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Plug-and-Play Optical Materials from Fluorescent Dyes and Macrocycles
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“This small-molecule ionic isolation lattices (SMILES) transfers the optical properties of typical cationic dyes directly and reliably from solution to high-density molecular crystals (Figure 8a).157,158”
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 [157]
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“SMILES crystals are formed with most cationic dyes, including cyanines, oxazines, and rhodamines, which deliver predictable optical properties and high fluorescence brightness with high dye densities (one dye per ∼4 nm3).”
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“An alternative approach is based on hierarchical coassembly using a scaffold ensuring spatial and electronic isolation to prohibit fluorescence quenching in an aggregate state.”
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 [157]
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Cites
Principles of Fluorescence Spectroscopy
Lakowicz, J. R. (1999) · Springer eBooks · doi:10.1007/978-1-4757-3061-6 · Cited by 26,948
A new generation of Ca2+ indicators with greatly improved fluorescence properties.
Grynkiewicz, G., Poenie, M., & Tsien, R. Y. (1985) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)83641-4 · Cited by 21,562
Principles of Fluorescence Spectroscopy
Lakowicz, J. R. (2006) · Springer eBooks · doi:10.1007/978-0-387-46312-4 · Cited by 19,795
Proteşescu, L., Yakunin, S., Bodnarchuk, M. I., Krieg, F., Caputo, R., Hendon, C. H., Yang, R., Walsh, A., & Kovalenko, M. V. (2015) · Nano Letters · doi:10.1021/nl5048779 · Cited by 9,243
Design and synthesis of an exceptionally stable and highly porous metal-organic framework
Li, H., Eddaoudi, M., O’Keeffe, M., & Yaghi, O. M. (1999) · Nature · doi:10.1038/46248 · Cited by 8,582
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
Zwischenmolekulare Energiewanderung und Fluoreszenz
Förster, T. (1948) · Annalen der Physik · doi:10.1002/andp.19484370105 · Cited by 8,285
Highly efficient phosphorescent emission from organic electroluminescent devices
Baldo, M. A., O’Brien, D. F., You, Y., Shoustikov, A., Sibley, S. P., Thompson, M. E., & Forrest, S. R. (1998) · Nature · doi:10.1038/25954 · Cited by 7,213
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
Theory of Concentration Quenching in Inorganic Phosphors
Dexter, D. L., & Schulman, J. H. (1954) · The Journal of Chemical Physics · doi:10.1063/1.1740265 · Cited by 2,264
Metals in Neurobiology: Probing Their Chemistry and Biology with Molecular Imaging
Que, E. L., Domaille, D. W., & Chang, C. J. (2008) · Chemical Reviews · doi:10.1021/cr078203u · Cited by 2,077
Hestand, N. J., & Spano, F. C. (2018) · Chemical Reviews · doi:10.1021/acs.chemrev.7b00581 · Cited by 1,984
Oriented 2D Covalent Organic Framework Thin Films on Single-Layer Graphene
Colson, J. W., Woll, A. R., Mukherjee, A., Levendorf, M. P., Spitler, E. L., Shields, V. B., Spencer, M. G., Park, J., & Dichtel, W. R. (2011) · Science · doi:10.1126/science.1202747 · Cited by 1,208
Polymer-encapsulated organic nanoparticles for fluorescence and photoacoustic imaging
Li, K., & Liu, B. (2014) · Chemical Society Reviews · doi:10.1039/c4cs00014e · Cited by 1,000
Yuan, W. Z., Lü, P., Chen, S., Lam, J. W. Y., Wang, Z., Liu, Y., Kwok, H. S., Ma, Y., & Tang, B. Z. (2010) · Advanced Materials · doi:10.1002/adma.200904056 · Cited by 973
X-ray analysis on the nanogram to microgram scale using porous complexes
Inokuma, Y., Yoshioka, S., Ariyoshi, J., Arai, T., Hitora, Y., Takada, K., Matsunaga, S., Rissanen, K. T., & Fujita, M. (2013) · Nature · doi:10.1038/nature11990 · Cited by 892
