Abstract
Polynuclear chromium ascorbate complexes were isolated and physicochemically analyzed in a comparative manner with their mononuclear analog (1). Characterization by elemental analysis, electronic, vibrational, 13C-n.m.r and mass spectroscopies, and variable temperature magnetic susceptibility studies, allowed structural proposals for the binuclear, [Cr 2(μ-OH)2(H2O)(C6H 7O6)3(OH)] • 4H2O (2), and trinuclear, [Cr3(μ-O)3(H2O) 6(C6H7O6)3] • 4 H2O (3) complexes. The pseudo-octahedral Cr III centers were suggested to be connected through hydroxo bridges in (2) and in (3) by oxo bridges forming a hexocyclic ring.
| Original language | English |
|---|---|
| Pages (from-to) | 451-459 |
| Number of pages | 9 |
| Journal | Transition Metal Chemistry |
| Volume | 30 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - May 2005 |
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