posted on 2012-05-10, 00:00authored byN. O. Mchedlov-Petrossyan, N. A. Vodolazkaya, R. V. Rodik, L. N. Bogdanova, T. A. Cheipesh, O. Yu. Soboleva, A. P. Kryshtal, L. V. Kutuzova, V. I. Kalchenko
The study of the aqueous solutions of the cationic hexameric
calixarene
5,11,17,23,29,35-hexakis (N,N-dimethyl-N-hydroxyethylammoniummethylene)-37,38,39,40,41,42-hexametoxycalix[6]arene
hexachloride demonstrates their colloidal nature. Within the concentration
range from 1 × 10–5 to 0.01 M, this compound
forms positively charged aggregates of a much larger size as compared
with those of tetrameric cationic calix[4]arene previously studied
by us. The aggregation was confirmed both by DLS and TEM experiments;
the last method revealed that the 102 to 103 nm sized particles consist of smaller primary aggregates. These
aggregates manifest themselves in displaying alteration of absorption
spectra and marked shifts of apparent ionization constants of common
acid–base indicators. These shifts resemble those registered
in micellar solutions of cationic surfactants and cationic polyelectrolyte
brushes. The pCl measurements also confirm the formation of calixarene
aggregates. The dye associations with the calixarene are governed
rather by interactions with the aggregates of the macrocycles than
by expected inclusion of the guest into the hosts cavity. Hence, on
using ionic calixarenes in aqueous media, not only inclusion phenomena
but also micellar effects should be taken into account.