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Snapshots of Dynamic Adaptation: Two-Dimensional Molecular Architectonics with Linear Bis-Hydroxamic Acid Modules  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Snapshots of Dynamic Adaptation: Two-Dimensional Molecular Architectonics with Linear Bis-Hydroxamic Acid Modules

作者:Jing, Chao[1,2];Zhang, Bodong[1];Synkule, Sabine[1];Ebrahimi, Maryam[1,3];Riss, Alexander[1];Auwaerter, Willi[1];Jiang, Li[1];Medard, Guillaume[4];Reichert, Joachim[1];Barth, Johannes V.[1];Papageorgiou, Anthoula C.[1]

机构:[1]Tech Univ Munich, Phys Dept E20, James Franck Str 1, D-85748 Garching, Germany;[2]East China Univ Sci & Technol, Key Lab Adv Mat, Sch Chem & Mol Engn, Shanghai 200237, Peoples R China;[3]Lakehead Univ, Dept Chem, 955 Oliver Rd, Thunder Bay, ON P7B 5E1, Canada;[4]Tech Univ Munich, Chair Prote & Bioanalyt, Emil Erlenmeyer Forum 5, D-85354 Freising Weihenstephan, Germany

年份:2019

卷号:58

期号:52

起止页码:18948

外文期刊名:ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

收录:;EI(收录号:20195107857736);WOS:【SCI-EXPANDED(收录号:WOS:000499180500001)】;

基金:We acknowledge funding by the Postdoctoral Council of China (2015 International Postdoctoral Exchange Fellowship Program, C.J.), the China Scholarship Council (B.Z., L.J.), the International Max Planck Research School of Advanced Photon Science (S.S.), the European Union's Horizon 2020 research and innovation programme (grant agreement no. 664878), the European Research Council Consolidator Grant NanoSurfs (no. 615233), and the Deutsche Forschungsgemeinschaft (Excellence Cluster Munich-Centre for Advanced Photonics and Heisenberg professorship, W.A.). Computations were performed on the shared Hierarchical Academic Research Computing Network (SHARCNET) and the Cedar, Graham, and Niagara clusters of Compute/Calcul Canada.

语种:英文

外文关键词:atomic force microscopy; host-guest systems; hydroxamic acid; scanning tunneling microscopy; two-dimensional nanostructures

摘要:Linear modules equipped with two terminal hydroxamic acid groups act as the building block of diverse two-dimensional supramolecular motifs and patterns with room-temperature stability on the close-packed single-crystal surfaces of silver and gold, revealing a complex self-assembly scenario. By combining multiple investigation techniques (scanning tunneling microscopy, atomic force microscopy, X-ray photoelectron spectroscopy, and density functional theory calculations), we analyze the characteristics of the ordered assemblies which range from close-packed structures to polyporous networks featuring an exceptionally extended primitive unit cell with a side length exceeding 7 nm. The polyporous network shows potential for hosting and promoting the formation of chiral supramolecules, whereas a transition from 1D chiral randomness to an ordered racemate is discovered in a different porous phase. We correlate the observed structural changes to the adaptivity of the building block and surface-induced changes in the chemical state of the hydroxamic acid functional group.

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