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Complex assembly from planar and twisted π-conjugated molecules towards alloy helices and core-shell structures

机译:从平面和扭曲的π共轭分子到合金螺旋和核-壳结构的复杂组装

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摘要

Integrating together two dissimilar π-conjugated molecules into controlled complex topological configurations remains a largely unsolved problem owing to the diversity of organic species and their respective different assembly features. Here, we find that two structurally similar organic semiconductors, 9,10-bis(phenylethynyl)anthracene (BA) and 5,12-bis(phenylethynyl)naphthacene (BN), co-assemble into two-component helices by control of the growth kinetics as well as the molar ratio of BA/BN. The helical superstructures made of planar and twisted bis(phenylethynyl) derivatives can be regarded as (BA)x(BN)1−x alloys, which are formed due to compatible structural relationship between BA and BN. Moreover, epitaxial growth of (BA)x(BN)1−x alloy layer on the surface of BA tube to form BA@(BA)x(BN)1−x core-shell structure is also achieved via a solute exchange process. The precise control over composition and morphology towards organic alloy helices and core-shell microstructures opens a door for understanding the complex co-assembly features of two or more different material partners with similar structures.
机译:由于有机物种的多样性及其各自不同的组装特征,将两个不同的π共轭分子整合到受控的复杂拓扑结构中仍然是一个悬而未决的问题。在这里,我们发现两个结构相似的有机半导体9,10-双(苯基乙炔基)蒽(BA)和5,12-双(苯基乙炔基)萘(BN)通过控制生长而共组装成两组分螺旋动力学以及BA / BN的摩尔比。由平面和扭曲的双(苯基乙炔基)衍生物制成的螺旋上层结构可以被视为(BA)x(BN)1-x合金,这是由于BA和BN之间具有相容的结构关系而形成的。此外,还通过溶质交换过程实现了在BA管表面上外延生长(BA)x(BN)1-x合金层以形成BA @(BA)x(BN)1-x核-壳结构。对有机合金螺旋和核-壳微结构的组成和形态的精确控制为理解具有相似结构的两个或多个不同材料伙伴的复杂共组装特征打开了一扇门。

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