Precisely Constructing Superlattices of Soft Giant Molecules via Regulating Volume Asymmetry

IF 15.6 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Journal of the American Chemical Society Pub Date : 2024-11-30 DOI:10.1021/jacs.4c09089
Huanyu Lei, Xian-You Liu, Yicong Wang, Xing-Han Li, Xiao-Yun Yan, Tong Liu, Jiahao Huang, Weiyi Li, Lichun Wang, Xiaoyi Kuang, Xiaran Miao, Fenggang Bian, Mingjun Huang, Yuchu Liu, Stephen Z.D. Cheng
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Abstract

Soft matters, particularly giant molecular self-assembly, have successfully replicated complex structures previously exclusive to metal alloys. These superlattices are constructed from mesoatoms─supramolecular spherical motifs of aggregated molecules, and the formation of superlattices critically depends on the volume distributions of these mesoatoms. Herein, we introduce two general methods to control volume asymmetry (i.e., the volumes’ ratio of the largest to smallest mesoatoms, VL/VS) within giant molecular self-assembly. Leveraging the spontaneous increase in the mesoatomic volume ratio in unary systems and self-sorted binary blends, we systematically adjust the volume asymmetry from 1.0 to 9.0 across 24 unary systems and 56 binary blends of giant molecules, uncovering the formation of various superlattices, including BCC, Frank-Kasper A15, σ, Laves C14, C15, NaZn13, AlB2, and notably, the first NaCl like superlattice in homogeneous soft matter self-assembly. A geometric-based analysis, combined with experimental results, further establishes a quantitative relationship between volume asymmetry and the corresponding superlattice formations, thus laying a solid foundation for superlattice engineering within giant molecular systems to mimic and even beyond metal alloys. The lattice parameters of various unit cells range from approximately 5 to 20 nm. Our investigation in giant molecules could guide the advancement of mesoscopic, periodic soft matter materials.

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通过调节体积不对称精确构建软巨分子超晶格
软物质,特别是巨大的分子自组装,已经成功地复制了以前只有金属合金才能复制的复杂结构。这些超晶格是由介原子──聚集分子的超分子球形基元构成的,超晶格的形成关键取决于这些介原子的体积分布。本文介绍了两种控制巨分子自组装中体积不对称(即最大与最小介原子的体积比,VL/VS)的一般方法。利用一元体系和自分选二元共混体系中介原子体积比的自发增加,我们系统地调整了24个一元体系和56个大分子二元共混体系的体积不对称从1.0到9.0,揭示了各种超晶格的形成,包括BCC、Frank-Kasper A15、σ、Laves C14、C15、NaZn13、AlB2,尤其是均匀软物质自组装中第一个类似NaCl的超晶格。基于几何的分析,结合实验结果,进一步建立了体积不对称与相应超晶格形成之间的定量关系,从而为模拟甚至超越金属合金的巨分子系统超晶格工程奠定了坚实的基础。各种单元胞的晶格参数范围约为5 ~ 20 nm。我们对大分子的研究可以指导介观、周期软物质材料的发展。
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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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