ChemInform Abstract: THE CHEMISTRY OF PYRROLIC COMPOUNDS. XL. A NEW SYNTHESIS OF PROTOPORPHYRINS III AND XIII AND A PROTON NMR STUDY OF THE PREFERRED PATHWAY OF ELECTRON DELOCALIZATION IN THE PORPHYRIN MACROCYCLE

1978 ◽  
Vol 9 (28) ◽  
Author(s):  
P. S. CLEZY ◽  
C. J. R. FOOKES ◽  
S. STERNHELL
1978 ◽  
Vol 31 (3) ◽  
pp. 639 ◽  
Author(s):  
PS Clezy ◽  
CJR Fookes ◽  
S Sternhell

The synthesis of protoporphyrins III and XIII as the dimethyl esters has been completed by an oxidative cyclization of biladiene-ac intermediates. Protoporphyrin III has been converted into deuteroporphyrin III and measurements of the proton coupling constant in the allylic unit, CH3-C=C-H, of this latter porphyrin point to the double bond of this system having a significantly diminished bond order. This finding is in accord with the view that the π-electron delocalization pathway in the porphyrin macrocycle involves the periphery of the molecule.


2000 ◽  
Vol 10 (PR7) ◽  
pp. Pr7-99-Pr7-102 ◽  
Author(s):  
G. Dosseh ◽  
D. Morineau ◽  
C. Alba-Simionesco
Keyword(s):  

1983 ◽  
Vol 14 (11) ◽  
Author(s):  
A. A. FOMICHEV ◽  
V. A. SVOREN' ◽  
N. F. SEPETOV ◽  
A. V. VARLAMOV ◽  
N. S. PROSTAKOV
Keyword(s):  

Langmuir ◽  
1994 ◽  
Vol 10 (3) ◽  
pp. 653-657 ◽  
Author(s):  
Omar A. El Seoud ◽  
Andrei Blasko ◽  
Clifford A. Bunton

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