journal article·2018Open access

A gold-nanoparticle stoppered [2]rotaxane

Anne Ulfkjær, Frederik W. Nielsen, Hana Al-Kerdi, Tamara Ruβ, Zaki K. Nielsen, Jens Ulstrup, Lanlan Sun, Kasper Moth-Poulsen, Jingdong Zhang, Michael Pittelkow

Nanoscale· Volume 10· Issue 19

Abstract

The construction of molecular machines has captured the imagination of scientists for decades. Despite significant progress in the synthesis and studies of the properties of small-molecule components (smaller than 2-5 kilo Dalton), challenges regarding the incorporation of molecular components into real devices are still eminent. Nano-sized molecular machines operate the complex biological machinery of life, and the idea of mimicking the amazing functions using artificial nano-structures is intriguing. Both in small-molecule molecular machine components and in many naturally occurring molecular machines, mechanically interlocked molecules and structures are key functional components. In this work, we describe our initial efforts to interface mechanically-interlocked molecules and gold-nanoparticles (AuNPs); the molecular wire connecting the AuNPs is covered in an insulating rotaxane-layer, thus mimicking the macroscopic design of a copper wire. Taking advantage of recent progress in the preparation of supramolecular complexes of the cucurbit[7]uril (CB[7]) macrocycle, we have prepared a bis-thiol functionalised pseudo-rotaxane that enables us to prepare a AuNP-stoppered [2]rotaxane in water. The pseudo-rotaxane is held together extremely tightly (Ka > 1013 M-1), Ka being the association constant. We have studied the solution and gas phase guest-host chemistry using NMR spectroscopy, mass spectroscopy, and electrochemistry. The bis-thiol functionalised pseudo-rotaxane holds further a ferrocene unit in the centre of the rotaxane; this ferrocene unit enables us to address the system in detail with and without CB[7] and AuNPs using electrochemical methods.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Supramolecular Chemistry and Complexes · Advanced biosensing and bioanalysis techniques · Molecular Sensors and Ion Detection

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

Affiliations

Department of Chemistry

University of Copenhagen

DK-2100 Copenhagen

Denmark

Technical University of Denmark

DK-2800 Kongens Lyngby

Department of Chemistry and Chemical Engineering

Chalmers University of Technology

SE-41296 Gothenburg

Sweden

Funding

Det Frie Forskningsråd · Lundbeckfonden · H2020 European Research Council

References (48)

