4.7 Article

Triply Helical Giant Domain with Homochirality in a Terpolymer Blend System

Journal

ACS MACRO LETTERS
Volume 10, Issue 7, Pages 978-983

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsmacrolett.1c00307

Keywords

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Funding

  1. JSPS KAKENHI [18H05209, 2019B1135]

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Hexagonally packed coaxial triply helical domains with mesoscopic length scale were successfully created in matrices from a blend system of S1IS2P tetrablock terpolymer/Sh homopolymer, where the intermediate S phase was found to have a helical nature due to S-2 chains filling the gap between the I and P helices. The grains composed of hexagonally packed helices exhibited homochirality.
Hexagonally packed coaxial triply helical domains with a mesoscopic length scale in matrices were created from an S1IS2P tetrablock terpolymer/Sh homopolymer blend system, wherein S-1, S-2, and Sh denote polystyrene, I is polyisoprene, and P represents poly(2-vinylpyridine). Two terpolymers, i.e., S1IS2P-3 (S-1/I/S-2/P = 0.50/0.17/0.19/0.14, M = 134k) and S1IS2P-4 (S-1/I/S-2/P = 0.58/0.16/0.10/0.16, M = 173k), were blended with Sh (M = 3k) at various concentrations. In the S1IS2P-3/S-h = 80/20 blend, the helical domain of P (o.d.= 19 nm; h.p. = 34 nm) was displayed by TEM, and the helical I phase (o.d. = 55 nm; i.d. = 29 nm; h.p. = 34 nm) was clearly demonstrated by 3D-TEM tomography. Essentially the same structure was confirmed to be created from the S1IS2P-4/S-h blend. These findings point out that S-2 chains fill the gap between the I and P helices, and hence the intermediate S phase also has a helical nature. Moreover, it is worth noting that grains composed of hexagonally packed helices reveal homochirality.

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