A gold-nanoparticle stoppered [2]rotaxane
Source abstract
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 ↗