Abstract

In this work, we developed a simple molecule with the effective generation of intense green emission in the amorphous thin-film. The synthesized novel molecule with excited-state intramolecular proton transfer (ESIPT), 3-Dimethylamino-1-(2-hydroxy-phenyl)-propenone (DHP), shows significantly enhanced green fluorescence in solid-state (fluorescence quantum yield Φf = 0.53), compared with the faint emission in the solution (Φf = 0.037). DHP molecules in amorphous thin-film effectively reinforce the radiative decay pathway, evidenced by enlarged Φf, shortened excited state lifetime τ. Taking advantage of the solid-state-induced emission enhancement characteristics, four-level ESIPT photocycle process and large Stokes shift, an efficient amplified spontaneous emission at 559.14 nm with a threshold of 12.41 mJ/cm2 is observed from the solid-state thin-film.

© 2019 Optical Society of America under the terms of the OSA Open Access Publishing Agreement

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  1. G. M. Farinola and R. Ragni, “Electroluminescent materials for white organic light emitting diodes,” Chem. Soc. Rev. 40(7), 3467–3482 (2011).
    [Crossref] [PubMed]
  2. K. P. Carter, A. M. Young, and A. E. Palmer, “Fluorescent Sensors for Measuring Metal Ions in Living Systems,” Chem. Rev. 114(8), 4564–4601 (2014).
    [Crossref] [PubMed]
  3. Z. Guo, S. Park, J. Yoon, and I. Shin, “Recent progress in the development of near-infrared fluorescent probes for bioimaging applications,” Chem. Soc. Rev. 43(1), 16–29 (2014).
    [Crossref] [PubMed]
  4. I. D. W. Samuel and G. A. Turnbull, “Organic Semiconductor Lasers,” Chem. Rev. 107(4), 1272–1295 (2007).
    [Crossref] [PubMed]
  5. A. J. C. Kuehne and M. C. Gather, “Organic Lasers: Recent Developments on Materials, Device Geometries, and Fabrication Techniques,” Chem. Rev. 116(21), 12823–12864 (2016).
    [Crossref] [PubMed]
  6. B. Z. Tang and A. Qin, Aggregation-Induced Emission: Fundamentals and Applications, Vol. 1 and 2, John Wiley & Sons, Chichester, UK 2013.
  7. Z. Zhao, J. W. Y. Lam, and B. Z. Tang, “Tetraphenylethene: a versatile AIE building block for the construction of efficient luminescent materials for organic light-emitting diodes,” J. Mater. Chem. 22(45), 23726 (2012).
    [Crossref]
  8. B. K. An, J. Gierschner, and S. Y. Park, “π-Conjugated Cyanostilbene Derivatives: A Unique Self-Assembly Motif for Molecular Nanostructures with Enhanced Emission and Transport,” Acc. Chem. Res. 45(4), 544–554 (2012).
    [Crossref] [PubMed]
  9. Y. Hong, J. W. Lam, and B. Z. Tang, “Aggregation-induced emission,” Chem. Soc. Rev. 40(11), 5361–5388 (2011).
    [Crossref] [PubMed]
  10. J. Luo, Z. Xie, J. W. Y. Lam, L. Cheng, H. Chen, C. Qiu, H. S. Kwok, X. Zhan, Y. Liu, D. Zhu, and B. Z. Tang, “Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole,” Chem. Commun. (Camb.) 18(18), 1740–1741 (2001).
    [Crossref] [PubMed]
  11. J. Mei, N. L. C. Leung, R. T. K. Kwok, J. W. Y. Lam, and B. Z. Tang, “Aggregation-Induced Emission: Together We Shine, United We Soar!” Chem. Rev. 115(21), 11718–11940 (2015).
    [Crossref] [PubMed]
  12. C. Zhang, C. L. Zou, Y. Yan, R. Hao, F. W. Sun, Z. F. Han, Y. S. Zhao, and J. Yao, “Two-Photon Pumped Lasing in Single-Crystal Organic Nanowire Exciton Polariton Resonators,” J. Am. Chem. Soc. 133(19), 7276–7279 (2011).
    [Crossref] [PubMed]
  13. T. Dutta, K. B. Woody, S. R. Parkin, M. D. Watson, and J. Gierschner, “Conjugated Polymers with Large Effective Stokes Shift: Benzobisdioxole-Based Poly(phenylene ethynylene)s,” J. Am. Chem. Soc. 131(47), 17321–17327 (2009).
    [Crossref] [PubMed]
  14. S. Park, J. E. Kwon, S. Y. Park, O. H. Kwon, J. K. Kim, S. J. Yoon, J. W. Chung, D. R. Whang, S. K. Park, D. K. Lee, D. J. Jang, J. Gierschner, and S. Y. Park, “Crystallization‐Induced Emission Enhancement and Amplified Spontaneous Emission from a CF3‐Containing Excited‐State Intramolecular‐Proton‐Transfer Molecule,” Adv. Opt. Mater. 5(18), 1700353 (2017).
    [Crossref]
  15. X. L. Liu, Z. C. Xu, and J. M. Cole, “Molecular Design of UV-vis Absorption and Emission Properties in Organic Fluorophores: Toward Larger Bathochromic Shifts, Enhanced Molar Extinction Coefficients, and Greater Stokes Shifts,” J. Phys. Chem. C 117(32), 16584–16595 (2013).
    [Crossref]
  16. X. L. Liu, J. M. Cole, and Z. C. Xu, “Substantial Intramolecular Charge Transfer Induces Long Emission Wavelengths and Mega Stokes Shifts in 6-Aminocoumarins,” J. Phys. Chem. C 121(24), 13274–13279 (2017).
    [Crossref]
  17. V. S. Padalkar and S. Seki, “Excited-state intramolecular proton-transfer (ESIPT)-inspired solid state emitters,” Chem. Soc. Rev. 45(1), 169–202 (2016).
    [Crossref] [PubMed]
  18. J. Zhao, S. Ji, Y. Chen, H. Guo, and P. Yang, “Excited state intramolecular proton transfer (ESIPT): from principal photophysics to the development of new chromophores and applications in fluorescent molecular probes and luminescent materials,” Phys. Chem. Chem. Phys. 14(25), 8803–8817 (2012).
    [Crossref] [PubMed]
  19. J. Wu, W. Liu, J. Ge, H. Zhang, and P. Wang, “New sensing mechanisms for design of fluorescent chemosensors emerging in recent years,” Chem. Soc. Rev. 40(7), 3483–3495 (2011).
    [Crossref] [PubMed]
  20. J. E. Kwon and S. Y. Park, “Advanced Organic Optoelectronic Materials: Harnessing Excited-State Intramolecular Proton Transfer (ESIPT) Process,” Adv. Mater. 23(32), 3615–3642 (2011).
    [Crossref] [PubMed]
  21. K. T. Kamtekar, A. P. Monkman, and M. R. Bryce, “Ordered Materials for Organic Electronics and Photonics,” Adv. Mater. 22, 572 (2010).
    [Crossref] [PubMed]
  22. K. Sakai, T. Ishikawa, and T. Akutagawa, “A blue-white-yellow color-tunable excited state intramolecular proton transfer (ESIPT) fluorophore: sensitivity to polar–nonpolar solvent ratios,” J. Mater. Chem. C Mater. Opt. Electron. Devices 1(47), 7866 (2013).
    [Crossref]
  23. H. Sasabe and J. Kido, “Multifunctional Materials in High-Performance OLEDs: Challenges for Solid-State Lighting,” Chem. Mater. 23(3), 621–630 (2011).
    [Crossref]
  24. F. Liang, L. Wang, D. Ma, X. Jing, and F. Wang, “Oxadiazole-containing material with intense blue phosphorescence emission for organic light-emitting diodes,” Appl. Phys. Lett. 81(1), 4–6 (2002).
    [Crossref]
  25. X. Cheng, F. Li, S. Han, Y. Zhang, C. Jiao, J. Wei, K. Ye, Y. Wang, and H. Zhang, “Emission behaviors of unsymmetrical 1,3-diaryl-β-diketones: A model perfectly disclosing the effect of molecular conformation on luminescence of organic solids,” Sci. Rep. 5(1), 9140 (2015).
    [Crossref] [PubMed]
  26. X. Cheng, K. Wang, S. Huang, H. Zhang, H. Zhang, and Y. Wang, “Organic Crystals with Near-Infrared Amplified Spontaneous Emissions Based on 2′-Hydroxychalcone Derivatives: Subtle Structure Modification but Great Property Change,” Angew. Chem. Int. Ed. Engl. 54(29), 8369–8373 (2015).
    [Crossref] [PubMed]
  27. X. Cheng, Y. Zhang, S. Han, F. Li, H. Zhang, and Y. Wang, “Multicolor Amplified Spontaneous Emissions Based on Organic Polymorphs That Undergo Excited-State Intramolecular Proton Transfer,” Chemistry 22(14), 4899–4903 (2016).
    [Crossref] [PubMed]
  28. W. Zhang, Y. Yan, J. Gu, J. Yao, and Y. S. Zhao, “Low-Threshold Wavelength-Switchable Organic Nanowire Lasers Based on Excited-State Intramolecular Proton Transfer,” Angew. Chem. Int. Ed. Engl. 54(24), 7125–7129 (2015).
    [Crossref] [PubMed]
  29. T. Yanaia, D. P. Tew, and N. C. Handy, “A new hybrid exchange-correlation functional using the Coulomb-attenuating method (CAM-B3LYP),” Chem. Phys. Lett. 393(1-3), 51–57 (2004).
    [Crossref]
  30. K. S. Levchenko, I. S. Semenova, V. N. Yarovenko, P. S. Shmelin, and M. M. Krayushkin, “Facile syntheses of 2-substituted 3-cyanochromones,” Tetrahedron Lett. 53(28), 3630–3632 (2012).
    [Crossref]
  31. S. Park, O. H. Kwon, S. Kim, S. Park, M. G. Choi, M. Cha, S. Y. Park, and D. J. Jang, “Imidazole-Based Excited-State Intramolecular Proton-Transfer Materials: Synthesis and Amplified Spontaneous Emission from A Large Single Crystal,” J. Am. Chem. Soc. 127(28), 10070–10074 (2005).
    [Crossref] [PubMed]
  32. K. Benelhadj, W. Muzuzu, J. Massue, P. Retailleau, A. Charaf-Eddin, A. D. Laurent, D. Jacquemin, G. Ulrich, and R. Ziessel, “White Emitters by Tuning the Excited-State Intramolecular Proton-Transfer Fluorescence Emission in 2-(2′-Hydroxybenzofuran)benzoxazole Dyes,” Chem. Eur. J 20(40), 12843–12857 (2014).
    [Crossref] [PubMed]
  33. Y. Kawamura, H. Yamamoto, K. Goushi, H. Sasabe, C. Adachi, and H. Yoshizaki, “Ultraviolet amplified spontaneous emission from thin films of 4,4′-bis(9-carbazolyl)-2,2′- biphenyl and the derivatives,” Appl. Phys. Lett. 84(15), 2724–2726 (2004).
    [Crossref]
  34. A. P. Demchenko, K. C. Tang, and P. T. Chou, “Excited-state proton coupled charge transfer modulated by molecular structure and media polarization,” Chem. Soc. Rev. 42(3), 1379–1408 (2013).
    [Crossref] [PubMed]

