American Chemical Society
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Helically Locked Tethered Twistacenes

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posted on 2018-06-15, 00:00 authored by Anjan Bedi, Linda J. W. Shimon, Ori Gidron
Twisting linear acenes out of planarity affects their electronic and optical properties, and induces chirality. However, it is difficult to isolate the effect of twisting from the substituent effect. Moreover, many twistacenes (twisted acenes) readily racemize in solution. Here, we introduce a series of twistacenes having an anthracene backbone diagonally tethered by an n-alkyl bridge, which induces a twist of various angles. This allows us to systematically monitor the effect of twisting on electronic and optical properties. We find that absorption is bathochromically shifted with increasing twist, while fluorescence quantum efficiency drops dramatically. The tethered twistacenes were isolated to their enantiomerically pure form, displaying strong chiroptical properties and anisotropy factor (g-value). No racemization was observed even upon prolonged heating, rendering these tethered twistacenes suitable as enantiopure helical building units for π-conjugated backbones.