Synthesis and Characterization of Some Novel Schiff Base Complexes of Oxovanadium(IV) Cation
Table 1
Physical and analytical data of the complexes.
Complex
Empirical formula
Decomp. temp. (°C)
C% found (Calcd)
H% found (Calcd)
N% found (Calcd)
V% found (Calcd)
S% found (Calcd)
BM (300°C)
VO(L1)SO4
C20H17N4VSO6F3
212
43.6 (43.7)
3.0 (3.1)
10.1 (10.2)
9.2 (9.3)
5.7 (5.8)
1.73
VO(L2)SO4
C20H17N4VS2O5F3
213
42.4 (42.5)
2.9 (3.0)
9.9 (9.9)
9.0 (9.0)
11.2 (11.3)
1.74
VO()SO4
C25H21N4VSO6F3
215
48.9 (48.9)
3.4 (3.5)
9.0 (9.1)
8.2 (8.3)
5.1 (5.2)
1.72
VO()SO4
C30H23N4VSO6F3
217
53.2 (53.3)
3.3 (3.4)
8.3 (8.3)
7.5 (7.5)
4.5 (4.6)
1.75
VO()SO4
C28H18N4VS2O6F6
219
45.6 (45.7)
2.4 (2.5)
7.5 (7.6)
6.8 (6.9)
8.6 (8.7)
1.74
VO()SO4
C35H25N4VSO6F3
227
57.0 (57.0)
3.3 (3.4)
7.5 (7.6)
6.9 (6.9)
4.3 (4.4)
1.73
VO()SO4
C25H21N4VS2O5F3
220
47.6 (47.7)
3.3 (3.4)
8.8 (8.9)
8.0 (8.1)
10.1 (10.2)
1.72
VO()SO4
C30H23N4VS2O5F3
218
52.0 (52.1)
3.3 (3.4)
8.1 (8.1)
7.4 (7.4)
9.2 (9.3)
1.76
VO()SO4
C28H18N4VS3O5F6
221
44.7 (44.8)
2.3 (2.4)
7.4 (7.5)
6.7 (6.8)
12.7 (12.8)
1.75
VO()SO4
C35H25N4VS2O5F3
218
55.7 (55.8)
3.2 (3.3)
7.4 (7.4)
6.8 (6.8)
8.4 (8.5)
1.74
L1: ligand derived by condensation of 4,4,4-trifluro-1-(2-furyl)-1,3-butanedione and p-phenylenediamine (1:2); L2: ligand derived by condensation of 4,4,4-trifluro-1-(2-thenyl)-1,3-butanedione and p-phenylenediamine (1:2); : macrocyclic ligand derived by condensation of L1 with acetylacetone; : macrocyclic ligand derived by condensation of L1 with benzoylacetone; : macrocyclic ligand derived by condensation of L1 with thenoyltrifluoroacetone; : macrocyclic ligand derived by condensation of L1 with dibenzoylmethane; : macrocyclic ligand derived by condensation of L2 with acetylacetone; : macrocyclic ligand derived by condensation of L2 with benzoylacetone; :macrocyclic ligand derived by condensation of L2 with thenoyltrifluoroacetone; : macrocyclic ligand derived by condensation of L2 with dibenzoylmethane.