Cited by 28
Xiao, T., Shen, Y., Bao, C., Diao, K., Ren, D., Qian, H., & Zhang, L. (2021) · RSC Advances · doi:10.1039/d1ra06239e · Cited by 28
Behera, S. K., Kainda, R., Basu, S., & Chaudhary, Y. S. (2022) · Applied Materials Today · doi:10.1016/j.apmt.2022.101407 · Cited by 29
Design of Aurone‐Based Dual‐State Emissive (DSE) Fluorophores
Berdnikova, D. V., Steup, S., Bolte, M., & Suta, M. (2023) · Chemistry - A European Journal · doi:10.1002/chem.202300356 · Cited by 27
Full Visible Spectrum and White Light Emission with a Single, Input-Tunable Organic Fluorophore
Zavaleta, A., Олегович, Л. А., Monteiro, J. H. S. K., Uchida, S., Bell, T. W., de Bettencourt‐Dias, A., Varganov, S. A., & Gallucci, J. C. (2020) · Journal of the American Chemical Society · doi:10.1021/jacs.0c08182 · Cited by 27
Redox-active tetraaryldibenzoquinodimethanes
Ishigaki, Y., Sugawara, K., Tadokoro, T., Hayashi, Y., Harimoto, T., & Suzuki, T. (2021) · Chemical Communications · doi:10.1039/d1cc02260a · Cited by 27
Bridged Aromatic Oxo‐ and Thioethers with Intense Emission in Solution and the Solid State
Riebe, S., Adam, S., Roy, B., Maisuls, I., Daniliuc, C. G., Dubbert, J., Strassert, C. A., Schapiro, I., & Voskuhl, J. (2021) · Chemistry - An Asian Journal · doi:10.1002/asia.202100492 · Cited by 27
Luminescent organic molecular frameworks from tetraphenylethylene-based building blocks
He, X., Bi, H., & Wei, P. (2023) · Journal of Materials Chemistry C · doi:10.1039/d2tc04713f · Cited by 27
Molecular Rotors: Fluorescent Sensors for Microviscosity and Conformation of Biomolecules
Páez-Pérez, M., & Kuimova, M. K. (2023) · Angewandte Chemie · doi:10.1002/ange.202311233 · Cited by 27
Saczuk, K., Dudek, M., Matczyszyn, K., & Deiana, M. (2024) · Nanoscale Horizons · doi:10.1039/d4nh00186a · Cited by 26
Machine Learning for Organic Fluorescent Materials
Zhong, J., Zhu, W., Shen, S., Zhou, N., Xi, M., Du, K., Wang, D., & Tang, B. Z. (2025) · Aggregate · doi:10.1002/agt2.70089 · Cited by 26
“However, the design and development of AIE still face challenges due to the complex relationship between its luminous properties and molecular structure and the lack of systematic theoretical guidance [96].”
