Second sphere coordination complexes via hydrogen bonding: Synthesis, spectroscopic characterisation of [trans-Co(en)2Cl2]CdX4 (X=Br or I) and single crystal X-ray structure determination of [trans-Co(en)2Cl2]CdBr4
β Scribed by Raj Pal Sharma; Rajni Sharma; Ritu Bala; Juan M. Salas; Miguel Quiros
- Publisher
- Elsevier Science
- Year
- 2006
- Tongue
- English
- Weight
- 251 KB
- Volume
- 794
- Category
- Article
- ISSN
- 0022-2860
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β¦ Synopsis
In an effort to explore [trans-Co(en) 2 Cl 2 ] C as anion receptor for tetrabromocadmate and tetraiodocadmate ion, green coloured single crystals of [trans-Co(en) 2 Cl 2 ]CdBr 4 I and [trans-Co(en) 2 Cl 2 ]CdI 4 II have been obtained by slowly mixing the separately dissolved transdichlorobis(ethylenediamine)cobalt(III) chloride with potassium tetrabromocadmate and tetraiodocadmate in aqueous medium in 2:1 molar ratio. The newly synthesized complex salt was characterized on the basis of elemental analysis and spectroscopic techniques (IR, UV/visible, 1 H and 13 C NMR). Single crystal X-ray structure determination of [trans-Co(en) 2 Cl 2 ] 2 CdBr 4 revealed that it crystallizes in the orthorhombic space group Pbca with aZ18.6201(10), bZ12.0872(6), cZ24.0877(12) A Λ, VZ5421.3(5) A Λ3, ZZ8, RZ0.0727. Supramolecular hydrogen bonding networks between ionic groups: bromide ions of tetrabromocadmate group and NH groups of coordinated ethylenediamine molecules, i.e. N-H/Br K interactions by second sphere coordination besides electrostatic forces of attraction have been observed. This suggests that [trans-Co(en) 2 Cl 2 ] C is a promising anion receptor for the tetrabromocadmate.
π SIMILAR VOLUMES
The authors deeply regret that the following error had not been detected before the publishing of the paper. In Table 1, compound 1, the unit cell constants and the cell volume should read: a = 13.3250(4), b = 10.0780(3), c = 13.5170(4), b = 98.888(2), and V = 1793.39(9).