Two structural isomers of the dicyanamide (dca, N(CN) ؊ 2 ) complex [Cu(dca) 2 (pyz)] n (pyz ؍ pyrazine) were prepared from aqueous solution and crystals were grown by slow di4usion and gel techniques. Crystal data: -[Cu(dca) 2 (pyz)] n , CuC 8 H 4 N 8 , monoclinic, Pn, Z ؍ 16, a ؍ 24.2549(7)
Synthesis, Structural Isomerism, and Magnetism of the Coordination Polymers [M(dca)2pyz], M=Mn, Fe, Co, Ni and Zn, dca=Dicyanamide (N(CN) −2), and pyz=Pyrazine
✍ Scribed by Paul Jensen; Stuart R. Batten; Boujemaa Moubaraki; Keith S. Murray
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- English
- Weight
- 465 KB
- Volume
- 159
- Category
- Article
- ISSN
- 0022-4596
No coin nor oath required. For personal study only.
✦ Synopsis
The coordination polymers [M(dca) 2 pyz] (M ؍ Mn, Fe, Co, Ni, Zn) have been synthesized and characterized by singlecrystal and powder X-ray di4raction. Two isomers have been observed. The compounds contain two interpenetrating 3D -Po related networks. Bidentate dca ligands bridge the metal atoms to form square-grid-like M(dca) 2 sheets, with the pyrazine ligands linking these sheets together to form the -Po-like 3D networks. The compounds contain interdigitated 2D sheets. The sheets consist of 1D chains of M(dca) 2 connected together by the pyrazine ligands. The compounds display an interesting phase change that simultaneously induces twinning of the crystals. At room temperature the structures are orthorhombic Pnma and contain dynamic disorder of the dca ligands. However, on cooling (e.g., to 123 K) the structures become monoclinic P2 1 /n with the dca ligands ordered, but since domains within each crystal order di4erently, this results in pseudo-merohedral twinning. Variable temperature and variable 5eld magnetic studies have shown that these compounds display weak antiferromagnetic coupling between the high-spin metal centers. Only in the case of -[Mn(dca) 2 pyz] is there evidence for 3D antiferromagnetic order occurring below 2.7 K.
📜 SIMILAR VOLUMES
## Abstract We report the synthesis, crystal structures, and spectral, thermal, and magnetic properties of a family of metal–organic perovskite ABX~3~, [C(NH~2~)~3~][M^II^(HCOO)~3~], in which A=C(NH~2~)~3~ is guanidinium, B=M is a divalent metal ion (Mn, Fe, Co, Ni, Cu, or Zn), and X is the formate