Porous Shape Persistent Fluorescent Polymer Films: An Approach to TNT Sensory Materials
Yang, J., & Swager, T. M. (1998) · Journal of the American Chemical Society · doi:10.1021/ja9742996 · Cited by 770
Fluorescent Polymer Nanoparticles Based on Dyes: Seeking Brighter Tools for Bioimaging
Reisch, A., & Klymchenko, A. S. (2016) · Small · doi:10.1002/smll.201503396 · Cited by 634
High-performance light-emitting diodes based on carbene-metal-amides
Di, D., Romanov, A. S., Yang, L., Richter, J. M., Rivett, J. P. H., Jones, S. T. E., Thomas, T. H., Abdi‐Jalebi, M., Friend, R. H., Linnolahti, M., et al. (2017) · Science · doi:10.1126/science.aah4345 · Cited by 616
High-performance light-emitting diodes based on carbene-metal-amides
Di, D., Romanov, A. S., Yang, L., Richter, J. M., Rivett, J., Jones, S. T. E., Thomas, T., Abdi Jalebi, M., Friend, R. H., Linnolahti, M., et al. (2017) · Apollo (University of Cambridge) · doi:10.17863/cam.10961 · Cited by 549
Bioconjugation of Ultrabright Semiconducting Polymer Dots for Specific Cellular Targeting
Wu, C., Schneider, T., Zeigler, M. B., Yu, J., Schiro, P. G., Burnham, D. R., McNeill, J., & Chiu, D. T. (2010) · Journal of the American Chemical Society · doi:10.1021/ja107196s · Cited by 530
Modular and predictable assembly of porous organic molecular crystals
Jones, J. T. A., Hasell, T., Wu, X., Bacsa, J., Jelfs, K. E., Schmidtmann, M., Chong, S. Y.-L., Adams, D. J., Trewin, A., Schiffmann, F., et al. (2011) · Nature · doi:10.1038/nature10125 · Cited by 523
Up-Conversion Fluorescence: Noncoherent Excitation by Sunlight
Baluschev, S. B., Miteva, T., Yakutkin, V. V., Nelles, G., Yasuda, A., & Wegner, G. (2006) · Physical Review Letters · doi:10.1103/physrevlett.97.143903 · Cited by 479
Lee, S., Chen, C., & Flood, A. H. (2013) · Nature Chemistry · doi:10.1038/nchem.1668 · Cited by 442
Self-citationChen, R. F., & Knutson, J. R. (1988) · Analytical Biochemistry · doi:10.1016/0003-2697(88)90412-5 · Cited by 424
Recent advances in solid‐state organic lasers
Chénais, S., & Forget, S. (2011) · Polymer International · doi:10.1002/pi.3173 · Cited by 389
On the efficiency limit of triplet–triplet annihilation for photochemical upconversion
Cheng, Y. Y., Khoury, T. H., Clady, R. G. C. R., Tayebjee, M. J. Y., Ekins‐Daukes, N. J., Crossley, M. J., & Schmidt, T. W. (2009) · Physical Chemistry Chemical Physics · doi:10.1039/b913243k · Cited by 382
Li, K., Qin, W., Ding, D., Tomczak, N., Geng, J., Liu, R., Liu, J., Zhang, X., Liu, H., Liu, B., et al. (2013) · Scientific Reports · doi:10.1038/srep01150 · Cited by 361
Fluorescence Quantum Yield of Aromatic Hydrocarbon Crystals
Katoh, R., Suzuki, K., Furube, A., Kotani, M., & Tokumaru, K. (2009) · The Journal of Physical Chemistry C · doi:10.1021/jp807684m · Cited by 259
Singh-Rachford, T. N., Haefelé, A., Ziessel, R. F., & Castellano, F. N. (2008) · Journal of the American Chemical Society · doi:10.1021/ja807056a · Cited by 241
Collective fluorescence switching of counterion-assembled dyes in polymer nanoparticles
Reisch, A., Didier, P., Richert, L., Oncul, S., Arntz, Y., Mély, Y., & Klymchenko, A. S. (2014) · Nature Communications · doi:10.1038/ncomms5089 · Cited by 226
Cyanine Conformational Restraint in the Far-Red Range
Michie, M. S., Götz, R., Franke, C., Bowler, M. M., Kumari, N., Magidson, V., Levitus, M., Lončarek, J., Sauer, M., & Schnermann, M. J. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.7b07272 · Cited by 172
Gray, V., Dzebo, D., Lundin, A., Alborzpour, J., Abrahamsson, M., Albinsson, B., & Moth‐Poulsen, K. (2015) · Journal of Materials Chemistry C · doi:10.1039/c5tc02626a · Cited by 170
