Luminescent metal-organic frameworks (MOFs) as a chemopalette: Tuning the thermochromic behavior of dual-emissive phosphorescence by adjusting the supramolecular microenvironments
Two classical copper(I)-cluster-based luminophores, namely, Cu 4I4 and [Cu3Pz3]2 (Pz=pyrazolate), are immobilized in a supramolecular system through the formation of metal-organic framework (MOF) materials. This series of luminescent MOF materials, namely, [Cu4I4(NH3)Cu 3(L1)3]n, [Cu4I4(NH 2CH3)Cu3(...
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| Main Authors: | , , , |
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| Format: | Article |
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Wiley
2013
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| Subjects: | |
| Online Access: | http://eprints.um.edu.my/12103/ https://doi.org/10.1002/chem.201204632 |
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| Summary: | Two classical copper(I)-cluster-based luminophores, namely, Cu 4I4 and [Cu3Pz3]2 (Pz=pyrazolate), are immobilized in a supramolecular system through the formation of metal-organic framework (MOF) materials. This series of luminescent MOF materials, namely, [Cu4I4(NH3)Cu 3(L1)3]n, [Cu4I4(NH 2CH3)Cu3(L1)3]n, and [Cu4I4Cu3(L2)3]n (L1=3-(4-pyridyl)-5-(p-tolyl)pyrazolate; L2=3-(4-pyridyl)-5-(2,4-dimethylphenyl) pyrazolate), exhibit diverse thermochromism attributed to the relative functioning efficacy of the two coordination luminophores. Such an intriguing chemopalette effect is regulated by the different supramolecular microenvironments between the two-dimensional layers of these MOFs, and in particular, by the fine-tuned Cu-Cu distances in the excimeric [Cu 3Pz3]2 luminophore. The structure-property elucidation of the thermochromic behavior allows one to understand these optical materials with unusual dual-emissive properties. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. |
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