Abstract
The copper(II)2,2'-bipyridine (bipy)-2-cyanoguanidine (cnge) complexes, [Cu(bipy)(cnge)(2)(FBF3)(2)] 1, [Cu(bipy)(cnge)Cl-2]. H2O 3, and [Cu(bipy)(2)(cnge)][BF4](2) . H2O 5, have been synthesised and structurally characterised. Their copper(II) co-ordination geometries vary from cis-distorted tetragonally elongated octahedral (for 1) through square pyramidal(for 3) to trigonal bipyramidal (for 5). That ill 1 comprises one bidentate chelating bipy and two monodentate cnge as equatorial ligands plus two BF4- anions as axial ligands, that in 3 comprises one bidentate chelating bipy, one monodentate cnge and one chlorine in equatorial positions with the other chlorine in the axial position, and that in 5 comprises two bidentate bipy ligands which straddle equatorial and axial sites and an equatorially located monodentate cnge ligand. The weak Cu-FBF3- co-ordinate bond in 1 is supported by an intramolecular N-H ... F hydrogen bond from an adjacent cnge amino moiety. A similar intramolecular N-H ... Cl interaction occurs in 3. Intermolecular hydrogen bonds exist in all three complexes; they include pairs of N-H ... N donor-acceptor interactions between centrosymmetrically related cnge ligands (in 3) and double N-H ... F contacts(in 5) as well as more conventional single N-H ... X (X = F, Cl, O or N) interactions.
| Original language | English |
|---|---|
| Pages (from-to) | 2667-2672 |
| Number of pages | 6 |
| Journal | JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS |
| Issue number | 15 |
| Publication status | Published - 7 Aug 1997 |
Keywords
- COORDINATIVELY UNSATURATED COPPER(I)
- CRYSTAL-STRUCTURE
- TETRAFLUOROBORATE
- CATION