Coaxial Helices in Chiral Supramolecular Aggregates from Highly Hindered Chiral Allenes

Abstract Chiral allenes self‐assembly following a cooperative mechanism into a supramolecular chiral aggregate consisting of two coaxial helices: the internal helix described by the allene stack and the external helix which consist in a 4‐helix described by the four allene substituents. More precisely, this supramolecular aggregate possesses six axially chiral elements within its structure—the allene, the allene stack (internal helix) and the stacks of the four allene substituents (external 4‐helix)—. Interestingly, slight variations in the magnitude of the tilting degree while keeping its P ‐ or M ‐ orientation (internal helix) can vary the orientation of the 4‐axial motifs at the external helix. Thus, while ( P )‐ 1 produces a supramolecular helix with a Θ ca. 15° ( P int ) and a M 1 / P 2 / M 1’ / P 2’ orientation of the four axial motifs at the periphery, ( P )‐ 2 produces a supramolecular helix with a Θ ca. 23° ( P int ) and a P 1 / P 2 / P 1’ / P 2’ orientation of the four axial motifs at the external helix. As a result, the ECD spectra and the AFM images of the ( P )‐ 1 and ( P )‐ 2 supramolecular aggregates dominated by the 1 and 1’ substituents of the chiral allene indicate opposite handedness although the chirality of the building block and the orientation of the allene stack are the same

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Publication Details

Journal
Angewandte Chemie
Published
2024-12-10
DOI
https://doi.org/10.1002/ange.202421310
Primary Topic
Synthesis and Properties of Aromatic Compounds
Type
article
Field-Weighted Citation Impact
0.00

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article

Coaxial Helices in Chiral Supramolecular Aggregates from Highly Hindered Chiral Allenes

Emilio Quiñoá, Rafael Rodríguez, Zulema Fernández, Marı́a Magdalena Cid et al.
1 links
Angewandte Chemie
Synthesis and Properties of Aromatic Compounds
article

Coaxial Helices in Chiral Supramolecular Aggregates from Highly Hindered Chiral Allenes

Emilio Quiñoá, Rafael Rodríguez, Zulema Fernández, Marı́a Magdalena Cid, Félix Freire
article en

Abstract

Abstract Chiral allenes self‐assembly following a cooperative mechanism into a supramolecular chiral aggregate consisting of two coaxial helices: the internal helix described by the allene stack and the external helix which consist in a 4‐helix described by the four allene substituents. More precisely, this supramolecular aggregate possesses six axially chiral elements within its structure—the allene, the allene stack (internal helix) and the stacks of the four allene substituents (external 4‐helix)—. Interestingly, slight variations in the magnitude of the tilting degree while keeping its P ‐ or M ‐ orientation (internal helix) can vary the orientation of the 4‐axial motifs at the external helix. Thus, while ( P )‐ 1 produces a supramolecular helix with a Θ ca. 15° ( P int ) and a M 1 / P 2 / M 1’ / P 2’ orientation of the four axial motifs at the periphery, ( P )‐ 2 produces a supramolecular helix with a Θ ca. 23° ( P int ) and a P 1 / P 2 / P 1’ / P 2’ orientation of the four axial motifs at the external helix. As a result, the ECD spectra and the AFM images of the ( P )‐ 1 and ( P )‐ 2 supramolecular aggregates dominated by the 1 and 1’ substituents of the chiral allene indicate opposite handedness although the chirality of the building block and the orientation of the allene stack are the same

Angewandte ChemieVol. 137(10)
Universidade de Santiago de Compostela (ES), Center for Research in Molecular Medicine and Chronic Diseases (ES), Universidade de Vigo (ES)
Universidade de Vigo, Xunta de Galicia, Centro Singular de Investigación de Galicia, European Regional Development Fund, Agencia Estatal de Investigación
Openalex Percentile: Top 83%
Synthesis and Properties of Aromatic Compounds
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