Haketa, Y., Sasaki, S., Ohta, N., Masunaga, H., Ogawa, H., Mizuno, N., Araoka, F., Takezoe, H., & Maeda, H. (2010) · Angewandte Chemie International Edition · doi:10.1002/anie.201006356 · Cited by 151
Andreiuk, B., Reisch, A., Bernhardt, E., & Klymchenko, A. S. (2019) · Chemistry - An Asian Journal · doi:10.1002/asia.201801592 · Cited by 151
Near-Infrared Fluorescent NanoGUMBOS for Biomedical Imaging
Bwambok, D. K., El‐Zahab, B., Challa, S. K., Li, M., Chandler, L., Baker, G. A., & Warner, I. M. (2009) · ACS Nano · doi:10.1021/nn9010126 · Cited by 120
Hua, B., Zhou, W., Yang, Z., Zhang, Z., Shao, L., Zhu, H., & Huang, F. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b11156 · Cited by 108
Concentration Quenching Behavior of Thermally Activated Delayed Fluorescence in a Solid Film
Kim, H. S., Park, S.-R., & Suh, M. C. (2017) · The Journal of Physical Chemistry C · doi:10.1021/acs.jpcc.7b02369 · Cited by 104
Solid state concentration quenching of organic fluorophores in PMMA
Green, A. P., & Buckley, A. (2014) · Physical Chemistry Chemical Physics · doi:10.1039/c4cp05244g · Cited by 87
Reisch, A., Trofymchuk, K., Runser, A., Fleith, G., Rawiso, M., & Klymchenko, A. S. (2017) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.7b12292 · Cited by 87
Bialas, D., Zitzler‐Kunkel, A., Kirchner, E., Schmidt, D., & Würthner, F. (2016) · Nature Communications · doi:10.1038/ncomms12949 · Cited by 85
Al‐Kaysi, R. O., Ahn, T. S., Müller, A. M., & Bardeen, C. J. (2006) · Physical Chemistry Chemical Physics · doi:10.1039/b605925b · Cited by 82
Ion-based materials comprising planar charged species
Dong, B., & Maeda, H. (2012) · Chemical Communications · doi:10.1039/c2cc34407f · Cited by 57
Ion Materials Comprising Planar Charged Species
Haketa, Y., Honsho, Y., Seki, S., & Maeda, H. (2012) · Chemistry - A European Journal · doi:10.1002/chem.201200951 · Cited by 52
Experimental demonstration of photon upconversion via cooperative energy pooling
Weingarten, D. H., LaCount, M. D., van de Lagemaat, J., Rumbles, G., Lusk, M. T., & Shaheen, S. E. (2017) · Nature Communications · doi:10.1038/ncomms14808 · Cited by 51
Weaver's historic accessible collection of synthetic dyes: a cheminformatics analysis
Kuenemann, M. A., Szymczyk, M., Chen, Y., Sultana, N., Hinks, D., Freeman, H. S., Williams, A. J., Fourches, D., & Vinueza, N. R. (2017) · Chemical Science · doi:10.1039/c7sc00567a · Cited by 50
Qiao, B., Hirsch, B. E., Lee, S., Pink, M., Chen, C., Laursen, B. W., & Flood, A. H. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.7b01937 · Cited by 49
Self-citationFluorescence Spectra of Organic Crystals
Birks, J. B., & Wright, G. T. (1954) · Proceedings of the Physical Society Section B · doi:10.1088/0370-1301/67/9/301 · Cited by 48
Organic Styryl Dye Nanoparticles: Synthesis and Unique Spectroscopic Properties
Yao, H., Yamashita, M., & Kimura, K. (2008) · Langmuir · doi:10.1021/la802879e · Cited by 45
Enhancement of triplet-sensitized upconversion in rigid polymers via singlet exciton sink approach
Raišys, S., Juršėnas, S., Simon, Y. C., Weder, C., & Kazlauskas, K. (2018) · Chemical Science · doi:10.1039/c8sc02151a · Cited by 44
Self-citationFateminia, S. M. A., Kacenauskaite, L., Zhang, C., Ma, S., Kenry, K., Manghnani, P. N., Chen, J., Xu, S., Hu, F., Xu, B., et al. (2018) · Small · doi:10.1002/smll.201803325 · Cited by 39
Self-citationPhotophysical and electron transfer studies of a stable carbocation
Dileesh, S., & Gopidas, K. R. (2000) · Chemical Physics Letters · doi:10.1016/s0009-2614(00)01091-5 · Cited by 37
Singharoy, A., Venkatakrishnan, B., Liu, Y., Mayne, C. G., Lee, S., Chen, C., Zlotnick, A., Schulten, K. J., & Flood, A. H. (2015) · Journal of the American Chemical Society · doi:10.1021/jacs.5b04407 · Cited by 29
