Issue 10, 2016

Slipped-cofacial J-type phthalocyanine dimers as potential non-linear absorbers for optical limiting applications

Abstract

We found, for the first time, that in the presence of HClO4, a slipped-cofacial magnesium J-type phthalocyanine dimer is subjected to demetallation, providing a thermally stable metal-free derivative, as proven by NMR and UV/Vis spectroscopy, as well as by MALDI-TOF mass spectrometry. Our thermoanalytical study demonstrated the high thermal stability of the dimeric ligand (up to 614 °C). The presence of tert-butyl substituents in the dimeric structures allowed us to discover, with the help of field emission scanning electron microscopy (FE-SEM), ordered phases, represented as threads composed of about 200 nm diameter circles, unlike the corresponding monomers, in which similar circles or triangles are scattered randomly. The interaction of the metal-free dimer with magnesium acetate gave an initial dimeric complex with intrinsic spectral properties. Simulation of the optical limiting (OL) properties using the finite field TDDFT (FF-TDDFT) approach (PBE/aug-cc-pVDZ) revealed that the limiting effect for J-type dimers is more pronounced in the visible region, whereas in the near-IR region, at low input fields, they can be used as linear optical filters.

Graphical abstract: Slipped-cofacial J-type phthalocyanine dimers as potential non-linear absorbers for optical limiting applications

Supplementary files

Article information

Article type
Paper
Submitted
15 Apr 2016
Accepted
04 Aug 2016
First published
04 Aug 2016

New J. Chem., 2016,40, 8262-8270

Slipped-cofacial J-type phthalocyanine dimers as potential non-linear absorbers for optical limiting applications

A. Yu. Tolbin, A. V. Dzuban, E. V. Shulishov, L. G. Tomilova and N. S. Zefirov, New J. Chem., 2016, 40, 8262 DOI: 10.1039/C6NJ01187J

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