Pickup, Oliver J S (2012) Ruthenium Carboxylate Complexes as Probes to Metal Ligand Interactions. MSc by research thesis, University of York.
Available under License Creative Commons Attribution-Noncommercial-No Derivative Works 2.0 UK: England & Wales.
A synthetic route to [Ru(κ2-O₂CC₆H₄-R)2(PPh₃)₂] complexes (where R= 4-F, 4-CH3, 4-OMe, 4-NMe2, 3-F, 3-CH3, 3-OMe, 3-NMe2) has been developed. From these species, novel ruthenium-carbonyl [Ru(κ2-O₂CC₆H₄-R)(κ1-O₂CC₆H₄-R)(CO)(PPh₃)₂] (where R= 4-F,4-CH3,4-OMe,4-NMe2,3-F,3-CH3,3-NMe2), and vinylidene complexes [Ru(κ2-O₂CC₆H₄-R)(κ1-O₂CC₆H₄-R)(=C=HPh)(PPh₃)₂] (where R= 4-F,4-CH3,4-OMe,4-NMe2,3-F,3-CH3,3-NMe2), have been synthesised. Hammett studies have shown the effect of changing the substituent on the carboxylate ligand on the M-C π-back bonding for the complexes of the general type [Ru(κ2-O₂CC₆H₄-R)(κ1-O₂CC₆H₄-R)(CO)(PPh₃)₂] and [Ru(κ2-O₂CC₆H₄-R)(κ1-O₂CC₆H₄-R)(=C=HPh)(PPh₃)₂]. The CO stretching frequencies in the IR spectra of the complexes [Ru(κ2-O₂CC₆H₄-R)(κ1-O₂CC₆H₄-R)(CO)(PPh₃)₂] demonstrate the more electron-donating substituents strengthen the bonding between the metal and the carbonyl ligand. A similar trend is observed in the case of the vinylidene-containing ruthenium complexes, demonstrating that the electronic properties of the ancillary ligands may profoundly affect the metal-vinylidene interaction.
|Item Type:||Thesis (MSc by research)|
|Academic Units:||The University of York > Chemistry (York)|
|Depositing User:||Mr Oliver J S Pickup|
|Date Deposited:||18 Sep 2012 10:58|
|Last Modified:||08 Aug 2013 08:49|