Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Rhenium complexes oxide halides

Rhenium(VI) complexes, 4,194 alkoxides, 4,196 amides, 4,194 amines, 4,199 carboxylates, 4,199 dimethylformamide, 4,199 dioxane, 4,198 halides, 4,195,199 2-hydroxypyridine, 4,199 imides, 4,194 magnetic behavior, 1,271 mixed sulfur-nitrogen compounds, 4,196 N heterocycles, 4,199 nitrides, 4,194 oxide halides, 4, 195 oxoanions,4,196 pyridine, 4,199 sulfates, 4,198 sulfur compounds, 4,196 tellurates, 4,198... [Pg.210]

Herrmann and co-workers showed that the 17-electron complex 62 may be subjected to electrochemical oxidation as well as reduction (54.55). The redox potentials of the respective halo complexes follow the expected trend for change in the halide ligands. In accordance with these electrochemical studies, both chemical oxidation and reduction reactions of 62 were found [Eqs. (49) and (50)]. Oxidation of the rhenium complex Re(CCMe3)(// -C5Me5)Cl2 by dioxygen results in cleavage of the neopentylidyne ligand from the metal center as pivalic anhydride and pivaloyl chloride. [Pg.261]

The following metal compounds are used for the preparation of the catalysts oxides, metal carbonyls, halides, alkyl and allyl complexes, as well as molybdenum, tungsten, and rhenium sulfides. Oxides of iridium, osmium, ruthenium, rhodium, niobium, tantalum, lanthanum, tellurium, and tin are effective promoters, although their catalytic activity is considerably lower. Oxides of aluminum, silicon, titanium, manganese, zirconium as well as silicates and phosphates of these elements are utilized as supports. Also, mixtures of oxides are used. The best supports are those of alumina oxide and silica. [Pg.706]

Rhenium Halides and Halide Complexes. Rhenium reacts with chlorine at ca 600°C to produce rheniumpentachloride [39368-69-9], Re2Cl2Q, a volatile species that is dimeric via bridging hahde groups. Rhenium reacts with elemental bromine in a similar fashion, but the metal is unreactive toward iodine. The compounds ReCl, ReBr [36753-03-4], and Rel [59301-47-2] can be prepared by careful evaporation of a solution of HReO and HX. Substantiation in a modem laboratory would be desirable. Lower oxidation state hahdes (Re X ) are also prepared from the pentavalent or tetravalent compounds by thermal decomposition or chemical reduction. [Pg.164]

Compounds of the formulas Re(CH3)6, ReO(CH3)4, Li e CH ] [60975-25-9], Re02(CH3)3 [56090-011-8], and Re03CH3 [70197-13-6] have been prepared. The first two compounds were obtained from reaction of rhenium halides or oxyhalides and methyllithium the last three were formed from the species by oxidation or reduction reactions. The use of these hydride and alkyl complexes as catalysts is under investigation. [Pg.164]

Finally, a mention should be made about the one peroxo system which will become more and more dominant the organometallic oxides of rhenium(VII). Such compounds have been found to be of outstanding catalytic activity for a number of oxygen transfer reactions with hydrogen peroxide.92 The best studied complex is methyltrioxorhenium(VII) (MTO) and its congeners. Figure 2.32 illustrates its synthesis. Epoxidation, aromatic oxidation and halide oxidation with these complexes have been studied with hydrogen peroxide and shown to be remarkably efficacious. [Pg.57]

Dinuclear Complexes Containing a Rhenium-Rhenium Bond and Oxide and/or Halide Bridges 176... [Pg.126]

It is in this oxidation state that the known chemistry of the two elements is most different. For rhenium di- and trinuclear cluster species predominate (Section 18-D-5), whereas for Tc there are only a few Tc and no Tc3+ complexes. Mononuclear Tc3+ species do occur. The only simple [MXJ3- complex known for either element is the [Tc(NCS)6]3 ion, but the mer-MCl3(PR3)3, MCl3py3, and [MX2(LL)2]+ complexes with X = halide, NCS , or MeS" and LL a diphosphine or diarsine are important.41 Some of these complexes can be reduced with retention of structure in the II and even I oxidation states.42... [Pg.993]

Rhenium (Re, at. mass 186.21) occurs mainly in oxidation states VII, V, and IV. Rhenium(VIl) compounds are the most stable. The colourless perrhenate, ReOT ion exhibits weak oxidizing properties. The chemical properties of rhenium resemble those of Mo and Mn. Rhenium(V) and (IV) form halide, oxalate, and tartrate complexes. [Pg.350]

The electrochemical properties of a number of isostructural rhe-nium(V) oxo, rhenium(V) imido, osmium(VI) nitrido, of formula [M(E)(X)(Y)(Tp )] (Tp = Tp or Tp, E = O, N-tolyl, N X, Y = hydrocarbyl, halide, triflate), have been described. The reactivity of these complexes as inner-sphere oxidants does not correlate with their peak reduction potentials, whereas the ease of the oxidation of these compounds well parallels their reactivity as oxidants.206... [Pg.124]


See other pages where Rhenium complexes oxide halides is mentioned: [Pg.115]    [Pg.97]    [Pg.280]    [Pg.318]    [Pg.165]    [Pg.165]    [Pg.3619]    [Pg.429]    [Pg.322]    [Pg.1058]    [Pg.97]    [Pg.207]    [Pg.279]    [Pg.283]    [Pg.299]    [Pg.303]    [Pg.337]    [Pg.367]    [Pg.164]    [Pg.93]    [Pg.143]    [Pg.143]    [Pg.147]    [Pg.163]    [Pg.167]    [Pg.168]    [Pg.193]    [Pg.224]    [Pg.185]    [Pg.1659]    [Pg.335]    [Pg.32]    [Pg.1058]    [Pg.261]    [Pg.669]    [Pg.143]   
See also in sourсe #XX -- [ Pg.4 , Pg.195 ]




SEARCH



Halide complexation

Halide oxidation

Halides complex

Halides oxides

Oxidation rhenium

Rhenium complexes

Rhenium complexes halides

Rhenium complexes mixed oxide-halides

Rhenium halides

Rhenium oxide

© 2024 chempedia.info