Abstract
The concept of the Thorpe-Ingold effect has been used to rationalize the helicity of the silylene-spaced divinylarene copolymers having chiral substituents. Diisopropylsilylene-spaced divinylbenzene copolymers having chiral 2-methylbutoxy substituents have been shown to exhibit a helical conformation. The presence of the bulky isopropyl substituents on silicon would render each of the monomeric units in these copolymers to favor a syn-syn conformation. The copolymer would thus be more folded to form helical morphology as revealed by the notable enhancement of the circular dichroic intensity. The reversible temperature-dependent circular dichroism (CD) profiles further support the stable helical conformation for the copolymers 4 b and 5 b.
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