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Ruthenium, tris methane

NgC 1 iH 12, Bis(pyrazol-1 -y 1)(N-methylimidazol-2-yl)methane, (pz)2(mim)CH, 34 33 N6CI2RUC72H48, Ruthenium(II), tris(4,7-diphe-nyl-l,10-phenantroline)-, chloride, 34 66 N6ClgNd405gCigH66, Neodymium(lll), tetrakis-( 3-hydroxo) hexaalaninedecaaquatetra-, perchlorate, 34 184... [Pg.253]

Fig. 24. Products of an Hi-promoted ruthenium catalyst in tri-n-propylphosphine oxide, as a function of reaction time (193) (A) ethanol ( ) methane (O) methanol ( ) ethylene glycol (A) n-propanol. Reaction conditions 75 ml solvent, 15 mmol Ru, 15 mmol HI, 850 atm, H2/CO = 1,230 C. Fig. 24. Products of an Hi-promoted ruthenium catalyst in tri-n-propylphosphine oxide, as a function of reaction time (193) (A) ethanol ( ) methane (O) methanol ( ) ethylene glycol (A) n-propanol. Reaction conditions 75 ml solvent, 15 mmol Ru, 15 mmol HI, 850 atm, H2/CO = 1,230 C.
Catalytic transformations involving the C-H bonds of thiophene are rare, but recently there has been a report on the catalytic addition of the C(2)-H bond of thiophene across ethylene to form 2-ethylthiophene <20040M5514>. Reaction of the ruthenium complex TpRu(CO)(NCMe)(Me) (where Tp = hydrido tris(pyrazolyl)borate) with thiophene produces the 2-thienyl complex 249 and methane. This complex catalyzes the formation of 2-ethylthiophene from a solution of thiophene and ethylene (Equation 121). The mechanism of this reaction has been explored. [Pg.828]

BrAsFjS, cyclo-Heptasulfur(l +), bromo-, hexaf1uoroarsenate(l -), 27 336 BrCH, Methane, bromo-, osmium and ruthenium complexes, 27 201, 205 BrCi Hj, Benzene, l-bromo-2,4,6-tri-tert-butyl-, 27 236... [Pg.375]

T riphenylphosphine—Diethyl azodi-carboxylate, 280, 645 Triphenylphosphine dibiomide, 645-646 Triphenylphosphine dichloride, 646-647 Triphenylphosphine dihaiides, 647-648 Triphenylphosphine diiodide, 648 Triphenylphosphine ditriflate, 648 Triphenylphosphite methiodide, 649 Triphenyl phosphite ozonide, 435 Triphenyl(prop-2-ynyl)phosphonium bromide, 494 Triphenylsilanol, 655, 656 Triphenylstannane, 649 Triphenyltin hydride, 649 Triphenylvinylsilane, 637 Triphosphopyridine nucleotide, 36-37 Tri- -propyl orthovanadate, 655 Tris-annelation, 410 Ttis(aquo)hexa-fi-acetato-p,-oxotri-ruthenium acetate, 425-426,650 Tris(dimethoxyboryl)methane, 328, 329 Tris(dimethylamino)borane, 554 Trishomocubanone, 108 Tris(neomenthyldiphenylphosphine)-chlororhodium, 416... [Pg.384]

C H24N4, 1,4,8,1 1-Tetrazacyclotetradecane, ruthenium complex, 29 166 CjqHj CIjPSIj, Phosphonous dichloride, [tris(trimethylsilyl)methyl)-, 27 239 CjoHjgSi], Methane, tris(trimethylsilyl)-, 27 238... [Pg.351]

Videla M, Jacinto JS et al (2006) New ruthenium nitrosyl complexes with tris(l-pyrazolyl) methane (tpm) and 2,2 -bipyridine (bpy) coligands. Structure, spectroscopy, and electrophilic and nucleophilic reactivities of bound nitrosyl. Inorg Chem 45 8608-8617... [Pg.105]

When activated carbon is used as support, the support degradation by Ru-catalyzed methanation imder ammonia synthesis conditions can occur, so it affects the fife of catalysts. Therefore, many researchers have tried to use metal oxides to replace the activated carbons as the supports for ruthenium catalysts. Supported catalysts with high dispersion and high activity can be obtained when noble metals in precursor forms are supported on hardly reduced metal oxide. The oxides which are commonly used as ruthenium catalyst support include oxides of alkaline earth metals, lanthanide,and alumina. ... [Pg.435]


See other pages where Ruthenium, tris methane is mentioned: [Pg.198]    [Pg.110]    [Pg.240]    [Pg.385]    [Pg.26]    [Pg.161]    [Pg.462]    [Pg.338]    [Pg.199]    [Pg.221]    [Pg.390]    [Pg.521]    [Pg.1085]    [Pg.250]    [Pg.10]    [Pg.284]   


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