Alkyl length dependent mechanofluorochromism of AIE-based phenothiazinyl fluorophenyl acrylonitrile derivatives. (January 2017)
- Record Type:
- Journal Article
- Title:
- Alkyl length dependent mechanofluorochromism of AIE-based phenothiazinyl fluorophenyl acrylonitrile derivatives. (January 2017)
- Main Title:
- Alkyl length dependent mechanofluorochromism of AIE-based phenothiazinyl fluorophenyl acrylonitrile derivatives
- Authors:
- Ma, Chunping
Zhang, Xiqi
Yang, Liutao
Li, Yang
Liu, Hongliang
Yang, Yang
Xie, Gaoyi
Ou, Yong-Cong
Wei, Yen - Abstract:
- Abstract: Four alkyl phenothiazinyl fluorophenyl acrylonitrile derivatives (PhC3F, PhC6F, PhC10F, andPhC12F ) with different length of alkyl chains were synthesized in high yield. The compounds showed obvious aggregation-induced emission (AIE) and alkyl length dependent mechanofluorochromic (MFC) properties.PhC3F with propyl chain andPhC12F with dodecyl chain showed obvious and reversible MFC behaviours, whilePhC6F with hexyl chain andPhC10F with decyl chain exhibited little MFC property. Small and wide-angle X-ray scattering indicated the MFC behaviour ofPhC3F andPhC12F were attributed to the phase transformation from crystalline to amorphous state, whilePhC6F maintained excellent crystalline performance before and after grinding, which was also evidenced by differential scanning calorimetry result. Quantum mechanical computations further revealedPhC6F had high molecular polarity, which greatly improved its crystalline performance, and made its original aggregated morphology hard to damage, then brought about little MFC diversification.PhC10F showed the highest molecular polarity and least MFC behaviour. We concluded that obvious MFC feature derived from appropriate crystalline performance, favourable molecular polarity and energy gap. Highlights: Four acrylonitrile derivatives with different length of alkyl chains were synthesized. The derivatives exhibited aggregation-induced emission feature. The derivatives showed alkyl length dependent mechanofluorochromism. TheAbstract: Four alkyl phenothiazinyl fluorophenyl acrylonitrile derivatives (PhC3F, PhC6F, PhC10F, andPhC12F ) with different length of alkyl chains were synthesized in high yield. The compounds showed obvious aggregation-induced emission (AIE) and alkyl length dependent mechanofluorochromic (MFC) properties.PhC3F with propyl chain andPhC12F with dodecyl chain showed obvious and reversible MFC behaviours, whilePhC6F with hexyl chain andPhC10F with decyl chain exhibited little MFC property. Small and wide-angle X-ray scattering indicated the MFC behaviour ofPhC3F andPhC12F were attributed to the phase transformation from crystalline to amorphous state, whilePhC6F maintained excellent crystalline performance before and after grinding, which was also evidenced by differential scanning calorimetry result. Quantum mechanical computations further revealedPhC6F had high molecular polarity, which greatly improved its crystalline performance, and made its original aggregated morphology hard to damage, then brought about little MFC diversification.PhC10F showed the highest molecular polarity and least MFC behaviour. We concluded that obvious MFC feature derived from appropriate crystalline performance, favourable molecular polarity and energy gap. Highlights: Four acrylonitrile derivatives with different length of alkyl chains were synthesized. The derivatives exhibited aggregation-induced emission feature. The derivatives showed alkyl length dependent mechanofluorochromism. The mechanofluorochromism was affected by molecular polarity and crystalline performance. … (more)
- Is Part Of:
- Dyes and pigments. Volume 136(2017)
- Journal:
- Dyes and pigments
- Issue:
- Volume 136(2017)
- Issue Display:
- Volume 136, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 136
- Issue:
- 2017
- Issue Sort Value:
- 2017-0136-2017-0000
- Page Start:
- 85
- Page End:
- 91
- Publication Date:
- 2017-01
- Subjects:
- Alkyl length dependent -- Mechanofluorochromism -- Aggregation-induced emission -- Acrylonitrile derivatives -- Molecular polarity -- Phase transformation
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.2016.08.031 ↗
- 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:
- 226.xml