Binding interaction of a fluoranthene–thiol on gold nanoparticles with β-cyclodextrin and DNA

In this paper, we report the preparation of a fluoranthene–thiol derivative, the assembly of the compound onto gold nanoparticles, and their binding to β-cyclodextrin and DNA. The synthesised fluoranthene–thiol is characterised using infra-red (IR), nuclear magnetic resonance (NMR), and mass spectro...

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Bibliographic Details
Main Authors: S. Eugene Thangaraj, Eva Janet Antony, Sameena Yousuf, P. Mosae Selvakumar, Premnath Dhanaraj, Israel V. M. V. Enoch
Format: Article
Language:English
Published: Taylor & Francis Group 2017-01-01
Series:Journal of Experimental Nanoscience
Subjects:
Online Access:http://dx.doi.org/10.1080/17458080.2016.1258496
Description
Summary:In this paper, we report the preparation of a fluoranthene–thiol derivative, the assembly of the compound onto gold nanoparticles, and their binding to β-cyclodextrin and DNA. The synthesised fluoranthene–thiol is characterised using infra-red (IR), nuclear magnetic resonance (NMR), and mass spectrometric techniques. The gold nanoparticles are characterised using transmission electron microscopy and energy dispersive X-ray spectroscopy microanalysis. The size of the nanoparticles is 5 ± 1 nm. The thiol–gold nanoparticles bind to β-cyclodextrin, and DNA and the fluorescence spectra show enhancement of fluorescence on the binding. The thiol–gold nanoparticles form a host–guest complex with β-cyclodextrin and the binding constant of the complex is 1330 mol−1 dm3. This reveals the openness of the thiol on the surface of the gold nanoparticles.
ISSN:1745-8080
1745-8099