Differential ion-pairing and temperature effects on intervalence charge transfer (IVCT) in a series of dinuclear ruthenium complexes
D'Alessandro, Deanna M., Junk, Peter C., and Keene, F. Richard (2005) Differential ion-pairing and temperature effects on intervalence charge transfer (IVCT) in a series of dinuclear ruthenium complexes. Supramolecular Chemistry, 17 (7). pp. 529-546.
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Thermochromism and anion-dependence studies on the intervalence charge transfer (IVCT) properties of the diastereoisomers of [lcubRu(bpy)2rcub2(μ-BL)]5+ lcubBL = dpb', dpq', and dpb: dpb' = dipyrido(2,3-a;3',2'-c)benzophenazine; dpq' = dipyrido(2,3-a;3',2'-c)phenazine; dpb = 2,3-bis(2-pyridyl)-1,4-benzoquinoxalinercub are reported. IVCT thermochromism studies revealed that the level of delocalisation may differ between the diastereoisomers for a system, and a slight temperature dependence in meso-[lcubRu(bpy)2rcub2(μ-dpb)]5+ which was dependent on the identity of the counter-anion lcub./GSCH_A_131036_images/GSCH_A_131036math001.gif or B(C6F5)4-rcub Anion effects on the IVCT properties of the diastereoisomeric forms of the three complexes were observed to be somewhat unpredictable.
X-ray crystal structure determinations on meso-[lcubRu(bpy)2rcub2(μ-dpb)]4+ (as the ./GSCH_A_131036_images/GSCH_A_131036math002.gif and [ZnCl4]2- salts), meso-[lcubRu(bpy)2rcub2(μ-dpb')]4+ (./GSCH_A_131036_images/GSCH_A_131036math003.gif salt) and meso-[lcubRu(bpy)2rcub2(μ-dpq')]4+([ZnCl4]2- salt) revealed considerable distortion in the bridging ligand, particularly in the dpb-bridged species where the distortion was also dependent on the anion.
|Item Type:||Article (Refereed Research - C1)|
|Date Deposited:||25 Jun 2009 02:26|
|FoR Codes:||03 CHEMICAL SCIENCES > 0302 Inorganic Chemistry > 030207 Transition Metal Chemistry @ 100%|
|SEO Codes:||97 EXPANDING KNOWLEDGE > 970103 Expanding Knowledge in the Chemical Sciences @ 100%|
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