Supercritical Carbon Dioxide-Soluble Ligands for Extracting Actinide Metal Ions from Porous Solids
The focus of the effort during the project period from 9/16/98 to 6/15/99 has been on the synthesis, aggregation, and coordination chemistry of silyl-containing diphosphonic acids that potentially could be useful as solvent extraction reagents in supercritical CO2. A homologous series of alkylenediphosphonic acids was esterified with 3-(trimethylsilyl)-1- propanol to the symmetrically-substituted diesters. The silicon-containing alcohol 3- (trimethylsilyl)-1-propanol was chosen for esterification of the diphosphonic acids because it contains both a silyl group and a trimethylene linker. Separating the trimethylsilyl from the organo-functional group by three carbon atoms is optimal for achieving chemical stability and synthetic accessibility. The synthesis of these compounds utilizes methodology that relies on dicyclohexylcarbodiimide as the esterification reagent to activate the acid.
- Research Organization:
- Argonne National Laboratory, Argonne, IL; Loyola University, Chicago, Chicago, Illinois; University of Notre Dame, Notre Dame , Indiana (US)
- Sponsoring Organization:
- USDOE Office of Environmental Management (EM) (US)
- DOE Contract Number:
- FG07-98ER14924; FG07-98ER14928
- OSTI ID:
- 831222
- Report Number(s):
- EMSP-64965-1999; R&D Project: EMSP 64965; TRN: US200430%%297
- Resource Relation:
- Other Information: PBD: 1 Jun 1999
- Country of Publication:
- United States
- Language:
- English
Similar Records
Synthesis and characterization of DI-[3-(trimethylsilyl)-1-propylene] alkylenediphosphonic acids.
Supercritical Carbon Dioxide-Soluble Ligands for Extracting Actinide Metal Ions from Porous Solids