Modification of Phosphoryl Substituents of Phthalocyanines As a Route to Targeted Tuning of Lipophilic-Hydrophilic Properties


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription Access

Abstract

О′,О′-Diethyl-[2-(3,4-dicyanophenoxy)phenyl]phosphonate has been synthesized for the first time and introduced in template condensation on lithium and zinc cations to prepare a series of new neutral and acidic phthalocyanines containing four fragments of 2-oxyphenylphosphonic acid. A scheme of modification of the peripheral substituents at the phosphoryl group was developed allowing a targeted synthesis of phthalocyanine ligands and complexes soluble in organic solvents or aqueous media.

About the authors

I. P. Kalashnikova

Institute of Physiologically Active Compounds

Author for correspondence.
Email: ikalashn@ipac.ac.ru
Russian Federation, Severnyi proezd 1, Chernogolovka, 142432

D. V. Baulin

Frumkin Institute of Physical Chemistry and Electrochemistry

Email: ikalashn@ipac.ac.ru
Russian Federation, Moscow

V. E. Baulin

Institute of Physiologically Active Compounds; Frumkin Institute of Physical Chemistry and Electrochemistry

Email: ikalashn@ipac.ac.ru
Russian Federation, Severnyi proezd 1, Chernogolovka, 142432; Moscow

A. Yu. Tsivadze

Frumkin Institute of Physical Chemistry and Electrochemistry

Email: ikalashn@ipac.ac.ru
Russian Federation, Moscow


Copyright (c) 2018 Pleiades Publishing, Ltd.

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies