2,3-Dihydroxybenzoic acid amides of tetraazaalkanes and tetaaza cycloalkanes
Abstract
This disclosure is directed to a compound of the formula given in the patent 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. No Drawings
- Inventors:
- Issue Date:
- OSTI Identifier:
- 7008117
- Patent Number(s):
- 4181654
- Application Number:
- PPN: US 5-927234
- Assignee:
- Dept. of Energy, Washington, DC (United States)
- DOE Contract Number:
- W-7405-ENG-48
- Resource Type:
- Patent
- Resource Relation:
- Patent File Date: 24 Jul 1978
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 32 ENERGY CONSERVATION, CONSUMPTION, AND UTILIZATION; ACTINIDES; MATERIALS RECOVERY; AMIDES; CHEMICAL REACTIONS; ELECTRON TRANSFER; ELEMENTS; MANAGEMENT; METALS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; PROCESSING; WASTE MANAGEMENT; WASTE PROCESSING; 320303* - Energy Conservation, Consumption, & Utilization- Industrial & Agricultural Processes- Equipment & Processes
Citation Formats
Weitl, F L, and Raymond, K N. 2,3-Dihydroxybenzoic acid amides of tetraazaalkanes and tetaaza cycloalkanes. United States: N. p., 1980.
Web.
Weitl, F L, & Raymond, K N. 2,3-Dihydroxybenzoic acid amides of tetraazaalkanes and tetaaza cycloalkanes. United States.
Weitl, F L, and Raymond, K N. Tue .
"2,3-Dihydroxybenzoic acid amides of tetraazaalkanes and tetaaza cycloalkanes". United States.
@article{osti_7008117,
title = {2,3-Dihydroxybenzoic acid amides of tetraazaalkanes and tetaaza cycloalkanes},
author = {Weitl, F L and Raymond, K N},
abstractNote = {This disclosure is directed to a compound of the formula given in the patent 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. No Drawings},
doi = {},
journal = {},
number = ,
volume = ,
place = {United States},
year = {1980},
month = {1}
}
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