2017 (2)

X. L. Liu, J. M. Cole, and Z. C. Xu, “Substantial Intramolecular Charge Transfer Induces Long Emission Wavelengths and Mega Stokes Shifts in 6-Aminocoumarins,” J. Phys. Chem. C 121(24), 13274–13279 (2017).
[Crossref]

S. Park, J. E. Kwon, S. Y. Park, O. H. Kwon, J. K. Kim, S. J. Yoon, J. W. Chung, D. R. Whang, S. K. Park, D. K. Lee, D. J. Jang, J. Gierschner, and S. Y. Park, “Crystallization‐Induced Emission Enhancement and Amplified Spontaneous Emission from a CF3‐Containing Excited‐State Intramolecular‐Proton‐Transfer Molecule,” Adv. Opt. Mater. 5(18), 1700353 (2017).
[Crossref]

2016 (3)

V. S. Padalkar and S. Seki, “Excited-state intramolecular proton-transfer (ESIPT)-inspired solid state emitters,” Chem. Soc. Rev. 45(1), 169–202 (2016).
[Crossref] [PubMed]

A. J. C. Kuehne and M. C. Gather, “Organic Lasers: Recent Developments on Materials, Device Geometries, and Fabrication Techniques,” Chem. Rev. 116(21), 12823–12864 (2016).
[Crossref] [PubMed]

X. Cheng, Y. Zhang, S. Han, F. Li, H. Zhang, and Y. Wang, “Multicolor Amplified Spontaneous Emissions Based on Organic Polymorphs That Undergo Excited-State Intramolecular Proton Transfer,” Chemistry 22(14), 4899–4903 (2016).
[Crossref] [PubMed]

2015 (4)

W. Zhang, Y. Yan, J. Gu, J. Yao, and Y. S. Zhao, “Low-Threshold Wavelength-Switchable Organic Nanowire Lasers Based on Excited-State Intramolecular Proton Transfer,” Angew. Chem. Int. Ed. Engl. 54(24), 7125–7129 (2015).
[Crossref] [PubMed]

X. Cheng, F. Li, S. Han, Y. Zhang, C. Jiao, J. Wei, K. Ye, Y. Wang, and H. Zhang, “Emission behaviors of unsymmetrical 1,3-diaryl-β-diketones: A model perfectly disclosing the effect of molecular conformation on luminescence of organic solids,” Sci. Rep. 5(1), 9140 (2015).
[Crossref] [PubMed]

X. Cheng, K. Wang, S. Huang, H. Zhang, H. Zhang, and Y. Wang, “Organic Crystals with Near-Infrared Amplified Spontaneous Emissions Based on 2′-Hydroxychalcone Derivatives: Subtle Structure Modification but Great Property Change,” Angew. Chem. Int. Ed. Engl. 54(29), 8369–8373 (2015).
[Crossref] [PubMed]

J. Mei, N. L. C. Leung, R. T. K. Kwok, J. W. Y. Lam, and B. Z. Tang, “Aggregation-Induced Emission: Together We Shine, United We Soar!” Chem. Rev. 115(21), 11718–11940 (2015).
[Crossref] [PubMed]

2014 (3)

K. P. Carter, A. M. Young, and A. E. Palmer, “Fluorescent Sensors for Measuring Metal Ions in Living Systems,” Chem. Rev. 114(8), 4564–4601 (2014).
[Crossref] [PubMed]

Z. Guo, S. Park, J. Yoon, and I. Shin, “Recent progress in the development of near-infrared fluorescent probes for bioimaging applications,” Chem. Soc. Rev. 43(1), 16–29 (2014).
[Crossref] [PubMed]

K. Benelhadj, W. Muzuzu, J. Massue, P. Retailleau, A. Charaf-Eddin, A. D. Laurent, D. Jacquemin, G. Ulrich, and R. Ziessel, “White Emitters by Tuning the Excited-State Intramolecular Proton-Transfer Fluorescence Emission in 2-(2′-Hydroxybenzofuran)benzoxazole Dyes,” Chem. Eur. J 20(40), 12843–12857 (2014).
[Crossref] [PubMed]

2013 (3)

A. P. Demchenko, K. C. Tang, and P. T. Chou, “Excited-state proton coupled charge transfer modulated by molecular structure and media polarization,” Chem. Soc. Rev. 42(3), 1379–1408 (2013).
[Crossref] [PubMed]

X. L. Liu, Z. C. Xu, and J. M. Cole, “Molecular Design of UV-vis Absorption and Emission Properties in Organic Fluorophores: Toward Larger Bathochromic Shifts, Enhanced Molar Extinction Coefficients, and Greater Stokes Shifts,” J. Phys. Chem. C 117(32), 16584–16595 (2013).
[Crossref]

K. Sakai, T. Ishikawa, and T. Akutagawa, “A blue-white-yellow color-tunable excited state intramolecular proton transfer (ESIPT) fluorophore: sensitivity to polar–nonpolar solvent ratios,” J. Mater. Chem. C Mater. Opt. Electron. Devices 1(47), 7866 (2013).
[Crossref]

2012 (4)

J. Zhao, S. Ji, Y. Chen, H. Guo, and P. Yang, “Excited state intramolecular proton transfer (ESIPT): from principal photophysics to the development of new chromophores and applications in fluorescent molecular probes and luminescent materials,” Phys. Chem. Chem. Phys. 14(25), 8803–8817 (2012).
[Crossref] [PubMed]

Z. Zhao, J. W. Y. Lam, and B. Z. Tang, “Tetraphenylethene: a versatile AIE building block for the construction of efficient luminescent materials for organic light-emitting diodes,” J. Mater. Chem. 22(45), 23726 (2012).
[Crossref]

B. K. An, J. Gierschner, and S. Y. Park, “π-Conjugated Cyanostilbene Derivatives: A Unique Self-Assembly Motif for Molecular Nanostructures with Enhanced Emission and Transport,” Acc. Chem. Res. 45(4), 544–554 (2012).
[Crossref] [PubMed]

K. S. Levchenko, I. S. Semenova, V. N. Yarovenko, P. S. Shmelin, and M. M. Krayushkin, “Facile syntheses of 2-substituted 3-cyanochromones,” Tetrahedron Lett. 53(28), 3630–3632 (2012).
[Crossref]

2011 (6)

G. M. Farinola and R. Ragni, “Electroluminescent materials for white organic light emitting diodes,” Chem. Soc. Rev. 40(7), 3467–3482 (2011).
[Crossref] [PubMed]

Y. Hong, J. W. Lam, and B. Z. Tang, “Aggregation-induced emission,” Chem. Soc. Rev. 40(11), 5361–5388 (2011).
[Crossref] [PubMed]

C. Zhang, C. L. Zou, Y. Yan, R. Hao, F. W. Sun, Z. F. Han, Y. S. Zhao, and J. Yao, “Two-Photon Pumped Lasing in Single-Crystal Organic Nanowire Exciton Polariton Resonators,” J. Am. Chem. Soc. 133(19), 7276–7279 (2011).
[Crossref] [PubMed]

J. Wu, W. Liu, J. Ge, H. Zhang, and P. Wang, “New sensing mechanisms for design of fluorescent chemosensors emerging in recent years,” Chem. Soc. Rev. 40(7), 3483–3495 (2011).
[Crossref] [PubMed]

J. E. Kwon and S. Y. Park, “Advanced Organic Optoelectronic Materials: Harnessing Excited-State Intramolecular Proton Transfer (ESIPT) Process,” Adv. Mater. 23(32), 3615–3642 (2011).
[Crossref] [PubMed]

H. Sasabe and J. Kido, “Multifunctional Materials in High-Performance OLEDs: Challenges for Solid-State Lighting,” Chem. Mater. 23(3), 621–630 (2011).
[Crossref]

2010 (1)

K. T. Kamtekar, A. P. Monkman, and M. R. Bryce, “Ordered Materials for Organic Electronics and Photonics,” Adv. Mater. 22, 572 (2010).
[Crossref] [PubMed]

2009 (1)

T. Dutta, K. B. Woody, S. R. Parkin, M. D. Watson, and J. Gierschner, “Conjugated Polymers with Large Effective Stokes Shift: Benzobisdioxole-Based Poly(phenylene ethynylene)s,” J. Am. Chem. Soc. 131(47), 17321–17327 (2009).
[Crossref] [PubMed]

2007 (1)

I. D. W. Samuel and G. A. Turnbull, “Organic Semiconductor Lasers,” Chem. Rev. 107(4), 1272–1295 (2007).
[Crossref] [PubMed]

2005 (1)

S. Park, O. H. Kwon, S. Kim, S. Park, M. G. Choi, M. Cha, S. Y. Park, and D. J. Jang, “Imidazole-Based Excited-State Intramolecular Proton-Transfer Materials: Synthesis and Amplified Spontaneous Emission from A Large Single Crystal,” J. Am. Chem. Soc. 127(28), 10070–10074 (2005).
[Crossref] [PubMed]

2004 (2)

Y. Kawamura, H. Yamamoto, K. Goushi, H. Sasabe, C. Adachi, and H. Yoshizaki, “Ultraviolet amplified spontaneous emission from thin films of 4,4′-bis(9-carbazolyl)-2,2′- biphenyl and the derivatives,” Appl. Phys. Lett. 84(15), 2724–2726 (2004).
[Crossref]

T. Yanaia, D. P. Tew, and N. C. Handy, “A new hybrid exchange-correlation functional using the Coulomb-attenuating method (CAM-B3LYP),” Chem. Phys. Lett. 393(1-3), 51–57 (2004).
[Crossref]

2002 (1)

F. Liang, L. Wang, D. Ma, X. Jing, and F. Wang, “Oxadiazole-containing material with intense blue phosphorescence emission for organic light-emitting diodes,” Appl. Phys. Lett. 81(1), 4–6 (2002).
[Crossref]

2001 (1)

J. Luo, Z. Xie, J. W. Y. Lam, L. Cheng, H. Chen, C. Qiu, H. S. Kwok, X. Zhan, Y. Liu, D. Zhu, and B. Z. Tang, “Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole,” Chem. Commun. (Camb.) 18(18), 1740–1741 (2001).
[Crossref] [PubMed]

Adachi, C.

Y. Kawamura, H. Yamamoto, K. Goushi, H. Sasabe, C. Adachi, and H. Yoshizaki, “Ultraviolet amplified spontaneous emission from thin films of 4,4′-bis(9-carbazolyl)-2,2′- biphenyl and the derivatives,” Appl. Phys. Lett. 84(15), 2724–2726 (2004).
[Crossref]

Akutagawa, T.

K. Sakai, T. Ishikawa, and T. Akutagawa, “A blue-white-yellow color-tunable excited state intramolecular proton transfer (ESIPT) fluorophore: sensitivity to polar–nonpolar solvent ratios,” J. Mater. Chem. C Mater. Opt. Electron. Devices 1(47), 7866 (2013).
[Crossref]

An, B. K.

