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Quantification of Cu2+ using 1,1′-oxalyldiimidazole chemiluminescence

Paper ID Volume ID Publish Year Pages File Format Full-Text
29054 44117 2006 5 PDF Available
Title
Quantification of Cu2+ using 1,1′-oxalyldiimidazole chemiluminescence
Abstract

Emission from two different peroxyoxalate chemiluminescence (PO-CL) reaction pathways (i.e., 1,1′-oxalyldiimidazole (ODI) and bis(2,4,6-trichlorophenyl)oxalate (TCPO) CL reactions) is significantly reduced in the presence of increasing Cu2+ concentrations. The CL intensity decrease in the ODI-CL reaction results from deactivation of the high-energy intermediate(s) by Cu2+, whereas the apparent quenching in the TCPO-CL reaction results from both this effect and formation of Cu2+–imidazole (ImH) complexes [Cu(ImH)n=1–4]2+. Because the reaction between Cu2+ and ImH occurs competitively with the formation of a high-energy intermediate (X) in TCPO-CL reactions, accurately determining Cu2+ concentrations with a TCPO-CL-based system is more difficult versus an ODI-CL-based system. Using ODI-CL, the detection limit of Cu2+ dissolved in water was determined to be 5.0 × 10−8 M (signal:noise = 3) in a 1 cm fluorescence flow micro-cell. ODI-CL-based systems are expected to be useful for the rapid quantification of many quenchers in environmental and biological samples because the interactions between the high-energy intermediate(s) and quencher are very rapid relative to other competitive reactions.

Keywords
Chemiluminescence; Copper; 1,1′-Oxalyldiimidazole (ODI); Peroxyoxalate; Quenching
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Quantification of Cu2+ using 1,1′-oxalyldiimidazole chemiluminescence
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Publisher
Database: Elsevier - ScienceDirect
Journal: Journal of Photochemistry and Photobiology A: Chemistry - Volume 182, Issue 1, 20 August 2006, Pages 28–32
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Bioengineering
Get Full-Text Now
Don't Miss Today's Special Offer
Price was $35.95
You save - $31
Price after discount Only $4.95
100% Money Back Guarantee
Full-text PDF Download
Online Support
Any Questions? feel free to contact us