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SPECTROSCOPIC INVESTIGATION ON THE TRICHLORO-, TETRAHALO- AND MIXED-TETRAHALO-CUPRATES OF THE PIPERIDINIUM AND MORPHOLINIUM CATIONS

1976; Taylor & Francis; Volume: 5; Issue: 4 Linguagem: Inglês

10.1080/00958977608073010

1029-0389

Giuseppe Marcotrigiano, Ledi Menabue, Gian Carlo Pellacani,

Crystal structures of chemical compounds

Abstract Some halo- and mixed-halo-cuprates of the type CuCl3 · L, CuCl4 · L2, CuCl3Br · L2, CuCl2Br2 · L2 and CuBr4 · L2, were prepared and characterized by means of far-i.r., i.r. and n.i.r. spectroscopy, magnetic moments and conductivity measurements. A band at 19000 cm−1, which appears only in the CuCl3 · L complexes, is characteristic of Cu2Cl2- 6 dimer or polymer species. For these complexes and for CuCl4(Morph)2 and CuCl3Br(Morph)2 (Morph = morpholinium cation) an approaching square-planar geometry, while for all the other complexes a distorted-tetrahedral geometry, may be suggested from their spectroscopic properties, compared to those of other tri- and tetra-halo-cuprates of known structure. An intermediate structure between these geometries may be proposed for the CuCl3 · Pipd complex. The planar geometry is probably stabilized by extensive NH … Cl hydrogen bonding interactions greater with the morpholinium cation than with the piperidinium cation. No thermochromic behaviour in the solid state in the 290–370° K temperature range is observed. The room-temperature magnetic moments agree with the proposed configurations.