B. K. An, J. Gierschner, and S. Y. Park, “π-Conjugated Cyanostilbene Derivatives: A Unique Self-Assembly Motif for Molecular Nanostructures with Enhanced Emission and Transport,” Acc. Chem. Res. 45(4), 544–554 (2012).
[Crossref] [PubMed]

Benelhadj, K.

K. Benelhadj, W. Muzuzu, J. Massue, P. Retailleau, A. Charaf-Eddin, A. D. Laurent, D. Jacquemin, G. Ulrich, and R. Ziessel, “White Emitters by Tuning the Excited-State Intramolecular Proton-Transfer Fluorescence Emission in 2-(2′-Hydroxybenzofuran)benzoxazole Dyes,” Chem. Eur. J 20(40), 12843–12857 (2014).
[Crossref] [PubMed]

Bryce, M. R.

K. T. Kamtekar, A. P. Monkman, and M. R. Bryce, “Ordered Materials for Organic Electronics and Photonics,” Adv. Mater. 22, 572 (2010).
[Crossref] [PubMed]

Carter, K. P.

K. P. Carter, A. M. Young, and A. E. Palmer, “Fluorescent Sensors for Measuring Metal Ions in Living Systems,” Chem. Rev. 114(8), 4564–4601 (2014).
[Crossref] [PubMed]

Cha, M.

S. Park, O. H. Kwon, S. Kim, S. Park, M. G. Choi, M. Cha, S. Y. Park, and D. J. Jang, “Imidazole-Based Excited-State Intramolecular Proton-Transfer Materials: Synthesis and Amplified Spontaneous Emission from A Large Single Crystal,” J. Am. Chem. Soc. 127(28), 10070–10074 (2005).
[Crossref] [PubMed]

Charaf-Eddin, A.

K. Benelhadj, W. Muzuzu, J. Massue, P. Retailleau, A. Charaf-Eddin, A. D. Laurent, D. Jacquemin, G. Ulrich, and R. Ziessel, “White Emitters by Tuning the Excited-State Intramolecular Proton-Transfer Fluorescence Emission in 2-(2′-Hydroxybenzofuran)benzoxazole Dyes,” Chem. Eur. J 20(40), 12843–12857 (2014).
[Crossref] [PubMed]

Chen, H.

J. Luo, Z. Xie, J. W. Y. Lam, L. Cheng, H. Chen, C. Qiu, H. S. Kwok, X. Zhan, Y. Liu, D. Zhu, and B. Z. Tang, “Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole,” Chem. Commun. (Camb.) 18(18), 1740–1741 (2001).
[Crossref] [PubMed]

Chen, Y.

J. Zhao, S. Ji, Y. Chen, H. Guo, and P. Yang, “Excited state intramolecular proton transfer (ESIPT): from principal photophysics to the development of new chromophores and applications in fluorescent molecular probes and luminescent materials,” Phys. Chem. Chem. Phys. 14(25), 8803–8817 (2012).
[Crossref] [PubMed]

Cheng, L.

J. Luo, Z. Xie, J. W. Y. Lam, L. Cheng, H. Chen, C. Qiu, H. S. Kwok, X. Zhan, Y. Liu, D. Zhu, and B. Z. Tang, “Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole,” Chem. Commun. (Camb.) 18(18), 1740–1741 (2001).
[Crossref] [PubMed]

Cheng, X.

X. Cheng, Y. Zhang, S. Han, F. Li, H. Zhang, and Y. Wang, “Multicolor Amplified Spontaneous Emissions Based on Organic Polymorphs That Undergo Excited-State Intramolecular Proton Transfer,” Chemistry 22(14), 4899–4903 (2016).
[Crossref] [PubMed]

X. Cheng, K. Wang, S. Huang, H. Zhang, H. Zhang, and Y. Wang, “Organic Crystals with Near-Infrared Amplified Spontaneous Emissions Based on 2′-Hydroxychalcone Derivatives: Subtle Structure Modification but Great Property Change,” Angew. Chem. Int. Ed. Engl. 54(29), 8369–8373 (2015).
[Crossref] [PubMed]

X. Cheng, F. Li, S. Han, Y. Zhang, C. Jiao, J. Wei, K. Ye, Y. Wang, and H. Zhang, “Emission behaviors of unsymmetrical 1,3-diaryl-β-diketones: A model perfectly disclosing the effect of molecular conformation on luminescence of organic solids,” Sci. Rep. 5(1), 9140 (2015).
[Crossref] [PubMed]

Choi, M. G.

S. Park, O. H. Kwon, S. Kim, S. Park, M. G. Choi, M. Cha, S. Y. Park, and D. J. Jang, “Imidazole-Based Excited-State Intramolecular Proton-Transfer Materials: Synthesis and Amplified Spontaneous Emission from A Large Single Crystal,” J. Am. Chem. Soc. 127(28), 10070–10074 (2005).
[Crossref] [PubMed]

Chou, P. T.

A. P. Demchenko, K. C. Tang, and P. T. Chou, “Excited-state proton coupled charge transfer modulated by molecular structure and media polarization,” Chem. Soc. Rev. 42(3), 1379–1408 (2013).
[Crossref] [PubMed]

Chung, J. W.

S. Park, J. E. Kwon, S. Y. Park, O. H. Kwon, J. K. Kim, S. J. Yoon, J. W. Chung, D. R. Whang, S. K. Park, D. K. Lee, D. J. Jang, J. Gierschner, and S. Y. Park, “Crystallization‐Induced Emission Enhancement and Amplified Spontaneous Emission from a CF3‐Containing Excited‐State Intramolecular‐Proton‐Transfer Molecule,” Adv. Opt. Mater. 5(18), 1700353 (2017).
[Crossref]

Cole, J. M.

X. L. Liu, J. M. Cole, and Z. C. Xu, “Substantial Intramolecular Charge Transfer Induces Long Emission Wavelengths and Mega Stokes Shifts in 6-Aminocoumarins,” J. Phys. Chem. C 121(24), 13274–13279 (2017).
[Crossref]

X. L. Liu, Z. C. Xu, and J. M. Cole, “Molecular Design of UV-vis Absorption and Emission Properties in Organic Fluorophores: Toward Larger Bathochromic Shifts, Enhanced Molar Extinction Coefficients, and Greater Stokes Shifts,” J. Phys. Chem. C 117(32), 16584–16595 (2013).
[Crossref]

Demchenko, A. P.

A. P. Demchenko, K. C. Tang, and P. T. Chou, “Excited-state proton coupled charge transfer modulated by molecular structure and media polarization,” Chem. Soc. Rev. 42(3), 1379–1408 (2013).
[Crossref] [PubMed]

Dutta, T.

T. Dutta, K. B. Woody, S. R. Parkin, M. D. Watson, and J. Gierschner, “Conjugated Polymers with Large Effective Stokes Shift: Benzobisdioxole-Based Poly(phenylene ethynylene)s,” J. Am. Chem. Soc. 131(47), 17321–17327 (2009).
[Crossref] [PubMed]

Farinola, G. M.

G. M. Farinola and R. Ragni, “Electroluminescent materials for white organic light emitting diodes,” Chem. Soc. Rev. 40(7), 3467–3482 (2011).
[Crossref] [PubMed]

Gather, M. C.

A. J. C. Kuehne and M. C. Gather, “Organic Lasers: Recent Developments on Materials, Device Geometries, and Fabrication Techniques,” Chem. Rev. 116(21), 12823–12864 (2016).
[Crossref] [PubMed]

Ge, J.

J. Wu, W. Liu, J. Ge, H. Zhang, and P. Wang, “New sensing mechanisms for design of fluorescent chemosensors emerging in recent years,” Chem. Soc. Rev. 40(7), 3483–3495 (2011).
[Crossref] [PubMed]

Gierschner, J.

S. Park, J. E. Kwon, S. Y. Park, O. H. Kwon, J. K. Kim, S. J. Yoon, J. W. Chung, D. R. Whang, S. K. Park, D. K. Lee, D. J. Jang, J. Gierschner, and S. Y. Park, “Crystallization‐Induced Emission Enhancement and Amplified Spontaneous Emission from a CF3‐Containing Excited‐State Intramolecular‐Proton‐Transfer Molecule,” Adv. Opt. Mater. 5(18), 1700353 (2017).
[Crossref]

B. K. An, J. Gierschner, and S. Y. Park, “π-Conjugated Cyanostilbene Derivatives: A Unique Self-Assembly Motif for Molecular Nanostructures with Enhanced Emission and Transport,” Acc. Chem. Res. 45(4), 544–554 (2012).
[Crossref] [PubMed]

T. Dutta, K. B. Woody, S. R. Parkin, M. D. Watson, and J. Gierschner, “Conjugated Polymers with Large Effective Stokes Shift: Benzobisdioxole-Based Poly(phenylene ethynylene)s,” J. Am. Chem. Soc. 131(47), 17321–17327 (2009).
[Crossref] [PubMed]

Goushi, K.

Y. Kawamura, H. Yamamoto, K. Goushi, H. Sasabe, C. Adachi, and H. Yoshizaki, “Ultraviolet amplified spontaneous emission from thin films of 4,4′-bis(9-carbazolyl)-2,2′- biphenyl and the derivatives,” Appl. Phys. Lett. 84(15), 2724–2726 (2004).
[Crossref]

Gu, J.

W. Zhang, Y. Yan, J. Gu, J. Yao, and Y. S. Zhao, “Low-Threshold Wavelength-Switchable Organic Nanowire Lasers Based on Excited-State Intramolecular Proton Transfer,” Angew. Chem. Int. Ed. Engl. 54(24), 7125–7129 (2015).
[Crossref] [PubMed]

Guo, H.

J. Zhao, S. Ji, Y. Chen, H. Guo, and P. Yang, “Excited state intramolecular proton transfer (ESIPT): from principal photophysics to the development of new chromophores and applications in fluorescent molecular probes and luminescent materials,” Phys. Chem. Chem. Phys. 14(25), 8803–8817 (2012).
[Crossref] [PubMed]

Guo, Z.

Z. Guo, S. Park, J. Yoon, and I. Shin, “Recent progress in the development of near-infrared fluorescent probes for bioimaging applications,” Chem. Soc. Rev. 43(1), 16–29 (2014).
[Crossref] [PubMed]

Han, S.

X. Cheng, Y. Zhang, S. Han, F. Li, H. Zhang, and Y. Wang, “Multicolor Amplified Spontaneous Emissions Based on Organic Polymorphs That Undergo Excited-State Intramolecular Proton Transfer,” Chemistry 22(14), 4899–4903 (2016).
[Crossref] [PubMed]

X. Cheng, F. Li, S. Han, Y. Zhang, C. Jiao, J. Wei, K. Ye, Y. Wang, and H. Zhang, “Emission behaviors of unsymmetrical 1,3-diaryl-β-diketones: A model perfectly disclosing the effect of molecular conformation on luminescence of organic solids,” Sci. Rep. 5(1), 9140 (2015).
[Crossref] [PubMed]

Han, Z. F.

