Handbook of Aggregation-Induced Emission, Volume 2. Группа авторов
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Название: Handbook of Aggregation-Induced Emission, Volume 2
Автор: Группа авторов
Издательство: John Wiley & Sons Limited
Жанр: Химия
isbn: 9781119642961
isbn:
The study of TPP dated back to the mid‐nineteenth century, while its real structure was established by Japp and Wilson in 1886. Since that, more studies are focused on synthetic methodologies and medicinal chemistry. It is until 2015 that Tang found TPP to be AIE‐active and have merits of easy synthesis, facile medication, good stability, and tunable electronic property, etc. This, therefore, evolves from a variety of functionalities based on tetraphenylpyrazines and makes its researches very attractive.
TPP can be synthesized by cyclization and Suzuki–Miyaura reactions. In the former case, several routes are provided to prepare TPP and its derivatives with mono‐, di‐, and tetrasubstitutions. For disubstituted TPP, the molecules even with substitutions at different sides can be obtained. By choosing a suitable method, TPP can be synthesized under a very simple and green condition and the purification of TPP can be carried out by recrystallization instead of chromatographic column. The Suzuki–Miyaura reaction can also give tetrasubstituted TPP efficiently and replenish the products that cannot be obtained by the former methods. Encouraged by this, a large amount of desired structures based on TPP can be designed.
TPP‐based luminescent materials show different functionalities to indicate their application potentials. Electron‐donating group‐modified TPPs often show high luminescent efficiencies in the aggregate state and can be utilized to fabricate OLEDs, with EQE approaching theoretic limit. By decorating TPP with an active group, the resulting AIEgen can function as a ratiometric fluorescent sensor to detect H2S with good selectivity and high sensitivity. Besides, by constructing TPP derivatives with different isomerization effects, a model can be established to elaborate the influence of molecular conjugation and porosity on the sensing properties. TPP can also catch the eyes of researchers in reticular chemistry. For example, the chiral TPP‐based organic cage can be obtained from the achiral TPP unit, which can form a host–guest complex with ACQ molecules to construct stable white‐light emission materials in the film state. Also, MOFs can be designed based on the TPP unit as ligand, which shows strong emissions due to coordination‐induced emission and antenna effect and displays a sensitive and selective ratiometric detection of arginine.
Overall, the researches on TPP are still in an embryonic stage. Many applications are worth being further explored. For example, pyrazines are widely found in natural products and known as antitumor, antibacterial, diuretic, anti‐TB, and antidiabetic drugs. Hydroxyl‐substituted TPPs are regarded as regulators of estrogen receptors. Thus, it is feasible to develop luminescent drugs and imaging agents to monitor the therapeutic process and life process. On the other hand, functional materials with diversified architectures are very easy to achieve based on TPP. The investigations of TPP‐based macrocycles, organic–inorganic coordinated cages, conjugated microporous polymers, covalent organic frameworks, and hydrogen‐bonded organic frameworks are still blank. We hope, with this chapter, a picture of the past, now, and future of TPP can be clearly painted and more sparks and opportunities can be motivated to boost the development of TPP‐based luminescent materials.
References
1 1 Zhao, Z., Chen, S., Chan, C. Y. K. et al. (2012) A facile and versatile approach to efficient luminescent materials for applications in organic light‐emitting diodes. Chemistry—An Asian Journal 7 (3): 484–488.
2 2 Zhou, J., Liu, Q., Feng, W. et al. (2015) Upconversion luminescent materials: advances and applications. Chemical Reviews 115 (1): 395–465.
3 3 Zhu, X., Su, Q., Feng, W. et al. (2017) Anti‐Stokes shift luminescent materials for bio‐applications. Chemical Society Reviews 46 (4): 1025–1039.
4 4 Grimsdale, A. C., Chan, K. L., Martin, R. E. et al. (2009) Synthesis of light‐emitting conjugated polymers for applications in electroluminescent devices. Chemical Reviews 109 (3): 897–1091.
5 5 Ding, D., Li, K., Liu, B. et al. (2013) Bioprobes based on AIE fluorogens. Accounts of Chemical Research 46 (11): 2441–2453.
