Improved syntheses of high hole mobility phthalocyanines: A case of steric assistance in the cyclo-oligomerisation of phthalonitriles

Beilstein J Org Chem. 2012:8:120-8. doi: 10.3762/bjoc.8.14. Epub 2012 Jan 24.

Abstract

It has been shown that the base-initiated cyclo-oligomerisation of phthalonitriles is favoured by bulky α-substituents making it possible to obtain the metal-free phthalocyanine directly and in high yield. The phthalocyanine with eight α-isoheptyl substituents gives a high time-of-flight hole mobility of 0.14 cm(2)·V(-1)·s(-1) within the temperature range of the columnar hexagonal phase, that is 169-189 °C.

Keywords: Thorpe–Ingold effect; high hole mobility; phthalocyanine; steric assistance; time-of-flight.