C. Zhang, C. L. Zou, Y. Yan, R. Hao, F. W. Sun, Z. F. Han, Y. S. Zhao, and J. Yao, “Two-Photon Pumped Lasing in Single-Crystal Organic Nanowire Exciton Polariton Resonators,” J. Am. Chem. Soc. 133(19), 7276–7279 (2011).
[Crossref] [PubMed]

Handy, N. C.

T. Yanaia, D. P. Tew, and N. C. Handy, “A new hybrid exchange-correlation functional using the Coulomb-attenuating method (CAM-B3LYP),” Chem. Phys. Lett. 393(1-3), 51–57 (2004).
[Crossref]

Hao, R.

C. Zhang, C. L. Zou, Y. Yan, R. Hao, F. W. Sun, Z. F. Han, Y. S. Zhao, and J. Yao, “Two-Photon Pumped Lasing in Single-Crystal Organic Nanowire Exciton Polariton Resonators,” J. Am. Chem. Soc. 133(19), 7276–7279 (2011).
[Crossref] [PubMed]

Hong, Y.

Y. Hong, J. W. Lam, and B. Z. Tang, “Aggregation-induced emission,” Chem. Soc. Rev. 40(11), 5361–5388 (2011).
[Crossref] [PubMed]

Huang, S.

X. Cheng, K. Wang, S. Huang, H. Zhang, H. Zhang, and Y. Wang, “Organic Crystals with Near-Infrared Amplified Spontaneous Emissions Based on 2′-Hydroxychalcone Derivatives: Subtle Structure Modification but Great Property Change,” Angew. Chem. Int. Ed. Engl. 54(29), 8369–8373 (2015).
[Crossref] [PubMed]

Ishikawa, T.

K. Sakai, T. Ishikawa, and T. Akutagawa, “A blue-white-yellow color-tunable excited state intramolecular proton transfer (ESIPT) fluorophore: sensitivity to polar–nonpolar solvent ratios,” J. Mater. Chem. C Mater. Opt. Electron. Devices 1(47), 7866 (2013).
[Crossref]

Jacquemin, D.

K. Benelhadj, W. Muzuzu, J. Massue, P. Retailleau, A. Charaf-Eddin, A. D. Laurent, D. Jacquemin, G. Ulrich, and R. Ziessel, “White Emitters by Tuning the Excited-State Intramolecular Proton-Transfer Fluorescence Emission in 2-(2′-Hydroxybenzofuran)benzoxazole Dyes,” Chem. Eur. J 20(40), 12843–12857 (2014).
[Crossref] [PubMed]

Jang, D. J.

S. Park, J. E. Kwon, S. Y. Park, O. H. Kwon, J. K. Kim, S. J. Yoon, J. W. Chung, D. R. Whang, S. K. Park, D. K. Lee, D. J. Jang, J. Gierschner, and S. Y. Park, “Crystallization‐Induced Emission Enhancement and Amplified Spontaneous Emission from a CF3‐Containing Excited‐State Intramolecular‐Proton‐Transfer Molecule,” Adv. Opt. Mater. 5(18), 1700353 (2017).
[Crossref]

S. Park, O. H. Kwon, S. Kim, S. Park, M. G. Choi, M. Cha, S. Y. Park, and D. J. Jang, “Imidazole-Based Excited-State Intramolecular Proton-Transfer Materials: Synthesis and Amplified Spontaneous Emission from A Large Single Crystal,” J. Am. Chem. Soc. 127(28), 10070–10074 (2005).
[Crossref] [PubMed]

Ji, S.

J. Zhao, S. Ji, Y. Chen, H. Guo, and P. Yang, “Excited state intramolecular proton transfer (ESIPT): from principal photophysics to the development of new chromophores and applications in fluorescent molecular probes and luminescent materials,” Phys. Chem. Chem. Phys. 14(25), 8803–8817 (2012).
[Crossref] [PubMed]

Jiao, C.

X. Cheng, F. Li, S. Han, Y. Zhang, C. Jiao, J. Wei, K. Ye, Y. Wang, and H. Zhang, “Emission behaviors of unsymmetrical 1,3-diaryl-β-diketones: A model perfectly disclosing the effect of molecular conformation on luminescence of organic solids,” Sci. Rep. 5(1), 9140 (2015).
[Crossref] [PubMed]

Jing, X.

F. Liang, L. Wang, D. Ma, X. Jing, and F. Wang, “Oxadiazole-containing material with intense blue phosphorescence emission for organic light-emitting diodes,” Appl. Phys. Lett. 81(1), 4–6 (2002).
[Crossref]

Kamtekar, K. T.

K. T. Kamtekar, A. P. Monkman, and M. R. Bryce, “Ordered Materials for Organic Electronics and Photonics,” Adv. Mater. 22, 572 (2010).
[Crossref] [PubMed]

Kawamura, Y.

Y. Kawamura, H. Yamamoto, K. Goushi, H. Sasabe, C. Adachi, and H. Yoshizaki, “Ultraviolet amplified spontaneous emission from thin films of 4,4′-bis(9-carbazolyl)-2,2′- biphenyl and the derivatives,” Appl. Phys. Lett. 84(15), 2724–2726 (2004).
[Crossref]

Kido, J.

H. Sasabe and J. Kido, “Multifunctional Materials in High-Performance OLEDs: Challenges for Solid-State Lighting,” Chem. Mater. 23(3), 621–630 (2011).
[Crossref]

Kim, J. K.

S. Park, J. E. Kwon, S. Y. Park, O. H. Kwon, J. K. Kim, S. J. Yoon, J. W. Chung, D. R. Whang, S. K. Park, D. K. Lee, D. J. Jang, J. Gierschner, and S. Y. Park, “Crystallization‐Induced Emission Enhancement and Amplified Spontaneous Emission from a CF3‐Containing Excited‐State Intramolecular‐Proton‐Transfer Molecule,” Adv. Opt. Mater. 5(18), 1700353 (2017).
[Crossref]

Kim, S.

S. Park, O. H. Kwon, S. Kim, S. Park, M. G. Choi, M. Cha, S. Y. Park, and D. J. Jang, “Imidazole-Based Excited-State Intramolecular Proton-Transfer Materials: Synthesis and Amplified Spontaneous Emission from A Large Single Crystal,” J. Am. Chem. Soc. 127(28), 10070–10074 (2005).
[Crossref] [PubMed]

Krayushkin, M. M.

K. S. Levchenko, I. S. Semenova, V. N. Yarovenko, P. S. Shmelin, and M. M. Krayushkin, “Facile syntheses of 2-substituted 3-cyanochromones,” Tetrahedron Lett. 53(28), 3630–3632 (2012).
[Crossref]

Kuehne, A. J. C.

A. J. C. Kuehne and M. C. Gather, “Organic Lasers: Recent Developments on Materials, Device Geometries, and Fabrication Techniques,” Chem. Rev. 116(21), 12823–12864 (2016).
[Crossref] [PubMed]

Kwok, H. S.

J. Luo, Z. Xie, J. W. Y. Lam, L. Cheng, H. Chen, C. Qiu, H. S. Kwok, X. Zhan, Y. Liu, D. Zhu, and B. Z. Tang, “Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole,” Chem. Commun. (Camb.) 18(18), 1740–1741 (2001).
[Crossref] [PubMed]

Kwok, R. T. K.

J. Mei, N. L. C. Leung, R. T. K. Kwok, J. W. Y. Lam, and B. Z. Tang, “Aggregation-Induced Emission: Together We Shine, United We Soar!” Chem. Rev. 115(21), 11718–11940 (2015).
[Crossref] [PubMed]

Kwon, J. E.

S. Park, J. E. Kwon, S. Y. Park, O. H. Kwon, J. K. Kim, S. J. Yoon, J. W. Chung, D. R. Whang, S. K. Park, D. K. Lee, D. J. Jang, J. Gierschner, and S. Y. Park, “Crystallization‐Induced Emission Enhancement and Amplified Spontaneous Emission from a CF3‐Containing Excited‐State Intramolecular‐Proton‐Transfer Molecule,” Adv. Opt. Mater. 5(18), 1700353 (2017).
[Crossref]

J. E. Kwon and S. Y. Park, “Advanced Organic Optoelectronic Materials: Harnessing Excited-State Intramolecular Proton Transfer (ESIPT) Process,” Adv. Mater. 23(32), 3615–3642 (2011).
[Crossref] [PubMed]

Kwon, O. H.

S. Park, J. E. Kwon, S. Y. Park, O. H. Kwon, J. K. Kim, S. J. Yoon, J. W. Chung, D. R. Whang, S. K. Park, D. K. Lee, D. J. Jang, J. Gierschner, and S. Y. Park, “Crystallization‐Induced Emission Enhancement and Amplified Spontaneous Emission from a CF3‐Containing Excited‐State Intramolecular‐Proton‐Transfer Molecule,” Adv. Opt. Mater. 5(18), 1700353 (2017).
[Crossref]

S. Park, O. H. Kwon, S. Kim, S. Park, M. G. Choi, M. Cha, S. Y. Park, and D. J. Jang, “Imidazole-Based Excited-State Intramolecular Proton-Transfer Materials: Synthesis and Amplified Spontaneous Emission from A Large Single Crystal,” J. Am. Chem. Soc. 127(28), 10070–10074 (2005).
[Crossref] [PubMed]

Lam, J. W.

Y. Hong, J. W. Lam, and B. Z. Tang, “Aggregation-induced emission,” Chem. Soc. Rev. 40(11), 5361–5388 (2011).
[Crossref] [PubMed]

Lam, J. W. Y.

J. Mei, N. L. C. Leung, R. T. K. Kwok, J. W. Y. Lam, and B. Z. Tang, “Aggregation-Induced Emission: Together We Shine, United We Soar!” Chem. Rev. 115(21), 11718–11940 (2015).
[Crossref] [PubMed]

Z. Zhao, J. W. Y. Lam, and B. Z. Tang, “Tetraphenylethene: a versatile AIE building block for the construction of efficient luminescent materials for organic light-emitting diodes,” J. Mater. Chem. 22(45), 23726 (2012).
[Crossref]

J. Luo, Z. Xie, J. W. Y. Lam, L. Cheng, H. Chen, C. Qiu, H. S. Kwok, X. Zhan, Y. Liu, D. Zhu, and B. Z. Tang, “Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole,” Chem. Commun. (Camb.) 18(18), 1740–1741 (2001).
[Crossref] [PubMed]

Laurent, A. D.

K. Benelhadj, W. Muzuzu, J. Massue, P. Retailleau, A. Charaf-Eddin, A. D. Laurent, D. Jacquemin, G. Ulrich, and R. Ziessel, “White Emitters by Tuning the Excited-State Intramolecular Proton-Transfer Fluorescence Emission in 2-(2′-Hydroxybenzofuran)benzoxazole Dyes,” Chem. Eur. J 20(40), 12843–12857 (2014).
[Crossref] [PubMed]

Lee, D. K.

