Issue 72, 2017

A pair of novel Zn(ii) enantiomeric coordination polymers based on a chiral multicarboxylate ligand: synthesis, crystal structures and molecular recognition properties

Abstract

A pair of Zn(II) enantiomeric coordination polymers, 1-R and 1-S, namely, [Zn4((R)-H3L)2(OH)2(H2O)2]·3H2O {H3L= (R)- or (S)-5-(1-carboxyethoxymethyl)-isophthalic acid}, were synthesized via solvothermal reactions. Their structures were determined by single-crystal X-ray diffraction analysis and further characterized by IR spectra, elemental analyses, thermogravimetric analysis (TGA), solid-state circular dichroism (CD) and powder X-ray diffraction (PXRD). The pair of enantiomers crystallized in the same chiral space group, featuring a 3,6-c net and kgd topological type structure with a point symbol of (43)2(46·66·83). Their CD spectra exhibit obvious positive or negative Cotton effects, indicating their homochirality. 1-R and 1-S also proved to be second-harmonic generation (SHG) active. Moreover, their fluorescent selective recognition towards nitro aromatic compounds and metal cations were also investigated.

Graphical abstract: A pair of novel Zn(ii) enantiomeric coordination polymers based on a chiral multicarboxylate ligand: synthesis, crystal structures and molecular recognition properties

Supplementary files

Article information

Article type
Paper
Submitted
31 Jul 2017
Accepted
21 Sep 2017
First published
26 Sep 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 45862-45868

A pair of novel Zn(II) enantiomeric coordination polymers based on a chiral multicarboxylate ligand: synthesis, crystal structures and molecular recognition properties

L. Gu, H. Zhang, W. Jiang, G. Hou, Y. Yu and D. Ma, RSC Adv., 2017, 7, 45862 DOI: 10.1039/C7RA08433A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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