Research Article

Synthesis and Spectroscopic Studies of Axially Ligated Zn(II)5,10,15,20-meso-tetra(p-chlorophenyl)porphyrin with Oxygen and Nitrogen Donors

Table 1

Main Infrared absorption frequencies corresponding to various groups in [X-ZnII-t(p-Cl)PP] [X = phenolates and pyridinates].

EntryCompound (N–H) (C–H) (C–N) (C=C) (C–O) (C=N) (C–Cl) (Zn–NPor) (Zn–NPy) (Zn–O) Other assignments
(cm−1)(cm−1)(cm−1)(cm−s1)(cm−1)(cm−1)(cm−1)(cm−1)(cm−1)(cm−1)

1H2t(p-Cl)PP34992966134015912342798.7
2Zn-t(p-Cl)PP2966.21341.11589.61207.52347798.3470
3phO-Zn-t(p-Cl)PP2960.41350.31584.11206.52339.3798.9474500.7
4p-OCH3phO-Zn-t(p-Cl)PP2962.71337.715901207.22342800.1489496.2ν(C–H) = 2851.1
ν(C–O–C)sym = 1020.2
ν(C–O–C)asym = 1261.3
5p-NH2 phO-Zn-t(p-Cl)PP2964.11351.61589.212052360799.3482496.3ν(NH2)sym = 3298
ν(NH2)asym = 3371
6p-NO2 phO-Zn-t(p-Cl)PP29631351.415901207.32360798.7471496.3ν(NO2)sym = 1345
ν(NO2)asym = 1520
7p-CH3py-Zn-t(p-Cl)PP2964109516402350799.5492617ν(CH3) = 2920
8p-NH2py-Zn-t(p-Cl)PP2965109416522354798.6495618ν(NH2)sym = 3280
ν(NH2)asym = 3450
9p-CNpy-Zn-t(p-Cl)PP2964.01096.11636.72358796490617.4ν(CN) = 2280