S. Park, J. E. Kwon, S. Y. Park, O. H. Kwon, J. K. Kim, S. J. Yoon, J. W. Chung, D. R. Whang, S. K. Park, D. K. Lee, D. J. Jang, J. Gierschner, and S. Y. Park, “Crystallization‐Induced Emission Enhancement and Amplified Spontaneous Emission from a CF3‐Containing Excited‐State Intramolecular‐Proton‐Transfer Molecule,” Adv. Opt. Mater. 5(18), 1700353 (2017).
[Crossref]

Leung, N. L. C.

J. Mei, N. L. C. Leung, R. T. K. Kwok, J. W. Y. Lam, and B. Z. Tang, “Aggregation-Induced Emission: Together We Shine, United We Soar!” Chem. Rev. 115(21), 11718–11940 (2015).
[Crossref] [PubMed]

Levchenko, K. S.

K. S. Levchenko, I. S. Semenova, V. N. Yarovenko, P. S. Shmelin, and M. M. Krayushkin, “Facile syntheses of 2-substituted 3-cyanochromones,” Tetrahedron Lett. 53(28), 3630–3632 (2012).
[Crossref]

Li, F.

X. Cheng, Y. Zhang, S. Han, F. Li, H. Zhang, and Y. Wang, “Multicolor Amplified Spontaneous Emissions Based on Organic Polymorphs That Undergo Excited-State Intramolecular Proton Transfer,” Chemistry 22(14), 4899–4903 (2016).
[Crossref] [PubMed]

X. Cheng, F. Li, S. Han, Y. Zhang, C. Jiao, J. Wei, K. Ye, Y. Wang, and H. Zhang, “Emission behaviors of unsymmetrical 1,3-diaryl-β-diketones: A model perfectly disclosing the effect of molecular conformation on luminescence of organic solids,” Sci. Rep. 5(1), 9140 (2015).
[Crossref] [PubMed]

Liang, F.

F. Liang, L. Wang, D. Ma, X. Jing, and F. Wang, “Oxadiazole-containing material with intense blue phosphorescence emission for organic light-emitting diodes,” Appl. Phys. Lett. 81(1), 4–6 (2002).
[Crossref]

Liu, W.

J. Wu, W. Liu, J. Ge, H. Zhang, and P. Wang, “New sensing mechanisms for design of fluorescent chemosensors emerging in recent years,” Chem. Soc. Rev. 40(7), 3483–3495 (2011).
[Crossref] [PubMed]

Liu, X. L.

X. L. Liu, J. M. Cole, and Z. C. Xu, “Substantial Intramolecular Charge Transfer Induces Long Emission Wavelengths and Mega Stokes Shifts in 6-Aminocoumarins,” J. Phys. Chem. C 121(24), 13274–13279 (2017).
[Crossref]

X. L. Liu, Z. C. Xu, and J. M. Cole, “Molecular Design of UV-vis Absorption and Emission Properties in Organic Fluorophores: Toward Larger Bathochromic Shifts, Enhanced Molar Extinction Coefficients, and Greater Stokes Shifts,” J. Phys. Chem. C 117(32), 16584–16595 (2013).
[Crossref]

Liu, Y.

J. Luo, Z. Xie, J. W. Y. Lam, L. Cheng, H. Chen, C. Qiu, H. S. Kwok, X. Zhan, Y. Liu, D. Zhu, and B. Z. Tang, “Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole,” Chem. Commun. (Camb.) 18(18), 1740–1741 (2001).
[Crossref] [PubMed]

Luo, J.

J. Luo, Z. Xie, J. W. Y. Lam, L. Cheng, H. Chen, C. Qiu, H. S. Kwok, X. Zhan, Y. Liu, D. Zhu, and B. Z. Tang, “Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole,” Chem. Commun. (Camb.) 18(18), 1740–1741 (2001).
[Crossref] [PubMed]

Ma, D.

F. Liang, L. Wang, D. Ma, X. Jing, and F. Wang, “Oxadiazole-containing material with intense blue phosphorescence emission for organic light-emitting diodes,” Appl. Phys. Lett. 81(1), 4–6 (2002).
[Crossref]

Massue, J.

K. Benelhadj, W. Muzuzu, J. Massue, P. Retailleau, A. Charaf-Eddin, A. D. Laurent, D. Jacquemin, G. Ulrich, and R. Ziessel, “White Emitters by Tuning the Excited-State Intramolecular Proton-Transfer Fluorescence Emission in 2-(2′-Hydroxybenzofuran)benzoxazole Dyes,” Chem. Eur. J 20(40), 12843–12857 (2014).
[Crossref] [PubMed]

Mei, J.

J. Mei, N. L. C. Leung, R. T. K. Kwok, J. W. Y. Lam, and B. Z. Tang, “Aggregation-Induced Emission: Together We Shine, United We Soar!” Chem. Rev. 115(21), 11718–11940 (2015).
[Crossref] [PubMed]

Monkman, A. P.

K. T. Kamtekar, A. P. Monkman, and M. R. Bryce, “Ordered Materials for Organic Electronics and Photonics,” Adv. Mater. 22, 572 (2010).
[Crossref] [PubMed]

Muzuzu, W.

K. Benelhadj, W. Muzuzu, J. Massue, P. Retailleau, A. Charaf-Eddin, A. D. Laurent, D. Jacquemin, G. Ulrich, and R. Ziessel, “White Emitters by Tuning the Excited-State Intramolecular Proton-Transfer Fluorescence Emission in 2-(2′-Hydroxybenzofuran)benzoxazole Dyes,” Chem. Eur. J 20(40), 12843–12857 (2014).
[Crossref] [PubMed]

Padalkar, V. S.

V. S. Padalkar and S. Seki, “Excited-state intramolecular proton-transfer (ESIPT)-inspired solid state emitters,” Chem. Soc. Rev. 45(1), 169–202 (2016).
[Crossref] [PubMed]

Palmer, A. E.

K. P. Carter, A. M. Young, and A. E. Palmer, “Fluorescent Sensors for Measuring Metal Ions in Living Systems,” Chem. Rev. 114(8), 4564–4601 (2014).
[Crossref] [PubMed]

Park, S.

S. Park, J. E. Kwon, S. Y. Park, O. H. Kwon, J. K. Kim, S. J. Yoon, J. W. Chung, D. R. Whang, S. K. Park, D. K. Lee, D. J. Jang, J. Gierschner, and S. Y. Park, “Crystallization‐Induced Emission Enhancement and Amplified Spontaneous Emission from a CF3‐Containing Excited‐State Intramolecular‐Proton‐Transfer Molecule,” Adv. Opt. Mater. 5(18), 1700353 (2017).
[Crossref]

Z. Guo, S. Park, J. Yoon, and I. Shin, “Recent progress in the development of near-infrared fluorescent probes for bioimaging applications,” Chem. Soc. Rev. 43(1), 16–29 (2014).
[Crossref] [PubMed]

S. Park, O. H. Kwon, S. Kim, S. Park, M. G. Choi, M. Cha, S. Y. Park, and D. J. Jang, “Imidazole-Based Excited-State Intramolecular Proton-Transfer Materials: Synthesis and Amplified Spontaneous Emission from A Large Single Crystal,” J. Am. Chem. Soc. 127(28), 10070–10074 (2005).
[Crossref] [PubMed]

S. Park, O. H. Kwon, S. Kim, S. Park, M. G. Choi, M. Cha, S. Y. Park, and D. J. Jang, “Imidazole-Based Excited-State Intramolecular Proton-Transfer Materials: Synthesis and Amplified Spontaneous Emission from A Large Single Crystal,” J. Am. Chem. Soc. 127(28), 10070–10074 (2005).
[Crossref] [PubMed]

Park, S. K.

S. Park, J. E. Kwon, S. Y. Park, O. H. Kwon, J. K. Kim, S. J. Yoon, J. W. Chung, D. R. Whang, S. K. Park, D. K. Lee, D. J. Jang, J. Gierschner, and S. Y. Park, “Crystallization‐Induced Emission Enhancement and Amplified Spontaneous Emission from a CF3‐Containing Excited‐State Intramolecular‐Proton‐Transfer Molecule,” Adv. Opt. Mater. 5(18), 1700353 (2017).
[Crossref]

Park, S. Y.

S. Park, J. E. Kwon, S. Y. Park, O. H. Kwon, J. K. Kim, S. J. Yoon, J. W. Chung, D. R. Whang, S. K. Park, D. K. Lee, D. J. Jang, J. Gierschner, and S. Y. Park, “Crystallization‐Induced Emission Enhancement and Amplified Spontaneous Emission from a CF3‐Containing Excited‐State Intramolecular‐Proton‐Transfer Molecule,” Adv. Opt. Mater. 5(18), 1700353 (2017).
[Crossref]

S. Park, J. E. Kwon, S. Y. Park, O. H. Kwon, J. K. Kim, S. J. Yoon, J. W. Chung, D. R. Whang, S. K. Park, D. K. Lee, D. J. Jang, J. Gierschner, and S. Y. Park, “Crystallization‐Induced Emission Enhancement and Amplified Spontaneous Emission from a CF3‐Containing Excited‐State Intramolecular‐Proton‐Transfer Molecule,” Adv. Opt. Mater. 5(18), 1700353 (2017).
[Crossref]

B. K. An, J. Gierschner, and S. Y. Park, “π-Conjugated Cyanostilbene Derivatives: A Unique Self-Assembly Motif for Molecular Nanostructures with Enhanced Emission and Transport,” Acc. Chem. Res. 45(4), 544–554 (2012).
[Crossref] [PubMed]

J. E. Kwon and S. Y. Park, “Advanced Organic Optoelectronic Materials: Harnessing Excited-State Intramolecular Proton Transfer (ESIPT) Process,” Adv. Mater. 23(32), 3615–3642 (2011).
[Crossref] [PubMed]

S. Park, O. H. Kwon, S. Kim, S. Park, M. G. Choi, M. Cha, S. Y. Park, and D. J. Jang, “Imidazole-Based Excited-State Intramolecular Proton-Transfer Materials: Synthesis and Amplified Spontaneous Emission from A Large Single Crystal,” J. Am. Chem. Soc. 127(28), 10070–10074 (2005).
[Crossref] [PubMed]

Parkin, S. R.

T. Dutta, K. B. Woody, S. R. Parkin, M. D. Watson, and J. Gierschner, “Conjugated Polymers with Large Effective Stokes Shift: Benzobisdioxole-Based Poly(phenylene ethynylene)s,” J. Am. Chem. Soc. 131(47), 17321–17327 (2009).
[Crossref] [PubMed]

Qiu, C.

J. Luo, Z. Xie, J. W. Y. Lam, L. Cheng, H. Chen, C. Qiu, H. S. Kwok, X. Zhan, Y. Liu, D. Zhu, and B. Z. Tang, “Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole,” Chem. Commun. (Camb.) 18(18), 1740–1741 (2001).
[Crossref] [PubMed]

Ragni, R.

G. M. Farinola and R. Ragni, “Electroluminescent materials for white organic light emitting diodes,” Chem. Soc. Rev. 40(7), 3467–3482 (2011).
[Crossref] [PubMed]

Retailleau, P.

