Perfluorinated porphyrazines 1: Synthesis and UV-vis spectral study of perfluorinated octaphenylporphyrazine and its indium(III) complex, [MPA(F5Ph)8](M = 2H, InIII(OH))

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.

1977 ◽  
Vol 30 (2) ◽  
pp. 443 ◽  
Author(s):  
DJ Collins ◽  
CW Tomkins

Treatment of a chloroform solution of ethyl 5-hydroxy-7a-methyl-1-oxo- 2,6,7,7a-tetrahydro-1H-indene-4-carboxylate with dry hydrogen chloride at room temperature gave ethyl 5-hydroxy-7a-methyl-1-oxo-cis-3a,6,7,7a- tetrahydro-1H-indene-4-carboxylate, and the corresponding trans-hydrindan in the ratio 9 : 1. Hydrogenation of this mixture gave ethyl 5-hydroxy-7a-methyl-1-oxo-cis-3a,6,7,7a-tetrahydroindan-4-carboxylate, and ethyl t-7a-methyl-1,5-dioxo-r-3a,4,5,6,7,7a-hexa-hydroindan-c-4a- carboxylate, which were characterized by conversion into the cis and trans isomers of 7a-methylperhydroindan-1,5-dione, respectively.


1984 ◽  
Vol 49 (3) ◽  
pp. 680-683 ◽  
Author(s):  
Bohumil Hájek ◽  
Dagmar Sýkorová ◽  
Jiří Chyba

The λ-C1-cis(N), δ-C1-cis(N), λ-C2-cis(N) and δ-C2-cis(N) isomers of the complex K[Co((S)-Pro)2CO3] were chromatographically separated and characterized by their electronic absorption spectra and CD spectra.


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