Parimal Paul, Beena Tyagi, Mohan M. Bhadbhade and Eringathodi Suresh
The reaction of 2,4,6-tris(2-pyridyl)-1,3,5-triazine (tptz) and
RhCl3·3H2O in refluxing ethanol–water
(1:
1) resulted in the hydrolysis of tptz to
bis(2-pyridylcarbonyl)amide anion (bpca) and afforded a complex of
composition [Rh(bpca)2][PF6] 1. However,
hydrolysis of tptz did not occur when it was treated with
RuCl3·3H2O under similar condition,
yielding instead the complex
[Ru(tptz)2][PF6]2·H2O
2. The molecular structures of 1 and 2 have been established by
single-crystal X-ray analysis. In complex 1 the
bis(2-pyridylcarbonyl)amido moiety functions as a tridentate ligand with
nitrogen donor atoms and is bound to RhIII in a mutually
perpendicular fashion forming a distorted-octahedral geometry around the
metal ion. In complex 2 two tridentate tptz are co-ordinated to
RuII in a similar manner as found for 1. From a comparison of
bond lengths and angles in the co-ordination spheres of 1 and 2 it is
suggested that the electron-withdrawing effect (L→M) of the metal
ion is the predominant factor, rather than angular strain at the
carbonyl carbon atoms, responsible for hydrolysis of tptz.
Electrochemical studies of 1 revealed a metal-based two-electron couple
(RhIII–RhI) at -1.15 V and two
ligand-based redox couples at -1.44 and -1.84 V. In the case
of 2 the RuII–RuIII couple appears at +1.77
V and the ligand-based reduction at -0.62 and -0.80 V which
are significantly positively shifted compared to those of free tptz.