K. Benelhadj, W. Muzuzu, J. Massue, P. Retailleau, A. Charaf-Eddin, A. D. Laurent, D. Jacquemin, G. Ulrich, and R. Ziessel, “White Emitters by Tuning the Excited-State Intramolecular Proton-Transfer Fluorescence Emission in 2-(2′-Hydroxybenzofuran)benzoxazole Dyes,” Chem. Eur. J 20(40), 12843–12857 (2014).
[Crossref] [PubMed]

Sakai, K.

K. Sakai, T. Ishikawa, and T. Akutagawa, “A blue-white-yellow color-tunable excited state intramolecular proton transfer (ESIPT) fluorophore: sensitivity to polar–nonpolar solvent ratios,” J. Mater. Chem. C Mater. Opt. Electron. Devices 1(47), 7866 (2013).
[Crossref]

Samuel, I. D. W.

I. D. W. Samuel and G. A. Turnbull, “Organic Semiconductor Lasers,” Chem. Rev. 107(4), 1272–1295 (2007).
[Crossref] [PubMed]

Sasabe, H.

H. Sasabe and J. Kido, “Multifunctional Materials in High-Performance OLEDs: Challenges for Solid-State Lighting,” Chem. Mater. 23(3), 621–630 (2011).
[Crossref]

Y. Kawamura, H. Yamamoto, K. Goushi, H. Sasabe, C. Adachi, and H. Yoshizaki, “Ultraviolet amplified spontaneous emission from thin films of 4,4′-bis(9-carbazolyl)-2,2′- biphenyl and the derivatives,” Appl. Phys. Lett. 84(15), 2724–2726 (2004).
[Crossref]

Seki, S.

V. S. Padalkar and S. Seki, “Excited-state intramolecular proton-transfer (ESIPT)-inspired solid state emitters,” Chem. Soc. Rev. 45(1), 169–202 (2016).
[Crossref] [PubMed]

Semenova, I. S.

K. S. Levchenko, I. S. Semenova, V. N. Yarovenko, P. S. Shmelin, and M. M. Krayushkin, “Facile syntheses of 2-substituted 3-cyanochromones,” Tetrahedron Lett. 53(28), 3630–3632 (2012).
[Crossref]

Shin, I.

Z. Guo, S. Park, J. Yoon, and I. Shin, “Recent progress in the development of near-infrared fluorescent probes for bioimaging applications,” Chem. Soc. Rev. 43(1), 16–29 (2014).
[Crossref] [PubMed]

Shmelin, P. S.

K. S. Levchenko, I. S. Semenova, V. N. Yarovenko, P. S. Shmelin, and M. M. Krayushkin, “Facile syntheses of 2-substituted 3-cyanochromones,” Tetrahedron Lett. 53(28), 3630–3632 (2012).
[Crossref]

Sun, F. W.

C. Zhang, C. L. Zou, Y. Yan, R. Hao, F. W. Sun, Z. F. Han, Y. S. Zhao, and J. Yao, “Two-Photon Pumped Lasing in Single-Crystal Organic Nanowire Exciton Polariton Resonators,” J. Am. Chem. Soc. 133(19), 7276–7279 (2011).
[Crossref] [PubMed]

Tang, B. Z.

J. Mei, N. L. C. Leung, R. T. K. Kwok, J. W. Y. Lam, and B. Z. Tang, “Aggregation-Induced Emission: Together We Shine, United We Soar!” Chem. Rev. 115(21), 11718–11940 (2015).
[Crossref] [PubMed]

Z. Zhao, J. W. Y. Lam, and B. Z. Tang, “Tetraphenylethene: a versatile AIE building block for the construction of efficient luminescent materials for organic light-emitting diodes,” J. Mater. Chem. 22(45), 23726 (2012).
[Crossref]

Y. Hong, J. W. Lam, and B. Z. Tang, “Aggregation-induced emission,” Chem. Soc. Rev. 40(11), 5361–5388 (2011).
[Crossref] [PubMed]

J. Luo, Z. Xie, J. W. Y. Lam, L. Cheng, H. Chen, C. Qiu, H. S. Kwok, X. Zhan, Y. Liu, D. Zhu, and B. Z. Tang, “Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole,” Chem. Commun. (Camb.) 18(18), 1740–1741 (2001).
[Crossref] [PubMed]

Tang, K. C.

A. P. Demchenko, K. C. Tang, and P. T. Chou, “Excited-state proton coupled charge transfer modulated by molecular structure and media polarization,” Chem. Soc. Rev. 42(3), 1379–1408 (2013).
[Crossref] [PubMed]

Tew, D. P.

T. Yanaia, D. P. Tew, and N. C. Handy, “A new hybrid exchange-correlation functional using the Coulomb-attenuating method (CAM-B3LYP),” Chem. Phys. Lett. 393(1-3), 51–57 (2004).
[Crossref]

Turnbull, G. A.

I. D. W. Samuel and G. A. Turnbull, “Organic Semiconductor Lasers,” Chem. Rev. 107(4), 1272–1295 (2007).
[Crossref] [PubMed]

Ulrich, G.

K. Benelhadj, W. Muzuzu, J. Massue, P. Retailleau, A. Charaf-Eddin, A. D. Laurent, D. Jacquemin, G. Ulrich, and R. Ziessel, “White Emitters by Tuning the Excited-State Intramolecular Proton-Transfer Fluorescence Emission in 2-(2′-Hydroxybenzofuran)benzoxazole Dyes,” Chem. Eur. J 20(40), 12843–12857 (2014).
[Crossref] [PubMed]

Wang, F.

F. Liang, L. Wang, D. Ma, X. Jing, and F. Wang, “Oxadiazole-containing material with intense blue phosphorescence emission for organic light-emitting diodes,” Appl. Phys. Lett. 81(1), 4–6 (2002).
[Crossref]

Wang, K.

X. Cheng, K. Wang, S. Huang, H. Zhang, H. Zhang, and Y. Wang, “Organic Crystals with Near-Infrared Amplified Spontaneous Emissions Based on 2′-Hydroxychalcone Derivatives: Subtle Structure Modification but Great Property Change,” Angew. Chem. Int. Ed. Engl. 54(29), 8369–8373 (2015).
[Crossref] [PubMed]

Wang, L.

F. Liang, L. Wang, D. Ma, X. Jing, and F. Wang, “Oxadiazole-containing material with intense blue phosphorescence emission for organic light-emitting diodes,” Appl. Phys. Lett. 81(1), 4–6 (2002).
[Crossref]

Wang, P.

J. Wu, W. Liu, J. Ge, H. Zhang, and P. Wang, “New sensing mechanisms for design of fluorescent chemosensors emerging in recent years,” Chem. Soc. Rev. 40(7), 3483–3495 (2011).
[Crossref] [PubMed]

Wang, Y.

X. Cheng, Y. Zhang, S. Han, F. Li, H. Zhang, and Y. Wang, “Multicolor Amplified Spontaneous Emissions Based on Organic Polymorphs That Undergo Excited-State Intramolecular Proton Transfer,” Chemistry 22(14), 4899–4903 (2016).
[Crossref] [PubMed]

X. Cheng, K. Wang, S. Huang, H. Zhang, H. Zhang, and Y. Wang, “Organic Crystals with Near-Infrared Amplified Spontaneous Emissions Based on 2′-Hydroxychalcone Derivatives: Subtle Structure Modification but Great Property Change,” Angew. Chem. Int. Ed. Engl. 54(29), 8369–8373 (2015).
[Crossref] [PubMed]

X. Cheng, F. Li, S. Han, Y. Zhang, C. Jiao, J. Wei, K. Ye, Y. Wang, and H. Zhang, “Emission behaviors of unsymmetrical 1,3-diaryl-β-diketones: A model perfectly disclosing the effect of molecular conformation on luminescence of organic solids,” Sci. Rep. 5(1), 9140 (2015).
[Crossref] [PubMed]

Watson, M. D.

T. Dutta, K. B. Woody, S. R. Parkin, M. D. Watson, and J. Gierschner, “Conjugated Polymers with Large Effective Stokes Shift: Benzobisdioxole-Based Poly(phenylene ethynylene)s,” J. Am. Chem. Soc. 131(47), 17321–17327 (2009).
[Crossref] [PubMed]

Wei, J.

X. Cheng, F. Li, S. Han, Y. Zhang, C. Jiao, J. Wei, K. Ye, Y. Wang, and H. Zhang, “Emission behaviors of unsymmetrical 1,3-diaryl-β-diketones: A model perfectly disclosing the effect of molecular conformation on luminescence of organic solids,” Sci. Rep. 5(1), 9140 (2015).
[Crossref] [PubMed]

Whang, D. R.

S. Park, J. E. Kwon, S. Y. Park, O. H. Kwon, J. K. Kim, S. J. Yoon, J. W. Chung, D. R. Whang, S. K. Park, D. K. Lee, D. J. Jang, J. Gierschner, and S. Y. Park, “Crystallization‐Induced Emission Enhancement and Amplified Spontaneous Emission from a CF3‐Containing Excited‐State Intramolecular‐Proton‐Transfer Molecule,” Adv. Opt. Mater. 5(18), 1700353 (2017).
[Crossref]

Woody, K. B.

T. Dutta, K. B. Woody, S. R. Parkin, M. D. Watson, and J. Gierschner, “Conjugated Polymers with Large Effective Stokes Shift: Benzobisdioxole-Based Poly(phenylene ethynylene)s,” J. Am. Chem. Soc. 131(47), 17321–17327 (2009).
[Crossref] [PubMed]

Wu, J.

J. Wu, W. Liu, J. Ge, H. Zhang, and P. Wang, “New sensing mechanisms for design of fluorescent chemosensors emerging in recent years,” Chem. Soc. Rev. 40(7), 3483–3495 (2011).
[Crossref] [PubMed]

Xie, Z.

J. Luo, Z. Xie, J. W. Y. Lam, L. Cheng, H. Chen, C. Qiu, H. S. Kwok, X. Zhan, Y. Liu, D. Zhu, and B. Z. Tang, “Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole,” Chem. Commun. (Camb.) 18(18), 1740–1741 (2001).
[Crossref] [PubMed]

Xu, Z. C.

X. L. Liu, J. M. Cole, and Z. C. Xu, “Substantial Intramolecular Charge Transfer Induces Long Emission Wavelengths and Mega Stokes Shifts in 6-Aminocoumarins,” J. Phys. Chem. C 121(24), 13274–13279 (2017).
[Crossref]

X. L. Liu, Z. C. Xu, and J. M. Cole, “Molecular Design of UV-vis Absorption and Emission Properties in Organic Fluorophores: Toward Larger Bathochromic Shifts, Enhanced Molar Extinction Coefficients, and Greater Stokes Shifts,” J. Phys. Chem. C 117(32), 16584–16595 (2013).
[Crossref]

Yamamoto, H.

Y. Kawamura, H. Yamamoto, K. Goushi, H. Sasabe, C. Adachi, and H. Yoshizaki, “Ultraviolet amplified spontaneous emission from thin films of 4,4′-bis(9-carbazolyl)-2,2′- biphenyl and the derivatives,” Appl. Phys. Lett. 84(15), 2724–2726 (2004).
[Crossref]

Yan, Y.

