Nickel-Organic Coordination Layers with Different Directional Cavities

The two new metal‐organic coordination frameworks [Ni2(pydc)2(4,4′‐bpy)(H2O)4]n·0.5n(4,4′‐bpy)2H2O (1) and [Ni2(pydc)2(2,2′‐bpy)2(H2O)2]n·2nH2O (2) (H2pydc = pyridine‐3,4‐dicarboxylic acid; bpy = bipyridine) have been synthesised under hydrothermal conditions and characterised by single‐crystal X‐ra...

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Veröffentlicht in:European Journal of Inorganic Chemistry 2006, Vol.2006 (23), p.4852-4856
Hauptverfasser: Zhou, Youfu, Yue, Chengyang, Yuan, Daqiang, Chen, Lian, Chen, Jiutong, Lan, Anjian, Jiang, Feilong, Hong, Maochun
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container_end_page 4856
container_issue 23
container_start_page 4852
container_title European Journal of Inorganic Chemistry
container_volume 2006
creator Zhou, Youfu
Yue, Chengyang
Yuan, Daqiang
Chen, Lian
Chen, Jiutong
Lan, Anjian
Jiang, Feilong
Hong, Maochun
description The two new metal‐organic coordination frameworks [Ni2(pydc)2(4,4′‐bpy)(H2O)4]n·0.5n(4,4′‐bpy)2H2O (1) and [Ni2(pydc)2(2,2′‐bpy)2(H2O)2]n·2nH2O (2) (H2pydc = pyridine‐3,4‐dicarboxylic acid; bpy = bipyridine) have been synthesised under hydrothermal conditions and characterised by single‐crystal X‐ray diffraction analysis. The structure of 1 contains parallel rectangular channels that accommodate large 4,4′‐bpy guests while that of 2 contains vertical channels coordinated to 2,2′‐bpy ligands. Their magnetic analyses show that they exhibit different magnetic interactions. The red shifts of the peak in their emission spectra relative to those of the the free ligands could be attributable to the metal–ligand coordination. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)
doi_str_mv 10.1002/ejic.200600539
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subjects Carboxylate ligands
Coordination polymers
Luminescence
Magnetic properties
Nickel
title Nickel-Organic Coordination Layers with Different Directional Cavities
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