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Biphenylene-bridged mesostructured organosilica as a novel hybrid host material for Ln(III) (Ln = Eu, Gd, Tb, Er, Yb) ions in the presence of 2-thenoyltrifluoroacetone

Authors
Biju, SilvanoseEom, Yu KyungBuenzli, Jean-Claude G.Kim, Hwan Kyu
Issue Date
2013
Publisher
ROYAL SOC CHEMISTRY
Citation
JOURNAL OF MATERIALS CHEMISTRY C, v.1, no.21, pp.3454 - 3466
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF MATERIALS CHEMISTRY C
Volume
1
Number
21
Start Page
3454
End Page
3466
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/106498
DOI
10.1039/c3tc30459k
ISSN
2050-7526
Abstract
A hierarchically ordered 4,4'-biphenylene-bridged mesoporous organosilica framework (Bp-PMO) has been synthesized with the aim of using it as a new hybrid host for Ln(III) ions. A series of novel organic-inorganic luminescent hybrid materials have been obtained by covalently linking Ln(III) complexes (Ln = Eu, Gd, Tb, Er, and Yb) to Bp-PMO functionalized with 2-thenoyltrifluoroacetone (HTTA). The visible and NIR photoluminescence studies of the hybrid materials show that Bp-PMO acts both as an inorganic host and an organic co-sensitizer for Ln(III) ions. The intrinsic quantum yield and lifetime data obtained for the hybrid material containing Eu-III (54.5% and 615 mu s) are among the highest values reported for hybrid materials containing Eu(III)tetrakis(beta-diketonate) complexes. The combination of Bp-PMO and HTTA also provides sizable sensitization for Tb-III, Er-III and Yb-III ions. The overall quantum yields and lifetime measurements for mixed metallic hybrid materials show that Ln -> Ln' energy transfer occurs in the mixed lanthanide systems. In addition, controlling the Ln/Ln' ratio allows one to tune the emission colour.
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