Abstract
The Au-C linkage has been demonstrated as a robust interface for coupling thin organic films on Au surfaces. However, the nature of the Au-C interaction remains elusive up to now. Surface-enhanced Raman spectroscopy was previously used to assign a band at 412 cm-1as a covalent sigma Au-C bond for films generated by spontaneous reduction of the 4-nitrobenzenediazonium salt on Au nanoparticles. However, this assignment is disputed based on our isotopic shift study. We now provide direct evidence for covalent Au-C bonds on the surface of Au nanoparticles using 13C cross-polarization/magic angle spinning solid-state NMR spectroscopy combined with isotope substitution. A 13C NMR shift at 165 ppm was identified as an aromatic carbon linked to the gold surface, while the shift at 148 ppm was attributed to C-C junctions in the arylated organic film. This demonstration of the covalent sigma Au-C bond fills the gap in metal-C bonds for organic films on surfaces, and it has great practical and theoretical significance in understanding and designing a molecular junction based on the Au-C bond.
Original language | English |
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Pages (from-to) | 362-368 |
Number of pages | 7 |
Journal | JACS Au |
Volume | 1 |
Issue number | 3 |
DOIs | |
State | Published - 22 Mar 2021 |
Keywords
- Au nanoparticles
- Au-C bond
- SERS
- aryldiazonium salts
- isotope labeling
- solid-state NMR