Phosphorus-Containing Macrocyclic Ionophores in Metal Ion Separations

2000 ◽  
Vol 39 (10) ◽  
pp. 3550-3565 ◽  
Author(s):  
Galina G. Talanova
1975 ◽  
Vol 53 (6) ◽  
pp. 809-816 ◽  
Author(s):  
W. Stafford Cripps ◽  
Christopher J. Willis

Perfluoropinacol, (CF3)2C(OH)C(OH)(CF3)2, ionizes by loss of two protons, and the resulting dinegative ion (PFP2−) chelates to Ni2+, Pd2+, Pt2+, and Cu2+. A variety of stable neutral complexes may be isolated if the tetracoordination of the metal ion is completed with two monodentate or one bidentate nitrogen- or phosphorus-containing ligands; square-planar structures are invariably found. The structures of these complexes are contrasted with those of analogous halides, and it is concluded that electronic effects are predominant in determining them, although steric influences may sometimes be important. The ligand field strength of the perfluoropinacolato ion is approximately equal to that of the thiocyanate ion.The nickel complexes Ni(PFP)22− and (PFP)Ni(RNHCH2CH2NHR) react with donor solvents (water, methanol, pyridine, etc.) to give equilibria between four- and five-coordinate solvated species; six-coordinate species are not observed. This unusual behavior is attributed to the steric hindrance imposed by the bulk of the PFP2− ligand.


Author(s):  
Richard A. Bartsch ◽  
Hong-Sik Hwang ◽  
Vladimir S. Talanov ◽  
Chunkyung Park ◽  
Galina G. Talanova

1999 ◽  
Vol 38 (6) ◽  
pp. 2182-2202 ◽  
Author(s):  
Josefina de Gyves ◽  
Eduardo Rodríguez de San Miguel

1989 ◽  
Vol 7 (5) ◽  
pp. 925-935 ◽  
Author(s):  
R.T. Paine ◽  
S.M. Blaha ◽  
A.A. Russell ◽  
G.S. Conary

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