Scheme 1
: Synthesis and chemical structures of ligands
L1
and
L2
1)
(N,N'E,N,N'E)-N,N'-(1,3-phenylenebis(methanylylidene))bis(5-nitrobenzo[d]thiazoL2-
amine
(L1).
A reaction between nitro-benzothiazole (2.0 mmol, 0.390 g) and 1,3-
benzenedicarboxaldehyde (1.0 mmol, 0.134 g) leads to the formation of
L1
; dark yellow
powder; yield, 0.482 g (92 %); mp-213 °C; FTIR (cm
-1
): 3314 (C-H aromatic), 1686 (C=N),
1525 (C=C), 1287 (N=O), 1231 (C-N), 1127 (C-C), 786 (C-H), 598 (C-S). UV/vis
(λ
max
):
229 nm, 342 nm.
1
H NMR (
ppm): 9.16 (s, 2H), 8.62 (s. 2H), 8.47 (s, 1H), 8.27 (d, 2H),
8.32 (d, 2H), 8.10 (d, 2H), 7.76 (t, 1H); Mass (ESI-MS, 100 %): 489.49 (Calculated: 488.04)
Anal. for C
22
H
12
N
6
O
4
S
2
; Elemental analysis: C 54.17; H 2.39; N 17.11; O 13.10; S 13.07
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