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Fluorescence modulation of cadmium sulfide quantum dots by azobenzene photochromic switches
Author(s) -
Hina Javed,
Kalsoom Fatima,
Zareen Akhter,
Muhammad Arif Nadeem,
Muhammad Siddiq,
Azhar Iqbal
Publication year - 2016
Publication title -
proceedings of the royal society a mathematical physical and engineering sciences
Language(s) - English
Resource type - Journals
eISSN - 1471-2946
pISSN - 1364-5021
DOI - 10.1098/rspa.2015.0692
Subject(s) - photochromism , azobenzene , cadmium sulfide , photochemistry , quantum dot , fluorescence , chemistry , isomerization , fluorophore , materials science , inorganic chemistry , nanotechnology , organic chemistry , molecule , catalysis , physics , quantum mechanics
We have investigated the attachment of azobenzene photochromic switches on the modified surface of cadmium sulfide (CdS) quantum dots (QDs). The modification of CdS QDs is done by varying the concentration of the capping agent (mercaptoacetic acid) and NH3 in order to control the size of the QDs. The X-ray diffraction studies revealed that the crystallite size of CdS QDs ranged from 6 to 10 nm. The azobenzene photochromic derivatives bis(4-hydroxybenzene-1-azo)4,4′(1,1′ diphenylmethane) (I) and 4,4′-diazenyldibenzoic acid (II) were synthesized and attached with surface-modified CdS QDs to make fluorophore–photochrome CdS-(I) and CdS-(II) dyad assemblies. Upon UV irradiation, the photochromic compounds (I) and (II) undergo a reversibletrans –cis isomerization. The photo-inducedtrans –cis transformation helps to transfer photo-excited electrons from the conduction band of the CdS QDs to the lowest unoccupied molecular orbital ofcis isomer of photochromic compounds (I) and (II). As a result, the fluorescence of CdS-(I) and CdS-(II) dyads is suppressed approximately five times compared to bare CdS QDs. The fluorescence modulation in such systems could help to design luminescent probes for bioimaging applications.

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