A π‐Conjugated, Covalent Phosphinine Framework. Issue 53 (13th August 2019)
- Record Type:
- Journal Article
- Title:
- A π‐Conjugated, Covalent Phosphinine Framework. Issue 53 (13th August 2019)
- Main Title:
- A π‐Conjugated, Covalent Phosphinine Framework
- Authors:
- Huang, Jieyang
Tarábek, Ján
Kulkarni, Ranjit
Wang, Cui
Dračínský, Martin
Smales, Glen J.
Tian, Yu
Ren, Shijie
Pauw, Brian R.
Resch‐Genger, Ute
Bojdys, Michael J. - Abstract:
- Abstract: Structural modularity of polymer frameworks is a key advantage of covalent organic polymers, however, only C, N, O, Si, and S have found their way into their building blocks so far. Here, the toolbox available to polymer and materials chemists is expanded by one additional nonmetal, phosphorus. Starting with a building block that contains a λ 5 ‐phosphinine (C5 P) moiety, a number of polymerization protocols are evaluated, finally obtaining a π‐conjugated, covalent phosphinine‐based framework (CPF‐1) through Suzuki–Miyaura coupling. CPF‐1 is a weakly porous polymer glass (72.4 m 2 g −1 BET at 77 K) with green fluorescence ( λ max =546 nm) and extremely high thermal stability. The polymer catalyzes hydrogen evolution from water under UV and visible light irradiation without the need for additional co‐catalyst at a rate of 33.3 μmol h −1 g −1 . These results demonstrate for the first time the incorporation of the phosphinine motif into a complex polymer framework. Phosphinine‐based frameworks show promising electronic and optical properties, which might spark future interest in their applications in light‐emitting devices and heterogeneous catalysis. Abstract : Phosphinine in π : For the first time since its synthesis in 1966, the six‐membered phosphinine ring is incorporated into a π‐conjugated polymer. The phosphinine‐based framework (CPF‐1) has a high concentration of paramagnetic species, high thermal stability, green fluorescence, and shows activity inAbstract: Structural modularity of polymer frameworks is a key advantage of covalent organic polymers, however, only C, N, O, Si, and S have found their way into their building blocks so far. Here, the toolbox available to polymer and materials chemists is expanded by one additional nonmetal, phosphorus. Starting with a building block that contains a λ 5 ‐phosphinine (C5 P) moiety, a number of polymerization protocols are evaluated, finally obtaining a π‐conjugated, covalent phosphinine‐based framework (CPF‐1) through Suzuki–Miyaura coupling. CPF‐1 is a weakly porous polymer glass (72.4 m 2 g −1 BET at 77 K) with green fluorescence ( λ max =546 nm) and extremely high thermal stability. The polymer catalyzes hydrogen evolution from water under UV and visible light irradiation without the need for additional co‐catalyst at a rate of 33.3 μmol h −1 g −1 . These results demonstrate for the first time the incorporation of the phosphinine motif into a complex polymer framework. Phosphinine‐based frameworks show promising electronic and optical properties, which might spark future interest in their applications in light‐emitting devices and heterogeneous catalysis. Abstract : Phosphinine in π : For the first time since its synthesis in 1966, the six‐membered phosphinine ring is incorporated into a π‐conjugated polymer. The phosphinine‐based framework (CPF‐1) has a high concentration of paramagnetic species, high thermal stability, green fluorescence, and shows activity in photocatalytic water splitting. … (more)
- Is Part Of:
- Chemistry. Volume 25:Issue 53(2019)
- Journal:
- Chemistry
- Issue:
- Volume 25:Issue 53(2019)
- Issue Display:
- Volume 25, Issue 53 (2019)
- Year:
- 2019
- Volume:
- 25
- Issue:
- 53
- Issue Sort Value:
- 2019-0025-0053-0000
- Page Start:
- 12342
- Page End:
- 12348
- Publication Date:
- 2019-08-13
- Subjects:
- fluorescence -- phosphinine -- polymers -- Suzuki–Miyaura coupling -- π-conjugated frameworks
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201900281 ↗
- 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:
- 26703.xml