Ferroelectric Order in the Chiral Coordination Polymers [Ln2(L*)2(ox)2(H2O)2] with Ln=Gd3+ or Dy3+, L*=((S, S)‐1,3‐bis(1‐Carboxylethyl)imidazolium and Ox=Oxalate.

Author:

Farger P.1ORCID,Leuvrey C.1,Lenertz M.1ORCID,Taupier G.12,Dorkenoo K. D.1,Ihiawakrim D.1ORCID,Cherifi‐Hertel S.1ORCID,Rogez G.1ORCID,Rabu P.1ORCID,Delahaye E.13ORCID

Affiliation:

1. Institut de Physique et Chimie des Matériaux de Strasbourg UMR 7504 Université de Strasbourg, CNRS 23 rue du Loess 67034 Strasbourg France

2. Synthèse Caractérisation ANalyse de la MATière (ScanMAT) - UAR CNRS 2025 CNRS Université de Rennes 1 Beaulieu - Bâtiment 10 A, 263 avenue du Général Leclerc 35042 Rennes France

3. Laboratoire de Chimie de Coordination CNRS Université de Toulouse UPS INPT 205 route de Narbonne 31077 Toulouse France

Abstract

AbstractWe evidence the ferroelectricity of two isostructural magnetic coordination networks obtained from a chiral imidazolium dicarboxylate salt ((S, S)‐1,3‐bis(1‐carboxylethyl)imidazolium or [HL*]) and Gd3+ or Dy3+ ions in presence of oxalic acid (H2ox). The two compounds exhibit a chiral structure P1 and ferroelectric properties. The crystallographic study shows that the Dy based‐compound is isostructural to the Gd analog. The non‐centrosymmetry of the two samples was further checked by means of nonlinear optical spectroscopy. The room temperature ferroelectric character of the compounds has been investigated through by an original method, derived from that used for thin films, made possible by preparing the sample as thin slices of resin containing inclusions of the coordination compounds.

Funder

Agence Nationale de la Recherche

Publisher

Wiley

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