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Bipy

The pale blue tris(2,2 -bipyridine)iron(3+) ion [18661-69-3] [Fe(bipy)2], can be obtained by oxidation of [Fe(bipy)2]. It cannot be prepared directiy from iron(III) salts. Addition of 2,2 -bipyridine to aqueous iron(III) chloride solutions precipitates the doubly hydroxy-bridged species [(bipy)2Fe(. t-OH)2Fe(bipy)2]Cl4 [74930-87-3]. [Fe(bipy)2] has an absorption maximum at 610 nm, an absorptivity of 330 (Mem), and a formation constant of 10. In mildly acidic to alkaline aqueous solutions the ion is reduced to the iron(II) complex. [Fe(bipy)2] is frequentiy used in studies of electron-transfer mechanisms. The triperchlorate salt [15388-50-8] is isolated most commonly. [Pg.440]

Other molybdenum(0) compounds of interest include MoCl2(NO)2 and MoCl2(NO)2(bipy) where bipy = 2,2 -bipyridine. The compound (C3H3)Mo(CO)2NO, similar in stmcture to Figure 7d, is also known. [Pg.474]

H2 or O2 from water in the presence of a sacrificial reductant or oxidant employ a mthenium complex, typically [Ru(bipy)2], as the photon absorber (96,97). A series of mixed binuclear mthenium complexes having a variety of bridging ligands have been the subject of numerous studies into the nature of bimolecular electron-transfer reactions and have been extensively reviewed (99—102). The first example of this system, reported in 1969 (103), is the Creutz-Taube complex [35599-57-6] [Ru2(pyz)(NH3. [Pg.178]

Like mthenium, amines coordinated to osmium in higher oxidation states such as Os(IV) ate readily deprotonated, as in [Os(en) (NHCH2CH2NH2)] [111614-75-6], This complex is subject to oxidative dehydrogenation to form an imine complex (105). An unusual Os(IV) hydride, [OsH2(en)2] [57345-94-5] has been isolated and characterized. The complexes of aromatic heterocycHc amines such as pyridine, bipytidine, phenanthroline, and terpyridine ate similar to those of mthenium. Examples include [Os(bipy )3 [23648-06-8], [Os(bipy)2acac] [47691-08-7],... [Pg.178]

Coordination Compounds. A large number of indium complexes with nitrogen ligands have been isolated, particularly where Ir is in the +3 oxidation state. Examples of ammine complexes include pr(NH3)3] " [24669-15-6], prCl(NH3)] " [29589-09-1], and / j -pr(03SCF3)2(en)2]" [90065-94-4], Compounds of A/-heterocychc ligands include trans- [xCX py)][ [24952-67-8], Pr(bipy)3] " [16788-86-6], and an unusual C-metalated bipyridine complex, Pr(bipy)2(C, N-bipy)] [87137-18-6]. Isolation of this latter complex produced some confusion regarding the chemical and physical properties of Pr(bipy)3]3+ (167). [Pg.181]

Classic A/-heterocychc ligands, eg, bipyridyl (bipy), terpyridyl, imidazole, pyrazine, phenanthroline, piperazine (including alkyl- and aryl-substituted derivatives), and polypyrazol-l-yl-borates (bis, tris, and tetra), have all been found to coordinate Th(IV) chlorides, perchlorates, and nitrates. The tripodal hydrotris(pyrazolyl)borates, HBPz, have been used to stabilize organometaHic complexes (31). Bis-porphyrin Th(IV) "sandwich" complexes have been... [Pg.37]

Allyl Complexes. Allyl complexes of uranium are known and are usually stabilized by cyclopentadienyl ligands. AEyl complexes can be accessed via the interaction of a uranium halide and an allyl grignard reagent. This synthetic method was utilized to obtain a rare example of a "naked" homoleptic allyl complex, U(T -C2H )4 [12701 -96-17, which decomposes at 0°C. Other examples, which are more stable than the homoleptic allyl complex have been synthesized, ie, U(allyl)2(OR)2 (R = alkyl), U(allyl)2X (X = halide), and U(allyl)(bipy)2. [Pg.335]

It has been established, that both DN and Ibp form complex compounds with ions Eu(III), Sm(III), Tb(III) and Dy(III), possessing luminescent properties. The most intensive luminescence is observed for complex compounds with ion Tb(III). It has been shown, that complexation has place in low acidic and neutral water solutions at pH 6,4-7,0. From the data of luminescence intensity for the complex the ratio of component Tb Fig was established equal to 1 2 by the continuous variations method. Presence at a solution of organic bases 2,2 -bipyridil, (Bipy) and 1,10-phenanthroline (Phen) causes the analytical signal amplification up to 250 (75) times as a result of the Bipy (Phen) inclusion in inner coordination sphere and formation of different ligands complexes with component ratio Tb Fig Bipy (Phen) = 1 2 1. [Pg.386]

Electrolysis, [Ni(bipy)3](BF3), Mg anode, DMF, rt, 40-99% yield.Aryl bromides and iodides are reduced under these conditions. [Pg.263]

A typical value for the N O distance in nitro complexes is 124 pm whereas in nitrito complexes the terminal N-O (121pm) is shorter than the internal N-O(M) 129 pm. In the bidentate chelating mode (iii) the 2 M O distances may be fairly similar as in [Cu(bipy)2(02N)]N03 or quite different as in [Cu(bipy)(02N)2] ... [Pg.464]


See other pages where Bipy is mentioned: [Pg.59]    [Pg.98]    [Pg.143]    [Pg.410]    [Pg.724]    [Pg.1108]    [Pg.10]    [Pg.264]    [Pg.256]    [Pg.439]    [Pg.440]    [Pg.470]    [Pg.9]    [Pg.177]    [Pg.177]    [Pg.177]    [Pg.178]    [Pg.178]    [Pg.179]    [Pg.181]    [Pg.182]    [Pg.182]    [Pg.183]    [Pg.184]    [Pg.185]    [Pg.329]    [Pg.329]    [Pg.330]    [Pg.334]    [Pg.383]    [Pg.1060]    [Pg.799]    [Pg.238]    [Pg.449]    [Pg.469]    [Pg.951]    [Pg.960]    [Pg.960]    [Pg.971]    [Pg.980]    [Pg.994]   
See also in sourсe #XX -- [ Pg.732 ]




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Bipy ligands

Bipy)2CL.Cl

Bipy, oxidation

Bipy-tb

Chromium complexes with bipy, phen, terpy

CoCl2/bipy

Complexes with bipy and phen

CuCl/bipy

Lanthanide complexes with bipy, phen

Preparation of Ag(bipy)

Ruthenium bipy complexes, quenching

SS-Bipy

Synthesis, Structure, and Properties of Bipy Complexes

Tris-bipy cryptates

With bipy-diol

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