In vitro removal of actinide (IV) ions
Abstract
A compound of the formula: ##STR1## wherein X is hydrogen or a conventional electron-withdrawing group, particularly --SO.sub.3 H or a salt thereof; n is 2, 3, or 4; m is 2, 3, or 4; and p is 2 or 3. The present compounds are useful as specific sequestering agents for actinide (IV) ions. Also described is a method for the 2,3-dihydroxybenzamidation of azaalkanes.
- Inventors:
-
- Martinez, CA
- Berkeley, CA
- Issue Date:
- Research Org.:
- Lawrence Livermore National Laboratory (LLNL), Livermore, CA (United States)
- OSTI Identifier:
- 864094
- Patent Number(s):
- 4309305
- Assignee:
- United States as represented by United States Department of (Washington, DC)
- Patent Classifications (CPCs):
-
C - CHEMISTRY C07 - ORGANIC CHEMISTRY C07D - HETEROCYCLIC COMPOUNDS
- DOE Contract Number:
- W-7405-ENG-48
- Resource Type:
- Patent
- Country of Publication:
- United States
- Language:
- English
- Subject:
- vitro; removal; actinide; compound; formula; str1; hydrogen; conventional; electron-withdrawing; particularly; -so; salt; compounds; useful; specific; sequestering; agents; described; method; 3-dihydroxybenzamidation; azaalkanes; sequestering agents; specific sequestering; particularly -so; conventional electron-withdrawing; /999/252/423/
Citation Formats
Weitl, Frederick L, and Raymond, Kenneth N. In vitro removal of actinide (IV) ions. United States: N. p., 1982.
Web.
Weitl, Frederick L, & Raymond, Kenneth N. In vitro removal of actinide (IV) ions. United States.
Weitl, Frederick L, and Raymond, Kenneth N. Fri .
"In vitro removal of actinide (IV) ions". United States. https://www.osti.gov/servlets/purl/864094.
@article{osti_864094,
title = {In vitro removal of actinide (IV) ions},
author = {Weitl, Frederick L and Raymond, Kenneth N},
abstractNote = {A compound of the formula: ##STR1## wherein X is hydrogen or a conventional electron-withdrawing group, particularly --SO.sub.3 H or a salt thereof; n is 2, 3, or 4; m is 2, 3, or 4; and p is 2 or 3. The present compounds are useful as specific sequestering agents for actinide (IV) ions. Also described is a method for the 2,3-dihydroxybenzamidation of azaalkanes.},
doi = {},
journal = {},
number = ,
volume = ,
place = {United States},
year = {1982},
month = {1}
}
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