Poly(isocyanide)s prepared by diastereoselective polymerisation of two chiral monomers, which differ only in the presence of a nitro-group adjacent to the stereogenic group, exhibit long range chiral induction, but a surprising influence of a remote substituent on the conformation and stability of the secondary structure in the macromolecules.
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Amabilino et al. (2004) studied this question.
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