W. Zhang, Y. Yan, J. Gu, J. Yao, and Y. S. Zhao, “Low-Threshold Wavelength-Switchable Organic Nanowire Lasers Based on Excited-State Intramolecular Proton Transfer,” Angew. Chem. Int. Ed. Engl. 54(24), 7125–7129 (2015).
[Crossref] [PubMed]

C. Zhang, C. L. Zou, Y. Yan, R. Hao, F. W. Sun, Z. F. Han, Y. S. Zhao, and J. Yao, “Two-Photon Pumped Lasing in Single-Crystal Organic Nanowire Exciton Polariton Resonators,” J. Am. Chem. Soc. 133(19), 7276–7279 (2011).
[Crossref] [PubMed]

Yanaia, T.

T. Yanaia, D. P. Tew, and N. C. Handy, “A new hybrid exchange-correlation functional using the Coulomb-attenuating method (CAM-B3LYP),” Chem. Phys. Lett. 393(1-3), 51–57 (2004).
[Crossref]

Yang, P.

J. Zhao, S. Ji, Y. Chen, H. Guo, and P. Yang, “Excited state intramolecular proton transfer (ESIPT): from principal photophysics to the development of new chromophores and applications in fluorescent molecular probes and luminescent materials,” Phys. Chem. Chem. Phys. 14(25), 8803–8817 (2012).
[Crossref] [PubMed]

Yao, J.

W. Zhang, Y. Yan, J. Gu, J. Yao, and Y. S. Zhao, “Low-Threshold Wavelength-Switchable Organic Nanowire Lasers Based on Excited-State Intramolecular Proton Transfer,” Angew. Chem. Int. Ed. Engl. 54(24), 7125–7129 (2015).
[Crossref] [PubMed]

C. Zhang, C. L. Zou, Y. Yan, R. Hao, F. W. Sun, Z. F. Han, Y. S. Zhao, and J. Yao, “Two-Photon Pumped Lasing in Single-Crystal Organic Nanowire Exciton Polariton Resonators,” J. Am. Chem. Soc. 133(19), 7276–7279 (2011).
[Crossref] [PubMed]

Yarovenko, V. N.

K. S. Levchenko, I. S. Semenova, V. N. Yarovenko, P. S. Shmelin, and M. M. Krayushkin, “Facile syntheses of 2-substituted 3-cyanochromones,” Tetrahedron Lett. 53(28), 3630–3632 (2012).
[Crossref]

Ye, K.

X. Cheng, F. Li, S. Han, Y. Zhang, C. Jiao, J. Wei, K. Ye, Y. Wang, and H. Zhang, “Emission behaviors of unsymmetrical 1,3-diaryl-β-diketones: A model perfectly disclosing the effect of molecular conformation on luminescence of organic solids,” Sci. Rep. 5(1), 9140 (2015).
[Crossref] [PubMed]

Yoon, J.

Z. Guo, S. Park, J. Yoon, and I. Shin, “Recent progress in the development of near-infrared fluorescent probes for bioimaging applications,” Chem. Soc. Rev. 43(1), 16–29 (2014).
[Crossref] [PubMed]

Yoon, S. J.

S. Park, J. E. Kwon, S. Y. Park, O. H. Kwon, J. K. Kim, S. J. Yoon, J. W. Chung, D. R. Whang, S. K. Park, D. K. Lee, D. J. Jang, J. Gierschner, and S. Y. Park, “Crystallization‐Induced Emission Enhancement and Amplified Spontaneous Emission from a CF3‐Containing Excited‐State Intramolecular‐Proton‐Transfer Molecule,” Adv. Opt. Mater. 5(18), 1700353 (2017).
[Crossref]

Yoshizaki, H.

Y. Kawamura, H. Yamamoto, K. Goushi, H. Sasabe, C. Adachi, and H. Yoshizaki, “Ultraviolet amplified spontaneous emission from thin films of 4,4′-bis(9-carbazolyl)-2,2′- biphenyl and the derivatives,” Appl. Phys. Lett. 84(15), 2724–2726 (2004).
[Crossref]

Young, A. M.

K. P. Carter, A. M. Young, and A. E. Palmer, “Fluorescent Sensors for Measuring Metal Ions in Living Systems,” Chem. Rev. 114(8), 4564–4601 (2014).
[Crossref] [PubMed]

Zhan, X.

J. Luo, Z. Xie, J. W. Y. Lam, L. Cheng, H. Chen, C. Qiu, H. S. Kwok, X. Zhan, Y. Liu, D. Zhu, and B. Z. Tang, “Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole,” Chem. Commun. (Camb.) 18(18), 1740–1741 (2001).
[Crossref] [PubMed]

Zhang, C.

C. Zhang, C. L. Zou, Y. Yan, R. Hao, F. W. Sun, Z. F. Han, Y. S. Zhao, and J. Yao, “Two-Photon Pumped Lasing in Single-Crystal Organic Nanowire Exciton Polariton Resonators,” J. Am. Chem. Soc. 133(19), 7276–7279 (2011).
[Crossref] [PubMed]

Zhang, H.

X. Cheng, Y. Zhang, S. Han, F. Li, H. Zhang, and Y. Wang, “Multicolor Amplified Spontaneous Emissions Based on Organic Polymorphs That Undergo Excited-State Intramolecular Proton Transfer,” Chemistry 22(14), 4899–4903 (2016).
[Crossref] [PubMed]

X. Cheng, F. Li, S. Han, Y. Zhang, C. Jiao, J. Wei, K. Ye, Y. Wang, and H. Zhang, “Emission behaviors of unsymmetrical 1,3-diaryl-β-diketones: A model perfectly disclosing the effect of molecular conformation on luminescence of organic solids,” Sci. Rep. 5(1), 9140 (2015).
[Crossref] [PubMed]

X. Cheng, K. Wang, S. Huang, H. Zhang, H. Zhang, and Y. Wang, “Organic Crystals with Near-Infrared Amplified Spontaneous Emissions Based on 2′-Hydroxychalcone Derivatives: Subtle Structure Modification but Great Property Change,” Angew. Chem. Int. Ed. Engl. 54(29), 8369–8373 (2015).
[Crossref] [PubMed]

X. Cheng, K. Wang, S. Huang, H. Zhang, H. Zhang, and Y. Wang, “Organic Crystals with Near-Infrared Amplified Spontaneous Emissions Based on 2′-Hydroxychalcone Derivatives: Subtle Structure Modification but Great Property Change,” Angew. Chem. Int. Ed. Engl. 54(29), 8369–8373 (2015).
[Crossref] [PubMed]

J. Wu, W. Liu, J. Ge, H. Zhang, and P. Wang, “New sensing mechanisms for design of fluorescent chemosensors emerging in recent years,” Chem. Soc. Rev. 40(7), 3483–3495 (2011).
[Crossref] [PubMed]

Zhang, W.

W. Zhang, Y. Yan, J. Gu, J. Yao, and Y. S. Zhao, “Low-Threshold Wavelength-Switchable Organic Nanowire Lasers Based on Excited-State Intramolecular Proton Transfer,” Angew. Chem. Int. Ed. Engl. 54(24), 7125–7129 (2015).
[Crossref] [PubMed]

Zhang, Y.

X. Cheng, Y. Zhang, S. Han, F. Li, H. Zhang, and Y. Wang, “Multicolor Amplified Spontaneous Emissions Based on Organic Polymorphs That Undergo Excited-State Intramolecular Proton Transfer,” Chemistry 22(14), 4899–4903 (2016).
[Crossref] [PubMed]

X. Cheng, F. Li, S. Han, Y. Zhang, C. Jiao, J. Wei, K. Ye, Y. Wang, and H. Zhang, “Emission behaviors of unsymmetrical 1,3-diaryl-β-diketones: A model perfectly disclosing the effect of molecular conformation on luminescence of organic solids,” Sci. Rep. 5(1), 9140 (2015).
[Crossref] [PubMed]

Zhao, J.

J. Zhao, S. Ji, Y. Chen, H. Guo, and P. Yang, “Excited state intramolecular proton transfer (ESIPT): from principal photophysics to the development of new chromophores and applications in fluorescent molecular probes and luminescent materials,” Phys. Chem. Chem. Phys. 14(25), 8803–8817 (2012).
[Crossref] [PubMed]

Zhao, Y. S.

W. Zhang, Y. Yan, J. Gu, J. Yao, and Y. S. Zhao, “Low-Threshold Wavelength-Switchable Organic Nanowire Lasers Based on Excited-State Intramolecular Proton Transfer,” Angew. Chem. Int. Ed. Engl. 54(24), 7125–7129 (2015).
[Crossref] [PubMed]

C. Zhang, C. L. Zou, Y. Yan, R. Hao, F. W. Sun, Z. F. Han, Y. S. Zhao, and J. Yao, “Two-Photon Pumped Lasing in Single-Crystal Organic Nanowire Exciton Polariton Resonators,” J. Am. Chem. Soc. 133(19), 7276–7279 (2011).
[Crossref] [PubMed]

Zhao, Z.

Z. Zhao, J. W. Y. Lam, and B. Z. Tang, “Tetraphenylethene: a versatile AIE building block for the construction of efficient luminescent materials for organic light-emitting diodes,” J. Mater. Chem. 22(45), 23726 (2012).
[Crossref]

Zhu, D.

J. Luo, Z. Xie, J. W. Y. Lam, L. Cheng, H. Chen, C. Qiu, H. S. Kwok, X. Zhan, Y. Liu, D. Zhu, and B. Z. Tang, “Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole,” Chem. Commun. (Camb.) 18(18), 1740–1741 (2001).
[Crossref] [PubMed]

Ziessel, R.

K. Benelhadj, W. Muzuzu, J. Massue, P. Retailleau, A. Charaf-Eddin, A. D. Laurent, D. Jacquemin, G. Ulrich, and R. Ziessel, “White Emitters by Tuning the Excited-State Intramolecular Proton-Transfer Fluorescence Emission in 2-(2′-Hydroxybenzofuran)benzoxazole Dyes,” Chem. Eur. J 20(40), 12843–12857 (2014).
[Crossref] [PubMed]

Zou, C. L.

