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Cobalt complexes triazole

Infrared data have been tabulated for benzotriazole and a wide range of its transition metal complexes or adducts (172). Far infrared spectra have been recorded for copper(II) benzotriazole adducts and bands at 270-320 cm-1 have been assigned to Cu-N vibrations (172). Infrared absorptions at approximately 825, 800, and 775 cm-1 in the spectra of cobalt(III)/4,5-disubstituted triazolate complexes have been attributed to triazolate ring vibrations (109). Infrared data have been reported and assignments made for palladium and platinum thiatriazoline-5-thionate complexes (37) and for the parent thione (127). Vibrational spectroscopy has been employed in an attempt to determine coordination sites for a range of 8-azapurine complexes (108). [Pg.178]

Despite the weak basicity of isoxazoles, complexes of the parent methyl and phenyl derivatives with numerous metal ions such as copper, zinc, cobalt, etc. have been described (79AHC(25) 147). Many transition metal cations form complexes with Imidazoles the coordination number is four to six (70AHC(12)103). The chemistry of pyrazole complexes has been especially well studied and coordination compounds are known with thlazoles and 1,2,4-triazoles. Tetrazole anions also form good ligands for heavy metals (77AHC(21)323). [Pg.51]

According to X-ray data, 2,5-diamino-l,3,4-triazole retains its diamino form in the heterovalent cobalt complex 375 (91IC4858) and in the polymeric complex with manganese thiocyanate (93ICA53). [Pg.291]

The NHCs have been used as ligands of different metal catalysts (i.e. copper, nickel, gold, cobalt, palladium, rhodium) in a wide range of cycloaddition reactions such as [4-1-2] (see Section 5.6), [3h-2], [2h-2h-2] and others. These NHC-metal catalysts have allowed reactions to occur at lower temperature and pressure. Furthermore, some NHC-TM catalysts even promote previously unknown reactions. One of the most popular reactions to generate 1,2,3-triazoles is the 1,3-dipolar Huisgen cycloaddition (reaction between azides and alkynes) [8]. Lately, this [3h-2] cycloaddition reaction has been aided by different [Cu(NHC)JX complexes [9]. The reactions between electron-rich, electron-poor and/or hindered alkynes 16 and azides 17 in the presence of low NHC-copper 18-20 loadings (in some cases even ppm amounts were used) afforded the 1,2,3-triazoles 21 regioselectively (Scheme 5.5 Table 5.2). [Pg.134]

Surface complexation to form a tetrahedral Co(L)X2 species is proposed to account for the adsorption of cobalt(II) chloride and bromide from acetone and ethanol solution onto silica gel modified with 3-amino-1,2,4,-triazole,526 supported by electronic and ESR spectroscopy. [Pg.54]

Involvement of two nucleophilic nitrogen atoms is thus typical for the amino heterocycles. The mutual disposition of the pyridine and amine nitrogen atoms allows the formation of chelate structures for the cobalt complexes of purine, 221 and 222. Structures with the N, iV -five-membered metal cycles were proven for the tri- and tetranuclear complexes of silver ) with 8-aminoquinoline (223) (92IC4370), and polymeric copper- and rhodium-acetate clusters (224). Another coordination mode can be found in the complexes of 4-amino-3,5-bis(pyridin-2-yl)-l,2,4-triazole, (225 or... [Pg.38]

Due to the low solubility of cobalt(II) fluoride in most solvents, formation of cobalt fluoro N-donor complexes (which are the only low-valent cobalt fluorides which are reliably reported) features a variety of starting materials. A common theme that runs throughout this work has been the use of [Co(BF4)2] as the fluoride source, and the subsequent controlled decomposition to obtain a metal-bound fluoride. This has been done, for example, with tris- (3,5-dimethyl-pyrazol-l-yl)methyl amine (amtd) to give [M2(amtd)2F(BF4)3(EtOH)Y(H20)] (M = Co, Cu, Zn x = 0-1.5, y = 1-2). The cobalt complex has been structurally characterised by X-ray diffraction [Fig. 3] [57]. Similarly, the combination of [M(BF4)2] (M = Mn, Co, Ni), [M(N03)2], NH4(NCS) and 3,5-diethyl-1,2,4-triazole (detrH) produces... [Pg.60]

Spin-state control in cobalt(II) complexes of pyridazine- or triazole-containing ligands 03CCR(245)17. [Pg.164]

POLSf-BIS(THIOC YANATO-AT)BIS-(i-(lW-l, 2,4-TRIAZOLE-AP,AT4)METAL(II) COMPLEXES WITH MANGANESE, IRON, COBALT, NICKEL, COPPER AND ZINC, AND BIS[TRIS(THIOCYANATO- V)TRIS( x-4//-l,2,4-TRIAZOLE-ATI)NICKEL(II)-A2 V2VVrlNICKEL(H)... [Pg.157]


See other pages where Cobalt complexes triazole is mentioned: [Pg.105]    [Pg.175]    [Pg.187]    [Pg.501]    [Pg.18]    [Pg.110]    [Pg.411]    [Pg.212]    [Pg.44]    [Pg.491]    [Pg.144]    [Pg.731]    [Pg.731]    [Pg.261]    [Pg.1290]    [Pg.156]    [Pg.522]    [Pg.424]    [Pg.177]    [Pg.447]    [Pg.318]    [Pg.266]   
See also in sourсe #XX -- [ Pg.32 , Pg.187 , Pg.188 ]

See also in sourсe #XX -- [ Pg.187 , Pg.188 ]




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