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Two ligand-length-tunable interpenetrating coordination networks with stable Zn-2 unit as three-connected uninode and supramolecular topologies
Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK), Inorganic and Structural Chemistry.
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2013 (English)In: CrystEngComm, ISSN 1466-8033, E-ISSN 1466-8033, Vol. 15, no 22, 4473-4482 p.Article in journal (Refereed) Published
Abstract [en]

Insight into the control of interpenetrating coordination networks has been strategized by using linear dicarboxylates with different lengths. In this work, we rely on two roles of triethanolamine (H-bonding donations and cooperative stabilization of Zn-2 unit) to target the syntheses of two unique interpenetrating coordination polymers. The two representative compounds, [Zn-4(teaH(2))(2)(bdc)(3)]center dot 2(MeOH) (1; bdc(2-) = 1,4-benzenedicarboxylate and teaH(2) 2 = triethanolamine anion) and [Zn-2(teaH(2))(bpdc)(1.5)] (2; bpdc(2-) = biphenyl-4,4'-dicarboxylate), contain a well-defined Zn-2 unit as three-connected uninode but are assembled into two different topology nets. Compound 1 represents the first example of a two-fold interpenetrating 2D -> 3D 4.6(5)-crb supramolecular architecture constructed from a two-fold interpenetrating 4.8(2)-fes subnet, whereas compound 2 shows an unreported self-catenated 3D -> 3D 6(15) supramolecular network that can be made by H-bond cross-linking of an eight-fold 10(3)-ths subnet. The photoluminescent properties of the two compounds have also been investigated.

Place, publisher, year, edition, pages
2013. Vol. 15, no 22, 4473-4482 p.
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Chemical Sciences
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URN: urn:nbn:se:su:diva-91328DOI: 10.1039/c3ce40117kISI: 000318944800010OAI: oai:DiVA.org:su-91328DiVA: diva2:633257
Note

AuthorCount:6;

Available from: 2013-06-26 Created: 2013-06-24 Last updated: 2017-12-06Bibliographically approved

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