Copper Complexes of Dicarboxy-Functionalized Tetramethylcyclam. Crystal Structures of Complexes with the Axial Ligands Perchlorate, Chloride, and Iodide
✍ Scribed by T. Schönherr; E. Weber; W. Seichter
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- German
- Weight
- 118 KB
- Volume
- 627
- Category
- Article
- ISSN
- 0372-7874
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✦ Synopsis
6,4,
4,
perchlorate (2 a) was synthesized via one-step cyclocondensation from bis(N,N'-dimethylethylenediamine-copper(II) perchlorate, formaldehyde and malonic acid. Anion exchange yielded the analogous copper(II) chloride (2 b) and iodide (2 c) complexes. Crystal structures of 2 a±2 c show a square-planar N 4 -co-ordination of the copper(II) ion with RRSS configuration of the nitrogens and perchlorate, chloride or iodide ions weakly co-ordinated axially. Relating to the macroring, the carboxy groups are in trans-position. In 2 a, the packing is typical of parallel strands of complex subunits effected by dimerization of the carboxy groups, while in 2 b and 2 c formation of the supramolecular strands involve hydrogen bond interactions between carboxy groups and halide anions.
📜 SIMILAR VOLUMES
off, washed with ether, and dried in vacuo; yield 27 g. b) H,C,N -+ PS,CI (M
## Abstract The reaction of Cu(AcO)~2~ · H~2~O and tridentate β‐iminoketone ligands yielded four new copper complexes: acetato{4‐{[2‐(dimethylamino)ethyl]amino}pent‐3‐en‐2‐onato}copper(II) (1), triacetato{4‐{[3‐(dimethylamino)‐propyl]amino}pent‐3‐en‐2‐onato}dicopper(II) (2), {4‐{[2‐(dimethylamino)e