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Tetrachloroferrate(III) Complexes of some Organic Diammonium Cations: Structures and Magnetic Properties
Authors:Bruce D. James Dr.  Jerzy Mrozinski Prof. Dr.  Julia Klak  Brian W. Skelton  Allan H. White
Affiliation:1. Department of Chemistry, La Trobe University, Vic. 3086, Australia, Tel.: +61 3 9479 2534, Fax.: +61 3 9479 1399;2. Bruce D. James, Department of Chemistry, La Trobe University, Vic. 3086, Australia, Tel.: +61 3 9479 2534, Fax.: +61 3 9479 1399;3. Jerzy Mrozinski, Faculty of Chemistry, University of Wroclaw, F. Joliot Curie 14, PL‐50‐383 Wroclaw, Poland, Tel.: +48 71 375 7307, Fax.: +48 71 328 2348;4. Wroclaw/Poland, University of Wroclaw, Department of Chemistry;5. Crawley/Western Australia, University of Western Australia, School of Biomedical, Biomolecular and Chemical Sciences, Chemistry M313
Abstract:With aqueous acidic iron(III) chloride, the three diamines ethylenediamine (en), tetramethylethylenediamine (tmeda) and 4:4′‐tetramethyldiaminodiphenylmethane (ddmp) yield the aquapentachloroferrate(III) and a pair of [FeCl4]? Cl? double salts, respectively. Their structures indicate that N–H···Cl hydrogen bonding is present, but the Fe···Fe distances are all quite long. The magnetic data show that, while all the materials display antiferromagnetic coupling on cooling, in none of the cases was any transition observed above 1.8 K.
Keywords:Iron  Aquapentachloroferrate(III)  Ethylenediammonium salt  Tetrachloroferrate(III) double salts  Tetramethylethylenediammonium  4:4′  ‐Tetramethyldiammoniumdiphenylmethane  Crystal structures  Magnetic properties
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