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A curved host and second guest cooperatively inhibit the dynamic motion of corannulene

Chemistry

A curved host and second guest cooperatively inhibit the dynamic motion of corannulene

Y. Yang, T. K. Ronson, et al.

This research conducted by Yang Yang, Tanya K. Ronson, Zifei Lu, Jieyu Zheng, Nicolas Vanthuyne, Alexandre Martinez, and Jonathan R. Nitschke unveils a novel artificial host-guest system where the binding of guests dramatically influences the host's structure and the dynamics of the guests themselves. Discover how a chiral cage enhances enantiomer detection while inhibiting molecular inversion.

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~3 min • Beginner • English
Abstract
Biomolecular systems show how host–guest binding can induce changes in molecular behavior, which in turn impact the functions of the system. Here we report an artificial host–guest system where dynamic adaptation during guest binding alters both host conformation and guest dynamics. The self-assembled cage host employed here possesses concave walls and a chirotopic cavity. Complementarity between the curved surfaces of fullerenes and the inner surface of the host cavity leads the host to reconfigure stereochemically in order to bind these guests optimally. The curved molecule corannulene undergoes rapid bowl-to-bowl inversion at room temperature. Its inversion barrier is increased upon binding, however, and increased further upon formation of a ternary complex, where corannulene and a cycloalkane are both bound together. The chiral nature of the host also leads to clear differences in the NMR spectra of ternary complexes involving corannulene and one or the other enantiomer of a chiral guest, which enables the determination of enantiomeric excess by NMR.
Publisher
Nature Communications
Published On
Jul 02, 2021
Authors
Yang Yang, Tanya K. Ronson, Zifei Lu, Jieyu Zheng, Nicolas Vanthuyne, Alexandre Martinez, Jonathan R. Nitschke
Tags
host-guest system
chiral cage
fullerenes
corannulene
enantiomeric excess
NMR
ternary complex
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