Answers are grounded in this paper and cite their sources.
The novel concept for the autoamplification of molecular chirality, wherein the amplification proceeds through the induction of supramolecular chirality, is presented. A solution of prochiral, ring-open diarylethenes is doped with a small amount of their chiral, ring-closed counterpart. The molecules co-assemble into helical fibers through hydrogen bonding and the handedness of the fibers is biased by the chiral, ring-closed diarylethene. Photochemical ring closure of the open diarylethene yields the ring-closed product, which is enriched in the template enantiomer.
No takes yet. Share an insight, caveat, or question.
Dijken et al. (2014) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: