Carbonyls, chromium iridium

C, Carbide iron complex, 26 246 ruthenium cluster complexes, 26 281-284 CHF,02, Acetic acid, trifluoro-tungsten complex, 26 222 CHFjOjS, Methanesulfonic acid, trifluoro-iridium, manganese, and rhenium complexes, 26 114, 115, 120 platinum complex, 26 126 CH2O2, Formic acid rhenium complex, 26 112 CH, Methyl iridium complex, 26 118 manganese complex, 26 156 rhenium complexes, 26 107 CHjO, Methanol platinum complexes, 26 135 tungsten complex, 26 45 CNajOuRusCn, Ruthenate(2- )ns-carbido-tetradecacarbonyl-disodium, 26 284 CO, Carbonyls chromium, 26 32, 34, 35 chromium, molybdenum, and tungsten, 26 343... 

Pyridazines form complexes with iodine, iodine monochloride, bromine, nickel(II) ethyl xanthate, iron carbonyls, iron carbonyl and triphenylphosphine, boron trihalides, silver salts, mercury(I) salts, iridium and ruthenium salts, chromium carbonyl and transition metals, and pentammine complexes of osmium(II) and osmium(III) (79ACS(A)125). Pyridazine N- oxide and its methyl and phenyl substituted derivatives form copper complexes (78TL1979). 

Mixed donor tridentate [NPS] ligated derivatives, chromium(III) complexes, 5, 370 Mixed iridium carbonyl dimers, preparation, 7, 289 Mixed isonitrile acetylides, liquid crystals, 12, 281 Mixed isonitrile phenyl complexes, liquid crystals, 12, 282 Mixed ligand triangular Pt carbonyl clusters, characteristics, 8, 411... 

Further restrictions to the scope of the present article concern certain molecules which can in one or more of their canonical forms be represented as carbenes, e.g. carbon monoxide such stable molecules, which do not normally show carbenoid reactivity, will not be considered. Nor will there be any discussion of so-called transition metal-carbene complexes (see, for example, Fischer and Maasbol, 1964 Mills and Redhouse, 1968 Fischer and Riedel, 1968). Carbenes in these complexes appear to be analogous to carbon monoxide in transition-metal carbonyls. Carbenoid reactivity has been observed only in the case of certain iridium (Mango and Dvoretzky, 1966) and iron complexes (Jolly and Pettit, 1966), but detailed examination of the nature of the actual reactive intermediate, that is to say, whether the complexes react as such or first decompose to give free carbenes, has not yet been reported. A chromium-carbene complex has been suggested as a transient intermediate in the reduction of gfem-dihalides by chromium(II) sulphate because of structural effects on the reaction rate and because of the structure of the reaction products, particularly in the presence of unsaturated compounds (Castro and Kray, 1966). The subject of carbene-metal complexes reappears in Section IIIB. 

Pyridazine forms a stable adduct with iodine, with semiconductor properties. " Similar complexes were prepared from iodine mono-ehloride, bromine, and nickel(II) ethyl xanthate. Complexes of pyrida-zines with iron carbonyls and with iron carbonyls and triphenylphosphine have been prepared and investigated. " Complexes of pyridazines with boron trihalides, silver salts, mercury(I) salts, iridium salts, " ruthenium salts, and chromium carbonyls are re-... 

The number of complexes of this type is considerably higher than for inclusion-and carbonyl complexes, because the components of the complexes can be varied much more Substituted cyclophanes from [22]- up to [26]cyclophanes, as well as indenophanes are used as ligands for metal fragments, which may consist of chromium, iron, ruthenium, rhodium, iridium or cobalt as metal units, and Cp-, Cp - and C R -units as stabilizing co-ligands. From Fig. 21 the importance of the oxidation state and position in the periodic table of the individual metals can be seen [48a] cobalt-III forms monocomplexes only, whereas the lower sited iridium-IIl also forms the biscomplexes for cobalt. 

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