5,10,15,20-TETRACYMANTRENYLPORPHYRIN ANA 5,10,15-TRICYMANTRENYLCORROL

Citation
Nm. Loim et al., 5,10,15,20-TETRACYMANTRENYLPORPHYRIN ANA 5,10,15-TRICYMANTRENYLCORROL, Russian chemical bulletin, 43(5), 1994, pp. 871-873
Citations number
8
Categorie Soggetti
Chemistry
Journal title
ISSN journal
10665285
Volume
43
Issue
5
Year of publication
1994
Pages
871 - 873
Database
ISI
SICI code
1066-5285(1994)43:5<871:5A5>2.0.ZU;2-3
Abstract
The reaction of pyrrol with cymantrenecarboxaldehyde in acetic acid re sults in 5,10,15,20-tetracymantenylporphyrin (1) and 5,10,15-tricymant renylcorrol (2). Porphyrin synthesis according to Lindsey's method onl y affords compound 1 in high yield. The NH-tautomerism in molecules 1 and 2 was investigated by dynamic NMR spectroscopy. It was shown that free rotation of the (CO)(3)MnC5H4 fragments around the bond with the carbon atoms in the meso-positions of the porhpyrin macrocycle occurs.