Guo, H., Lin, J., Zheng, L., & Yang, F. (2021) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2021.119744 · Cited by 26
Advancements in Biosensors Based on the Assembles of Small Organic Molecules and Peptides
Deng, D., Chang, Y. K., Liu, W., Ren, M., Xia, N., & Hao, Y. (2023) · Biosensors · doi:10.3390/bios13080773 · Cited by 26
Su, H., Shang, W., Li, G., Yan, W., Yan, X., Tang, B. Z., & Qin, W. (2024) · Advanced Functional Materials · doi:10.1002/adfm.202414976 · Cited by 26
Abedi, S. A. A., Chi, W., Tan, D., Shen, T., Wang, C., Ang, E. C. X., Tan, C., Anariba, F., & Liu, X. (2021) · The Journal of Physical Chemistry A · doi:10.1021/acs.jpca.1c06263 · Cited by 25
Kumsampao, J., Chaiwai, C., Sukpattanacharoen, C., Nalaoh, P., Chawanpunyawat, T., Chasing, P., Namuangruk, S., Kungwan, N., Sudyoadsuk, T., & Promarak, V. (2021) · Advanced Photonics Research · doi:10.1002/adpr.202100141 · Cited by 25
Biosensors for the Detection of Enzymes Based on Aggregation-Induced Emission
Gao, F., Liu, G., Qiao, M., Li, Y., & Yi, X. (2022) · Biosensors · doi:10.3390/bios12110953 · Cited by 25
Zhao, Y., Hao, H., Wang, H., Sun, L., Zhang, N., Zhang, X. K., & Liang, J. (2023) · Microchemical Journal · doi:10.1016/j.microc.2023.108626 · Cited by 25
Ma, D., Zhuang, W., Liu, Q., Chen, J., Li, S., Li, S., & Chen, M. (2023) · Chemical Engineering Journal · doi:10.1016/j.cej.2023.146792 · Cited by 25
Morselli, G., Eggenweiler, T. H., Villa, M., Prescimone, A., & Wenger, O. S. (2025) · Journal of the American Chemical Society · doi:10.1021/jacs.5c08541 · Cited by 24
Li, X., Zhang, X., Zhang, F., Luo, X., & Luo, H. (2022) · Advanced Synthesis & Catalysis · doi:10.1002/adsc.202200251 · Cited by 24
Dai, L., Mao, W., Hu, L., Song, J., Zhang, Y., Huang, T., & Wang, M. (2022) · Dyes and Pigments · doi:10.1016/j.dyepig.2022.110436 · Cited by 24
Fluorescent Silk Obtained by Feeding Silkworms with Fluorescent Materials †
Wu, Z., Sun, Z., & Xiong, H. (2023) · Chinese Journal of Chemistry · doi:10.1002/cjoc.202300043 · Cited by 24
DNA Framework-Engineered Assembly of Cyanine Dyes for Structural Identification of Nucleic Acids
Li, C., Chen, J., Man, T., Chen, B., Li, J., Li, Q., Yang, X., Wan, Y., Fan, C., & Shen, J. (2024) · JACS Au · doi:10.1021/jacsau.3c00826 · Cited by 24
Visual detection of viscosity through activatable molecular rotor with aggregation-induced emission
Xu, L., Wu, K., Han, R., Sui, Y., Huang, C., Huang, W., & Liu, L. (2021) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2021.120016 · Cited by 23
Turley, A. T., Saha, P. K., Danos, A., Bismillah, A. N., Monkman, A. P., Yufit, D. S., Curchod, B. F. E., Etherington, M. K., & McGonigal, P. R. (2022) · Angewandte Chemie International Edition · doi:10.1002/anie.202202193 · Cited by 23
AIPE-active cationic Ir( iii ) complexes for efficient detection of 2,4,6-trinitrophenol and oxygen
He, P., Chen, Y., Li, X., Yan, Y., & Liu, C. (2022) · Dalton Transactions · doi:10.1039/d2dt03537e · Cited by 23
Ma, H., Li, R., Meng, H., Tian, M., Zhang, X., Liu, Y., Li, L., Yuan, J., & Wei, Y. (2023) · Small · doi:10.1002/smll.202204778 · Cited by 23
Can We See SEI Directly by Naked Eyes?
