A method for intelligently optimizing hierarchical assembly structure sequences by assembly hybrid G-diagram

Author(s):  
Xiaoxi Kou ◽  
Yan Cao ◽  
Hu Qiao
2020 ◽  
Author(s):  
Ian Colliard ◽  
Gregory Morrosin ◽  
Hans-Conrad zur Loye ◽  
May Nyman

Superatoms are nanometer-sized molecules or particles that can form ordered lattices, mimicking their atomic counterparts. Hierarchical assembly of superatoms gives rise to emergent properties in superlattices of quantum-dots, p-block clusters, and fullerenes. Here, we introduce a family of uranium-oxysulfate cluster anions whose hierarchical assembly in water is controlled by two parameters; acidity and the countercation. In acid, larger Ln<sup>III</sup> (Ln=La-Ho) link hexamer (U<sub>6</sub>) oxoclusters into body-centered cubic frameworks, while smaller Ln<sup>III</sup> (Ln=Er-Lu &Y) promote linking of fourteen U<sub>6</sub>-clusters into hollow superclusters (U<sub>84</sub> superatoms). U<sub>84</sub> assembles into superlattices including cubic-closest packed, body-centered cubic, and interpenetrating networks, bridged by interstitial countercations, and U<sub>6</sub>-clusters. Divalent transition metals (TM=Mn<sup>II </sup>and Zn<sup>II</sup>), with no added acid, charge-balance and promote the fusion of 10 U<sub>6</sub> and 10 U-monomers into a wheel–shaped cluster (U<sub>70</sub>). Dissolution of U<sub>70</sub> in organic media reveals (by small-angle Xray scattering) that differing supramolecular assemblies are accessed, controlled by TM-linking of U<sub>70</sub>-clusters. <br>


2021 ◽  
Vol 12 (38) ◽  
pp. 12619-12630
Author(s):  
Guo-Guo Weng ◽  
Ben-Kun Hong ◽  
Song-Song Bao ◽  
Yujie Wen ◽  
Lan-Qing Wu ◽  
...  

Superhelices of terbium phosphonates formed following a new type of “chain-twist-growth” mechanism involving flexible cyclohexyl groups.


ACS Nano ◽  
2021 ◽  
Author(s):  
Erin N. Lang ◽  
Ashlin G. Porter ◽  
Tianhong Ouyang ◽  
Anni Shi ◽  
Tyler R. Hayes ◽  
...  

2021 ◽  
Vol 628 ◽  
pp. 119230
Author(s):  
Shuhao Wang ◽  
Shaosuo Bing ◽  
Yunhao Li ◽  
Yong Zhou ◽  
Lin Zhang ◽  
...  

Langmuir ◽  
2008 ◽  
Vol 24 (21) ◽  
pp. 12483-12488 ◽  
Author(s):  
Wui Siew Tan ◽  
Christina L. Lewis ◽  
Nicholas E. Horelik ◽  
Daniel C. Pregibon ◽  
Patrick S. Doyle ◽  
...  

Small ◽  
2021 ◽  
pp. 2100862
Author(s):  
Liang Huang ◽  
Yuxing Zhang ◽  
Tao Liao ◽  
Kui Xu ◽  
Chenxing Jiang ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Ling Xin ◽  
Xiaoyang Duan ◽  
Na Liu

AbstractIn living organisms, proteins are organized prevalently through a self-association mechanism to form dimers and oligomers, which often confer new functions at the intermolecular interfaces. Despite the progress on DNA-assembled artificial systems, endeavors have been largely paid to achieve monomeric nanostructures that mimic motor proteins for a single type of motion. Here, we demonstrate a DNA-assembled building block with rotary and walking modules, which can introduce new motion through dimerization and oligomerization. The building block is a chiral system, comprising two interacting gold nanorods to perform rotation and walking, respectively. Through dimerization, two building blocks can form a dimer to yield coordinated sliding. Further oligomerization leads to higher-order structures, containing alternating rotation and sliding dimer interfaces to impose structural twisting. Our hierarchical assembly scheme offers a design blueprint to construct DNA-assembled advanced architectures with high degrees of freedom to tailor the optical responses and regulate multi-motion on the nanoscale.


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