An AIE-Active conjugated macrocyclic tetramaleimide for "Turn-On" far red/near-infrared fluorescent bioimaging. (June 2021)
- Record Type:
- Journal Article
- Title:
- An AIE-Active conjugated macrocyclic tetramaleimide for "Turn-On" far red/near-infrared fluorescent bioimaging. (June 2021)
- Main Title:
- An AIE-Active conjugated macrocyclic tetramaleimide for "Turn-On" far red/near-infrared fluorescent bioimaging
- Authors:
- Zeng, Wei
Zhu, Ling-Yun
Chen, Yong
Lin, Mei-Jin - Abstract:
- Abstract: A novel water-soluble conjugated macrocyclic tetramaleimide (WCMT-1) with far red/near-infrared (FR/NIR) fluorescence emission has been rationally designed and successfully synthesized. WCMT-1 with the twisted donor (D) and acceptor (A) structures make it possess both aggregation-induce emission (AIE) and twist intramolecular charge transfer (TICT) characteristics. Due to the AIE effects, WCMT-1 exhibits a strong fluorescence in non-polar solvents (the quantum yield of WCMT-1 reaches to 33.7% in toluene and 32.5% in CCl4 ), but it is quenched in an aqueous solution caused by the TICT process. However, by the introduction of sodium lauryl sulfonate (SLS) into the WCMT-1 aqueous solution, the in situ generated WCMT-1&SLS supra-amphiphile resulted in remarkable recovery of FR/NIR fluorescence. Furthermore, combined with its large Stokes shift and good water solubility, the bioimaging experiments towards HeLa and HepG2 cells have also been conducted to give a good performance. Graphical abstract: A water-soluble conjugated macrocyclic tetramaleimide with D-A structural features and AIE-activated FR/NIR emission properties has been developed and the "turn-on" fluorescent bioimaging has been conducted. Image 1 Highlights: A novel water-soluble conjugated macrocyclic tetramaleimide (WCMT-1) with far red/near-infrared (FR/NIR) fluorescence emission has been synthesized. WCMT-1 possesses both aggregation-induce emission (AIE) and twist intramolecular charge transfer (TICT)Abstract: A novel water-soluble conjugated macrocyclic tetramaleimide (WCMT-1) with far red/near-infrared (FR/NIR) fluorescence emission has been rationally designed and successfully synthesized. WCMT-1 with the twisted donor (D) and acceptor (A) structures make it possess both aggregation-induce emission (AIE) and twist intramolecular charge transfer (TICT) characteristics. Due to the AIE effects, WCMT-1 exhibits a strong fluorescence in non-polar solvents (the quantum yield of WCMT-1 reaches to 33.7% in toluene and 32.5% in CCl4 ), but it is quenched in an aqueous solution caused by the TICT process. However, by the introduction of sodium lauryl sulfonate (SLS) into the WCMT-1 aqueous solution, the in situ generated WCMT-1&SLS supra-amphiphile resulted in remarkable recovery of FR/NIR fluorescence. Furthermore, combined with its large Stokes shift and good water solubility, the bioimaging experiments towards HeLa and HepG2 cells have also been conducted to give a good performance. Graphical abstract: A water-soluble conjugated macrocyclic tetramaleimide with D-A structural features and AIE-activated FR/NIR emission properties has been developed and the "turn-on" fluorescent bioimaging has been conducted. Image 1 Highlights: A novel water-soluble conjugated macrocyclic tetramaleimide (WCMT-1) with far red/near-infrared (FR/NIR) fluorescence emission has been synthesized. WCMT-1 possesses both aggregation-induce emission (AIE) and twist intramolecular charge transfer (TICT) characteristics. A remarkable recovery of FR/NIR fluorescence for WCMT-1 in aqueous solution could be achieved by the introduction of sodium lauryl sulfonate (SLS). The bioimaging experiments towards HeLa cells and HepG2 cells for WCMT-1&SLS have also been conducted. This study suggests that WCMT-1 is a promising bioprobe for organic-solvent-free bioimaging. … (more)
- Is Part Of:
- Dyes and pigments. Volume 190(2021)
- Journal:
- Dyes and pigments
- Issue:
- Volume 190(2021)
- Issue Display:
- Volume 190, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 190
- Issue:
- 2021
- Issue Sort Value:
- 2021-0190-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-06
- Subjects:
- Conjugated macrocyclic -- Far red/near-infrared (FR/NIR) -- Aggregation-induce emission (AIE) -- Bioimaging
Dyes and dyeing -- Periodicals
Pigments -- Periodicals
667.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01437208 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.dyepig.2021.109324 ↗
- Languages:
- English
- ISSNs:
- 0143-7208
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3635.600000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23814.xml