journal article·2019Open access

Six state molecular revolver mounted on a rigid platform

Jan Homberg, Marcin Lindner, Lukas Gerhard, Kevin Edelmann, Timo Frauhammer, Yasmine Nahas, Michal Valášek, Marcel Mayor, Wulf Wulfhekel

Nanoscale· Volume 11· Issue 18

Abstract

The rotation of entire molecules or large moieties happens at 100 ps time scales and the transition process itself is experimentally inaccessible to scanning probe techniques. However, the reversible switching of a molecule between more than two metastable states allows to assign a rotational switching direction. Rotational switching is a phenomenon that is particularly interesting with regard to possible applications in molecular motors. In this work, single tetraphenylmethane molecules deposited on a Au(111) surface were studied in a low temperature scanning tunneling microscope (STM). These molecules comprise rotational axes mounted on a tripodal sulfur-anchored stand and with the STM tip, we were able to induce transitions between six rotational states of the molecular motif. We were able to identify critical parameters for the onset of rotational switching and to characterize the influence of the local environment. The subtle difference between fcc and hcp stacking and the rotational state of neighboring molecules clearly influence the population of the rotational states.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Mechanical and Optical Resonators · Various Chemistry Research Topics · Molecular Junctions and Nanostructures

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

Affiliations

Institute of Nanotechnology

Karlsruhe Institute of Technology

Germany

Physikalisches Institut

Department of Chemistry

University of Basel

Funding

Deutsche Forschungsgemeinschaft · Baden-Württemberg Stiftung

References (42)

Show source-provided references
1. Kühne · Proc. Natl. Acad. Sci. U. S. A. · 2010 · 107 · 2133210.1073/pnas.1008991107 ↗
2. Iancu · Proc. Natl. Acad. Sci. U. S. A. · 2006 · 103 · 1371810.1073/pnas.0603643103 ↗
3. Auwärter · Nat. Nanotechnol. · 2012 · 7 · 4110.1038/nnano.2011.211 ↗
4. Otsuki · J. Am. Chem. Soc. · 2010 · 132 · 687010.1021/ja907077e ↗
5. Zhang · Nat. Nanotechnol. · 2016 · 11 · 70610.1038/nnano.2016.69 ↗
6. Godlewski · ACS Nano · 2016 · 10 · 849910.1021/acsnano.6b03590 ↗
7. Perera · Nat. Nanotechnol. · 2013 · 8 · 4610.1038/nnano.2012.218 ↗
8. Quek · Nat. Nanotechnol. · 2009 · 4 · 23010.1038/nnano.2009.10 ↗
9. Kiguchi · J. Am. Chem. Soc. · 2014 · 136 · 732710.1021/ja413104g ↗
10. Qiu · Phys. Rev. Lett. · 2004 · 93 · 19680610.1103/PhysRevLett.93.196806 ↗
11. Alemani · J. Am. Chem. Soc. · 2006 · 128 · 1444610.1021/ja065449s ↗
12. Wirth · J. Phys. Chem. C · 2015 · 119 · 487410.1021/jp5122036 ↗
13. Gerhard · Nat. Commun. · 2017 · 8 · 1467210.1038/ncomms14672 ↗
14. Comstock · Phys. Rev. Lett. · 2007 · 99 · 03830110.1103/PhysRevLett.99.038301 ↗
15. Browne · Annu. Rev. Phys. Chem. · 2009 · 60 · 40710.1146/annurev.physchem.040808.090423 ↗
16. Kim · Nano Lett. · 2012 · 12 · 373610.1021/nl3015523 ↗
17. Blum · Nat. Mater. · 2005 · 4 · 16710.1038/nmat1309 ↗
18. Wu · J. Phys. Chem. C · 2008 · 112 · 524110.1021/jp7114548 ↗
19. Liljeroth · Science · 2007 · 317 · 120310.1126/science.1144366 ↗
20. Henningsen · J. Phys. Chem. C · 2007 · 111 · 1484310.1021/jp0741861 ↗
21. Valášek · Beilstein J. Nanotechnol. · 2016 · 7 · 37410.3762/bjnano.7.34 ↗
22. Valášek · Chem. – Eur. J. · 2017 · 23 · 1353810.1002/chem.201703349 ↗
23. Kitagawa · J. Org. Chem. · 2006 · 71 · 136210.1021/jo051863j ↗
24. Ie · J. Am. Chem. Soc. · 2011 · 133 · 301410.1021/ja109577f ↗
25. Zhu · J. Am. Chem. Soc. · 2013 · 135 · 1579410.1021/ja4048569 ↗
26. Valášek · J. Org. Chem. · 2014 · 79 · 734210.1021/jo501029t ↗
27. Hauptmann · New J. Phys. · 2015 · 17 · 01301210.1088/1367-2630/17/1/013012 ↗
28. Lindner · Chem. – Eur. J. · 2016 · 22 · 1321810.1002/chem.201602019 ↗
29. Lindner · Angew. Chem., Int. Ed. · 2017 · 56 · 829010.1002/anie.201703586 ↗
30. Fischer · Phys. Rev. Lett. · 1999 · 82 · 173210.1103/PhysRevLett.82.1732 ↗
31. Barth · Phys. Rev. B: Condens. Matter Mater. Phys. · 1990 · 42 · 930710.1103/PhysRevB.42.9307 ↗
32. Repain · Appl. Surf. Sci. · 2000 · 162–163 · 3010.1016/S0169-4332(00)00166-5 ↗
33. Pearson · Proc. R. Soc. London · 1895 · 58 · 24010.1098/rspl.1895.0041 ↗
34. Repp · Phys. Rev. Lett. · 2000 · 85 · 298110.1103/PhysRevLett.85.2981 ↗
35. Kulawik · Surf. Sci. · 2005 · 590 · L25310.1016/j.susc.2005.05.068 ↗
36. Gross · Phys. Rev. Lett. · 2004 · 93 · 05610310.1103/PhysRevLett.93.056103 ↗
37. LaShell · Phys. Rev. Lett. · 1996 · 77 · 341910.1103/PhysRevLett.77.3419 ↗
38. Lingenfelder · Angew. Chem., Int. Ed. · 2007 · 46 · 449210.1002/anie.200700194 ↗
39. Reinert · Phys. Rev. B: Condens. Matter Mater. Phys. · 2001 · 63 · 11541510.1103/PhysRevB.63.115415 ↗
40. Kumagai · Nat. Chem. · 2014 · 6 · 4110.1038/nchem.1804 ↗
41. Elste · Appl. Phys. A · 2008 · 93 · 34510.1007/s00339-008-4826-2 ↗
42. Miyamachi · Nat. Commun. · 2012 · 3 · 93810.1038/ncomms1940 ↗