Journal
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
Volume 189, Issue -, Pages 80-85Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.saa.2017.07.059
Keywords
Metalloporphyrins; Mixed beta-octasubstituted Zn(II)-porphyrins; Solvent effect; Electronic absorption; Ligand binding; Equilibrium constants
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Funding
- Department of Science and Technology, Govt. of India [R/S1/IC-30/2007]
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A series of mixed beta-octasubstituted Zn(II)-porphyrins, 2,3,12,13-tetra(chloro/cyano/methyl)-5,7,8,10,15,17,18,20-octaphenylporphinato zinc(II), ZnTPP(Ph)(4)X-4 (X=CN, Cl and CH3) have been examined by electronic absorption spectroscopy in various solvents. These Zn(II)-porphyrins exhibited varying degree of red-shift of absorption bands as high as 20-30 nm in 'B' band and 50-60 nm in longest wavelength band, 'Q(0,0)' band in polar solvents relative to that found in nonpolar solvents. The red-shift of B and Q(0,0) bands showed an unusual trend, ZnTPP(Ph)(4)(CN)(4)>ZnTPP(Ph)(4)(CH3)(4)>ZnTPP(Ph)(4)Cl-4 but fails to follow an anticipated anodic shift in first porphyrin ring oxidation (vs Ag/AgCl) potential: ZnTPP(Ph)(4)(CN)(4) (1.02V)>ZnTPP(Ph)(4)Cl-4 (0.74V)>ZnTPP(Ph)(4)(CH3)(4) (0.38V). Such a trend suggests the combined effect of non-planarity of the macrocycle and electronic effect of the peripheral substituents. The equilibrium constants for the binding of nitrogenous bases with the Zn(II)-porphyrins showed as high as twenty fold increase for ZnTPP(Ph)(4)X-4 (X=Br and CN) relative to ZnTPP(Ph)(4)(CH3)(4) and follow the order: ZnTPP(Ph)(4)(CN)(4)>ZnTPP(Ph)(4)Br-4>ZnTPP(Ph)(4)(CH3)(4)<= ZnTPP which is approximately in line with an increase in anodic shift of their first ring redox potentials (ZnTPP(Ph)(4)(CN)(4) (1.02V)>ZnTPP(Ph)(4)Br-4 (0.72V)>ZnTPP (0.84V)>ZnTPP(Ph)(4)(CH3)(4)) (0.38V). (C) 2017 Elsevier B.V. All rights reserved.
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