Si−C(N) σ Linkages and N → Si Dative Bonding at Pyridine/Si(111)-7 × 7
Source abstract
Abstract
We experimentally demonstrated that pyridine/Si(111)-7 x 7 can act as an electron donor/acceptor pair as a result of the charge transfer from the electron-rich N atom of pyridine to the electron-deficient adatom of the Si surface, evidenced by the upshift of 1.8 eV (state A) for the N(1s) core level upon the formation of a datively bonded complex compared to physisorbed molecules. Another state (B) whose N(1s) binding energy downshifts by 1.2 eV was assigned to an adduct through Si-C and Si-N covalent linkages, formed via a [4 + 2]-like addition mechanism on Si(111)-7 x 7. Binding molecules through the formation of the dative bond resulted from significant electron transfer opens a new approach for the creation of Si-based molecular architectures and modification of semiconductor interfacial properties with unsaturated organic molecules.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Boron and Carbon Nanomaterials Research · Semiconductor materials and devices · Semiconductor materials and interfaces
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, National University of Singapore, 10 Kent Ridge, Singapore 119260
References (29)
Show source-provided references
1. Yates J. T., Jr. · Science · 1998 · 279 · 33610.1126/science.279.5349.336 ↗
2. Wolkow R. A. · Annu. Rev. Phys. Chem. · 1999 · 50 · 44110.1146/annurev.physchem.50.1.413 ↗
3. Lu X. · J. Phys. Chem. B · 2001 · 105 · 10075
4. Takayanagi K. · J. Vac. Sci. Technol., A · 1985 · 3 · 150610.1116/1.573160 ↗
5. Cao Y. · J. Am. Chem. Soc. · 2000 · 122 · 1813
6. Cao Y. · Angew. Chem. Int. Ed. · 2000 · 39 · 2744
7. Tao F. · J. Am. Chem. Soc. · 2002 · 124 · 7180
8. Tao F. · J. Am. Chem. Soc. · 2001 · 123 · 9403
9. Tao F. · J. Am. Chem. Soc. · 2003 · 125 · 6696
10. Tao F. · J. Phys. Chem. B · 2002 · 106 · 3895
11. Qiao Q. H. · Chem. Phys. Lett. · 2000 · 325 · 512
12. Cao X. · J. Am. Chem. Soc. · 2001 · 123 · 10996
13. Cao X. · J. Phys. Chem. B · 2002 · 106 · 1842
14. Wang G. T. · J. Phys. Chem. B · 2003 · 107 · 298610.1021/jp021751l ↗
15. Wang G. T. · J. Phys. Chem. B · 2001 · 105 · 3299
16. Wang G. T. · J. Phys. Chem. B · 2001 · 105 · 12565
17. Tao F. · J. Phys. Chem. B · 2003 · 107 · 6390
18. Cho Y. E. · J. Am. Chem. Soc. · 2003 · 125 · 7515
19. Cohen M. R. · Surf. Sci. · 1991 · 245 · 1110.1016/0039-6028(91)90462-2 ↗
20. Swartz W. E. · Spectrochim. Acta A · 1974 · 30 · 157210.1016/0584-8539(74)80166-2 ↗
21. Jack J. J. · Anal. Chem. · 1971 · 43 · 73610.1021/ac60301a017 ↗
22. Long D. A. · Trans. Faraday Soc. · 1963 · 59 · 78310.1039/TF9635900783 ↗
23. Wiberg K. B. · J. Phys. Chem. · 1984 · 88 · 607510.1021/j150668a068 ↗
24. Taguchi Y. · J. Chem. Phys. · 1991 · 95 · 687610.1063/1.461498 ↗
25. Cao Y. · J. Phys. Chem. B · 1999 · 103 · 5702
26. Qiao M. H. · Chem. Phys. Lett. · 2000 · 325 · 512
27. Stidham H. D. · Spectrochim. Acta · 1965 · 21 · 3210.1016/0371-1951(65)80102-3 ↗
28. Hagemann H. · Spectrochim. Acta, Part A · 1985 · 41 · 75610.1016/0584-8539(85)80185-9 ↗
29. Carreira L. A. · J. Chem. Phys. · 1973 · 59 · 81210.1063/1.1680096 ↗