C. Zhang, C. L. Zou, Y. Yan, R. Hao, F. W. Sun, Z. F. Han, Y. S. Zhao, and J. Yao, “Two-Photon Pumped Lasing in Single-Crystal Organic Nanowire Exciton Polariton Resonators,” J. Am. Chem. Soc. 133(19), 7276–7279 (2011).
[Crossref] [PubMed]

Acc. Chem. Res. (1)

B. K. An, J. Gierschner, and S. Y. Park, “π-Conjugated Cyanostilbene Derivatives: A Unique Self-Assembly Motif for Molecular Nanostructures with Enhanced Emission and Transport,” Acc. Chem. Res. 45(4), 544–554 (2012).
[Crossref] [PubMed]

Adv. Mater. (2)

J. E. Kwon and S. Y. Park, “Advanced Organic Optoelectronic Materials: Harnessing Excited-State Intramolecular Proton Transfer (ESIPT) Process,” Adv. Mater. 23(32), 3615–3642 (2011).
[Crossref] [PubMed]

K. T. Kamtekar, A. P. Monkman, and M. R. Bryce, “Ordered Materials for Organic Electronics and Photonics,” Adv. Mater. 22, 572 (2010).
[Crossref] [PubMed]

Adv. Opt. Mater. (1)

S. Park, J. E. Kwon, S. Y. Park, O. H. Kwon, J. K. Kim, S. J. Yoon, J. W. Chung, D. R. Whang, S. K. Park, D. K. Lee, D. J. Jang, J. Gierschner, and S. Y. Park, “Crystallization‐Induced Emission Enhancement and Amplified Spontaneous Emission from a CF3‐Containing Excited‐State Intramolecular‐Proton‐Transfer Molecule,” Adv. Opt. Mater. 5(18), 1700353 (2017).
[Crossref]

Angew. Chem. Int. Ed. Engl. (2)

X. Cheng, K. Wang, S. Huang, H. Zhang, H. Zhang, and Y. Wang, “Organic Crystals with Near-Infrared Amplified Spontaneous Emissions Based on 2′-Hydroxychalcone Derivatives: Subtle Structure Modification but Great Property Change,” Angew. Chem. Int. Ed. Engl. 54(29), 8369–8373 (2015).
[Crossref] [PubMed]

W. Zhang, Y. Yan, J. Gu, J. Yao, and Y. S. Zhao, “Low-Threshold Wavelength-Switchable Organic Nanowire Lasers Based on Excited-State Intramolecular Proton Transfer,” Angew. Chem. Int. Ed. Engl. 54(24), 7125–7129 (2015).
[Crossref] [PubMed]

Appl. Phys. Lett. (2)

Y. Kawamura, H. Yamamoto, K. Goushi, H. Sasabe, C. Adachi, and H. Yoshizaki, “Ultraviolet amplified spontaneous emission from thin films of 4,4′-bis(9-carbazolyl)-2,2′- biphenyl and the derivatives,” Appl. Phys. Lett. 84(15), 2724–2726 (2004).
[Crossref]

F. Liang, L. Wang, D. Ma, X. Jing, and F. Wang, “Oxadiazole-containing material with intense blue phosphorescence emission for organic light-emitting diodes,” Appl. Phys. Lett. 81(1), 4–6 (2002).
[Crossref]

Chem. Commun. (Camb.) (1)

J. Luo, Z. Xie, J. W. Y. Lam, L. Cheng, H. Chen, C. Qiu, H. S. Kwok, X. Zhan, Y. Liu, D. Zhu, and B. Z. Tang, “Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole,” Chem. Commun. (Camb.) 18(18), 1740–1741 (2001).
[Crossref] [PubMed]

Chem. Eur. J (1)

K. Benelhadj, W. Muzuzu, J. Massue, P. Retailleau, A. Charaf-Eddin, A. D. Laurent, D. Jacquemin, G. Ulrich, and R. Ziessel, “White Emitters by Tuning the Excited-State Intramolecular Proton-Transfer Fluorescence Emission in 2-(2′-Hydroxybenzofuran)benzoxazole Dyes,” Chem. Eur. J 20(40), 12843–12857 (2014).
[Crossref] [PubMed]

Chem. Mater. (1)

H. Sasabe and J. Kido, “Multifunctional Materials in High-Performance OLEDs: Challenges for Solid-State Lighting,” Chem. Mater. 23(3), 621–630 (2011).
[Crossref]

Chem. Phys. Lett. (1)

T. Yanaia, D. P. Tew, and N. C. Handy, “A new hybrid exchange-correlation functional using the Coulomb-attenuating method (CAM-B3LYP),” Chem. Phys. Lett. 393(1-3), 51–57 (2004).
[Crossref]

Chem. Rev. (4)

J. Mei, N. L. C. Leung, R. T. K. Kwok, J. W. Y. Lam, and B. Z. Tang, “Aggregation-Induced Emission: Together We Shine, United We Soar!” Chem. Rev. 115(21), 11718–11940 (2015).
[Crossref] [PubMed]

K. P. Carter, A. M. Young, and A. E. Palmer, “Fluorescent Sensors for Measuring Metal Ions in Living Systems,” Chem. Rev. 114(8), 4564–4601 (2014).
[Crossref] [PubMed]

I. D. W. Samuel and G. A. Turnbull, “Organic Semiconductor Lasers,” Chem. Rev. 107(4), 1272–1295 (2007).
[Crossref] [PubMed]

A. J. C. Kuehne and M. C. Gather, “Organic Lasers: Recent Developments on Materials, Device Geometries, and Fabrication Techniques,” Chem. Rev. 116(21), 12823–12864 (2016).
[Crossref] [PubMed]

Chem. Soc. Rev. (6)

Z. Guo, S. Park, J. Yoon, and I. Shin, “Recent progress in the development of near-infrared fluorescent probes for bioimaging applications,” Chem. Soc. Rev. 43(1), 16–29 (2014).
[Crossref] [PubMed]

Y. Hong, J. W. Lam, and B. Z. Tang, “Aggregation-induced emission,” Chem. Soc. Rev. 40(11), 5361–5388 (2011).
[Crossref] [PubMed]

G. M. Farinola and R. Ragni, “Electroluminescent materials for white organic light emitting diodes,” Chem. Soc. Rev. 40(7), 3467–3482 (2011).
[Crossref] [PubMed]

V. S. Padalkar and S. Seki, “Excited-state intramolecular proton-transfer (ESIPT)-inspired solid state emitters,” Chem. Soc. Rev. 45(1), 169–202 (2016).
[Crossref] [PubMed]

A. P. Demchenko, K. C. Tang, and P. T. Chou, “Excited-state proton coupled charge transfer modulated by molecular structure and media polarization,” Chem. Soc. Rev. 42(3), 1379–1408 (2013).
[Crossref] [PubMed]

J. Wu, W. Liu, J. Ge, H. Zhang, and P. Wang, “New sensing mechanisms for design of fluorescent chemosensors emerging in recent years,” Chem. Soc. Rev. 40(7), 3483–3495 (2011).
[Crossref] [PubMed]

Chemistry (1)

X. Cheng, Y. Zhang, S. Han, F. Li, H. Zhang, and Y. Wang, “Multicolor Amplified Spontaneous Emissions Based on Organic Polymorphs That Undergo Excited-State Intramolecular Proton Transfer,” Chemistry 22(14), 4899–4903 (2016).
[Crossref] [PubMed]

J. Am. Chem. Soc. (3)

S. Park, O. H. Kwon, S. Kim, S. Park, M. G. Choi, M. Cha, S. Y. Park, and D. J. Jang, “Imidazole-Based Excited-State Intramolecular Proton-Transfer Materials: Synthesis and Amplified Spontaneous Emission from A Large Single Crystal,” J. Am. Chem. Soc. 127(28), 10070–10074 (2005).
[Crossref] [PubMed]

C. Zhang, C. L. Zou, Y. Yan, R. Hao, F. W. Sun, Z. F. Han, Y. S. Zhao, and J. Yao, “Two-Photon Pumped Lasing in Single-Crystal Organic Nanowire Exciton Polariton Resonators,” J. Am. Chem. Soc. 133(19), 7276–7279 (2011).
[Crossref] [PubMed]

T. Dutta, K. B. Woody, S. R. Parkin, M. D. Watson, and J. Gierschner, “Conjugated Polymers with Large Effective Stokes Shift: Benzobisdioxole-Based Poly(phenylene ethynylene)s,” J. Am. Chem. Soc. 131(47), 17321–17327 (2009).
[Crossref] [PubMed]

J. Mater. Chem. (1)

Z. Zhao, J. W. Y. Lam, and B. Z. Tang, “Tetraphenylethene: a versatile AIE building block for the construction of efficient luminescent materials for organic light-emitting diodes,” J. Mater. Chem. 22(45), 23726 (2012).
[Crossref]

J. Mater. Chem. C Mater. Opt. Electron. Devices (1)

K. Sakai, T. Ishikawa, and T. Akutagawa, “A blue-white-yellow color-tunable excited state intramolecular proton transfer (ESIPT) fluorophore: sensitivity to polar–nonpolar solvent ratios,” J. Mater. Chem. C Mater. Opt. Electron. Devices 1(47), 7866 (2013).
[Crossref]

J. Phys. Chem. C (2)

X. L. Liu, Z. C. Xu, and J. M. Cole, “Molecular Design of UV-vis Absorption and Emission Properties in Organic Fluorophores: Toward Larger Bathochromic Shifts, Enhanced Molar Extinction Coefficients, and Greater Stokes Shifts,” J. Phys. Chem. C 117(32), 16584–16595 (2013).
[Crossref]

X. L. Liu, J. M. Cole, and Z. C. Xu, “Substantial Intramolecular Charge Transfer Induces Long Emission Wavelengths and Mega Stokes Shifts in 6-Aminocoumarins,” J. Phys. Chem. C 121(24), 13274–13279 (2017).
[Crossref]

Phys. Chem. Chem. Phys. (1)

J. Zhao, S. Ji, Y. Chen, H. Guo, and P. Yang, “Excited state intramolecular proton transfer (ESIPT): from principal photophysics to the development of new chromophores and applications in fluorescent molecular probes and luminescent materials,” Phys. Chem. Chem. Phys. 14(25), 8803–8817 (2012).
[Crossref] [PubMed]

Sci. Rep. (1)

X. Cheng, F. Li, S. Han, Y. Zhang, C. Jiao, J. Wei, K. Ye, Y. Wang, and H. Zhang, “Emission behaviors of unsymmetrical 1,3-diaryl-β-diketones: A model perfectly disclosing the effect of molecular conformation on luminescence of organic solids,” Sci. Rep. 5(1), 9140 (2015).
[Crossref] [PubMed]

Tetrahedron Lett. (1)

K. S. Levchenko, I. S. Semenova, V. N. Yarovenko, P. S. Shmelin, and M. M. Krayushkin, “Facile syntheses of 2-substituted 3-cyanochromones,” Tetrahedron Lett. 53(28), 3630–3632 (2012).
[Crossref]

Other (1)

B. Z. Tang and A. Qin, Aggregation-Induced Emission: Fundamentals and Applications, Vol. 1 and 2, John Wiley & Sons, Chichester, UK 2013.

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Figures (4)

Fig. 1
Fig. 1 (a) Schematic diagram of ESIPT photocycle. (b) Normalized absorption (blue) and emission spectra (green) in CHCl3 (1 × 105 M) and emission spectra (red) for doped thin-film of DHP. The inset demonstrates the chemical structure of DHP.
Fig. 2
Fig. 2 (a) Normalized PL decay transients for DHP in doped thin-film. (b) Normalized PL decay transients for DHP in CHCl3 solution (1 × 105 M) of E* form. (c) Normalized PL decay transients for DHP in CHCl3 solution (1 × 105 M) K* form.
Fig. 3
Fig. 3 (a) Optimized geometries for DHP. (b) Potential energy surfaces in the gas phase and representation of the LE and ESIPT states of DHP .
Fig. 4
Fig. 4 (a) The edge-emission spectra of doped thin-films for DHP excited by different energy. Output intensity at λASE. (b) Full Widths at Half-maximum (FWHM) as a function of pump energy for DHP.

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