کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1312671 | 975482 | 2009 | 7 صفحه PDF | دانلود رایگان |

A novel series of linear chain coordination polymers, [NH4][MII(H2PO2)3(H2O)] where M = Mn, Co, Ni, has been obtained by the reaction of divalent metals salts with ammonium pyrophosphite, [NH4][H2PO2], in a methanol–water mixture. They crystallise in the monoclinic P21/n cell and contain polar chains aligned with opposing polarity. Both bridging and terminal monodentate coordination modes are exhibited by the H2PO2-. Two types of hydrogen-bond between a coordinated water and a monodentate H2PO2- connect the chains into a 3D-network. The compounds have been further characterised by IR and UV–Vis spectroscopies, TGA, and their magnetic properties measured. All three compounds exhibit weak antiferromagnetic nearest neighbour interaction. A similar study on the known [FeIII(H2PO2)3] is also reported. Its magnetic susceptibility fits a model for a 1D-antiferromagnet with 2 J/k of 1.20(1) K and g of 2.019(2).
Zig-zag chains of divalent transition metals have been characterised by X-ray crystallography, thermal, optical and magnetic measurements in the salts [NH4][MII(H2PO2)3(H2O)], (Mn, Co and Ni). They are all weakly coupled paramagnets.Figure optionsDownload as PowerPoint slide
Journal: Inorganica Chimica Acta - Volume 362, Issue 5, 1 April 2009, Pages 1428–1434