Premium
Pyridyl‐Functionalised 3 H ‐1,2,3,4‐Triazaphospholes: Synthesis, Coordination Chemistry and Photophysical Properties of Low‐Coordinate Phosphorus Compounds
Author(s) -
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
Publication year - 2015
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201500988
Subject(s) - chemistry , quantum yield , photoexcitation , ligand (biochemistry) , excited state , coordination complex , conjugated system , cycloaddition , photochemistry , fluorescence , crystallography , metal , organic chemistry , polymer , biochemistry , physics , receptor , quantum mechanics , nuclear physics , catalysis
Novel conjugated, pyridyl‐functionalised triazaphospholes with either t Bu or SiMe 3 substituents at the 5‐position of the N 3 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 I complex of the type [(N^N)Re(CO) 3 Br] through the coordination of nitrogen atom N 2 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.