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      Improving ruthenium-based ECL through nonionic surfactants and tertiary amines

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          Abstract

          The influence of surfactants and coreactants on Ru(bpy) 3 2+ electrogenerated chemiluminescence (ECL) was investigated comparatively.

          Abstract

          The influence of surfactants and coreactants on Ru(bpy) 3 2+ electrogenerated chemiluminescence (ECL) was investigated comparatively. Specifically, the influence that the two tertiary amines, N-butyldiethanolamine (NBEA) and 2-(dibutylamino)ethanol (DBAE) have on the ECL reaction, alone and in the presence of the two surfactants Triton™ X-100 and Zonyl® FSN, was investigated, in comparison with that of the well-studied and established coreactant tripropylamine (TPA). Experiments were conducted on poly(methyl methacrylate) substrates coated with plasma-evaporated gold as used in many miniaturized systems. Upon optimization and study of the various combinations, the combination of NBEA/Zonyl FSN provided superior ECL signal characteristics. A limit of detection (LOD) of 2.2 nM Ru(bpy) 3 2+ was obtained. Compared with the LOD of 0.59 μM for the commonly used TPA/Triton™ X-100 system, the resulting LOD is enhanced by a factor of 250. In addition, significantly more stable signals lead to an increase in sensitivity by a factor of 50. This makes the NBEA/Zonyl® FSN system an attractive ECL strategy, especially for miniaturized analytical systems. Furthermore, it became clear that previously postulated effects of surfactants on the enhancement of coreactant-based ECL do not translate to other surfactants and coreactants. We could demonstrate that more complicated mechanisms are at play as the ECL intensity for Ru(bpy) 3 2+/NBEA was the highest in the presence of Zonyl® FSN, whereas the ECL signal decreased significantly upon introduction of the surfactant with DBAE as coreactant.

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          Most cited references30

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          Electrochemiluminescence (ECL).

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            Electrogenerated chemiluminescence and its biorelated applications.

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              Electrogenerated chemiluminescence 69: the tris(2,2'-bipyridine)ruthenium(II), (Ru(bpy)3(2+))/tri-n-propylamine (TPrA) system revisited-a new route involving TPrA*+ cation radicals.

              The reaction occurring on electrooxidation of Ru(bpy)(3)(2+) (bpy = 2,2'-bipyridine) and tri-n-propylamine (TPrA) leads to the production of Ru(bpy)(3)(2+) and light emission. The accepted mechanism of this widely used reaction involves the reaction of Ru(bpy)(3)(3+) and a reduced species derived from the free radical of the TPrA. However, this mechanism does not account for many of the observed features of this reaction. A new route involving the intermediacy of TPrA cation radicals (TPrA(*+)) in the generation of Ru(bpy)(3)(2+) was established, based on results of scanning electrochemical microscopy (SECM)-electrogenerated chemiluminescence (ECL) experiments, as well as cyclic voltammetry simulations. A half-life of approximately 0.2 ms was estimated for TPrA(*+) in neutral aqueous solution. Direct evidence for TPrA(*+) in this medium was obtained via flow cell electron spin resonance (ESR) experiments at approximately 20 degrees C. The ESR spectra of the TPrA(*+) species consisted of a relatively intense and sharp septet with a splitting of approximately 20 G and a g value of 2.0038.
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                Author and article information

                Contributors
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                Journal
                ANALAO
                The Analyst
                Analyst
                Royal Society of Chemistry (RSC)
                0003-2654
                1364-5528
                2017
                2017
                : 142
                : 14
                : 2648-2653
                Affiliations
                [1 ]Institute of Analytical Chemistry
                [2 ]Chemo- and Biosensors
                [3 ]University of Regensburg
                [4 ]Germany
                [5 ]Department of Biological and Environmental Engineering
                Article
                10.1039/C7AN00197E
                001399d0-8601-4311-af99-acb5b66b8a2e
                © 2017
                History

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