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A series of lanthanide coordination polymers with 4′-(4-carboxyphenyl)-2,2′:6′,2″-terpyridine: Syntheses, crystal structures and luminescence properties
A series of lanthanide coordination polymers, [Ln(cptpy) 3] n [Ln = Sm ( 1), Eu ( 2), Tb ( 3), Dy ( 4), Hcptpy = 4′-(4-carboxyphenyl)-2,2′:6′,2″-terpyridine] have been prepared under hydrothermal conditions and characterized by IR, Elemental analysis, single crystal X-ray diffraction. Compounds 1– 4...
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Published in: | Inorganic chemistry communications 2011-03, Vol.14 (3), p.484-488 |
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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: | A series of lanthanide coordination polymers, [Ln(cptpy)
3]
n
[Ln
=
Sm (
1), Eu (
2), Tb (
3), Dy (
4), Hcptpy
=
4′-(4-carboxyphenyl)-2,2′:6′,2″-terpyridine] have been prepared under hydrothermal conditions and characterized by IR, Elemental analysis, single crystal X-ray diffraction. Compounds
1–
4 are isostructural with 1D framework, in which all Ln
III atoms are nine-coordinated and (cptpy)
− anions adopt two different coordination modes. The network packed through π···π stacking interactions and C–H···π interactions to form a 3D supramolecular structure without solvent molecules. In addition, the thermal stabilities and luminescence properties were also studied.
A series of lanthanide coordination polymers, [Ln(cptpy)
3]
n
[Ln
=
Sm (
1), Eu (
2), Tb (
3), Dy (
4), Hcptpy
=
4′-(4-carboxyphenyl)-2,2′:6′,2″-terpyridine] have been prepared under hydrothermal conditions and characterized. Their photoluminescence properties were also studied. The thermal stabilities and lifetime of
2 were further studied.
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► A series of lanthanide coordination polymers, [Ln(cptpy)
3]
n have been prepared. ► The 3D supramolecular structure is formed through π···π and C–H···π interactions. ► The (cptpy)
- anion can efficiently sensitize Eu
III luminescence. |
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ISSN: | 1387-7003 1879-0259 |
DOI: | 10.1016/j.inoche.2011.01.007 |