journal article·2021

Coordination-directed self-assembly of molecular motors: towards a two-wheel drive nanocar

Menglian Li, Shaorui Li, Kexin Zhang, Xin Chi, Hang Zhou, Hai-Bing Xu, Yuexing Zhang, Quan Li, Dong Wang, Ming-Hua Zeng

Nanoscale· Volume 13· Issue 39
Publisher page

Abstract

Designing and constructing hierarchical and stimuli-responsive motorized nanocar systems to perform useful tasks on-demand is highly imperative towards molecular nanotechnology. In this work, a most simplified two-wheel nanocar was successfully prepared through a facile strategy of coordination-directed self-assembly. The nanocar meso-AgL2 features a central pseudo square-planar Ag(I) which was bridged by two enantiomeric motors as the wheels that ensure the car moves in the same direction when observed externally. Thanks to the electronic push-pull characteristic of L and 3ILCT triplet sensitization, this nanocar can be driven by visible light up to 500 nm. Furthermore, it could be disassembled into individual motor elements through the addition of pyridine, thus allowing dynamic regulation over the function of the nanocar. Importantly, our STM imaging results showed very organized tilted layered structures for meso-AgL2 on highly oriented pyrolytic graphite (HOPG) that are quite similar to its crystalline ones, paving the way for future single molecule manipulations. The nanocar reported here represents the first example of integrating individual motors into a hierarchical motorized nanocar system via the facile coordination-directed self-assembly method and may offer a good starting point to realize its robotic functions, e.g., metal transportation and release.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Supramolecular Chemistry and Complexes · Porphyrin and Phthalocyanine Chemistry · Magnetism in coordination complexes

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Ministry-of-Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, College of Chemistry & Chemical Engineering, Hubei University, Wuhan 430062, P. R. China

Key Laboratory of Molecular Nanostructure and Nanotechnology and Beijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences (CAS), Beijing 100190, P. R. China

University of Chinese Academy of Sciences, Beijing 100049, P. R. China

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, P. R. China

Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Guilin, 541004, P. R. China

Funding

National Natural Science Foundation of China · Natural Science Foundation of Guangxi Province

References (38)

Show source-provided references
1. Feringa · Angew. Chem., Int. Ed. · 2017 · 56 · 1106010.1002/anie.201702979 ↗
2. Wang · Science · 2011 · 331 · 142910.1126/science.1199844 ↗
3. Chen · Chem. Commun. · 2016 · 52 · 676510.1039/C6CC02382G ↗
4. Chen · J. Am. Chem. Soc. · 2014 · 136 · 321910.1021/ja412110t ↗
5. Pijper · Angew. Chem., Int. Ed. · 2007 · 46 · 369310.1002/anie.200604941 ↗
6. Li · Nat. Nanotechnol. · 2015 · 10 · 16110.1038/nnano.2014.315 ↗
7. Foy · Nat. Nanotechnol. · 2017 · 12 · 54010.1038/nnano.2017.28 ↗
8. López · Nature · 2017 · 548 · 56710.1038/nature23657 ↗
9. Liu · Angew. Chem., Int. Ed. · 2021 · 60 · 1612910.1002/anie.202104285 ↗
10. Zhang · Matter · 2020 · 3 · 35510.1016/j.matt.2020.05.014 ↗
11. Krause · Nat. Rev. Chem. · 2020 · 4 · 55010.1038/s41570-020-0209-9 ↗
12. Kistemaker · Mater. Chem. Front. · 2021 · 5 · 290010.1039/D0QM01091J ↗
13. Chen · Nat. Chem. · 2018 · 10 · 13210.1038/nchem.2887 ↗
14. Leung · J. Am. Chem. Soc. · 2018 · 140 · 1772410.1021/jacs.8b10778 ↗
15. Leung · Angew. Chem., Int. Ed. · 2019 · 58 · 1098510.1002/anie.201905445 ↗
16. Danowski · J. Am. Chem. Soc. · 2020 · 142 · 904810.1021/jacs.0c03063 ↗
17. Morin · Org. Lett. · 2006 · 8 · 171310.1021/ol060445d ↗
18. Kudernac · Nature · 2011 · 479 · 20810.1038/nature10587 ↗
19. Davis · Tetrahedron Lett. · 2011 · 52 · 155310.1016/j.tetlet.2011.01.116 ↗
20. Wezenberg · Angew. Chem. · 2015 · 127 · 1161910.1002/ange.201505781 ↗
21. Faulkner · J. Am. Chem. Soc. · 2016 · 138 · 1359710.1021/jacs.6b06467 ↗
22. Movahedi · J. Mol. Struct. · 2017 · 1139 · 40710.1016/j.molstruc.2017.03.042 ↗
23. Wiedbrauk · J. Am. Chem. Soc. · 2016 · 138 · 1221910.1021/jacs.6b05981 ↗
24. Maerz · Chem. – Eur. J. · 2014 · 20 · 1398410.1002/chem.201403661 ↗
25. Guentner · Chem. – Eur. J. · 2016 · 22 · 1643310.1002/chem.201604237 ↗
26. Shao · J. Am. Chem. Soc. · 2019 · 141 · 836410.1021/jacs.9b03932 ↗
27. Shi · J. Am. Chem. Soc. · 2021 · 143 · 44210.1021/jacs.0c11752 ↗
28. McCann · BioMetals · 2004 · 17 · 63510.1007/s10534-004-1229-5 ↗
29. Massoud · New J. Chem. · 2011 · 35 · 64010.1039/c0nj00697a ↗
30. Pallenberg · Polyhedron · 1997 · 16 · 271110.1016/S0277-5387(97)00051-X ↗
31. Pollard · Adv. Funct. Mater. · 2007 · 17 · 71810.1002/adfm.200601025 ↗
32. García-López · Asian J. Org. Chem. · 2015 · 4 · 130810.1002/ajoc.201500325 ↗
33. Sun · Chem. Soc. Rev. · 2020 · 49 · 388910.1039/D0CS00038H ↗
34. Harris · Chem. Commun. · 2013 · 49 · 670310.1039/c3cc43191f ↗
35. Han · Chem. Soc. Rev. · 2014 · 43 · 184810.1039/C3CS60473J ↗
36. Wang · Nat. Commun. · 2020 · 11 · 467510.1038/s41467-020-18487-5 ↗
37. Lewis · Chem. Soc. Rev. · 2017 · 46 · 257710.1039/C7CS00199A ↗
38. Aucagne · J. Am. Chem. Soc. · 2006 · 128 · 218610.1021/ja056903f ↗