Anion effects on calixarene monolayers: a Hofmeister series study
Barbara Lonetti1, Pierandrea Lo Nostro, Barry W Ninham
1Department of Chemistry and CSGI, University of Florence, via della Lastruccia 3, 50019 Sesto Fiorentino, Florence, Italy.
Abstract:
Due to their amphiphilic structure, calixarenes adsorb at the air/water interface and form stable Langmuir films. We have explored the effect of salts on calix[6]- and calix[8]arene spreading isotherms at the air/water interface. A wide range of different potassium salts was used in the subphase: KCl, KI, KBr, KSCN, KNO(3), CH(3)COOK, K(2)SO(4), and K(3)PO(4). The differences in Langmuir isotherms are due to the presence of different anions in the subphase, to the different conformations of the ligands at the interface, and to the different complexing affinities of calix[6]- and calix[8]arene for potassium ions. The two systems show a significant specific ion effect that can be discussed in terms of Hofmeister series. Characteristic monolayer parameters, e.g., limiting area (A(lim)), collapse pressure (pi(coll)), modulus of compressibility (C(s)(-1)), and surface potential (DeltaV), are discussed in terms of some physicochemical parameters that reflect dispersion forces: in particular, anion polarizabilities, lyotropic number (N), molar surface tension increment (sigma), and partial molar volume (nu(s)).
Related Concept Videos
Aromatic Hydrocarbon Anions: Structural Overview
Due to the absence of continuous overlap of p...
π Electron Effects on Chemical Shift: Overview
Electrophilic Addition to Alkynes: Halogenation
Halogenation is another class of electrophilic addition reactions where a halogen molecule gets added across a π bond. In alkynes, the presence of two π bonds allows for the addition of two equivalents of halogens (bromine or chlorine). The addition of the first halogen molecule forms a trans-dihaloalkene as the major product and the cis isomer as the minor product. Subsequent addition of the second equivalent yields the tetrahalide.
π Molecular Orbitals of the Allyl Cation and Anion
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group with both...
π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds


