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来自高度受阻手性丙二烯的手性超分子聚集体中的同轴螺旋

Coaxial Helices in Chiral Supramolecular Aggregates from Highly Hindered Chiral Allenes.

作者信息

Lago-Silva María, Fernández-Míguez Manuel, Fernández Zulema, Cid María Magdalena, Quiñoá Emilio, Rodríguez Rafael, Freire Félix

机构信息

Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares (CiQUS), Universidade de Santiago de Compostela, E-15782, Santiago de Compostela, Spain.

Departamento de Química Orgánica, Universidade de Santiago de Compostela, E-15782, Santiago de Compostela, Spain.

出版信息

Angew Chem Int Ed Engl. 2025 Mar 3;64(10):e202421310. doi: 10.1002/anie.202421310. Epub 2024 Dec 18.

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) and a M/P/M/P orientation of the four axial motifs at the periphery, (P)-2 produces a supramolecular helix with a Θ ca. 23° (P) and a P/P/P/P 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.

摘要

手性联烯通过协同机制自组装成一种超分子手性聚集体,该聚集体由两个同轴螺旋组成:内部螺旋由联烯堆叠形成,外部螺旋由四个联烯取代基形成的四螺旋组成。更确切地说,这种超分子聚集体在其结构中具有六个轴向手性元素——联烯、联烯堆叠(内部螺旋)和四个联烯取代基的堆叠(外部四螺旋)。有趣的是,在保持其P或M取向(内部螺旋)的同时,倾斜度大小的轻微变化会改变外部螺旋上4-轴向基序的取向。因此,(P)-1产生一个超分子螺旋,其θ约为15°(P),外围四个轴向基序的取向为M/P/M/P,而(P)-2产生一个超分子螺旋,其θ约为23°(P),外部螺旋上四个轴向基序的取向为P/P/P/P。结果,由手性联烯的1和1'取代基主导的(P)-1和(P)-2超分子聚集体的ECD光谱和AFM图像显示出相反的手性,尽管构建单元的手性和联烯堆叠的取向是相同的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e833/11878346/c285210456a5/ANIE-64-e202421310-g001.jpg

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