Issue 33, 2018

A paraelectric–ferroelectric phase transition of an organically templated zinc oxalate coordination polymer

Abstract

Water-presence dependent switchable ferroelectricity was discovered in the hybrid organic–inorganic zinc oxalate 1D coordination polymer (DABCOH2)[Zn(C2O4)2]·3H2O (DZnOH, where DABCOH2: diprotonated 1.4-diazoniabicyclo[2.2.2]octane). The compound undergoes a reversible para–ferroelectric phase transition at 207 K from room temperature centrosymmetric phase I (space group P21/n) to low-temperature non-centrosymmetric phase II (space group P21). The microscopic mechanism of the phase transition is directly associated with the reconstruction of the hydrogen-bond network. On heating, the crystals exhibit a reversible single-crystal to single-crystal transformation concerned with the removal of all water molecules giving anhydrous DABCO zinc oxalate (DABCOH2)[Zn(C2O4)2] (DZnO). The dehydrated compound does not show ferroelectric properties.

Graphical abstract: A paraelectric–ferroelectric phase transition of an organically templated zinc oxalate coordination polymer

Supplementary files

Article information

Article type
Communication
Submitted
12 Jul 2018
Accepted
19 Jul 2018
First published
23 Jul 2018

Dalton Trans., 2018,47, 11308-11312

A paraelectric–ferroelectric phase transition of an organically templated zinc oxalate coordination polymer

K. Pasińska, A. Piecha-Bisiorek, V. Kinzhybalo, A. Ciżman, A. Gągor and A. Pietraszko, Dalton Trans., 2018, 47, 11308 DOI: 10.1039/C8DT02859A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements