Nature of supramolecular complexes controlled by the structure of the guest molecules: Formation of octa acid based capsuleplex and cavitandplex

Jayaraj, Nithyanandhan ; Zhao, Yaopeng ; Parthasarathy, Anand ; Porel, Mintu ; Liu, Robert S. H. ; Ramamurthy, V. (2009) Nature of supramolecular complexes controlled by the structure of the guest molecules: Formation of octa acid based capsuleplex and cavitandplex Langmuir, 25 (18). pp. 10575-10586. ISSN 0743-7463

Full text not available from this repository.

Official URL: http://pubs.acs.org/doi/abs/10.1021/la901367k

Related URL: http://dx.doi.org/10.1021/la901367k

Abstract

Factors that govern inclusion of organic molecules within octa acid (OA), a synthetic deep cavity cavitand, have been delineated by examining the complexation behavior of a number of organic molecules with varying dimensions and functionalities with OA. The formation of two types of complexes has been noted: the one which we call cavitandplex is a partially open complex in which a part of the guest molecule remains exposed to water, and the other termed capsuleplex is formed through assembly of two OA molecules. In capsuleplex, the guest is protected from water. Generally, guest molecules that possess ionic head groups form cavitandplex, and all others form capsuleplex. Capsuleplex may contain one or two guest molecules within the capsule. Small organic molecules (<10 Å in length) may form both 2:1 and 2:2 capsuleplex, while longer ones (>12 Å) preferentially form 2:1 capsuleplex. Extensive 1H NMR experiments have been carried out to characterize host-guest complexes. In the absence of the guest, OA tends to aggregate in water. The extent of aggregation depends on the concentration of OA and the presence of salts in solution. We expect the information obtained from this study to be of great value in predicting the nature of complexes with a given guest and facilitating appropriate guest chosen by researchers.

Item Type:Article
Source:Copyright of this article belongs to American Chemical Society.
ID Code:55881
Deposited On:19 Aug 2011 07:51
Last Modified:19 Aug 2011 07:51

Repository Staff Only: item control page