Symmetric, twinned, and double-decker phthalocyanines substituted by trialkylated pentaerythritol

Authors

MUZAFFER KÖÇ
AYŞE GÜL GÜREK
FABIENNE DUMOULIN
VEFA AHSEN

DOI

10.3906/kim-1202-64

Abstract

Trialkylated pentaerythritol was chosen as a bulky substituent for a set of 3 free-base phthalocyanines: a symmetric, a twinned, and a double-decker derivative. The bulkiness of this substituent lowered the aggregation of the phthalocyanines. The electronic absorptions were comparatively investigated: the twinned phthalocyanine exhibited a significant near-infrared shifted absorption. The neutral radical Eu(III) complex was oxidized by bromine. These 3 phthalocyanines are promising for use as molecular materials.

Keywords

Phthalocyanine, twinned, alkylated pentaerythritol, europium, double-decker, electronic near-infrared delocalization

First Page

493

Last Page

502

Recommended Citation

KÖÇ, MUZAFFER; GÜREK, AYŞE GÜL; DUMOULIN, FABIENNE; and AHSEN, VEFA (2012) "Symmetric, twinned, and double-decker phthalocyanines substituted by trialkylated pentaerythritol," Turkish Journal of Chemistry: Vol. 36: No. 4, Article 1. https://doi.org/10.3906/kim-1202-64
Available at: https://journals.tubitak.gov.tr/chem/vol36/iss4/1