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Silyl complexes bimetallic

Dienols with 2 equiv. of 1 gave the corresponding bimetallic alkoxide organozir-conocene complexes however, protolysis allowed recovery of the alcohol functionality (Scheme 8-29) [107]. Alcohols can also be easily converted to ethers. Alkyl, aryl, silyl [85,112,183, 210] and THP [17, 153, 211, 219] ethers are stable under hydrozirconation conditions side products were observed only with the trimethylsUyl group [220, 221]. [Pg.271]

In contrast, Fe-Hg-X complexes show little tendency to form halide bridged species and less is known about complexes containing Zn. We first reported the formation of Fe-Si-O-M four membered ring systems with soft metals M = Ag, Rh, Pd, and Pt, and then prepared bimetallic complexes with more oxophilic metals in order to better understand the conditions for the occurrence of this unusual (t-alkoxy-silyl bridging mode. We have expanded our studies on Cd-containing complexes [3b-d] to Group 13 elements and we report here about the synthesis and reactivity of new, stable heterometallic Fe-M (M =... [Pg.199]

Siloxane compounds, in vitreous silica manufacture, 22 414 Siloxane materials, 20 240 Siloxane oligomers, in silicone polymerization, 22 555-556 Siloxanols, silylation and, 22 703 Silsesquioxane hybrids, 13 549 Silsesquioxanes, 15 188, 22 589-590 SilvaGas process, 3 696, 697 Silver (Ag), 22 636-667. See also Silver compounds. See Ag entries Argentothiosulfate complexes Batch desilverizing Lead-silver alloys Palladium-silver alloy membranes analytical methods for, 22 650-651 applications of, 22 636-637, 657-662 as bactericide, 22 656, 657, 660 barium alloys with, 3 344 in bimetallic monetary system, 22 647-648 in cast dental gold alloys, 8 307t coke formation on, 5 266 colloidal precipitation color, 7 343t colloidal suspensions, 7 275 color, 7 334, 335... [Pg.843]

Braunstein and coworkers have shown (vide supra) that in the bimetallic Fe—Pt complex (CO)3(SiR3)Fe(yU.-PPh2)Pt(PPh3)CO(Fe—Pt), a silyl migration occurred from the Fe to the Pt center (Scheme 17)102. Remarkably, the first example of a well-characterized insertion of a transition-metal fragment into a strained silicon-carbon bond of a silicon-bridged [l]ferrocenophane was recently reported by Sheridan, Lough and Manners. The... [Pg.2110]

Also, the silylated phosphoranediimine CH2[P(Ph2)=NSiMc3]2 (49) acts as a powerful ligand with two nitrogens as donor sites. The 1 1 molar ratio reaction of A1Mc3 with (49) has been reported to yield a cyclic complex (50) via elimination of methane. A bimetallic complex can be obtained either by the reaction of (50) and one equivalent of AlMe3 or by the reaction of (49) and two equivalents of AlMe3. ... [Pg.197]

Treatment of Cp"Cr(Ti -Cot), Cp" = Cp, Cp with (EtCN)3M(CO)3, M = Mo, W and Fe2(CO)9 affords the complexes [(Cp Cr)(CO)3M][ i-Cot], M = Fe, Cr, W, Cp = Cp and I(Cp Cr)(CO)3Crl/i-Cot, Cot = Cyclooctatetrane, which have been spectroscopically characterised. Bimetallic complexes containing bis(tetramethylcyclopentadienyl) dimethylsilane bridges have been prepared from the reaction of arene tricarbonyl molybdenum complexes with the silyl substituted cyclopentadienyl derivative. The synthesis of pinanylcyclopentadienes followed by metallation and reaction with Mo(CO)s and Mel gives the chiral (-)-[(ii -C5Me4-3-pinanyl)(CO)3Me], which has been structurally characterised. The chiral methallyl complexes CpMo(NO)X(Ti -2-methallyl) X = camphorsulfonate have been resolved and the reactions of the... [Pg.383]

The additions of bimetallic reagents such as the silicon-metal and tin-metal compounds to the carbon-carbon multiple bonds have been extensively studied however, there are few reports concerning the metal-boron compounds as shown above. Miyaura and co-workers have examined the addition reaction of tetraafkoxydiboron to alkynes and found that only the platinum complexes such as Pt(PPh3)4 exhibited excellent catalytic activity (Scheme 24). Pd(PPh3)4 and Pd(OAc)2-isocyanide complexes, which have been the best catalysts for the silyl- and stannyhnetallation, were ineffective because their oxidative addition to palladium(0)-phosphine complexes is very slow. ... [Pg.1174]


See other pages where Silyl complexes bimetallic is mentioned: [Pg.2037]    [Pg.2046]    [Pg.2072]    [Pg.211]    [Pg.2037]    [Pg.2046]    [Pg.2072]    [Pg.201]    [Pg.153]    [Pg.243]    [Pg.1533]    [Pg.243]    [Pg.227]    [Pg.1533]    [Pg.553]    [Pg.557]    [Pg.322]    [Pg.640]    [Pg.266]    [Pg.270]    [Pg.796]    [Pg.35]    [Pg.58]    [Pg.4435]    [Pg.109]    [Pg.2074]    [Pg.98]    [Pg.434]    [Pg.294]    [Pg.392]    [Pg.53]   
See also in sourсe #XX -- [ Pg.2072 , Pg.2073 ]

See also in sourсe #XX -- [ Pg.2072 , Pg.2073 ]




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