Near-Infrared Electrochemiluminescence from Bistridentate Ruthenium(II) Di(quinoline-8-yl)pyridine Complexes in Aqueous Media

Chempluschem. 2020 Feb;85(2):346-352. doi: 10.1002/cplu.201900637. Epub 2020 Feb 6.

Abstract

We report the synthesis, photophysics, electrochemistry and electrochemiluminescence (ECL) of two dqp (dqp=2,6-di(quinoline-8-yl)pyridine) based ruthenium(II) complexes, bearing either a n-butyl ester (1) or the corresponding carboxylic acid functionality (2). The complexes were prepared from [Ru(dqp)(MeCN)3 ][PF6 ]2 by reaction with the dqp precursor using microwave irradiation. In both cases, photoluminescence spectra present strong 3 MLCT-based red/near-infrared (NIR) emissions centred at about 710 nm. The photoluminescence quantum yields were 6.1 % and 1.8 % for 1 and 2 respectively while the excited state lifetimes were 3.60 μs and 2.37 μs. Both complexes are ECL active, although ECL efficiency (ΦECL ) of 1 was substantially higher than 2, due to its more favourable electrochemical properties. Importantly, 1 also gave strong ECL in aqueous media, which is rare for near-infrared emitters. The results suggest the possibility of very interesting ECL sensing applications for this class of emitter in biological media.

Keywords: bistridendate ligands; electrochemiluminescence; near-infrared emission; photoluminescence; ruthenium(II).

Publication types

  • Research Support, Non-U.S. Gov't