Mechanofluorochromism, polymorphism and thermochromism of novel D–π–A piperidin-1-yl-substitued isoquinoline derivatives. Issue 40 (2nd October 2019)
- Record Type:
- Journal Article
- Title:
- Mechanofluorochromism, polymorphism and thermochromism of novel D–π–A piperidin-1-yl-substitued isoquinoline derivatives. Issue 40 (2nd October 2019)
- Main Title:
- Mechanofluorochromism, polymorphism and thermochromism of novel D–π–A piperidin-1-yl-substitued isoquinoline derivatives
- Authors:
- Chen, Yating
Zhang, Xinyu
Wang, Mengzhu
Peng, Jingqing
Zhou, Yunbing
Huang, Xiaobo
Gao, Wenxia
Liu, Miaochang
Wu, Huayue - Abstract:
- Abstract : Two novel D–π–A isoquinoline derivatives using triphenylamine/9-phenyl-9 H -carbazole as an electron donor were found to exhibit polymorphic, thermochromic, and/or mechanofluorochromic activities. Abstract : Two novel D–π–A isoquinoline derivatives IQ-TPA and IQ-PC using triphenylamine and 9-phenyl-9 H -carbazole as an electron donor, respectively, were synthesized to investigate their applications in mechanofluorochromic (MFC) materials. The design was inspired by an accidentally obtained piperidine-1-substituted isoquinoline intermediate emitting strong blue solid-state fluorescence, which was obtained from the reaction of a 4 H -pyran derivative with piperidine by a complex ring-opening/closing mechanism. These two compounds with highly twisted conformations both had two crystalline polymorphs in which the piperidin-1-yl group was located on different sides of the isoquinoline core. The different emissions of the polymorphs were confirmed to originate from their different molecular conformations. For IQ-TPA, yellow-emitting IQ-TPA-y could be converted into green-emitting IQ-TPA-g and exhibited hypsochromic MFC and thermochromic properties by the transformation between different crystalline states, respectively. Regarding IQ-PC, the two polymorphs did not exhibit MFC activities owing to the strong intermolecular interactions in the crystalline state, while the transition from green-emitting IQ-PC-g to yellow-emitting IQ-PC-y could be achieved by an annealingAbstract : Two novel D–π–A isoquinoline derivatives using triphenylamine/9-phenyl-9 H -carbazole as an electron donor were found to exhibit polymorphic, thermochromic, and/or mechanofluorochromic activities. Abstract : Two novel D–π–A isoquinoline derivatives IQ-TPA and IQ-PC using triphenylamine and 9-phenyl-9 H -carbazole as an electron donor, respectively, were synthesized to investigate their applications in mechanofluorochromic (MFC) materials. The design was inspired by an accidentally obtained piperidine-1-substituted isoquinoline intermediate emitting strong blue solid-state fluorescence, which was obtained from the reaction of a 4 H -pyran derivative with piperidine by a complex ring-opening/closing mechanism. These two compounds with highly twisted conformations both had two crystalline polymorphs in which the piperidin-1-yl group was located on different sides of the isoquinoline core. The different emissions of the polymorphs were confirmed to originate from their different molecular conformations. For IQ-TPA, yellow-emitting IQ-TPA-y could be converted into green-emitting IQ-TPA-g and exhibited hypsochromic MFC and thermochromic properties by the transformation between different crystalline states, respectively. Regarding IQ-PC, the two polymorphs did not exhibit MFC activities owing to the strong intermolecular interactions in the crystalline state, while the transition from green-emitting IQ-PC-g to yellow-emitting IQ-PC-y could be achieved by an annealing treatment. This indicated that different electron-donating groups led to different solid-state fluorescence stimulus-responsive properties. This work provides some useful information for the development of traditional fluorescent molecules with MFC, polymorphic, and thermochromic properties. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 7:Issue 40(2019)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 7:Issue 40(2019)
- Issue Display:
- Volume 7, Issue 40 (2019)
- Year:
- 2019
- Volume:
- 7
- Issue:
- 40
- Issue Sort Value:
- 2019-0007-0040-0000
- Page Start:
- 12580
- Page End:
- 12587
- Publication Date:
- 2019-10-02
- 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/c9tc03942b ↗
- 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
British Library STI - ELD Digital store - Ingest File:
- 12018.xml