Abstract
AbstractThis work presents a general approach for synthesis of substituted [5]‐helical dispiroindeno[2,1‐c]fluorenes based on Rh‐catalyzed intramolecular cyclotrimerization of triynes. This approach was further extended for the first synthesis of configurationally stable [7]‐helical dispiroindeno[2,1‐c]fluorenes. A series of variously substituted derivatives was prepared and their photophysical and electrochemical properties were evaluated. Their fluorescence emission maxima were in the region of 351–428 nm and quantum yields up to 88 % are the highest measured among the full‐carbon helical compounds.
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