Abstract
A series of 2,2′:4,4″:4′,4‴-quaterpyridinium ligands bearing different N-substituents (methyl, Me; phenyl, Ph; 4-acetylphenyl, AcPh; 2-pyrimidyl, Pym; 3,5-bis-methoxycarbonyl-phenyl, MCP) have been prepared. These compounds feature powerful electron acceptor moieties and hence have been combined with different electron-rich metal centres to give complexes suitable for quadratic nonlinear optical properties. A series of dipolar ruthenium(II) ammine complex salts of the form [RuII(NH 3)4LA][PF6]4 and octupolar complex salts of the form [MII(LA) 3][PF6]8 (M = Ru(II)/Fe(II), LA = a 2,2′:4,4″:4′,4″-quaterpyridinium ligand) have been prepared. These compounds exhibit multiple intense, low energy metal-to-ligand charge-transfer (MLCT) absorptions in the visible region and reversible M(III/II) redox processes. First hyperpolarizabilities have been determined directly by using hyper-Rayleigh scattering and indirectly via calculation from Stark (electroabsorption) spectroscopic data.
Original language | English |
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Title of host publication | Proceedings of SPIE - The International Society for Optical Engineering|Proc SPIE Int Soc Opt Eng |
Editors | M.G. Kuzyk, M. Eich, R.A. Norwood |
Pages | 341-350 |
Number of pages | 9 |
Volume | 5212 |
Publication status | Published - 2003 |
Event | Linear and Nonlinear Optics of Organic Materials III - San Diego, CA Duration: 1 Jul 2003 → … |
Conference
Conference | Linear and Nonlinear Optics of Organic Materials III |
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City | San Diego, CA |
Period | 1/07/03 → … |
Keywords
- Hyper-Rayleigh scattering
- Pyridinium salts
- Quaterpyridyl
- Ruthenium complexes
- Stark spectroscopy