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Three-component D-A hybrid heterostructures with enhanced photochromic, photomodulated luminescence and selective anion-sensing properties
As an emerging class of hybrid complexes, donor-acceptor (D-A) hybrid heterostructures with advantages of both photoactive organic and inorganic components have provided an excellent platform for the fabrication of multifunctional photoactive materials. In this context, we have demonstrated three no...
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Published in: | Dalton transactions : an international journal of inorganic chemistry 2020-10, Vol.49 (37), p.1383-1389 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | As an emerging class of hybrid complexes, donor-acceptor (D-A) hybrid heterostructures with advantages of both photoactive organic and inorganic components have provided an excellent platform for the fabrication of multifunctional photoactive materials. In this context, we have demonstrated three novel host-guest D-A hybrid heterostructures, {[Ln(BCEbpy)(H
2
O)
4
][Co
III
(CN)
6
]·4H
2
O}
n
(
1
(Eu),
2
(Dy),
3
(Sm)), based on the anionic Co(CN)
6
3−
and cationic coordination layers assembled from a viologen functionalized tecton and Ln(NO)
3
. Due to the introduction of an electron donor, Co
III
(CN)
6
3−
, the unique hybrid exhibits a highly sensitive and reversible photochromic transformation from light-yellow to brown upon UV-Vis irradiation. More interestingly, accompanied with this photochromic process, hybrid
1
simultaneously possesses a photomodulated fluorescence behaviour. In addition, hybrid
1
shows high sensitivity and selectivity towards Cr
2
O
7
2−
anions with a fairly small LOD of
ca.
9.6 × 10
−6
M.
Three novel three-component hybrid heterostructures with inorganic [Co
III
(CN)
6
]
3−
anions as electron donors and viologen tectons as electron acceptors exhibit combined properties of photochromism, photomodulated luminescence and anion sensing. |
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ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/d0dt02390f |