Triphenylethylene-based fluorophores: Facile preparation and full-color emission in both solution and solid states. (September 2016)
- Record Type:
- Journal Article
- Title:
- Triphenylethylene-based fluorophores: Facile preparation and full-color emission in both solution and solid states. (September 2016)
- Main Title:
- Triphenylethylene-based fluorophores: Facile preparation and full-color emission in both solution and solid states
- Authors:
- Wen, Wei
Shi, Zi-Fa
Cao, Xiao-Ping
Xu, Nian-Sheng - Abstract:
- Abstract: A series of triphenylethylene-based luminophoric molecules were efficiently synthesized. The substituent effect of the fluorophores on their photophysical properties was then investigated. Consequently, it was found that longer conjugated system and larger molecular dipole of the donor–π–acceptor fluorophores could result in bathochromic shifts of UV–vis absorption and emission bands, so do the Stokes shifts. Especially, full-color fluorescent emissions in both solution and solid states could be achieved by changing conjugation length and substituents with different electron-donating or accepting abilities in the triphenylethylene skeleton. The density functional theory calculations further demonstrated that with the increase of the electron-donating or accepting abilities of the substituents, the energy gaps of the fluorophores gradually decreased, which elucidated the substituent effect of the organic fluorophores on their photophysical properties. Graphical abstract: Tunable fluorescent emission . A series of triphenylethylene-based luminophoric molecules with full-color fluorescent emissions in both solution and solid states were efficiently synthesized. Highlights: A series of triphenylethylene-based luminophoric molecules were synthesized by a Horner-Wadsworth-Emmons olefination or an Knoevenagel condensation reaction. The fluorophores exhibit fluorescent emission in both solution and solid states. The fluorescent emission wavelength could cover the entireAbstract: A series of triphenylethylene-based luminophoric molecules were efficiently synthesized. The substituent effect of the fluorophores on their photophysical properties was then investigated. Consequently, it was found that longer conjugated system and larger molecular dipole of the donor–π–acceptor fluorophores could result in bathochromic shifts of UV–vis absorption and emission bands, so do the Stokes shifts. Especially, full-color fluorescent emissions in both solution and solid states could be achieved by changing conjugation length and substituents with different electron-donating or accepting abilities in the triphenylethylene skeleton. The density functional theory calculations further demonstrated that with the increase of the electron-donating or accepting abilities of the substituents, the energy gaps of the fluorophores gradually decreased, which elucidated the substituent effect of the organic fluorophores on their photophysical properties. Graphical abstract: Tunable fluorescent emission . A series of triphenylethylene-based luminophoric molecules with full-color fluorescent emissions in both solution and solid states were efficiently synthesized. Highlights: A series of triphenylethylene-based luminophoric molecules were synthesized by a Horner-Wadsworth-Emmons olefination or an Knoevenagel condensation reaction. The fluorophores exhibit fluorescent emission in both solution and solid states. The fluorescent emission wavelength could cover the entire visible spectral region. … (more)
- Is Part Of:
- Dyes and pigments. Volume 132(2016)
- Journal:
- Dyes and pigments
- Issue:
- Volume 132(2016)
- Issue Display:
- Volume 132, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 132
- Issue:
- 2016
- Issue Sort Value:
- 2016-0132-2016-0000
- Page Start:
- 282
- Page End:
- 290
- Publication Date:
- 2016-09
- Subjects:
- Fluorescence -- Full-color emission -- Materials science -- Solid-state luminescence -- Triphenylethylene
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.2016.04.014 ↗
- 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:
- 1270.xml