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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
19
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pubmed:dateCreated |
1998-1-14
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pubmed:abstractText |
The perfluorosulfonated ionomer Nafion shows potential utility as a polymer film to enhance the electrochemical detection of [ReI(DMPE)3]+, where DMPE = 1,2-bis-(dimethylphosphino)ethane. [ReI(DMPE)3]+, a nonradioactive radiopharmaceutical analog for heart imaging, partitions strongly into Nafion films on glassy carbon. Well-defined, chemically reversible cyclic voltammograms are obtained for the [ReI(DMPE)3]+/[ReII(DMPE)3]2+ couple with Eo' shifted positively by 60 mV relative to its value on bare glassy carbon. [ReI(DMPE)3]+ partitions into Nafion more strongly than the oxidized form, [ReII-(DMPE)3]2+. The detection limit for [ReI(DMPE)3]+ by cyclic voltammetry was improved by 2-3 orders of magnitude by the Nafion film. Differential pulse voltammetry for oxidation of [ReI(DMPE)3]+ at the Nafion-modified electrode has a detection limit of 2.5 x 10(-9) M compared to 1.0 x 10(-7) M at the bare electrode. A preconcentration factor of 1 x 10(6) for partitioning of [ReI(DMPE)3]+ from 0.05 M NaCl into Nafion on a glassy carbon electrode was measured.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Fluorocarbon Polymers,
http://linkedlifedata.com/resource/pubmed/chemical/Organometallic Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphines,
http://linkedlifedata.com/resource/pubmed/chemical/Radiopharmaceuticals,
http://linkedlifedata.com/resource/pubmed/chemical/perfluorosulfonic acid
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0003-2700
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
69
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4045-50
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading | |
pubmed:year |
1997
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pubmed:articleTitle |
Electrochemical behavior of [ReI(DMPE)3]+, where DMPE = 1,2-bis(dimethylphosphino)ethane, at perfluorosulfonated ionomer-modified electrodes.
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pubmed:affiliation |
Department of Chemistry, University of Cincinnati, Ohio 45221-0172, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.
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