A Luminescent Nitrogen‐Containing Polycyclic Aromatic Hydrocarbon Synthesized by Photocyclodehydrogenation with Unprecedented Regioselectivity. Issue 49 (22nd October 2015)
- Record Type:
- Journal Article
- Title:
- A Luminescent Nitrogen‐Containing Polycyclic Aromatic Hydrocarbon Synthesized by Photocyclodehydrogenation with Unprecedented Regioselectivity. Issue 49 (22nd October 2015)
- Main Title:
- A Luminescent Nitrogen‐Containing Polycyclic Aromatic Hydrocarbon Synthesized by Photocyclodehydrogenation with Unprecedented Regioselectivity
- Authors:
- Gu, Xinggui
Wang, Hong
Roose, Jesse
He, Zikai
Zhou, Yue
Yan, Yongli
Cai, Yuanjing
Shi, Heping
Zhang, Yilin
Sung, Herman H. Y.
Lam, Jacky W. Y.
Miao, Qian
Zhao, Yongsheng
Wong, Kam Sing
Williams, Ian D.
Tang, Ben Zhong - Abstract:
- Abstract: We present a nitrogen‐containing polycyclic aromatic hydrocarbon (N‐PAH), namely 12‐methoxy‐9‐(4‐methoxyphenyl)‐5, 8‐diphenyl‐4‐(pyridin‐4‐yl)pyreno[1, 10, 9‐ h, i, j ]isoquinoline ( c ‐TPE‐ON), which exhibits high quantum‐yield emission both in solution (blue) and in the solid state (yellow). This molecule was unexpectedly obtained by a three‐fold, highly regioselective photocyclodehydrogenation of a tetraphenylethylene‐derived AIEgen. Based on manifold approaches involving UV/Vis, photoluminescence, and NMR spectroscopy as well as HRMS, we propose a reasonable mechanism for the formation of the disk‐like N‐PAH that is supported by density functional theory calculations. In contrast to most PAHs that are commonly used, our system does not suffer from entire fluorescence quenching in the solid state due to the peripheral aromatic rings preventing π–π stacking interactions, as evidenced by single‐crystal X‐ray analysis. Moreover, its rod‐like microcrystals exhibit excellent optical waveguide properties. Hence, c ‐TPE‐ON comprises a N‐PAH with unprecedented luminescent properties and as such is a promising candidate for fabricating organic optoelectronic devices. Our design and synthetic strategy might lead to a more general approach to the preparation of solution‐ and solid‐state luminescent PAHs. Abstract : Unprecedented luminescence : A luminescent nitrogen‐containing polycyclic aromatic hydrocarbon (N‐PAH) has been synthesized from a vinylene‐based AIEgen by aAbstract: We present a nitrogen‐containing polycyclic aromatic hydrocarbon (N‐PAH), namely 12‐methoxy‐9‐(4‐methoxyphenyl)‐5, 8‐diphenyl‐4‐(pyridin‐4‐yl)pyreno[1, 10, 9‐ h, i, j ]isoquinoline ( c ‐TPE‐ON), which exhibits high quantum‐yield emission both in solution (blue) and in the solid state (yellow). This molecule was unexpectedly obtained by a three‐fold, highly regioselective photocyclodehydrogenation of a tetraphenylethylene‐derived AIEgen. Based on manifold approaches involving UV/Vis, photoluminescence, and NMR spectroscopy as well as HRMS, we propose a reasonable mechanism for the formation of the disk‐like N‐PAH that is supported by density functional theory calculations. In contrast to most PAHs that are commonly used, our system does not suffer from entire fluorescence quenching in the solid state due to the peripheral aromatic rings preventing π–π stacking interactions, as evidenced by single‐crystal X‐ray analysis. Moreover, its rod‐like microcrystals exhibit excellent optical waveguide properties. Hence, c ‐TPE‐ON comprises a N‐PAH with unprecedented luminescent properties and as such is a promising candidate for fabricating organic optoelectronic devices. Our design and synthetic strategy might lead to a more general approach to the preparation of solution‐ and solid‐state luminescent PAHs. Abstract : Unprecedented luminescence : A luminescent nitrogen‐containing polycyclic aromatic hydrocarbon (N‐PAH) has been synthesized from a vinylene‐based AIEgen by a photocyclodehydrogenation reaction with unexpected regioselectivity. The N‐PAH exhibits excellent optical properties both in solution and in the solid state (see figure). … (more)
- Is Part Of:
- Chemistry. Volume 21:Issue 49(2015)
- Journal:
- Chemistry
- Issue:
- Volume 21:Issue 49(2015)
- Issue Display:
- Volume 21, Issue 49 (2015)
- Year:
- 2015
- Volume:
- 21
- Issue:
- 49
- Issue Sort Value:
- 2015-0021-0049-0000
- Page Start:
- 17973
- Page End:
- 17980
- Publication Date:
- 2015-10-22
- Subjects:
- aggregation -- luminescence -- optical waveguides -- polycycles -- regioselectivity
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201503147 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1496.xml