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Updated: Jul 29, 2026

Controlling the Size, Shape and Stability of Supramolecular Polymers in Water
Published on: August 2, 2012
Conformational preferences and supramolecular aggregation in 2-nitrophenylthiolates:
1School of Chemistry, University of St Andrews, St Andrews, Fife KY16 9ST, Scotland. cg@st-andrews.ac.uk.
Abstract:
In the title compound, C(12)H(15)NO(7)S, the molecular conformation shows a concerted disrotatory twist of the nitro group and the galactose fragment out of the plane of the aryl ring. The molecules are linked by O-H.O hydrogen bonds [O.O range 2.725 (2)-3.024 (2) A and O-H.O range 155-175 degrees ] to form a three-dimensional framework.
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