A chiral substituted acetylene, (s)-2-octyl propiolate, was stereoregularly polymerized using a catalyst, [Rh(nbd)Cl]2, at 40 °C in methanol to give the corresponding helical polymer, Ps2OcP. The changes of (1)H and (13)C NMR spectra in line shapes and splitting patterns were consistently interpreted in terms of restricted rotation around the ester O-*C bond, ~O-*C(ε)H(ε)(R)~, R = a branched CH(ε)3 in the ester side chains rather than the helix inversion with the aid of a 3-site jump model. Three peaks due to the branched methyl H(ε) proton and its C(η) carbon observed at 0 °C suggested the formation of three rotamers called A, B, and C, based on the presence of the contracted helix and stretched helix forms that have an intrinsic helical pitch. Furthermore, an accordion-like helix oscillation (HELIOS) along the main chain axis was proposed to explain the temperature dependence spectral changes observed in (1)H and (13)C NMR, UV-vis, and circular dicromism (CD) spectra. The temperature dependence UV-vis and CD spectra of Ps2OcP corroborate the presence of contracted and stretched one-handed helix sense polymers in solution in which the helical pitches and their persistence lengths depend on the temperature.
p-n-Heptylphenylacetylene (pHepPA) was stereoregularly polymerized in n-hexane at 25 C using [Rh(nbd)Cl] 2 catalyst (nbd: norbornadiene) and NEt 3 , affording the purplered Poly(R) in 97% yield. A 80 C heat treatment transformed Poly(R) to the black Poly(B). The Poly(R) X-ray diffraction (XRD) pattern revealed a hexagonal crystal structure comprising contracted cis-cisoid helices [ Hexa Poly(R) CC ]. The 80 C heat treatment generated two tetragonal crystals: Tetra Poly(B) CC containing contracted cis-cisoid helices and Tetra Poly(B) CT containing stretched cis-transoid helices. The helical diameters before and after heat treatment were estimated using XRD and were consistent with molecular mechanics calculations (MMFF94 force field method). When heated at 80 C in the solid phase, the k max in the diffuse reflective UV-vis spectra of Hexa Poly(R) CC shifted from 482 to 560 nm. Additionally, an endothermic transition occurred in the Hexa Poly(R) CC differential scanning calorimetric trace at 80 C. Therefore, these data corroborated the assertion that Hexa Poly(R) CC thermally converted to Tetra Poly(B) CC and Tetra Poly(B) CT .
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