Abstract:The synthesis and characterisation of a series of ruthenium polypyridyl complexes containing pyridyltriazole ligands in different coordination modes are described. The electrochemical and electronic properties of the compounds with respect to the coordination mode of the pyridyltriazole ligand are reported. Upon photolysis of the complex containing the 1‐methyl‐3‐(pyridin‐2‐yl)‐1,2,4‐triazole ligand, irreversible ligand isomerisation is observed.
“…The work serves as affirmation of formation of monodentate intermediates from bidentate ligands in the process of net loss of the bidentate ligand. Irreversible photoisomerization of Ru(II) complexes of the closely related 1-methyl-3-(pyridin-2-yl)-1,2,4-triazole was also reported by Fanni et al 65 …”
Section: Photoisomerization Processes Of Ru(ii) Imine Complexessupporting
This article is a short review that presents a short review of photosubstitution reactions of Ru(II) imine complexes and illustrates their use in the development of therapeutic agents. The review begins with an overview of the photophysical behavior and common photoreactions of Ru(II) imine complexes, with select examples from the literature since the 1960s. It is followed by a more detailed picture of the application of knowledge gained over the years in the development of Ru(II) complexes for photobiology and photodynamic therapy.
“…The work serves as affirmation of formation of monodentate intermediates from bidentate ligands in the process of net loss of the bidentate ligand. Irreversible photoisomerization of Ru(II) complexes of the closely related 1-methyl-3-(pyridin-2-yl)-1,2,4-triazole was also reported by Fanni et al 65 …”
Section: Photoisomerization Processes Of Ru(ii) Imine Complexessupporting
This article is a short review that presents a short review of photosubstitution reactions of Ru(II) imine complexes and illustrates their use in the development of therapeutic agents. The review begins with an overview of the photophysical behavior and common photoreactions of Ru(II) imine complexes, with select examples from the literature since the 1960s. It is followed by a more detailed picture of the application of knowledge gained over the years in the development of Ru(II) complexes for photobiology and photodynamic therapy.
“…However, for complexes containing protonated or methylated triazole ligands the 3 MC level is stabilised and photolability observed. 11,12,13 As a result photoinduced ligand dissociation processes are observed where the triazole ligand is not anionic. For [Ru(bpy) 2 (Hpytr)] 2+ there are two coordination isomers possible where the Hpytr ligand is bound either via the N2 or the N4 nitrogen atom of the triazole ring (Fig.…”
is observed. The activation parameters for the population of the 3 MC state from the lowest 3 MLCT manifold, as obtained from temperature dependent emission lifetime studies, are reported and their relevance to the observed photochemical behaviour is considered. The results obtained are discussed in relation the analogous pyridine-triazole complexes.
“…This is related to the strong sigma donor capacity of the deprotonated triazole ring. This leads to a considerable increase in the energy of the deactivating 3 MC level (Figure 1) ( Figure 9) [47]. This shows interactions between the pyridine group and the phenanthroline ligand in the starting material and pyridine mesityl interaction for the photoproduct.…”
Section: For the Earlier Mentioned Compound Fac-[re(bpy)(co)mentioning
In this contribution a range of photo induced ligand rearrangements observed for first and second row transition metal and organometallic compounds are discussed. The processes discussed include photoinduced ligand exchange, linkage isomerisation and changes occurring within the coordination sphere of the compounds such as cis-trans and fac-mer isomerisations. The relevance of these processes for photocatalytic cycles or their application as synthetic tools is discussed where appropriate.
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