Invited for the cover of this issue is Shinji Toyota and co-workers at Tokyo Institute of Technology and Okayama University of Science. The image depicts a spirally rising dragon to represent the helical molecular structures in the manuscript. Read the full text of the article at 10.
View Article and Find Full Text PDFPolycyclic aromatic compounds consisting of four or five fused anthracene units were synthesized by PtCl -catalyzed cycloisomerization as novel long expanded helicenes. These compounds have helical structures with significant stacking of the terminal anthracene moieties at 0.33 nm interlayer distance.
View Article and Find Full Text PDFPolycyclic aromatic hydrocarbons consisting of three fused anthracene units were designed as new π-conjugated compounds having helical structures. These expanded helicenes were synthesized by Pt-catalyzed cycloisomerization of the corresponding ethynyl-substituted precursors. The nonplanar and helical structure was confirmed by X-ray analysis and DFT calculations, and the barrier to helical inversion was estimated to be 34 kJ mol .
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