Wang, M., Liang, H., Wang, C., Wang, A., Song, Y., Wang, J., Wang, B., Wei, Y., He, X., & Yang, Y. (2023) · Advanced Materials · doi:10.1002/adma.202306683 · Cited by 23
Deng, H., Li, X., Pan, L., Tang, M., Wang, B., Zhang, Y., Zhang, H., Kong, X., Wang, S., & Zhu, W. (2024) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.4c03484 · Cited by 22
Burkinshaw, S. M. (2021) · Coloration Technology · doi:10.1111/cote.12550 · Cited by 22
Tyrosine-Decorated Gold Nanoclusters Chelated Cerium(III) for Fluorescence Detection of Dopamine
Wu, F., Zhu, J., Weng, G., Li, J.-J., & Zhao, J. (2021) · ACS Applied Nano Materials · doi:10.1021/acsanm.1c02982 · Cited by 23
Xiao, T., Qian, H., Li, X., Wu, Z., Li, Z., & Sun, X. (2023) · Dyes and Pigments · doi:10.1016/j.dyepig.2023.111289 · Cited by 22
Zeng, W., Zhu, L., Chen, Y., & Lin, M. (2021) · Dyes and Pigments · doi:10.1016/j.dyepig.2021.109324 · Cited by 22
Li, Q., Huang, K., Qiu, Q., Zhang, X., Qin, D., & Zeng, X. (2021) · Dyes and Pigments · doi:10.1016/j.dyepig.2021.109537 · Cited by 22
Mechanophoric hydrogels: when mechanical stress produces useful responses
Soares, F. A., & Besenius, P. (2025) · Organic Chemistry Frontiers · doi:10.1039/d4qo02060j · Cited by 21
“35 More complex mechanisms of fluorescence like the Förster Resonance Energy Transfer (FRET) or more recently the Excited State Intramolecular Proton Transfer (ESIPT) are also encountered.”
Li, Z., Zhang, J., Wu, Z., Lei, H., Zhao, Y., Qi, W., Gao, X., Jiang, F., Liu, Y., Chen, L., et al. (2025) · Advanced Science · doi:10.1002/advs.202510147 · Cited by 21
Strategies for enhancing the signal-to-noise ratio in optical lateral flow immunoassay: A review
Yuan, J., Huang, L., & Wang, J. (2025) · TrAC Trends in Analytical Chemistry · doi:10.1016/j.trac.2025.118494 · Cited by 21
Sun, Z., Ni, Y., Prakasam, T., Liu, W., Wu, H., Zhang, Z., Di, H., Baldridge, K. K., Trabolsi, A., & Olson, M. A. (2021) · Chemistry - A European Journal · doi:10.1002/chem.202100601 · Cited by 21
Biesen, L., May, L., Nirmalananthan‐Budau, N., Hoffmann, K., Resch‐Genger, U., & Mueller, T. J. J. (2021) · Chemistry - A European Journal · doi:10.1002/chem.202102052 · Cited by 21
Zhu, M., Zhong, M., Chen, M., Huang, S., Li, Y., & Cao, F. (2022) · Optical Materials · doi:10.1016/j.optmat.2022.112059 · Cited by 21
Mobed, A., & Hasanzadeh, M. (2022) · RSC Advances · doi:10.1039/d1ra09393b · Cited by 25
Tang, F., Wang, Q., Gao, Y.-N., Zhang, Y., Liang, Y., Lu, Z., Liu, R., & Ding, A. (2022) · Bioconjugate Chemistry · doi:10.1021/acs.bioconjchem.2c00140 · Cited by 21
Ramdass, A., Sathish, V., & Thanasekaran, P. (2022) · Results in Chemistry · doi:10.1016/j.rechem.2022.100337 · Cited by 22
Chen, J., Stenspil, S. G., Kaziannis, S., Kacenauskaite, L., Lenngren, N., Kloz, M., Flood, A. H., & Laursen, B. W. (2022) · ACS Applied Nano Materials · doi:10.1021/acsanm.2c01899 · Cited by 21
Ibrahim, N., Loumaigne, M., Grolleau, J., Allain, M., & Frère, P. (2022) · Molecular Systems Design & Engineering · doi:10.1039/d2me00058j · Cited by 21
Mitochondria MicroRNA Spatial Imaging via pH-Responsive Exonuclease-Assisted AIE Nanoreporter
Du, J., Qiao, Y., Meng, X., Wei, W., Dai, W., Yang, L., Yang, C., & Dong, H. (2022) · Analytical Chemistry · doi:10.1021/acs.analchem.2c00941 · Cited by 21
