Recent advances in aggregation-induced emission (AIE)-based chemosensors for the detection of organic small molecules
Literature Information
Ming Hui Chua, Kang Le Osmund Chin, Xiaogang Liu
The discovery of the aggregation-induced emission (AIE) phenomenon in many classes of organic molecules has revolutionized our understanding of the photoluminescence properties of materials. These breakthroughs have opened up new possibilities for real-life applications and state-of-the-art technologies. AIE luminogens (AIEgens) have emerged as highly useful tools, effectively overcoming the limitations of conventional aggregation-caused quenching (ACQ) luminogens. They find applications in various fields such as biomedical uses, optoelectronics, stimuli-responsive materials, and chemosensing. In particular, the development of highly sensitive and selective AIE fluorescent probes has significantly complemented conventional instrumental analysis methods, offering low-cost, convenient, and rapid detection of target analytes. With intensive research efforts in this area, a wide range of small molecule analytes, including biologically important molecules, drug molecules, volatile organic compounds, and explosives, can now be detected. This review aims to provide an overview of the progress made in the development of AIE-based organic small molecule probes over the past five years.
Recommended Journals
Related Literature
Polymerization-induced polymer aggregation or polymer aggregation-enhanced polymerization? A computer simulation study
Si-Min Kong, Yao-Hong Xue, Xiao-Li Liu, Xiao-Xi Jia, Feng-Chao Cui
DOI: 10.1039/C8CP03069C
Theoretical insights into photo-induced electron transfer at BiOX (X = F, Cl, Br, I) (001) surfaces and interfaces
Tan Li, Xiaochao Zhang, Changming Zhang, Rui Li, Jianxin Liu, Rui Lv, Hui Zhang, Peide Han, Caimei Fan, Zhanfeng Zheng
DOI: 10.1039/C8CP05671D
Computational investigation of gas detection and selectivity on TiS3 nanoflakes supported by experimental evidence
Masoud Aryanpour, Nassim Rafiefard, Seyed Hossein Hosseini-Shokouh, Somayeh Fardindoost
DOI: 10.1039/C8CP05026K
Exciton localization in excited-state dynamics of a tetracene trimer: a surface hopping LC-TDDFTB study
Evgenii Titov, Alexander Humeniuk, Roland Mitrić
DOI: 10.1039/C8CP05240A
How the methyl group position influences the ultrafast deactivation in aromatic radicals
DOI: 10.1039/C8CP06087H
Base adsorption mechanism over zeolite catalysts at different Al contents probed by the tapered element oscillating microbalance (TEOM)
Pierre Bräuer, Carmine D’Agostino
DOI: 10.1039/C8CP05001E
Thermodiffusion of citrate-coated γ-Fe2O3 nanoparticles in aqueous dispersions with tuned counter-ions – anisotropy of the Soret coefficient under a magnetic field
M. Kouyaté, G. Demouchy, G. Mériguet, S. Nakamae, V. Peyre, M. Roger, A. Cēbers, J. Depeyrot, E. Dubois, R. Perzynski
DOI: 10.1039/C8CP06858E
Time-gated triplet-state optical spectroscopy to decipher organic luminophores embedded in rigid matrices
Atul D. Sontakke, Jean-Marie Mouesca, Victor Castaing, Mathieu Salaün, Isabelle Gautier-Luneau, Vincent Maurel, Alain Ibanez, Bruno Viana
DOI: 10.1039/C8CP03952F
Anomalous molecular infiltration in graphene laminates
Riccardo Checchetto, Paolo Bettotti, Gianfranco Carotenuto, Werner Egger, Christoph Hugenschmidt, Antonio Miotello
DOI: 10.1039/C8CP03879A
Impact of H-termination on the nitrogen reduction reaction of molybdenum carbide as an electrochemical catalyst
Qinye Li, Siyao Qiu, Lizhong He, Xiwang Zhang
DOI: 10.1039/C8CP04474K
You might also like
Are there alternatives to 1-(4-Chlorophenyl)-N-hydroxymethanimine (CAS: 3848-36-0) in synthesis?
When considering alternatives to 1-(4-Chlorophenyl)-N-hydroxymethanimine (CAS: 3...
How should (1R,9S,10S,12S,14E,16S,19R,20R,21S,22R)-3,9,21-Trihydroxy-5,10,12,14,16,20,22-heptamethyl-23,24-dioxatetracyclo[17.3.1.1~6,9~.0~2,7~]tetracosa-2,5,7,14-tetraen-4-one (CAS: 183202-73-5) be stored?
This compound should be stored in a cool, dry place away from direct sunlight. I...
How is 3-(4-Bromophenyl)-5-(2-fluorophenyl)-1,2,4-oxadiazole (CAS: 419553-16-5) typically synthesized?
3-(4-Bromophenyl)-5-(2-fluorophenyl)-1,2,4-oxadiazole is synthesized through a m...
How is 5-Chloro-2-(4-chlorophenyl)-4-methyl-6-[3-(1-piperidinyl)propoxy]pyrimidine (CAS: 1639220-19-1) typically synthesized?
5-Chloro-2-(4-chlorophenyl)-4-methyl-6-[3-(1-piperidinyl)propoxy]pyrimidine (CAS...
What industries use 2-Chloro-4-(difluoromethoxy)pyridine (CAS: 1206978-15-5)?
2-Chloro-4-(difluoromethoxy)pyridine is used in the pharmaceutical industry for ...
What regulatory guidelines apply to 3-Chloro-6-methylpyridazine (CAS: 1121-79-5)?
3-Chloro-6-methylpyridazine (CAS: 1121-79-5) is classified under the Globally Ha...
Are there alternatives to Methyl 4,5-dimethyl-2-nitrobenzoate in synthesis?
Several alternatives can be used in the synthesis of Methyl 4,5-dimethyl-2-nitro...
Are there alternatives to (2E,2'E)-3,3'-(1,4-Phenylene)bisacrylaldehyde in synthesis?
Alternatives to (2E,2'E)-3,3'-(1,4-Phenylene)bisacrylaldehyde include other acry...
What is 3-Amino-5-chloropyridin-2-ol hydrochloride (CAS: 1261906-29-9)?
3-Amino-5-chloropyridin-2-ol hydrochloride is an organic compound with the CAS n...
What precautions should be taken when handling 6,7-Difluoro-2,3-dihydro-4H-chromen-4-one (CAS: 1092349-93-3)?
When handling 6,7-Difluoro-2,3-dihydro-4H-chromen-4-one, it is essential to wear...















