RESUMO
Synthesis of helically chiral aromatics resulting from fusion of pyrene and [4]- or [5]helicene has been accomplished using photoredox catalysis employing a Cu-based sensitizer as the key step. Photocyclisation experiments for the synthesis of the target compounds were carried out in batch and using continuous flow strategies. The solid-state structures, UV/Vis absorption spectra and fluorescence spectra of the pyrene-helicene hybrids were investigated and compared to that of the parent [5]helicene to discern the effects of merging a pyrene moiety within a helicene skeleton. The studies demonstrated that pyrene-helicene hybrids adopt co-planar or stacked arrangements in the solid state, in contrast to the solid-state structure of the parent [5]helicene. The UV/Vis and fluorescence spectra of the pyrene-helicene hybrids exhibited strong red-shifts when compared to the parent [5]helicene. DFT calculations suggest that the strategy of extending the π surface in the y axis of the helicenes increased their HOMO levels while also decreasing their LUMO levels, resulting in significantly reduced band gaps.
RESUMO
Conditions for the palladium-catalyzed direct arylation of a wide range of heterocycles with aryl bromides are reported. Those conditions employ a stoichiometric ratio of both coupling partners, as well as a substoichiometric quantity of pivalic acid, which results in significantly faster reactions. An evaluation of the influence of the nature of the aryl halide has also been carried out.
Assuntos
Compostos Heterocíclicos/química , Compostos Heterocíclicos/síntese química , Hidrocarbonetos Bromados/química , Paládio/química , Catálise , Estrutura Molecular , EstereoisomerismoRESUMO
A photochemical synthesis of [5]helicene employing a copper-based sensitizer 7 has been developed that avoids the disadvantages associated with the traditional UV light mediated method. The visible light mediated synthesis uses common glassware and a simple household light bulb without the competing formation of [2 + 2] cycloadducts, regioisomers, or the overoxidation product benzo[ghi]perylene 3. Preliminary results show that the reaction time can be significantly reduced through the use of a continuous flow strategy.