68380-65-4Relevant articles and documents
Crown calix[4]arenes, method of preparation and use for selective extraction of caesium
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, (2008/06/13)
PCT No. PCT/FR98/00401 Sec. 371 Date Jan. 27, 1999 Sec. 102(e) Date Jan. 27, 1999 PCT Filed Mar. 2, 1998 PCT Pub. No. WO98/39321 PCT Pub. Date Sep. 11, 1998The invention relates to new calixarenes of formula: in which R1 represents a crown ether chain that includes at least two aryl or cycloalkyl rings, R2 is a hydroxyl or alkoxy group, or the two R2 groups together form a crown ether chain such as R1, and R3 represents a hydrogen atom or an alkyl group. The calixarenes are used to selectively extract caesium from aqueous solutions that notably have high concentrations of sodium.
A new calix[4]arene-bis(crown ether) derivative displaying an improved caesium over sodium selectivity: Molecular dynamics and experimental investigation of alkali-metal ion complexation
Lamare, Veronique,Dozol, Jean-Francois,Fuangswasdi, Saowarux,Arnaud-Neu, Francoise,Thuery, Pierre,Nierlich, Martine,Asfari, Zouhair,Vicens, Jacques
, p. 271 - 284 (2007/10/03)
In the light of computational studies suggesting enhanced cation-binding abilities for various benzo derivatives of calix[4]arene-bis-crown-6 macrocycles, the synthesis and properties of one of these ligands, BC6B2, have been investigated. In this compound, di(1,2-phenylene)-annelated glycolic chains link the 1,3- and 2,4-phenyl rings of the calixarene, thereby forcing it into the 1,3-alternate conformation. The detailed structures of BC6B2·CH3NO2 1 and Cs2(NO3)2BC6B2·CHCl 3·H2O 2 have been established by X-ray crystallography. Studies of coordination and solvent extraction of the alkali-metal ions have been used to compare this ligand with a number of related systems known previously.
Macroring-Neutral Molecule Complexation. Synthesis of Biconcave Pyridino Hosts, Complex Formation, and X-ray Crystal Structures of Two Inclusion Compounds
Weber, Edwin,Koehler, Hans-Juergen,Reuter, Hans
, p. 1236 - 1242 (2007/10/02)
A series of pyridino macrocycles 1-3(a-e) incorporating rigid bi- and triaryl ether segments in different ring positions have been synthesized.The effect of incorporation of these building blocks into a given macroring framework on the host properties for