Triazolate complexes nickel

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)... 

Dimethyl-1,2,4-triazolium iodide with nickel(II) acetate gives the carbene complex l2Ni( 1,4-dimethyl-l,2,4-triazol-5-ylidene)2 (97OM2209). 

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). 

A range of L-cysteine derivatives bearing a 1,2,4-triazolyl residue on the sulfur atom has been prepared by the asymmetric Michael addition of 4,5-dialkyl-3-mercapto-l,2,4-triazoles to a nickel Schiff base complex. The enantiomeric excesses of the product aminoacids were measured and found to be greater than 98.5% in some cases <2004TA705, 2004RCB932, 2004IZV894>. 

Four main types of antioxidants are commonly used in polypropylene stabilizer systems although many other types of chemical compounds have been suggested. These types include hindered phenolics, thiodi-propionate esters, aryl phosphites, and ultraviolet absorbers such as the hydroxybenzophenones and benzotriazoles. Other chemicals which have been reported include aromatic amines such as p-phenylenediamine, hydrocarbon borates, aminophenols, Zn and other metal dithiocarbamates, thiophosphates, and thiophosphites, mercaptals, chromium salt complexes, tin-sulfur compounds, triazoles, silicone polymers, carbon black, nickel phenolates, thiurams, oxamides, metal stearates, Cu, Zn, Cd, and Pb salts of benzimidazoles, succinic acid anhydride, and others. The polymeric phenolic phosphites described here are another type. 

The preparation of thioacethydrazide, MeCSNHNHj, has now been accomplished, both from the known nickel complex and from carboxymethyl dithio-acetate [MeC(=S)SCH2C02Hl and hydrazine. It is stable at —30 °C, but at room temperature it changes into l,4-dihydro-3,6-dimethyl-l,2,4,5-tetrazine and at its melting point (95—96 °C) into 4-amino-3,5-dimethyl-1,2,4-triazole. 

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