Design of multi-functional AIEgens: tunable emission, circularly polarized luminescence and self-assembly by dark through-bond energy transfer. Issue 33 (8th August 2018)
- Record Type:
- Journal Article
- Title:
- Design of multi-functional AIEgens: tunable emission, circularly polarized luminescence and self-assembly by dark through-bond energy transfer. Issue 33 (8th August 2018)
- Main Title:
- Design of multi-functional AIEgens: tunable emission, circularly polarized luminescence and self-assembly by dark through-bond energy transfer
- Authors:
- Feng, Hai-Tao
Gu, Xinggui
Lam, Jacky W. Y.
Zheng, Yan-Song
Tang, Ben Zhong - Abstract:
- Abstract : A pair of chiral R / S -TPE-BINOL derivatives with dark resonance energy transfer was synthesized using a tetraphenylethylene derivative as a dark energy donor which also endows the target molecules with aggregation-induced emission characteristics, BODIPY as an energy acceptor and BINOL as a chiral source. Abstract : A pair of chiral R / S -TPE-BINOL derivatives with dark resonance energy transfer was facilely synthesized by coupling of a tetraphenylethylene (TPE) derivative, BODIPY dye and R / S -1, 1′-bi-2-binaphthol (BINOL), where TPE not only was selected as a dark energy donor, but also can endow the target molecules with aggregation-induced emission (AIE) characteristics; BODIPY served as an energy acceptor; BINOL, one of the most popular axially chiral compounds, was employed as a chiral source. Due to the chiral feature of R / S -TPE-BINOL, obvious CD and CPL signals were observed in the solution and aggregated states. Generally, for organic dyes, high dissymmetric factor ( g em ) values are often accompanied by low emission efficiencies. To improve emission efficiency, an effective strategy of dark through-bond energy transfer was adopted. This method makes it possible to avoid fluorescence leakage originating from donor emission. The energy of TPE can be completely transferred to the BODIPY unit before non-radiative relaxation with an energy transfer efficiency of up to 99% and a high quantum yield of 91%. Remarkably, these enantiomers couldAbstract : A pair of chiral R / S -TPE-BINOL derivatives with dark resonance energy transfer was synthesized using a tetraphenylethylene derivative as a dark energy donor which also endows the target molecules with aggregation-induced emission characteristics, BODIPY as an energy acceptor and BINOL as a chiral source. Abstract : A pair of chiral R / S -TPE-BINOL derivatives with dark resonance energy transfer was facilely synthesized by coupling of a tetraphenylethylene (TPE) derivative, BODIPY dye and R / S -1, 1′-bi-2-binaphthol (BINOL), where TPE not only was selected as a dark energy donor, but also can endow the target molecules with aggregation-induced emission (AIE) characteristics; BODIPY served as an energy acceptor; BINOL, one of the most popular axially chiral compounds, was employed as a chiral source. Due to the chiral feature of R / S -TPE-BINOL, obvious CD and CPL signals were observed in the solution and aggregated states. Generally, for organic dyes, high dissymmetric factor ( g em ) values are often accompanied by low emission efficiencies. To improve emission efficiency, an effective strategy of dark through-bond energy transfer was adopted. This method makes it possible to avoid fluorescence leakage originating from donor emission. The energy of TPE can be completely transferred to the BODIPY unit before non-radiative relaxation with an energy transfer efficiency of up to 99% and a high quantum yield of 91%. Remarkably, these enantiomers could self-assemble into bowl-like hollow microspheres in a mixed solvent of THF/water to give a stable fluorescent suspension with tunable emission from the green to yellow region. Moreover, TPE-BOD was selected as the fluorescent probe for specific staining of lipid droplets in living cells. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 6:Issue 33(2018)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 6:Issue 33(2018)
- Issue Display:
- Volume 6, Issue 33 (2018)
- Year:
- 2018
- Volume:
- 6
- Issue:
- 33
- Issue Sort Value:
- 2018-0006-0033-0000
- Page Start:
- 8934
- Page End:
- 8940
- Publication Date:
- 2018-08-08
- Subjects:
- Materials -- Periodicals
Chemistry, Analytic -- Periodicals
Optical materials -- Research -- Periodicals
Electronics -- Materials -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/tc# ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c8tc02504e ↗
- Languages:
- English
- ISSNs:
- 2050-7526
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205300
British Library DSC - BLDSS-3PM
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