Research Article

Axially Ligated Zirconium(IV) Tetraphenylporphyrin: Synthesis, Characterization, and Biological Activity

Table 4

1H NMR data of Zr(TPP)(Y)(X) in CDCl3.

PorphyrinsImino protonsβ-Pyrrole protonsMeso-aryl protonsacac protonsPhenolate protons

Zr(TPP)(acac)(phO)8.94 (s)8.26 (d, 4H, Ho)  
7.79 (d, 4H, Ho)  
7.68–7.79 (m, 12H, Hm, p)
1.46 (s, 6H, )  
4.56 (s, H, HCH)
7.04 (d, 2H, Ho)  
7.14–7.27 (m, 3H, Hm, p)

Zr(TPP)(acac)(p-NH2phO)8.42 (s)7.45 (d, 4H, Ho)  
7.28 (d, 4H, Ho)  
7.11–7.19 (m, 12H, Hm, p)
1.52 (s, 6H, )  
3.85 (s, H, HCH)
6.87 (d, 2H, Ho)  
6.71 (d, 2H, Hm)  
4.85 (s, 2H, HNH)

Zr(TPP)(acac)(p-OCH3phO)8.47 (s)7.50 (d, 4H, Ho)  
7.40 (d, 4H, Ho)  
7.16–7.24 (m, 12H, Hm, p)
1.55 (s, 6H, )
3.89 (s, H, HCH)
6.98 (m, 4H, Ho, m)  
3.43 (s, 3H, )

Zr(TPP)(acac)(p-CH3phO)8.47 (s)7.48 (d, 4H, Ho)  
7.74 (d, 4H, Ho)  
7.15–7.23 (m, 12H, Hm, p)
1.50 (s, 6H, )  
3.89 (s, H, HCH)
6.98 (m, 4H, Ho, m)  
2.18 (s, 3H, )

Zr(TPP)(acac)(p-ClphO)9.34 (s)8.37 (d, 4H, Ho)   
8.18 (d, 4H, Ho)
7.83–7.92 (m, 12H, Hm, p)
1.79 (s, 6H, )  
4.59 (s, H, HCH)
7.12 (d, 2H, Ho)  
7.36 (d, 2H, Hm)

Zr(TPP)(acac)(p-NO2phO)9.36 (s)8.49 (d, 4H, Ho)  
8.21 (d, 4H, Ho)  
7.88–7.97 (m, 12H, Hm, p)
1.81 (s, 6H, )  
4.63 (s, H, HCH)
7.21 (d, 2H, Ho)  
7.42 (d, 2H, Hm)

Zr(TPP)(acac)(o,p-Cl2phO)8.51 (s)8.48 (d, 4H, Ho)  
8.21 (d, 4H, Ho)  
7.95–8.05 (m, 12H, Hm, p)
1.80 (s, 6H, )  
4.64 (s, H, HCH)
7.12 (s, 1H, Ho)  
7.66–7.82 (m, 2H, Hm)

Zr(TPP)(acac)(o,p-(NO2)2phO)9.57 (s)8.57 (d, 4H, Ho)  
8.29 (d, 4H, Ho)  
8.05–8.13 (m, 12H, Hm, p)
2.11 (s, 6H, )  
4.72 (s, H, HCH)
7.22 (s, 1H, Ho)  
7.72–7.86 (m, 2H, Hm)