Structure and Antibacterial Activity of Bi-cyclohexanone Pentaerythritol Ketal
- DOI
- 10.2991/ame-16.2016.213How to use a DOI?
- Keywords
- Cyclohexanone pentaerythritol ketal, X-ray structure, antibacterial activity
- Abstract
Cyclohexanone pentaerythritol ketal was synthesized from cyclohexanone and pentaerythritol by condensation using NaHSO4 as catalyst and characterized by NMR and MS spectrum. Furthermore, the structure of the tile compound was confirmed by single-crystal X-ray diffraction. It crystallizes in orthorhombic space group, P 21, with a unit cell dimensions of a = 11.1214(9) Å, b = 13.9216(6) Å and c = 11.6658(10) Å. In the crystal, there are two independent molecules with different conformation, varying both in bond lengths and angles. In each molecular, there are four six-membered cycles, two cyclohexyl groups and two 1,3-dioxane groups. The four six-membered cycles all display a typical stable boat conformation. The stacking interaction is responsible for the crystal's 1-D supra-molecular structure. The thermal gravimetric analysis (TGA) indicates the title compound is stable below 200°C, and the remaining weight ratio is less than 9% above 300°C. This compound was evaluated for their in vitro antimicrobial activity against six bacteria (S. aureus, S. epidermidis, M. luteus, E. coli, K. pneumoniae, A. fumigatus). It some anti-inflammatory activity against the tested bacteria and the inhibition is depending on the concentration.
- Copyright
- © 2016, the Authors. Published by Atlantis Press.
- Open Access
- This is an open access article distributed under the CC BY-NC license (http://creativecommons.org/licenses/by-nc/4.0/).
Cite this article
TY - CONF AU - Li Huang PY - 2016/06 DA - 2016/06 TI - Structure and Antibacterial Activity of Bi-cyclohexanone Pentaerythritol Ketal BT - Proceedings of the 2nd Annual International Conference on Advanced Material Engineering (AME 2016) PB - Atlantis Press SP - 1315 EP - 1320 SN - 2352-5401 UR - https://doi.org/10.2991/ame-16.2016.213 DO - 10.2991/ame-16.2016.213 ID - Huang2016/06 ER -