Published March 2007 | Version v1
Journal article

Crystal structure and magnetic properties of hydrated and dehydrated nickel(II)-pyromellitate

  • 1. Department of Physics and Electronics, Kyushu Institute of Technology, Kitakyushu, Fukuoka 804-8550 (Japan)
  • 2. Laboratoire de Chimie de Coordination Organique, UMR 7140-CNRS, Universite Louis Pasteur, 67000 Strasbourg (France)

Description

Ni2(H2O)4PM.2H2O, where PM is benzene-1,2,4,5-tetracarboxylate, forms square-grid layers with Ni-OCO-Ni bridges that are connected to one another by the benzene moiety. It consists of ferromagnetic layers coupled antiferromagnetically to their neighbors with a long-range Neel ordering at 3 K. A critical field of 1300 Oe suffices to reverse all the moments to a ferromagnetic state. On dehydration to Ni2(H2O)2PM the structure is transformed irreversibly to chains connected by benzene and the magnetic behavior is that of a paramagnet with very weak coupling. By the rehydration of the latter to Ni2(H2O)2PM.2H2O, the structure hardly changes but the magnetism recovers showing T N at 3 K

Additional details

Identifiers

DOI
10.1016/j.jmmm.2006.10.455;
PII
S0304-8853(06)01664-7;

Publishing Information

Journal Title
Journal of Magnetism and Magnetic Materials
Journal Volume
310
Journal Issue
2
Journal Page Range
p. 1435-1437
ISSN
0304-8853
CODEN
JMMMDC

Conference

Title
17. international conference on magnetism
Dates
20-25 Aug 2006
Place
Kyoto (Japan)

INIS

Country of Publication
Netherlands
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
39029751
Subject category
S36: MATERIALS SCIENCE;
Resource subtype / Literary indicator
Conference
Descriptors DEI
BENZENE; COUPLING; CRITICAL FIELD; CRYSTAL STRUCTURE; DEHYDRATION; HYDRATES; LAYERS; MAGNETIC PROPERTIES; MAGNETISM; NICKEL COMPLEXES; POLYMERS; PRESSURE DEPENDENCE
Descriptors DEC
AROMATICS; COMPLEXES; HYDROCARBONS; MAGNETIC FIELDS; ORGANIC COMPOUNDS; PHYSICAL PROPERTIES; TRANSITION ELEMENT COMPLEXES

Optional Information

Copyright
Copyright (c) 2006 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.