Home Extraction of americium and europium by CMPO-substituted adamantylcalixarenes
Article
Licensed
Unlicensed Requires Authentication

Extraction of americium and europium by CMPO-substituted adamantylcalixarenes

  • V. A. Babain , M. Yu. Alyapyshev , M. D. Karavan , V. Böhmer , L. Wang , E. A. Shokova , A. E. Motornaya , I. M. Vatsouro and V. V. Kovalev
Published/Copyright: September 25, 2009

Summary

Eight p-adamantylcalix[4]arene derivatives, bearing four CMPO-like functions [(CH2)nNHC(O)CH2- P(O)Ph2] at the wide (4a,b, n = 0, 1) or narrow (5a–c and 6a–c, n = 2–4) rims were synthesized for the first time. Studies of the extraction of americium(III) and europium(III) from 3 M HNO3 solutions to organic phases (dichloromethane, m-nitro-trifluoromethylbenzene) showed: (i) The extraction ability for all the adamantylcalixarene ligands is much better than for their monomeric analogues –N-(1-adamantyl)-, N-(1-adamantylmethyl)- and N,N-(dibutyl)carbamoylmethyldiphenylphosphine oxides 7a, 7b, 8; (ii) The extraction percentage increases strongly with increasing length of the spacer for all types of ligands 4–6, and best extraction results were found for 4b (n = 1) and 5c (n = 4); (iii) The separation coefficient DAm/DEu for the investigated compounds did not exceed 2, which is close to the narrow rim CMPO calixarenes, studied earlier; (iv) Variation of the spacer length between CMPO groups attached to the 1,3- and 2,4-positions of the calixarene platform in 6 did not lead to appreciably improved extractants, neither with respect to the extraction abilities (D) nor to the selectivities (DAm/DEu).

Received: 2004-12-1
Accepted: 2005-4-19
Published Online: 2009-9-25
Published in Print: 2005-12-1

© Oldenbourg Wissenschaftsverlag, München

Downloaded on 17.9.2025 from https://www.degruyterbrill.com/document/doi/10.1524/ract.2005.93.12.749/html
Scroll to top button