Crown Ethers with Fluctuating Ring Size (“Breathing Crown Ethers”)

1979 ◽  
Vol 18 (4) ◽  
pp. 311-312 ◽  
Author(s):  
Gerhard Schröder ◽  
Walter Witt
Keyword(s):  
2018 ◽  
Vol 316 (2) ◽  
pp. 535-541 ◽  
Author(s):  
Olga A. Zakurdaeva ◽  
Andrey F. Asachenko ◽  
Maxim A. Topchiy ◽  
Sergey V. Nesterov

Author(s):  
Patricia Paviet-Hartmann ◽  
Ana Nunez Gomez-Aleixandre ◽  
Joshua Pak ◽  
Amparo Glez Espartero ◽  
Frederic Poineau ◽  
...  

As it is envisioned today, the first segment of the UREX+ process uses low nitric acid concentrations for U(VI) extraction where pertechnetate anion, TcO4−, can be co-extracted with the uranyl and nitrate into TBP-hydrocarbon solutions. A reductant complexant, acetohydroxamic acid (AHA) is added to the process through the scrub to limit the extractability of plutonium and neptunium. Recent work performed in our laboratory (Ref. 1) demonstrated that TcO4− undergoes reductive nitrosylation by AHA under a variety of conditions. The resulting divalent technetium is complexed by AHA to form the pseudo-octahedral trans-aquonitrosyl-(diacetohydroxamic)-technetium(II) complex ([Tc(II)(NO)(AHA)2H2O]+). In this paper, we are reporting the extraction of [Tc(II)(NO)(AHA)2H2O]+ complex by new designed macrocompounds as well as commercially available crown ethers from 18-crown-6 to 24-crown-8 in ring size and of varying derivatization. Several organic diluents with different dielectric constants are used to enhance the distribution coefficient of technetium (II). The experimental efforts are focused on determining the best extraction conditions by varying the macrocomponds nature and concentration, and the organic phase composition.


2010 ◽  
Vol 52 (4) ◽  
pp. 363-365
Author(s):  
V. V. Yakshin ◽  
O. M. Vilkova ◽  
N. A. Tsarenko ◽  
L. I. Atamas’ ◽  
I. G. Tananaev ◽  
...  

2011 ◽  
Vol 40 (2) ◽  
pp. 384-392 ◽  
Author(s):  
Adrián Roca-Sabio ◽  
Marta Mato-Iglesias ◽  
David Esteban-Gómez ◽  
Andrés de Blas ◽  
Teresa Rodríguez-Blas ◽  
...  

2006 ◽  
Vol 84 (10) ◽  
pp. 1273-1279 ◽  
Author(s):  
Hua Mao ◽  
John B Thorne ◽  
Jennifer S Pharr ◽  
Robert E Gawley

Convenient macrocyclization synthetic routes for the preparation of different-sized monoaza anthracylmethyl crown ether chemosensors (15-crown-5, 18-crown-6, 21-crown-7, 24-crown-8, and 27-crown-9) are described. Evaluation of these crowns as chemosensors for saxitoxin revealed that the larger crowns have moderately higher binding constants, with the 27-crown-9 chemosensor having the largest binding constant (2.29 × 105 (mol/L)–1). Fluorescence enhancements of 100% were observed at saxitoxin concentrations of 5 µmol/L, which is close to the detection limit in mouse bioassay.Key words: anthracene, crown ethers, saxitoxin, paralytic shellfish poison (PSP), binding constants; chemosensors.


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