Metal–metal bonding and structures of trinickel and tricobalt dipyridylamido complexes from surface-enhanced Raman spectra
Version of Record online: 26 JAN 2010
Copyright © 2010 John Wiley & Sons, Ltd.
Journal of Raman Spectroscopy
Volume 41, Issue 12, pages 1694–1699, December 2010
How to Cite
Lai, S.-H., Hsiao, C.-J., Huang, Y.-M., Chen, I.-C., Wang, W.-Z. and Peng, S.-M. (2010), Metal–metal bonding and structures of trinickel and tricobalt dipyridylamido complexes from surface-enhanced Raman spectra. J. Raman Spectrosc., 41: 1694–1699. doi: 10.1002/jrs.2604
- Issue online: 16 DEC 2010
- Version of Record online: 26 JAN 2010
- Manuscript Accepted: 3 DEC 2009
- Manuscript Received: 22 OCT 2009
- National Science Council and Ministry of Education, Taiwan
- metal-string complex;
We recorded surface-enhanced Raman scattering (SERS) spectra of metal-string complexes Co3(dpa)4 Cl2 [di(2-pyridyl)amido (dpa)], Ni3(dpa)4 Cl2 and the oxidized form of the Ni3 complex to determine their vibrational wavenumbers and to investigate their structures. For SERS measurements these complexes were adsorbed on silver nanoparticles in aqueous solution to eliminate the constraint of a crystal lattice and the complexes remain in thermal equilibrium. From our analysis of the vibrational normal modes we assigned the SERS lines at 242 and 276 cm−1 to Ni3 and Co3 symmetric-stretching modes of the symmetric form. For Co3 (dpa)4Cl2 a Raman line at 383 cm−1 was assigned to the CoCo stretching mode of the unsymmetric form. The wavenumber of the Ni3 symmetric-stretching mode of the oxidized form [Ni3(dpa)4]3+ is 274 cm−1, greater than that for neutral Ni3(dpa)4Cl2, in agreement with a prediction of delocalized molecular-orbital theory that an electron is removed from an antibonding orbital after oxidation. The experimental data show that the SERS technique serves as an excellent tool to observe the variation of metal–metal bonding during an oxidation or reduction reaction. Copyright © 2010 John Wiley & Sons, Ltd.