It was shown on the basis of NMR-H spectra that the addition of proton to dianions of Zn-octaethylchlorine, Zn-octaethylporphin, and Zn-monoasaethioporphyrin results in the formation of products with the structure of alpha-dihydroflorine, alpha-florine, and gamma-florine respectively. This indicates that electron density greatly increases when the anions are formed in the centres which had a decreased density in the initial molecule.

Download full-text PDF

Source

Publication Analysis

Top Keywords

[intermediate reduction
4
reduction products
4
products porphyrins
4
porphyrins structure]
4
structure] basis
4
basis nmr-h
4
nmr-h spectra
4
spectra addition
4
addition proton
4
proton dianions
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!