Controlled Molecular Arrangement of Cinnamic Acid in Layered Double Hydroxide through pi-pi Interaction for Controlled Release

Author:

Kim Taeho1ORCID,Paek Seung-Min2ORCID,Wang Kang-Kyun3,Park Jin Kuen4ORCID,Salles Fabrice5ORCID,Oh Jae-Min1ORCID

Affiliation:

1. Department of Energy and Materials Engineering, Dongguk University, Seoul 04620, Republic of Korea

2. Department of Chemistry, Kyungpook National University, Daegu 41566, Republic of Korea

3. BI Bio-Photonics Co., Ltd., Gimpo-si 10090, Republic of Korea

4. Department of Chemistry, Hankuk University of Foreign Studies, Yongin 17035, Republic of Korea

5. Institute Charles Gerhardt des Matériaux (ICGM), Université de Montpellier, CNRS, ENSCM, 34090 Montpellier, France

Abstract

Cinnamic acid (CA) was successfully incorporated into Zn-Al layered double hydroxide (LDH) through coprecipitation. The CA moiety was stabilized in the interlayer space through not only electrostatic interaction but also intermolecular π-π interaction. It was noteworthy that the CA arrangement was fairly independent of the charge density of LDH, showing the important role of the layer–CA and CA-CA interactions in molecular stabilization. Computer simulations using the Monte Carlo method as well as analytical approaches including infrared, UV-vis spectroscopy, and differential scanning calorimetry showed the existence of intermolecular interaction. In order to reinforce molecular stabilization, a neutral derivative of CA, cinnamaldehyde (CAD), was additionally incorporated into LDH. It was clearly shown that CAD played a role as a π-π interaction mediator to enhance the stabilization of CA. The time-dependent release of CA from LDH was first governed by the layer charge density of LDH; however, the existence of CAD provided additional stabilization to the CA arrangement to slow down the release kinetics.

Funder

National Research Foundation of Korea

Ministry of Science and ICT & Korean National Police Agency

Publisher

MDPI AG

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