Remarkable pressure-induced emission enhancement based on intermolecular charge transfer in halogen bond-driven dual-component co-crystals. Issue 48 (28th November 2018)
- Record Type:
- Journal Article
- Title:
- Remarkable pressure-induced emission enhancement based on intermolecular charge transfer in halogen bond-driven dual-component co-crystals. Issue 48 (28th November 2018)
- Main Title:
- Remarkable pressure-induced emission enhancement based on intermolecular charge transfer in halogen bond-driven dual-component co-crystals
- Authors:
- Li, Aisen
Wang, Jing
Liu, Yingjie
Xu, Shuping
Chu, Ning
Geng, Yijia
Li, Bao
Xu, Bin
Cui, Haining
Xu, Weiqing - Abstract:
- Abstract : Remarkable pressure-induced emission enhancement from dark to bright based on intermolecular charge transfer (CT) is presented in this study. Abstract : A series of two-component co-crystals driven by I⋯N interactions based on the bipyridine (BIPY) chromophore with one among three different co-former building blocks, iodopentafluorobenzene (IPFB), 1, 4-diiodotetrafluorobenzene (DITFB) and 1, 3, 5-trifluoro-2, 4, 6-triiodobenzene (IFB), were prepared and analysed via infared spectroscopy and single-crystal X-ray diffraction. By comparing the I⋯N distances in the co-crystal structures, we found that the higher the –F ratio in the building blocks the closer the contact of the I⋯N bond, enhancing the intermolecular interactions in these co-crystals as well. That is, the positive electrostatic potential on the iodine atom(s) in the co-formers was enhanced by the presence of strong electron-withdrawing groups. The distinct spectroscopic behaviours (fluorescence and Raman spectra) among the two-component BIPY co-crystal systems in response to hydrostatic pressure were also investigated. Interestingly, the fluorescence of BIPY–DITFB presented intriguing abnormal evolution from dark to bright, suggesting a new charge transfer state due to the decreased intermolecular distance and the enhanced I⋯N interactions. Theoretical simulations by Materials Studio also showed the shortened I⋯N distance and the increased angle of C–I⋯N, evidencing the enhanced I⋯N interactions. InAbstract : Remarkable pressure-induced emission enhancement from dark to bright based on intermolecular charge transfer (CT) is presented in this study. Abstract : A series of two-component co-crystals driven by I⋯N interactions based on the bipyridine (BIPY) chromophore with one among three different co-former building blocks, iodopentafluorobenzene (IPFB), 1, 4-diiodotetrafluorobenzene (DITFB) and 1, 3, 5-trifluoro-2, 4, 6-triiodobenzene (IFB), were prepared and analysed via infared spectroscopy and single-crystal X-ray diffraction. By comparing the I⋯N distances in the co-crystal structures, we found that the higher the –F ratio in the building blocks the closer the contact of the I⋯N bond, enhancing the intermolecular interactions in these co-crystals as well. That is, the positive electrostatic potential on the iodine atom(s) in the co-formers was enhanced by the presence of strong electron-withdrawing groups. The distinct spectroscopic behaviours (fluorescence and Raman spectra) among the two-component BIPY co-crystal systems in response to hydrostatic pressure were also investigated. Interestingly, the fluorescence of BIPY–DITFB presented intriguing abnormal evolution from dark to bright, suggesting a new charge transfer state due to the decreased intermolecular distance and the enhanced I⋯N interactions. Theoretical simulations by Materials Studio also showed the shortened I⋯N distance and the increased angle of C–I⋯N, evidencing the enhanced I⋯N interactions. In contrast, BIPY–IFB showed only slightly enhanced fluorescence intensity at 550 nm consistent with BIPY–DITFB. Once the pressure was relieved, both the Raman and fluorescence spectra for BIPY co-crystal systems entirely self-recovered. Remarkable emission enhancement in a solid-state co-crystal has been rarely reported in previous publications and in fact, this study paves a unique way for designing and developing novel stimuli-responsive photo-functional materials. … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 20:Issue 48(2018)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 20:Issue 48(2018)
- Issue Display:
- Volume 20, Issue 48 (2018)
- Year:
- 2018
- Volume:
- 20
- Issue:
- 48
- Issue Sort Value:
- 2018-0020-0048-0000
- Page Start:
- 30297
- Page End:
- 30303
- Publication Date:
- 2018-11-28
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c8cp06363j ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9148.xml