Abstract
Structural analyses of [Pd(C11H10N2O2)2]Cl 2.4H2O, (I), and [Au(C11H10N2O2)Cl2]Cl, (II), revealed that both metals are in square-planar coordination environments. The Pd atom in (I) is coordinated equatorially by four N-atom donors and has two long-range Pd⋯O interactions which lead to approximate pseudo-octahedral geometry. The Au complex achieves a coordination number of four with two N and two Cl donors, however, a weak long-range intramolecular axial interaction accounts for the fifth coordination site to make the species pseudo-square pyramidal.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 707-710 |
| Number of pages | 4 |
| Journal | Acta Crystallographica Section C: Crystal Structure Communications |
| Volume | 53 |
| Issue number | 6 |
| DOIs | |
| State | Published - Jun 15 1997 |
All Science Journal Classification (ASJC) codes
- General Biochemistry, Genetics and Molecular Biology
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