A spectrophotometric and thermodynamic study of the sitting-atop complex formation from reaction between free base meso-tetraarylporphyrins and zirconyl nitrate in chloroform solution

Author(s):  
Hossein Dehghani ◽  
Mohammad Reza Mansournia
2003 ◽  
Vol 44 (29) ◽  
pp. 5515-5517 ◽  
Author(s):  
Jeroni Morey ◽  
Pablo Ballester ◽  
Miquel Angel Barceló ◽  
Antoni Costa ◽  
Pere M Deyà

2013 ◽  
Vol 17 (08n09) ◽  
pp. 905-912 ◽  
Author(s):  
Pavel A. Stuzhin ◽  
Maksim Yu. Goryachev ◽  
Svetlana S. Ivanova ◽  
Anna Nazarova ◽  
Igor Pimkov ◽  
...  

Novel perfluorinated porphyrazine has been prepared as indium(III) complex of octa(pentafluorophenyl)porphyrazine by cyclotetramerization of 1,2-dicyano-1,2-bis(pentafluorophenyl)-ethylene (mixture of cis- and trans-isomers) with basic indium(III) acetate in a melt. The In III complex is stable in trifluoroacetic and sulfuric acids, but is easily demetalated with formation of the free-base in a chloroform solution containing HCl or slighly acidified with CF 3 COOH in the presence of tetraalkylammonium chloride as a catalyst. Perfluorination of octaphenylporphyrazine macrocycle leads to a hypsochromic shift of the Q-band maxima in the electronic absorption spectra, to drastic decrease of the basicity of meso-nitrogen atoms of porphyrazine macrocycle and to increase of the acidity of the internal NH -groups.


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