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HERO ID
7623425
Reference Type
Journal Article
Title
A novel photo-responsive azobenzene-containing nanoring host for fullerene-guest facile encapsulation and release
Author(s)
Yuan, K; Guo, YJ; Zhao, X; ,
Year
2014
Is Peer Reviewed?
1
Journal
Physical Chemistry Chemical Physics
ISSN:
1463-9076
EISSN:
1463-9084
Publisher
ROYAL SOC CHEMISTRY
Location
CAMBRIDGE
Page Numbers
27053-27064
Language
English
PMID
25382786
DOI
10.1039/c4cp03687e
Web of Science Id
WOS:000345453200077
URL
http://xlink.rsc.org/?DOI=C4CP03687E
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Abstract
Azobenzenes in particular have been proved to have a robust photo-response, in which their configuration can transform between the trans- and cis-form upon UV-visible irradiation. Accordingly, azobenzene-containing molecules are frequently applied in the design of the guests, involving so-called host-guest chemistry. In this paper, a novel photo-responsive nanoring host molecule ([4]AB) has been designed by introducing four azobenzene groups onto the ring, and interactions between the designed nanoring host and fullerenes C60 and C70 guests were investigated at both the M06-L/MIDI! as well as M06-2X/6-31G(d) level of theory. By analyzing the geometric characteristics and host-guest binding energies, it is revealed that the designed [4]AB with diameter ca. 13.4 Å is an ideal host molecule for the encapsulation of guests C60 and C70 fullerene. Meanwhile, inferred from UV-vis-NIR spectroscopy, the guest C60 and C70 could be facilely released from the cavity of the [4]AB via configuration transformation between trans- and cis-form of the host under 474 and 506 nm photo-irradiation, respectively. Frontier orbital features, weak interaction regions, infrared spectroscopy and (1)H NMR spectra have also been theoretically simulated. The present work would provide a new strategy for facile reversible encapsulation and release of fullerene guest by a novel nanoring host.
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