Bipyridyls complexes with metals

Ligands based upon bipyridyl have extensive application in coordination chemistry and have long been a popular subject for study. These ligands can form stable complexes with metals from... 

Organometallic compounds apart, oxidation states below - -2 are best represented by complexes with tris-bidentate nitrogen-donor ligands such as 2,2 -bipyridyl. Reduction by LiAlH4 in thf yields tris(bipyridyl) complexes in which the formal oxidation state of vanadium is -1-2 to —1. Magnetic moments are compatible with low-spin configurations of the metal but. 

Analytical chemistry of metal complexes with nitrogen-containing ligands of the 2,2 -bipyridyl type. A. T. Pilipenko and E. R. Falendysh, Russ. Chem. Rev. (Engl. Transl.), 1972, 41, 991-1008 (249). 

A CT transition which is very similar to the -> MMCT transition has been observed by Vogler et al. [55] for complexes [M(2,2 -bipyridyl)X3] with X = Cl, Br, I and M = Sb, Bi. These authors report MLCT transitions involving the promotion of an electron from the lone pair to the n orbital of the bipyridyl ligand. For example, for M = Sb and X = Br they observe an orange color for the complex due to an absorption band with a maximum at 435 nm. In the complexes considered by us the transition is to an antibonding n orbital (with pronounced d character) on the filled-shell transition-metal complex ion. 

The inverted region in electron transfer reactions is studied for the reaction of electronically-excited ruthenium(II) tris-bipyridyl ions with various metal(III) tris-bipyridyl complexes. Numerical calculations for the diffusion-reaction equation are summarized for the case where electron transfer occurs over a range of distances. Comparison is made with the experimental data and with a simple approximation. The analysis reveals some of the factors which can cause a flattening of the In k versus AG curve in the inverted... 

Bipyridyl (continued) as ligand, 12 135-1% catalysis, 12 157-159 electron-transfer reactions, 12 153-157 formation, dissociation, and racemization of complexes, 12 149-152 kinetic studies, 12 149-159 metal complexes with, in normal oxidation states, 12 175-189 nonmetal complexes with, 12 173-175 oxidation-reduction potentials, 12 144-147... 

Suitably substituted diazines also form chelate complexes, e.g. 2,3,5,6-tetrakis(a-pyridyl)pyrazine yields red tridentate complexes with Fe11. In the fast development of metallosupramolecular chemistry, many other polydentate ligands, based on 2,2 -bipyridyl units, have been obtained and studied (94CI(L)56). Thus, two molecules of oligopyridine (58) interact with various metal ions (Fe2+, Co2+, Cu2+ etc.) to form a double-helical [M2L2]4+ complex in which each metal is bonded to a tridentate region from each ligand. 

Metal acetylacetonates quench triplet species generated by flash photolysis of aromatic ketones and hydrocarbons.330-333 More recently, these reactions have been studied from a synthetic standpoint. Triplet state benzophenone sensitizes photoreduction of Cu(MeCOCHCOMe)2 by alcohols to give black, presumably polymeric, [Cu(MeCOCHCOMe)] . This reacts with Lewis bases to provide complexes of the type CuL2(MeCOCHCOMe) (L = bipyridyl/2, ethylenediamine/2, carbon monoxide, Ph3P). Disubstituted alkynes yield Cu(C2 R2 XMeCOCHCOMe) but terminal alkynes form CuQR acetylides.334 The bipyridyl complex of copper(I) acetylacetonate catalyzes the reduction of oxygen to water and the oxidation of primary and secondary alcohols to aldehydes and ketones.335... 

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