Preparation and computational investigation of molecular imprinted polymers for Clidinium Bromide

Abstract

Molecular imprinted polymers (MIPs) are polymers that possess recognition sites specific for a predetermined target molecule (Template). Inspired by the idea of biological natural receptors, they behave like synthetic molecular recognition elements. They have been developed into a promising tool in several crucial applications, including analytical methods, drug delivery, and catalysis. The non-covalent imprinting is more commonly used approach in the preparation of MIPs because of its simplicity. In this approach, intermolecular interactions between the template molecule (T) and the functional monomer (FM) are the forces that govern the performance of the resulting MIP. Hence, studying these interactions is very important to elucidate and understand the imprinting mechanism. This paper focuses on preparation of two MIPs for a Clidinium Bromide (CB), using two different types of FMs. These MIPs are characterized by using IR and SEM techniques. Adsorption isotherm properties to CB are assayed for them. Then the structures of the pre-polymerization complexes of prepared MIPs were investigated using Density Functional Theory (DFT) calculations at B3LYP/6-31G level in a vacuum and other media. Finally, Bader's Quantum Theory of Atoms in Molecules (QTAIM) was used to prove the existence and nature of intermolecular interactions between CB and FM. The theoretical results were in complete agreement with experiments and indicated that the use of AM as FM is preferred over MA in the MIP preparation for CB.