A simple strategy for the efficient design of mitochondria-targeting NIR-II phototheranostics
Li, Y., He, M., Liu, Z., Chuah, C., Tang, Y., Duo, Y., & Tang, B. Z. (2023) · Journal of Materials Chemistry B · doi:10.1039/d2tb02295h · Cited by 23
Yu, Y., Chao, X., Xie, M., Zhou, Y., Ma, C., Zhou, H., Sun, Q., Pan, Y., Yang, W., & Xue, S. (2023) · Dyes and Pigments · doi:10.1016/j.dyepig.2023.111306 · Cited by 21
Chen, C., Sun, Y., Zhao, Y. C., VanderLinden, R. T., Tuo, W., Zhang, F., Zhang, S., Sepehrpour, H., Yan, C., Wang, J., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2102602118 · Cited by 21
Zhang, W., Liu, M.-Q., & Luo, Y. (2025) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2025.216555 · Cited by 20
Li, J., Daniliuc, C. G., Kartha, K. K., Fernández, G., Kehr, G., & Erker, G. (2021) · Journal of the American Chemical Society · doi:10.1021/jacs.0c12236 · Cited by 20
Halder, S., Nayak, B., Bhattacharjee, B., Ramesh, A., & Das, G. C. (2021) · Journal of Materials Chemistry C · doi:10.1039/d1tc02089g · Cited by 20
A novel aggregation-induced enhanced emission aromatic molecule: 2-aminophenylboronic acid dimer
Li, X., Wang, D., Zhang, Y., Lu, W., Yang, S., Hou, G., Zhao, Z., Qin, H., Zhang, Y., Li, M., et al. (2021) · Chemical Science · doi:10.1039/d1sc03765j · Cited by 20
Biesen, L., Krenzer, J., Nirmalananthan‐Budau, N., Resch‐Genger, U., & Mueller, T. J. J. (2022) · Chemical Science · doi:10.1039/d2sc00415a · Cited by 20
Tao, M., Mao, J., Bao, Y., Liu, F., Mai, Y., Guan, S., Luo, S., Huang, Y., Li, Z., Zhong, Y., et al. (2023) · Advanced Science · doi:10.1002/advs.202205435 · Cited by 18
Ye, X., Wang, S., Zhou, P., Zhang, D., & Zhu, P. (2023) · Physical Chemistry Chemical Physics · doi:10.1039/d3cp00654a · Cited by 20
Xu, T., Yin, X. X., Zhai, C., Chen, D., Yang, X., Hu, S., Hu, K., Shang, Y., Dong, J., Yao, Z., et al. (2023) · Chemical Science · doi:10.1039/d3sc04006b · Cited by 20
Burkinshaw, S. M. (2023) · Coloration Technology · doi:10.1111/cote.12745 · Cited by 20
Humeniuk, A., & Glover, W. J. (2024) · Journal of Chemical Theory and Computation · doi:10.1021/acs.jctc.3c01018 · Cited by 20
López‐Gandul, L., Rodríguez, R., Vanthuyne, N., Crassous, J., & Sánchez, L. (2024) · Nanoscale · doi:10.1039/d4nr02110j · Cited by 20
Zeng, C., Wang, H., Wang, B., Hu, P., Zhao, K., & Donnio, B. (2024) · Chemistry of Materials · doi:10.1021/acs.chemmater.4c01213 · Cited by 20
Rouillon, J., Blahut, J., Jean, M., Albalat, M., Vanthuyne, N., Lesage, A., Ali, L. M. A., Hadj‐Kaddour, K., Onofre, M., Gary‐Bobo, M., et al. (2020) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.0c15810 · Cited by 20
Room-Temperature Phosphorescence Vapochromism through Conformational Control
Fermi, A., Gahlot, S., Jorand, E., D’Agostino, S., Dai, Y., Negri, F., Moustrou, C., Gingras, M., & Ceroni, P. (2025) · Journal of the American Chemical Society · doi:10.1021/jacs.5c07339 · Cited by 19
Xiao, T., Tang, L., Ren, D., Diao, K., Li, Z., & Sun, X. (2022) · Chemistry - A European Journal · doi:10.1002/chem.202203463 · Cited by 19
Chemical fuel-driven gelation with dissipative assembly-induced emission
Cheng, M. H., Chen, D., Zhang, L., Xiao, T., Jiang, J., & Wang, L. (2023) · Organic Chemistry Frontiers · doi:10.1039/d2qo01888h · Cited by 19
