Imine Derivatives on Au(111): Evidence for “Inverted” Thermal Isomerization
Source abstract
Abstract
Molecules that undergo reversible isomerization between trans and cis states, typically upon illumination with light at appropriate wavelengths, represent an important class of molecular switches. In this combined scanning tunneling microscopy (STM) and high-resolution electron energy loss spectroscopy (HREELS) study, we report on self-assembled arrays of imine derivatives on a Au(111) surface. Most of the molecules are found in the trans state after deposition at room temperature, but many of them change their conformation upon heating, which we assign to switching to the cis state. As for many molecular switches, the trans isomer is the energetically more stable compound in solution, resulting in thermal cis to trans relaxation upon sufficient heating. On the surface, however, the number of cis isomers increases with temperature, pointing toward an "inverted" thermal isomerization behavior. The reason for this surface-mediated effect could be a stronger coupling, as compared to the trans state, of the central imine part of the molecule to the gold surface, which is sterically only possible in the cis state.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Molecular Junctions and Nanostructures · Surface Chemistry and Catalysis · Graphene research and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Physics Department, Freie Universität Berlin, Arnimallee 14, Berlin, Germany
Fritz-Haber-Institute of the Max-Planck Society, Faradayweg 4-6, Berlin, Germany
Chemistry Department, Freie Universität Berlin, Takustraße 3, Berlin, Germany
References (48)
Show source-provided references
1. Joachim C. · Nature · 2000 · 408 · 54110.1038/35046000 ↗
2. Heath J. R. · Phys. Today · 2003 · 56 · 4310.1063/1.1583533 ↗
3. Feringa B. L. · 200110.1002/3527600329 ↗
4. van der Molen S. J. · J. Phys.: Condens. Matter · 2010 · 22 · 133001
5. Lehn J. M. · Chem.—Eur. J. · 2006 · 12 · 591010.1002/chem.200600489 ↗
6. Schultz T. · J. Am. Chem. Soc. · 2003 · 125 · 809810.1021/ja021363x ↗
7. Chang C.-W. · J. Am. Chem. Soc. · 2004 · 126 · 1010910.1021/ja049215p ↗
8. Iancu V. · Proc. Natl. Acad. Sci. U.S.A. · 2006 · 103 · 1371810.1073/pnas.0603643103 ↗
9. Liljeroth P. · Science · 2007 · 317 · 120310.1126/science.1144366 ↗
10. Alemani M. · J. Am. Chem. Soc. · 2006 · 128 · 1444610.1021/ja065449s ↗
11. Choi B.-Y. · Phys. Rev. Lett. · 2006 · 96 · 15610610.1103/PhysRevLett.96.156106 ↗
12. Henzl J. · Angew. Chem., Int. Ed. · 2006 · 45 · 60310.1002/anie.200502229 ↗
13. Hagen S. · Chem. Phys. Lett. · 2007 · 444 · 8510.1016/j.cplett.2007.07.005 ↗
14. Comstock M. J. · Phys. Rev. Lett. · 2007 · 99 · 03830110.1103/PhysRevLett.99.038301 ↗
15. Selvanathan S. · Appl. Phys. A: Mater. Sci. Process. · 2008 · 93 · 24710.1007/s00339-008-4827-1 ↗
16. Dri C. · Nat. Nanotechnol. · 2008 · 3 · 64910.1038/nnano.2008.269 ↗
17. Alemani M. · J. Phys. Chem. C · 2008 · 112 · 1050910.1021/jp711134p ↗
18. Kumar A. S. · Nano Lett. · 2008 · 8 · 164410.1021/nl080323+ ↗
19. Hagen S. · J. Chem. Phys. · 2008 · 129 · 16410210.1063/1.2997343 ↗
20. Henningsen N. · Appl. Phys. A: Mater. Sci. Process. · 2008 · 93 · 24110.1007/s00339-008-4840-4 ↗
21. McNellis E. R. · Phys. Chem. Chem. Phys. · 2010 · 12 · 640410.1039/c001978j ↗
22. Mercurio G. · Phys. Rev. Lett. · 2010 · 104 · 03610210.1103/PhysRevLett.104.036102 ↗
23. Nägele T. · Chem. Phys. Lett. · 1997 · 272 · 48910.1016/S0009-2614(97)00531-9 ↗
24. Grill L. · J. Phys.: Condens. Matter · 2008 · 20 · 053001
25. Bombis C. · Phys. Rev. Lett. · 2010 · 104 · 18550210.1103/PhysRevLett.104.185502 ↗
26. Óvari L. · J. Phys. Chem. C · 2007 · 111 · 1537010.1021/jp075274o ↗
27. Piantek M. · J. Am. Chem. Soc. · 2009 · 131 · 1272910.1021/ja901238p ↗
28. Wolf M. · Surf. Sci. · 2009 · 603 · 150610.1016/j.susc.2008.11.049 ↗
29. Hugel T. · Science · 2002 · 296 · 110310.1126/science.1069856 ↗
30. Hagen S. · Appl. Phys. A: Mater. Sci. Process. · 2008 · 93 · 25310.1007/s00339-008-4831-5 ↗
31. Fischer E. · J. Chem. Phys. · 1957 · 27 · 80810.1063/1.1743834 ↗
32. Berns U. · Z. Naturforsch. · 1976 · 31 · 95310.1515/znb-1976-0712 ↗
33. Asano T. · J. Org. Chem. · 1993 · 58 · 441810.1021/jo00068a042 ↗
34. King N. R. · J. Mater. Chem. · 1997 · 7 · 62510.1039/a607980f ↗
35. Óvári L. · J. Chem. Phys. · 2010 · 133 · 04470710.1063/1.3460647 ↗
36. Hagen S. · New J. Phys. · 2010 · 12 · 12502210.1088/1367-2630/12/12/125022 ↗
37. Wettermark G. · J. Phys. Chem. · 1965 · 69 · 158410.1021/j100889a023 ↗
38. Levy N. · Nano Lett. · 2009 · 9 · 93510.1021/nl802632g ↗
39. Skrabal P. · Helv. Chim. Acta · 1975 · 58 · 80010.1002/hlca.19750580318 ↗
40. Ezumi K. · Chem. Lett. · 1974 · 3 · 139310.1246/cl.1974.1393 ↗
41. Traetteberg M. · J. Mol. Struct. · 1978 · 48 · 39510.1016/0022-2860(78)87250-0 ↗
42. Bürgi H. B. · Helv. Chim. Acta · 1970 · 53 · 174710.1002/hlca.19700530724 ↗
43. Meic Z. · Pure Appl. Chem. · 1989 · 61 · 212910.1351/pac198961122129 ↗
44. Leyssner F. · J. Phys. Chem. C · 2010 · 114 · 123110.1021/jp909684x ↗
45. Gahl, C.et al.Manuscript in preparation.
46. Anderson D. G. · J. Am. Chem. Soc. · 1965 · 87 · 143310.1021/ja01085a004 ↗
47. Gaenko A. V. · Theor. Chem. Acc. · 2007 · 118 · 27110.1007/s00214-007-0319-1 ↗
48. Collman J. P. · 1987