Self-citationConcentration quenching of fluorescence in solutions
Chaudhuri, K. D. (1959) · The European Physical Journal A · doi:10.1007/bf01337496 · Cited by 28
Maeda, H., Hane, W., Bando, Y., Terashima, Y., Haketa, Y., Shibaguchi, H., Kawai, T., Naito, M., Takaishi, K., Uchiyama, M., et al. (2013) · Chemistry - A European Journal · doi:10.1002/chem.201301737 · Cited by 27
Soulié, M., Carayon, C., Saffon‐Merceron, N., Blanc, S. P.-L., & Fery‐Forgues, S. (2016) · Physical Chemistry Chemical Physics · doi:10.1039/c6cp05848e · Cited by 24
Material gain concentration quenching in organic dye-doped polymer thin films
Vogelbacher, F., Zhou, X., Huang, J., Li, M., Jiang, K., Song, Y., Unterrainer, K., & Hainberger, R. (2019) · Optical Materials Express · doi:10.1364/ome.9.001208 · Cited by 16
Die Aenderung des Fluorescenzvermögens mit der Concentration
Walter, B. (1888) · Annalen der Physik · doi:10.1002/andp.18882700606 · Cited by 16
Simperler, A., Mikenda, W., & Schwarz, K. (2001) · Chemistry - A European Journal · doi:10.1002/1521-3765(20010417)7:8 · Cited by 14
A dye laser with a polyurethane matrix
Bezrodnyi, V. I., Derevyanko, N. A., Ishchenko, A. A., & Karabanova, L. V. (2001) · Technical Physics · doi:10.1134/1.1387547 · Cited by 13
Die Aenderungen des Fluorescenzvermögens mit der Concentration
Walter, B. (1889) · Annalen der Physik · doi:10.1002/andp.18892720212 · Cited by 12
Concentration quenching of laser dyes fluorescence in variety of solid matrices and liquid solutions
Kravchenko, Y. V., Koldunov, M. F., & Petukhov, V. A. (2017) · Optical and Quantum Electronics · doi:10.1007/s11082-017-0963-1 · Cited by 6
IV. On some new colouring matters
Church, A. H., & Perkin, W. H. (1857) · Proceedings of the Royal Society of London · doi:10.1098/rspl.1856.0015 · Cited by 2
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Metadata
- Authors
- Benson, C. R., Kacenauskaite, L., VanDenburgh, K. L., Zhao, W., Qiao, B., Sadhukhan, T., Pink, M., Chen, J., Borgi, S., Chen, C.-H., Davis, B. J., Simon, Y. C., Raghavachari, K., Laursen, B. W., & Flood, A. H.
- Affiliations
- Indiana University Bloomington (US)
- University of Copenhagen (DK)
- University of Southern Mississippi (US)
- Corresponding author
- Laursen, Bo W.
- Flood, Amar H.
- ORCID
- Venue
- Chem
- Publisher
- Elsevier BV
- Published
- 2020-08
- Volume
- 6
- Issue
- 8
- Pages
- 1978-1997
- ISSN
- 2451-9294 (ISSN-L)
- OpenAlex
- W3047531788
- Cited by
- 226
- References
- 63
- Citations by year
- 2026: 13 · 2025: 41 · 2024: 47 · 2023: 42 · 2022: 39 · 2021: 40 · 2020: 3
- FWCI
- 12.06
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Chem (publishedVersion)
- Research at the University of Copenhagen (University of Copenhagen) (publishedVersion, cc-by-nc-nd)
- Aquila Digital Community (University of Southern Mississippi) (submittedVersion)
- Funders
- Forskerakademiet (DFF-6111-00483)
- National Science Foundation (DMR-1533988, DGE-149999)
- College of Arts and Sciences, Boston University
- Københavns Universitet
- Indiana University
- Topics
- Physical Sciences › Materials Science › Materials Chemistry › Luminescence and Fluorescent Materials
- Physical Sciences › Chemistry › Organic Chemistry › Supramolecular Chemistry and Complexes
- Physical Sciences › Chemistry › Physical and Theoretical Chemistry › Crystallography and molecular interactions
- Keywords
- fluorescent dyes, fluorescence quenching, concentration quenching, organic light-emitting diodes, polymer additives, xanthene, oxazines, cyanine dyes, wide band gap, optical materials
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