Show source-provided references
1. Stoddart · Angew. Chem., Int. Ed. · 2017 · 56 · 1109410.1002/anie.201703216 ↗
2. Kelly · Nature · 1999 · 401 · 15010.1038/43639 ↗
3. Koumura · Nature · 1999 · 401 · 15210.1038/43646 ↗
4. Lee · Nature · 2009 · 458 · 31410.1038/nature07847 ↗
5. Fielden · Angew. Chem., Int. Ed. · 2017 · 56 · 1116610.1002/anie.201702531 ↗
6. Lim · J. Phys.: Condens. Matter · 2015 · 27 · 354101
7. Hegemann · Acc. Chem. Res. · 2015 · 48 · 190910.1021/acs.accounts.5b00156 ↗
8. Jang · J. Am. Chem. Soc. · 2005 · 127 · 156310.1021/ja044530x ↗
9. Zhang · Adv. Mater. · 2017 · 29 · 160494810.1002/adma.201604948 ↗
10. Zhang · ChemPhysChem · 2016 · 17 · 175910.1002/cphc.201501048 ↗
11. Boal · J. Am. Chem. Soc. · 2000 · 122 · 73410.1021/ja993900s ↗
12. Nowak · Angew. Chem., Int. Ed. · 2015 · 54 · 419210.1002/anie.201409667 ↗
13. Cecconello · Nano Lett. · 2013 · 13 · 627510.1021/nl403884w ↗
14. Daniel · Chem. Rev. · 2004 · 104 · 29310.1021/cr030698+ ↗
15. Katz · Angew. Chem., Int. Ed. · 2004 · 43 · 604210.1002/anie.200400651 ↗
16. Alkilany · Acc. Chem. Res. · 2013 · 46 · 65010.1021/ar300015b ↗
17. Dewi · ACS Nano · 2015 · 9 · 143410.1021/nn5058408 ↗
18. Sun · Chem. Soc. Rev. · 2014 · 43 · 737810.1039/C4CS00143E ↗
19. Fernandez · APL Mater. · 2014 · 2 · 01070210.1063/1.4858295 ↗
20. Gschneidtner · J. Mater. Chem. C · 2013 · 1 · 712710.1039/c3tc31483a ↗
21. Guttman · Appl. Phys. Lett. · 2011 · 99 · 06311310.1063/1.3624899 ↗
22. Petersen · J. Phys. Chem. B · 2010 · 114 · 1177110.1021/jp105948v ↗
23. Karmakar · Nanoscale · 2012 · 4 · 231110.1039/c2nr11195k ↗
24. Rekharsky · Proc. Natl. Acad. Sci. U. S. A. · 2007 · 104 · 2073710.1073/pnas.0706407105 ↗
25. Lloyd-Jones · Synthesis · 2008 · 661
26. Glidewell · J. Organomet. Chem. · 1997 · 527 · 25910.1016/S0022-328X(96)06644-2 ↗
27. Marquez · IEEE Trans. Nanobioscience · 2004 · 3 · 3910.1109/TNB.2004.824269 ↗
28. Jeon · J. Am. Chem. Soc. · 2005 · 127 · 1298410.1021/ja052912c ↗
29. Cao · Angew. Chem., Int. Ed. · 2014 · 53 · 98810.1002/anie.201309635 ↗
30. C. A. Schalley , Analytical Methods in Supramolecular Chemistry , Wiley , 2007
31. Green · Biochem. J. · 1963 · 89 · 58510.1042/bj0890585 ↗
32. Bardelang · Cryst. Growth Des. · 2011 · 11 · 559810.1021/cg201173j ↗
33. Mecozzi · Chem. – Eur. J. · 1998 · 4 · 101610.1002/(SICI)1521-3765(19980615)4:6<1016::AID-CHEM1016>3.0.CO;2-B ↗
34. Yang · Isr. J. Chem. · 2011 · 51 · 55110.1002/ijch.201100032 ↗
35. Yi · Org. Biomol. Chem. · 2013 · 11 · 28710.1039/C2OB26834E ↗
36. Connelly · Chem. Rev. · 1996 · 96 · 87710.1021/cr940053x ↗
37. Ong · Organometallics · 2003 · 22 · 418110.1021/om030305x ↗
38. Cui · Langmuir · 2009 · 25 · 1376310.1021/la9015096 ↗
39. Senler · Supramol. Chem. · 2014 · 26 · 67710.1080/10610278.2014.930148 ↗
40. Engstrom · Anal. Chem. · 1984 · 56 · 13610.1021/ac00266a005 ↗
41. Randles · Trans. Faraday Soc. · 1948 · 44 · 32710.1039/TF9484400327 ↗
42. A. J. Bard and L. R.Faulkner , Electrochemical Methods: Fundamentals and Applications , Wiley , 2 nd edn, 2001
43. Gadde · Curr. Org. Chem. · 2011 · 15 · 2710.2174/138527211793797800 ↗
44. D. K. Gosser , Cyclic Voltammetry: Simulation and Analysis of Reaction Mechanisms , Wiley , 1993
45. Nicholson · Anal. Chem. · 1965 · 37 · 135110.1021/ac60230a016 ↗
46. A. M. Kuznetsov and J.Ulstrup , Electron transfer in chemistry and biology - An introduction to the theory , Wiley , 1998
47. Laviron · J. Electroanal. Chem. · 1979 · 101 · 1910.1016/S0022-0728(79)80075-3 ↗
48. Leung · J. Am. Chem. Soc. · 2016 · 138 · 298910.1021/jacs.6b01382 ↗