Mechanofluorochromic properties of aggregation-induced emission-active tetraphenylethene-containing cruciform luminophores. (September 2018)
- Record Type:
- Journal Article
- Title:
- Mechanofluorochromic properties of aggregation-induced emission-active tetraphenylethene-containing cruciform luminophores. (September 2018)
- Main Title:
- Mechanofluorochromic properties of aggregation-induced emission-active tetraphenylethene-containing cruciform luminophores
- Authors:
- Wang, Yonghui
Xu, Defang
Gao, Huaizhi
Wang, Ying
Liu, Xingliang
Han, Aixia
Zhang, Chao
Zang, Ling - Abstract:
- Abstract: Two twisted donor–acceptor cruciform luminophores (DHCS-TPE andDMCS-TPE ) that were composed of two π-conjugated segments connected via a central benzene core have been prepared. Such cruciforms showed unique intramolecular charge transfer (ICT) emission, obvious aggregation-induced emission (AIE) properties (αAIE = 19 and 20, respectively) and high solid state efficiency (0.913 and 0.424, respectively). Especially, the two compounds exhibited substituent-dependent mechanofluorochromic (MFC) behavior. The as-prepared powders of the more twistedDMCS-TPE could emit strong blue-green light centered at 474 nm, and the fluorescence color changed into yellowish green (531 nm) after grinding, a red shift of 57 nm was observed. Such mechanochromism was reversible upon the treatment of grinding and fuming with DCM. The high contrast MFC behavior ofDMCS-TPE originated from the planarization of the molecular conformation and subsequent planar intramolecular charge transfer (PICT) under external force. By sharp contrast, the less twistedDHCS-TPE exhibited no MFC behavior. The reason is that the less twisted molecular conformation ofDHCS-TPE generates strong intermolecular forces and close packing. Thus compared toDMCS-TPE, the crystalline solid powders ofDHCS-TPE possess higher lattice energy and better structural stability. The grinding of the crystalline solid powders ofDHCS-TPE cannot lead to amorphization and mechanochromic luminescence. Graphical abstract: Highlights:Abstract: Two twisted donor–acceptor cruciform luminophores (DHCS-TPE andDMCS-TPE ) that were composed of two π-conjugated segments connected via a central benzene core have been prepared. Such cruciforms showed unique intramolecular charge transfer (ICT) emission, obvious aggregation-induced emission (AIE) properties (αAIE = 19 and 20, respectively) and high solid state efficiency (0.913 and 0.424, respectively). Especially, the two compounds exhibited substituent-dependent mechanofluorochromic (MFC) behavior. The as-prepared powders of the more twistedDMCS-TPE could emit strong blue-green light centered at 474 nm, and the fluorescence color changed into yellowish green (531 nm) after grinding, a red shift of 57 nm was observed. Such mechanochromism was reversible upon the treatment of grinding and fuming with DCM. The high contrast MFC behavior ofDMCS-TPE originated from the planarization of the molecular conformation and subsequent planar intramolecular charge transfer (PICT) under external force. By sharp contrast, the less twistedDHCS-TPE exhibited no MFC behavior. The reason is that the less twisted molecular conformation ofDHCS-TPE generates strong intermolecular forces and close packing. Thus compared toDMCS-TPE, the crystalline solid powders ofDHCS-TPE possess higher lattice energy and better structural stability. The grinding of the crystalline solid powders ofDHCS-TPE cannot lead to amorphization and mechanochromic luminescence. Graphical abstract: Highlights: Two twisted donor–acceptor π-conjugated cruciform luminophores showed unique ICT properties. They exhibited evident aggregation-induced emission characteristics and high solid state efficiency. Their different mechanofluorochromic behavior was controlled by the molecular conformation induced by substituents. … (more)
- Is Part Of:
- Dyes and pigments. Volume 156(2018)
- Journal:
- Dyes and pigments
- Issue:
- Volume 156(2018)
- Issue Display:
- Volume 156, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 156
- Issue:
- 2018
- Issue Sort Value:
- 2018-0156-2018-0000
- Page Start:
- 291
- Page End:
- 298
- Publication Date:
- 2018-09
- Subjects:
- Cruciform -- Tetraphenylethene -- Intramolecular -- Charge-transfer -- Aggregation-induced -- Emission -- Mechanofluorochromism
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.2018.04.021 ↗
- 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:
- 10898.xml