A New Platform of B/N‐Doped Cyclophanes: Access to a π‐Conjugated Block‐Type B3N3 Macrocycle with Strong Dipole Moment and Unique Optoelectronic Properties. (19th March 2022)
- Record Type:
- Journal Article
- Title:
- A New Platform of B/N‐Doped Cyclophanes: Access to a π‐Conjugated Block‐Type B3N3 Macrocycle with Strong Dipole Moment and Unique Optoelectronic Properties. (19th March 2022)
- Main Title:
- A New Platform of B/N‐Doped Cyclophanes: Access to a π‐Conjugated Block‐Type B3N3 Macrocycle with Strong Dipole Moment and Unique Optoelectronic Properties
- Authors:
- Li, Pengfei
Shimoyama, Daisuke
Zhang, Niu
Jia, Yawei
Hu, Guofei
Li, Chenglong
Yin, Xiaodong
Wang, Nan
Jäkle, Frieder
Chen, Pangkuan - Abstract:
- Abstract: We herein describe a new design principle to achieve B/N‐doped cyclophane where an electron‐donor block of three triarylamines (Ar3 N) and an acceptor block of three triarylboranes (Ar3 B) are spatially separated on opposite sides of the π‐extended ring system. DFT computations revealed the distinct electronic structure of the block ‐type macrocycle MC‐ b ‐B3N3 with a greatly enhanced dipole moment and reduced HOMO–LUMO energy gap in comparison to its analogue with alternating B and N sites, MC‐ alt ‐B3N3 . The unique arrangement of borane acceptor Ar3 B and amine donor Ar3 N components in MC‐ b ‐B3N3 induces exceptionally strong intramolecular charge transfer in the excited state, which is reflected in a largely red‐shifted luminescence at 612 nm in solution. The respective linear open‐chain oligomer L‐ b ‐B3N3 was also synthesized for comparison. Our new approach to donor–acceptor macrocycles offers important fundamental insights and opens up a new avenue to unique optoelectronic materials. Abstract : An unusual block ‐type π‐conjugated macrocycle MC ‐ b ‐B3N3 that shows a strong dipole moment and a narrow HOMO–LUMO gap is introduced. Compared with other cyclic hexamers, its unique orientation of electron‐donor block and acceptor block resulted in largely red‐shifted orange emission both in solution and in the solid state.
- Is Part Of:
- Angewandte Chemie. Volume 134:Number 20(2022)
- Journal:
- Angewandte Chemie
- Issue:
- Volume 134:Number 20(2022)
- Issue Display:
- Volume 134, Issue 20 (2022)
- Year:
- 2022
- Volume:
- 134
- Issue:
- 20
- Issue Sort Value:
- 2022-0134-0020-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-03-19
- Subjects:
- Boron -- Conjugated Macrocycles -- Donor–Acceptor Blocks -- Luminescence -- Optoelectronic Materials
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ange.202200612 ↗
- Languages:
- English
- ISSNs:
- 0044-8249
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0902.000000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23319.xml