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Abstract
The selective synthesis of multiply functionalized phthalocyanines (Pcs) as single regioisomers remains challenging. We report our approach for the selective synthesis of C4h Pcs bearing different α- and β-substituents. These C4h phthalocyanines demonstrate a more general route to octa-substituted Pcs with both function and controlled symmetry.
Supplementary materials
Title
Electronic Supplementary Information
Description
General experimental details, synthetic details, NMR data, photophysical data and X-ray crystallography data
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