The secondary structure of Rh-based stereoregular cis -poly( N -propargylamides) was proposed on the basis of the UV−vis, CD, and IR spectra, the wormlike touched-bead model theory, and a semiempirical molecular orbital calculation. The IR spectra demonstrated the formation of well-ordered intramolecular hydrogen bonding between the pendant amide groups. The relatively red-shified absorption and the intense CD effects indicate that the main chain twists only slightly from coplanarity to exist in a helical conformation with a large helix pitch. Analyzing the intrinsic viscosity of a polymer, (±)-poly( N -propargyl-2-ethylhexanamide), on the basis of the wormlike touched-bead model theory, showed a large helix pitch per monomer unit ( h, 0.2 nm), which also supports the above characteristics that the main chain loosely twists. A semiempirical calculation with the AM1 method showed that the helical conjugated backbone is surrounded by two helically arranged hydrogen-bond strands.
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Nomura et al. (2002) studied this question.
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