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Hydroxyl radical reaction and lantha...
~
Cullen, Thomas Donovan.
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Hydroxyl radical reaction and lanthanide ion complexation kinetics of DTPA.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Hydroxyl radical reaction and lanthanide ion complexation kinetics of DTPA./
作者:
Cullen, Thomas Donovan.
面頁冊數:
63 p.
附註:
Source: Masters Abstracts International, Volume: 52-03.
Contained By:
Masters Abstracts International52-03(E).
標題:
Chemistry, Organic. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=1524188
ISBN:
9781303521652
Hydroxyl radical reaction and lanthanide ion complexation kinetics of DTPA.
Cullen, Thomas Donovan.
Hydroxyl radical reaction and lanthanide ion complexation kinetics of DTPA.
- 63 p.
Source: Masters Abstracts International, Volume: 52-03.
Thesis (M.S.)--California State University, Long Beach, 2013.
The rate constants for hydroxyl radical reaction with multiple protonated forms of free diethylenetriaminepentaacetic acid {DTP A) as well as with DTPA complexed with a number of lanthanide metal ions were determined using electron pulse radio lysis and transient absorption spectroscopy. The rate constants for the most protonated DTP A species were ≈ 2.5 x 10 9 M-1s-1, but for H2-DTPA 3- a higher value of 4.1 x 109 M-1s -1 at 20-23 °C was obtained. Thermodynamic parameters were also determined for these protonated DTPA species. The metal-complexed DTPA rate constants at pH 3.0-5.0 were typically faster than for the free DTP A values, and varied depending on the metal IOn.
ISBN: 9781303521652Subjects--Topical Terms:
516206
Chemistry, Organic.
Hydroxyl radical reaction and lanthanide ion complexation kinetics of DTPA.
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Hydroxyl radical reaction and lanthanide ion complexation kinetics of DTPA.
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63 p.
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Source: Masters Abstracts International, Volume: 52-03.
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Adviser: Stephen P. Mezyk.
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Thesis (M.S.)--California State University, Long Beach, 2013.
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The rate constants for hydroxyl radical reaction with multiple protonated forms of free diethylenetriaminepentaacetic acid {DTP A) as well as with DTPA complexed with a number of lanthanide metal ions were determined using electron pulse radio lysis and transient absorption spectroscopy. The rate constants for the most protonated DTP A species were ≈ 2.5 x 10 9 M-1s-1, but for H2-DTPA 3- a higher value of 4.1 x 109 M-1s -1 at 20-23 °C was obtained. Thermodynamic parameters were also determined for these protonated DTPA species. The metal-complexed DTPA rate constants at pH 3.0-5.0 were typically faster than for the free DTP A values, and varied depending on the metal IOn.
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The complexation kinetics ofDTPA with multiple lanthanide metal ions was measured using a stopped-flow system. The measured rate constants ranged from 103-104 M-1s-1. Thermodynamic parameters were also determined for both the complexation ofEu 3+ and Lu3+. It was observed that as the ionic radius of the metal ion being complexed increased, so did the complexation rate constant.
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This study will increase understanding of the chemistry occurring within TALSPEAK, which is necessary in order to optimize this process.
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