6 6 Chen, C., Ou, H., Liu, R. et al. (2020) Regulating the photophysical property of organic/polymer optical agents for promoted cancer phototheranostics. Advanced Materials 32 (3): 1806331.
7 7 Yang, Z., Mao, Z., Xie, Z. et al. (2017) Recent advances in organic thermally activated delayed fluorescence materials. Chemical Society Reviews 46 (3): 915–1016.
8 8 Lee, J. H., Chen, C. H., Lee, P. H. et al. (2019) Blue organic light‐emitting diodes: current status, challenges, and future outlook. Journal of Materials Chemistry C 7 (20), 5874–5888.
9 9 Luo, J., Xie, Z., Lam, J. W. Y. et al. (2001) Aggregation‐induced emission of 1‐methyl‐1,2,3,4,5‐pentaphenylsilole. Chemical Communications 381 (18): 1740–1741.
10 10 Wang, J., Gu, X., Zhang, P. et al. (2017) Ionization and anion−π+ interaction: a new strategy for structural design of aggregation‐induced emission luminogens. Journal of the American Chemistry Society 139 (46): 16974–16979.
11 11 Wang, Y., Chen, M., Alifu, N. et al. (2017) Aggregation‐induced emission luminogen with deep‐red emission for through‐skull three‐photon fluorescence imaging of mouse. ACS Nano 11 (10): 10452–10461.
12 12 Niu, G., Zheng, X., Zhao, Z. et al. (2019) Functionalized acrylonitriles with aggregation‐induced emission: structure tuning by simple reaction–condition variation, efficient red emission, and two‐photon bioimaging. Journal of the American Chemistry Society 141 (38): 15111–15120.
13 13 Mei, J., Leung, N. L. C., Kwok, R. T. K. et al. (2015) Aggregation‐induced emission: together we shine, united we soar! Chemical Reviews 115 (21): 11718–11940.
14 14 Chen, M., Xie, W., Li, D. et al. (2018) Utilizing a pyrazine‐containing aggregation‐induced emission luminogen as an efficient photosensitizer for imaging‐guided two‐photon photodynamic therapy. Chemistry‐A European Journal 24 (62): 16603–16608.
15 15 Chen, Y., Zhang, W., Zhao, Z. et al. (2018) An easily accessible ionic aggregation‐induced emission luminogen with hydrogen‐bonding‐switchable emission and wash‐free imaging ability. Angewandte Chemie International Edition 57 (18): 5011–5015.
16 16 Wang, D., Su, H., Kwok, R. T. K. et al. (2017) Facile synthesis of red/NIR AIE luminogens with simple structures, bright emissions, and high photostabilities, and their applications for specific imaging of lipid droplets and image‐guided photodynamic therapy. Advanced Functional Materials 27 (46): 1704039.
17 17 Huang, J., Yang, X., Li, X. et al. (2012) Bipolar AIE‐active luminogens comprised of an oxadiazole core and terminal TPE moieties as a new type of host for doped electroluminescence. Chemical Communications 48 (77): 9586–9588.
18 18 Shi, H., Xin, D., Gu, X. et al. (2016) The synthesis of novel AIE emitters with the triphenylethene‐carbazole skeleton and para‐/meta‐substituted arylboron groups and their application in efficient non‐doped OLEDs. Journal of Materials Chemistry C 4 (6), 1228–1237.
19 19 Xu, B., Chi, Z., Li, H. et al. (2011) Synthesis and properties of aggregation‐induced emission compounds containing triphenylethene and tetraphenylethene moieties. The Journal of Physical Chemistry C 115 (35): 17574–17581.
20 20 Han, T., Zhang, Y. J., Feng, X. et al. (2013) Reversible and hydrogen bonding‐assisted piezochromic luminescence for solid‐state tetraaryl‐buta‐1,3‐diene. Chemical Communications 49 (63): 7049–7051.
21 21 Yang, Z., Qin, W., Leung, N. L. C. et al. (2016) A mechanistic study of AIE processes of TPE luminogens: intramolecular rotation vs. configurational isomerization. Journal of Materials Chemistry СКАЧАТЬ