Controlled Release Kinetics in Hydroxy Double Salts: Effect of Host Anion Structure
Author(s) -
Stephen Majoni,
Jeanne M. Hossenlopp
Publication year - 2014
Publication title -
advances in physical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.269
H-Index - 17
eISSN - 1687-7993
pISSN - 1687-7985
DOI - 10.1155/2014/710487
Subject(s) - layered double hydroxides , intercalation (chemistry) , chemistry , substituent , ion , kinetics , hydroxide , metal , inorganic chemistry , controlled release , stereochemistry , organic chemistry , materials science , nanotechnology , physics , quantum mechanics
Nanodimensional layered metal hydroxides such as layered double hydroxides (LDHs) and hydroxy double salts (HDSs) can undergo anion exchange reactions releasing intercalated anions. Because of this, these metal hydroxides have found applications in controlled release delivery of bioactive species such as drugs and pesticides. In this work, isomers of hydroxycinnamate were used as model compounds to systematically explore the effects of anion structure on the rate and extent of anion release in HDSs. Following intercalation and subsequent release of the isomers, it has been demonstrated that the nature and position of substituent groups on intercalated anions have profound effects on the rate and extent of release. The extent of release was correlated with the magnitude of dipole moments while the rate of reaction showed strong dependence on the extent of hydrogen bonding within the layers. The orthoisomer showed a more sustained and complete release as compared to the other isomers
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