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B-hydrides

Fig. 11. X-ray diffraction pattern of a Ni99Cul alloy partially transformed into its (3-hydride (0 NiCuH) before (a) and after (b) hydride decomposition. Arrows point to the diffraction peaks representing the rich in copper alloy phsae desegregated from the initial alloy after a multiple hydrogen absorption-desorption treatment. After Palczew-ska and Majchrzak (48). Fig. 11. X-ray diffraction pattern of a Ni99Cul alloy partially transformed into its (3-hydride (0 NiCuH) before (a) and after (b) hydride decomposition. Arrows point to the diffraction peaks representing the rich in copper alloy phsae desegregated from the initial alloy after a multiple hydrogen absorption-desorption treatment. After Palczew-ska and Majchrzak (48).
Hydrozirconation of iminoboranes -B=N-R leads to a four-membered ring with a Zr-H-B hydride bridge [209]. [Pg.268]

Carbonylation is an exceedingly broad subject, but the main reaction patterns can be easily rationalized by recalling the classification used earlier for coupling reactions involving (a) metallacycles (b) hydride-promoted reactions and (c) oxidative addition of organic halides to zero-valent nickel. In fact, one or other of these steps is necessary to form a species able to undergo carbonylation. [Pg.225]

Two significant items were confirmed in this work (a) Molybdenum, and most probably tungsten, can expand its sphere of coordination beyond 6 and (b) hydride shifts transforming olefins to allyls or 7r-allyls, via v -> (t and 77 - Tj3 processes, respectively, are feasible in metals that are known to produce active metathesis catalysts. [Pg.456]

In the case of hydrogenation using [Ru(BINAP)Cl2]n as the catalyst precursor, the reaction seems to occur by a monohydride mechanism as shown in Scheme 6-31. On exposure to hydrogen, RuC12 loses chloride to form RuHCl species A, which in turn reversibly forms the keto ester complex B. Hydride transfer occurs in B from the Ru center to the coordinated ketone to form C. The reaction of D with hydrogen completes the catalytic cycle.67... [Pg.361]

Figure 1. a. cw-enediol mediated isomerization (36,37) b. hydride shift mechanism... [Pg.488]

Hydrides. Both ionic covalent compounds of H with another element usually metallic. These will generally be described under the other element eg Al-hydride in Vol 1, p A145 B-hydrides in Vol 2, pp B253-56. However certain... [Pg.211]

B. Hydrides AHa.—HeH has been investigated at SCF level, using a CGTO basis set. The ground-state PE surface was computed in this work.378... [Pg.127]

First b-hydride elimination occurs with the formation of (c), and then migratory insertion results in the formation of (d). Elimination of the acetaldehyde and a hydrogen ion then leaves Pd (0). The Pd (0) is converted back to Pd(II) by the auxiliary Cu(II)-catalysed air oxidation. [Pg.225]

For the analysis influence of design weight on COP we shall present (13) in the simplified kind, assuming, that the heat capacity of hydride and a material of a design of a sorber is approximately identical both weights low-temperature A and high-temperature B hydride are equal ... [Pg.393]

Figure 6.7 (Below) Metal-mediated alkene isomerization via (a) allyl or (b) hydride intermediates... Figure 6.7 (Below) Metal-mediated alkene isomerization via (a) allyl or (b) hydride intermediates...
Hammes-Schiffer, S. Watney, J. B. Hydride transfer catalysed by Escherichia coli and Bacillus subtilis dihydrofolate reductase coupled motions and distal mntations, Philos. Trans. R. Soc. London Ser. B 2006, 361, 1365-1373. [Pg.593]

Ans. (a) Hydrogen ion (b) Hydride ion (c) Sodium hydride (d) Beryllium hydride... [Pg.100]

Scheme 23. (a) Cycloaddition and (b) hydride-transfer pathways via -promoted ET from BNAH... [Pg.130]

Figure 2. (a) Addition-Elimination (A-E) and (b) Hydride-Transfer (H-T) methanol electro-oxidation mechanisms by Methanol Dehydrogenase Enzyme proposed in the literature. [Pg.249]

Key to method (A) exchange reaction with tin heterocycle (B) hydride addition to diyne (C) oxidation of saturated ketone (D) bromination-dehydrobromination by pyrolysis (E) reaction of RLi or ArLi with exocyclic M-Cl of preformed diene (F) ring expansion reaction from cyclopentadiene derivative (G) LiAlHi reduction of exocyclic M-Cl (H) carbene insertion into five-membered cyclo-pentadiene derivative. Doering-Hoffman method (I) 1,6-cycloaddition of GeCU. [Pg.167]

Kalina, D. G., Marks, T. J. Wachter, W. A. "Photochemical Synthesis of Low-Valent Organothorium Complexes. Evidence for Photoinduced B-Hydride Elimination," J. Amer. Chem. [Pg.372]

This reaction followed by three further steps, namely (a) a fast hydrogen transfer from the (S-carbon of the chain to the metal, (b) hydride transfer... [Pg.798]

In Section 8C -1. we considered methods for introducing solution samples b hydride genetiilion, Aioniiza-li()fi of the hydrides requires only thai they be healed in a quartz lube, as shtwvn in Figure... [Pg.236]


See other pages where B-hydrides is mentioned: [Pg.198]    [Pg.186]    [Pg.155]    [Pg.157]    [Pg.86]    [Pg.813]    [Pg.816]    [Pg.74]    [Pg.113]    [Pg.62]    [Pg.161]    [Pg.155]    [Pg.157]    [Pg.282]    [Pg.469]    [Pg.816]    [Pg.53]    [Pg.462]    [Pg.143]    [Pg.452]    [Pg.177]    [Pg.103]    [Pg.316]    [Pg.590]    [Pg.45]    [Pg.46]    [Pg.171]   


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