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Catecholamines, hydrogen peroxide determination

The most commonplace substrates in energy-transfer analytical CL methods are aryl oxalates such as to(2,4,6-trichlorophenyl) oxalate (TCPO) and z s(2,4-dinitrophenyl) oxalate (DNPO), which are oxidized with hydrogen peroxide [7, 8], In this process, which is known as the peroxyoxalate-CL (PO-CL) reaction, the fluorophore analyte is a native or derivatized fluorescent organic substance such as a polynuclear aromatic hydrocarbon, dansylamino acid, carboxylic acid, phenothiazine, or catecholamines, for example. The mechanism of the reaction between aryl oxalates and hydrogen peroxide is believed to generate dioxetane-l,2-dione, which may itself decompose to yield an excited-state species. Its interaction with a suitable fluorophore results in energy transfer to the fluorophore, and the subsequent emission can be exploited to develop analytical CL-based determinations. [Pg.179]


See other pages where Catecholamines, hydrogen peroxide determination is mentioned: [Pg.1448]    [Pg.1448]    [Pg.587]    [Pg.30]    [Pg.30]    [Pg.113]    [Pg.564]    [Pg.564]    [Pg.339]    [Pg.537]   
See also in sourсe #XX -- [ Pg.625 , Pg.626 , Pg.647 ]




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Catecholamines, hydrogen peroxide

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