EDP Sciences logo
Menu
All issues Volume 8 (2024) Emergent Scientist, 8 (2024) 1 References
Open Access
Issue
Emergent Scientist
Volume 8, 2024
Article Number 1
Number of page(s) 18
Section Chemistry
DOI https://doi.org/10.1051/emsci/2023004
Published online 25 January 2024
  1. M. Qayyum, T. Bushra, Z.A. Khan, H. Gul, S. Majeed, C. Yu, U. Farooq, A.J. Shaikh, S.A. Shahzad, Synthesis and tetraphenylethylene-based aggregation-induced emission probe for rapid detection of nitroaromatic compounds in aqueous media, ACS Omega 6, 25447–25460 (2021) [CrossRef] [Google Scholar]
  2. S. Majeed, T.A. Khan, M.T. Waseem, H.M. Junaid, A.M. Khan, S.A. Shahzad, A ratiometric fluorescent, colorimetric, and paper sensor for sequential detection of Cu2+ and Glutathione in food: AIEE and reversible piezo fluorochromic activity, J. Photochem. Photobiol. Chem. 431, 114062 (2022) [CrossRef] [Google Scholar]
  3. L. Wilbraham, M. Louis, D. Alberga, A. Brosseau, R. Guillot, F. Ito, F. Labat, R. Métivier, C. Allain, I. Ciofini, Revealing the origins of mechanically induced fluorescence changes in organic molecular crystals, Adv. Mater. 30, 1800817 (2018) [CrossRef] [Google Scholar]
  4. S.A. Jenekhe, J.A. Osaheni, Excimers and exciplexes of conjugated polymers, Science 265, 765–768 (1994) [CrossRef] [Google Scholar]
  5. F. Song, B. Liu, B.Z. Tang, Celebration of the 20th anniversary of aggregation-induced emission with research highlights from royal society of chemistry journals, J. Mater. Chem. C 8, 7972–7974 (2020) [CrossRef] [Google Scholar]
  6. J. Luo, Z. Xie, J.W.Y. Lam, L. Cheng, B.Z. Tang, H. Chen, C. Qiu, H.S. Kwok, X. Zhan, Y. Liu, D. Zhu, Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole, Chem. Commun. 18, 1740–1741 (2001) [CrossRef] [Google Scholar]
  7. Z.-F. Chang, L.-M. Jing, C. Wei, Y.-P. Dong, Y.-C. Ye, Y.S. Zhao, J.-L. Wang, Hexaphenylbenzene-based, π-conjugated snowflake-shaped luminophores: tunable aggregation-induced emission effect and piezofluo-rochromism, Chem. – Eur. J. 21, 8504–8510 (2015) [CrossRef] [Google Scholar]
  8. B. Prusti, M. Chakravarty, Disparity in piezofluo-rochromism for twisted mono-carbazole-based AIEgens resulting from interchanging electron-rich substituents: effect of coplanarity on twisted π-conjugates., Mater. Adv. 2, 1752–1759 (2021) [CrossRef] [Google Scholar]
  9. B. Xu, Z. Chi, J. Zhang, X. Zhang, H. Li, X. Li, S. Liu, Y. Zhang, J. Xu, Piezofluoro-chromic and aggregation-induced-emission compounds containing triphenylethylene and tetraphenylethylene moieties, Chem. – Asian J. 6, 1470–1478 (2011) [CrossRef] [Google Scholar]
  10. Y. Cao, W. Xi, L. Wang, H. Wang, L. Kong, H. Zhou, J. Wu, Y. Tian, Reversible piezofluorochromic nature and mechanism of aggregation-induced emission-active compounds based on simple modification, RSC Adv. 4, 24649–24652 (2014) [CrossRef] [Google Scholar]
  11. Z.-Q. Yao, J. Xu, B. Zou, Z. Hu, K. Wang, Y.-J. Yuan, Y.-P. Chen, R. Feng, J.-B. Xiong, J. Hao, X.-H. Bu, A dual-stimuli-responsive coordination network featuring reversible wide-range luminescence-tuning behavior, Angew. Chem. Int. Ed. 58, 5614–5618 (2019) [CrossRef] [Google Scholar]
  12. J. Sturalan, M.K. Etherington, A.N. Bismillah, H.F. Hig-ginbotham, W. Trewby, J.A. Aguilar, E.H.C. Bromley, A.-J. Avestro, A.P. Monkman, P.R. McGonigal, Excited-state aromatic interactions in the aggregation-induced emission of molecular rotors, J. Am. Chem. Soc. 139, 17882–17889 (2017) [CrossRef] [Google Scholar]
  13. P. Das, A. Kumar, A. Chowdhury, P.S. Mukherjee, Aggregation-induced emission and white luminescence from a combination of π- conjugated donor-acceptor organic Luminogens, ACS Omega 3, 13757–13771 (2018) [CrossRef] [Google Scholar]
  14. D.W. Cho, D.W. Cho, Excimer and exciple emissions of 1,8-naphthalimides caused by aggregation in extremely polar or nonpolar solvents, New J. Chem. 38, 2233–36 (2014) [CrossRef] [Google Scholar]
  15. J.G. Baragi, M.I. Aralaguppi, T.M. Aminabhavi, M.Y. Kariduraganavar, A.S. Kittur, Density, viscosity, refractive index, and speed of sound for binary mixtures of anisole with 2-chloroethanol, 1,4-dioxane, tetrachloroethylene, tetrachloroethane, DMF, DMSO, and diethyl oxalate at (298.15, 303.15, and 308.15) K, J. Chem. Eng. Data 50, 910–916 (2005) [CrossRef] [Google Scholar]
  16. NIST. Chemical Substance Database, 2023. Retrieved July 8, 2023, from https://webbook.nist.gov/chemistry/fluid/ [Google Scholar]
  17. E. Ramachandran, R. Dhamodharan, Rational design of phenothiazine (PTz) and ethylenedioxythiophene (EDOT) based donor–acceptor compounds with a molecular aggregation breaker for solid state emission in red and NIR regions, J. Mater. Chem. C 3, 8642–8648 (2015) [CrossRef] [Google Scholar]
  18. S.S.M. Fernandes, M. Belsley, A.I. Pereira, D. Ivanou, A. Mendes, L.L.G. Justino, H.D. Burrows, M.M.M. Raposo, Push–pull N,N-diphenylhydrazones bearing bithiophene or thienothiophene spacers as nonlinear optical second harmonic generators and as photosensitizers for nanocrystalline TiO2 dye-sensitized solar cells, ACS Omega 3, 12893–12904 (2018) [CrossRef] [Google Scholar]
  19. Conor Parks et al., Solubility curves and nucleation rates from molecular dynamics for polymorph prediction – moving beyond lattice energy minimization, Phys. Chem. Chem. Phys. 19, 5285–5295 (2017) [CrossRef] [Google Scholar]

Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.

Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.

Initial download of the metrics may take a while.