Bathochromic shift of the Q-bands of octakis(p-t-butylbenzyloxy)phthalocyanines with magnesium(II), nickel(II) and copper(II) in a solvent mixture of chloroform and acetic acid

Author:

Kasuga Kuninobu1,Yashiki Katsuyori1,Sugimori Tamotsu1,Handa Makoto1

Affiliation:

1. Department of Materials Science, Faculty of Science and Engineering, Shimane University, Matsue 690-8504, Japan

Abstract

1,4,8,11,15,18,22,25-octakis(p-t-butylbenzyloxy)phthalocyanine complexes of magnesium(II), nickel(II) and copper(II) were prepared by refluxing the propanol solution of 3,6-di(p-t-butylbenzyloxy)phthalonitrile in the presence of magnesium turnings. The complexes showed intense Q-bands between 740 and 750 nm in chloroform. The magnesium(II) complex showed an additional weak band at 807 nm in chloroform, while the nickel(II) and copper(II) did not. The Q-band of the magnesium(II) species was red-shifted with increase of acetic acid in the solvent mixture of chloroform and acetic acid; 745, (765, 807) and (810, 868 nm) in chloroform, 0.1% (v/v) acetic acid and 60% (v/v) acetic acid, respectively. The magnesium(II) complex has bands at 900 and 999 nm in trifluoroacetic acid. In the solvent mixture of 1% (v/v) acetic acid, the red-shift of the Q-band was larger for the magnesium(II) derivative, a little for the nickel(II) and scarcely for the copper(II), respectively. The shift was explained by protonation of the external nitrogen atoms of the phthalocyanine ring.

Publisher

World Scientific Pub Co Pte Lt

Subject

General Chemistry

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