Ganz, D., Geng, P., & Wagenknecht, H. (2023) · ACS Chemical Biology · doi:10.1021/acschembio.3c00079 · Cited by 19
Clusteroluminescence of Unconjugated Polymers: A Review
Сахно, Т. В., Sakhno, Y. E., & Kuchmiy, S. Y. (2023) · Theoretical and Experimental Chemistry · doi:10.1007/s11237-023-09768-3 · Cited by 18
Furuta, M., Arii, S., Umeda, H., Matsukawa, R., Shizu, K., Kaji, H., Kawashima, S. A., Hori, Y., Tomita, T., Sohma, Y., et al. (2024) · Advanced Science · doi:10.1002/advs.202401346 · Cited by 18
Mateen, F., Hwang, T. G., Boesel, L. F., Choi, W. J., Kim, J. P., Gong, X. N., Park, J. M., & Hong, S. (2021) · International Journal of Energy Research · doi:10.1002/er.6939 · Cited by 19
“Typical AIE fluorophores (AIEgen) are organic molecules that contain freely rotatable functional moieties such as tetraphenylethene (TPE) or triphenylamine (TPA) and are non-emissive in good solvents but exhibit enhanced emission when dispersed in polymers or in solid-state.(31,32) In 2014, Banal and et al firstly rep…”
BackgroundPotopnyk, M. A., Kravets, M., Luboradzki, R., Volyniuk, D. Y., Sashuk, V., & Gražulevičius, J. V. (2020) · Organic & Biomolecular Chemistry · doi:10.1039/d0ob02225j · Cited by 18
One-step light-up metabolic probes for in situ discrimination and killing of intracellular bacteria
Yu, E. Y., Lee, M. M. S., Chau, J. H. C., Lam, K. W. K., Park, H., Kwok, R. T. K., Lam, J. W. Y., Li, Y., & Tang, B. Z. (2022) · Materials Chemistry Frontiers · doi:10.1039/d1qm01495a · Cited by 18
Xu, W., Hu, D., Wang, Z., Wang, G., Liu, K., Liang, J., Miao, R., & Fang, Y. (2022) · The Journal of Physical Chemistry Letters · doi:10.1021/acs.jpclett.2c01228 · Cited by 18
Geng, P., List, E., Rönicke, F., & Wagenknecht, H. (2022) · Chemistry - A European Journal · doi:10.1002/chem.202203156 · Cited by 18
Goyal, H., Annan, I., Ahluwalia, D., Bag, A., & Gupta, R. (2023) · Sensors · doi:10.3390/s23041798 · Cited by 18
Metadata
- Authors
- Würthner, F.
- Affiliations
- University of Würzburg (DE)
- Corresponding author
- Würthner, Frank
- ORCID
- Würthner, Frank
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2020-07-13
- Volume
- 59
- Issue
- 34
- Pages
- 14192-14196
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W3042602012
- Cited by
- 696
- References
- 63
- Citations by year
- 2026: 68 · 2025: 130 · 2024: 133 · 2023: 131 · 2022: 120 · 2021: 95 · 2020: 19
- FWCI
- 4.68
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Angewandte Chemie International Edition (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Physical Sciences › Materials Science › Materials Chemistry › Luminescence and Fluorescent Materials
- Physical Sciences › Chemistry › Physical and Theoretical Chemistry › Photochemistry and Electron Transfer Studies
- Physical Sciences › Engineering › Electrical and Electronic Engineering › Organic Light-Emitting Diodes Research
- Keywords
- aggregation-induced emission, fluorescence enhancement, J-aggregate formation, tetraphenylethylene, stilbenes, poly(phenylene vinylene), cyanine dyes, thiazole orange, DNA intercalation, OLED materials, nucleic acid probes, bioimaging, fluorescence sensing
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review