Pyridyl‐Functionalised 3H‐1, 2, 3, 4‐Triazaphospholes: Synthesis, Coordination Chemistry and Photophysical Properties of Low‐Coordinate Phosphorus Compounds. Issue 31 (26th June 2015)
- Record Type:
- Journal Article
- Title:
- Pyridyl‐Functionalised 3H‐1, 2, 3, 4‐Triazaphospholes: Synthesis, Coordination Chemistry and Photophysical Properties of Low‐Coordinate Phosphorus Compounds. Issue 31 (26th June 2015)
- Main Title:
- Pyridyl‐Functionalised 3H‐1, 2, 3, 4‐Triazaphospholes: Synthesis, Coordination Chemistry and Photophysical Properties of Low‐Coordinate Phosphorus Compounds
- Authors:
- Sklorz, Julian A. W.
Hoof, Santina
Rades, Nadine
De Rycke, Nicolas
Könczöl, László
Szieberth, Dénes
Weber, Manuela
Wiecko, Jelena
Nyulászi, László
Hissler, Muriel
Müller, Christian - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Novel conjugated, pyridyl‐functionalised triazaphospholes with either <italic>t</italic>Bu or SiMe<sub>3</sub> substituents at the 5‐position of the N<sub>3</sub>PC heterocycle have been prepared by a [3+2] cycloaddition reaction and compared with structurally related, triazole‐based systems. Photoexcitation of the 2‐pyridyl‐substituted triazaphosphole gives rise to a significant fluorescence emission with a quantum yield of up to 12 %. In contrast, the all‐nitrogen triazole analogue shows no emission at all. DFT calculations indicate that the 2‐pyridyl substituted systems have a more rigid and planar structure than their 3‐ and 4‐pyridyl isomers. Time‐dependent (TD) DFT calculations show that only the 2‐pyridyl‐substituted triazaphosphole exhibits similar planar geometry, with matching conformational arrangements in the lowest energy excited state and the ground state; this helps to explain the enhanced emission intensity. The chelating P, N‐hybrid ligand forms a Re<sup>I</sup> complex of the type [(N^N)Re(CO)<sub>3</sub>Br] through the coordination of nitrogen atom N<sup>2</sup> to the metal centre rather than through the phosphorus donor. Both structural and spectroscopic data indicate substantial π‐accepting character of the triazaphosphole, which is again in contrast to that of the all‐nitrogen‐containing triazoles. The synthesis and photophysical properties of a new class of phosphorus‐containing<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Novel conjugated, pyridyl‐functionalised triazaphospholes with either <italic>t</italic>Bu or SiMe<sub>3</sub> substituents at the 5‐position of the N<sub>3</sub>PC heterocycle have been prepared by a [3+2] cycloaddition reaction and compared with structurally related, triazole‐based systems. Photoexcitation of the 2‐pyridyl‐substituted triazaphosphole gives rise to a significant fluorescence emission with a quantum yield of up to 12 %. In contrast, the all‐nitrogen triazole analogue shows no emission at all. DFT calculations indicate that the 2‐pyridyl substituted systems have a more rigid and planar structure than their 3‐ and 4‐pyridyl isomers. Time‐dependent (TD) DFT calculations show that only the 2‐pyridyl‐substituted triazaphosphole exhibits similar planar geometry, with matching conformational arrangements in the lowest energy excited state and the ground state; this helps to explain the enhanced emission intensity. The chelating P, N‐hybrid ligand forms a Re<sup>I</sup> complex of the type [(N^N)Re(CO)<sub>3</sub>Br] through the coordination of nitrogen atom N<sup>2</sup> to the metal centre rather than through the phosphorus donor. Both structural and spectroscopic data indicate substantial π‐accepting character of the triazaphosphole, which is again in contrast to that of the all‐nitrogen‐containing triazoles. The synthesis and photophysical properties of a new class of phosphorus‐containing extended π systems are described.</p> </abstract> … (more)
- Is Part Of:
- Chemistry. Volume 21:Issue 31(2015)
- Journal:
- Chemistry
- Issue:
- Volume 21:Issue 31(2015)
- Issue Display:
- Volume 21, Issue 31 (2015)
- Year:
- 2015
- Volume:
- 21
- Issue:
- 31
- Issue Sort Value:
- 2015-0021-0031-0000
- Page Start:
- 11096
- Page End:
- 11109
- Publication Date:
- 2015-06-26
- Subjects:
- Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201500988 ↗
- 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:
- 4149.xml