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Metal Y

Ifydroxamic acids reagents for the solvent extraction and spectrophotometric determination of metals. Y. K. Agrawal and S. A. Patel, Rev. Anal. Chem., 1980, 4, 237-278 (167). [Pg.45]

Figure 2. Formation of ternary borides and phase equilibria within ternary boride systems of the type M-M-B or M-Y-B (M = metal, Y = honmetal). , complete isothermal section established B, part of a diagram only. Numbers in the lower part of each square correspond to the refs, to the ternary section. The number of ternary compounds observed is indicated in the right upper corner of each square. Figure 2. Formation of ternary borides and phase equilibria within ternary boride systems of the type M-M-B or M-Y-B (M = metal, Y = honmetal). , complete isothermal section established B, part of a diagram only. Numbers in the lower part of each square correspond to the refs, to the ternary section. The number of ternary compounds observed is indicated in the right upper corner of each square.
A new class of oxidation catalysts is prepared by complexation of metal-Y zeolites with tetradentate N,N -bis(2-pyridinecarboxamide) derivatives (Scheme 7.3). [Pg.254]

Sc(OTf)3 is an effective catalyst in aldol reactions of silyl enol ethers with aldehydes.49 Compared with other typical rare-earth-metal (Y, Yb) trifiates, Sc(OTf)3 has the strongest activity in the reaction of 1-trimethylsiloxycyclohexane with benzaldehyde in dichloromethane. Although the reaction scarcely proceeded at —78°C in the presence of Y(OTf)3 or Yb(OTf)3, the aldol adduct was obtained in 81% yield in the presence of Sc(OTf)3 (Scheme 9). [Pg.403]

In order to describe the different conformations in type 16-20 molecules, the torsion angles (Ep)M-Sb-Y-Sb (Ep = assumed direction of the lone pair at antimony M = transition metal Y = CH2, O, S) were used. The Ep-Sb-Y-Sb torsion angles, which are considered in complexes with monodentate (type 16) coordination of the Sb ligand, were calculated from the corresponding pairs of torsion angles C-Sb-Y-Sb (Scheme 8). [Pg.107]

Other recent examples of complexes with acyclic M-Sb-Y-Sb-M (M = transition metal Y = CH2, O, S) frames are [Br(CO)4Mn( i-Me2Sb-CH2-SbMe2)Mn(CO)4Br)],96 [(MeC5H4)(CO)2Mn( i-Ph2Sb-Y-SbPh2)Mn... [Pg.113]

The rare earth elements (REE) are the lanthanides (defined as those elements with valence electrons in 4/orbitals), La, Ce, Pr, Nd, (Pm), Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, and Yb. Often included for analysis, because they behave in a chemically similar way, although strictly not REE, are the Group 3 transition metals Y and Lu. The radioactive lanthanide element promethium (Pm) is excluded from analysis, since it is not found in samples because of its short half-life. [Pg.210]

Debido a que el hidrdgeno tienen un solo elec-trdn, se puede comportar como metal y perder un electrdn o comportarse como un no metal y ganar un electrdn. [Pg.18]

Los elementos del bloque p incluyen metales, metaloides, no metales y gases inertes. [Pg.18]

Los metales y los haldgenos se pueden clasificar de acuerdo con su capacidad de reaccionar. Estas clasificaciones, conocidas como series de activi-dad, sirven para determinar la posibilidad de que ocurran reacciones de sustitucion sencilla. [Pg.27]

The 6-3IG basis set is presently available for first-row transition metals only (Sc-Zn). STO-3G and 3-2IG basis sets are also available for second-row metals (Y-Cd), but are not recommended for use with correlated models. The LACVP pseudopotential is available for all three transition series and PM3 parameterizations have been developed for most important metals in all three rows. [Pg.140]

The value of the Volta potential difference between a metal a and a solution can be obtained by performing two measurements, in one of which the electrode a is in contact with the solution (Fig. A6.1), whereas, in the second, it is separated from the latter by a space filled with ionized unreactive gas at a low pressure (Fig. A6.2). Electrode a and another electrode of a metal y, reversible to ions Mz+ in solution, are connected to a potentiometer P by wires P and P made of the same metal. [Pg.314]

The reactions of chlorobenzene and benzaldehyde with ammonia over metal Y zeolites have been studied by a pulse technique. For aniline formation from the reaction of chlorobenzene and ammonia, the transition metal forms of Y zeolites show good activity, but alkali and alkaline earth metal forms do not. For CuY, the main products are aniline and benzene. The order of catalytic activity of the metal ions isCu> Ni > Zn> Cr> Co > Cd > Mn > Mg, Ca, Na 0. This order has no relation to the order of electrostatic potential or ionic radius, but is closely related to the order of electronegativity or ammine complex formation constant of metal cations. For benzonitrile formation from benzaldehyde and ammonia, every cation form of Y zeolite shows high activity. [Pg.498]

R,R rare earth metal Y electronic specific heat coefficient... [Pg.36]

For metals y can be neglected at low temperatures (but not at T < IK). Express entropy for metals at low temperatures as a function of heat capacity. [Pg.47]

The allylmetallation of vinyl metals, y-heterosubstituted with a methoxy-methyl ether as the chelating group, leads to the corresponding gembismetal-lic derivatives,20 but now, warming the reaction mixture to room temperature promotes an internal nucleophilic substitution, leading to a metallated cyclopropane which can react with different electrophiles21 (Equation 7.5 and Protocol 9). [Pg.121]

Metal y dynes per cm. Tem- perature dy/dT Temperature range for dy/dT Reference... [Pg.164]

Metals Y Performance Building Y InfoTech Thermoforming Rubber ... [Pg.156]


See other pages where Metal Y is mentioned: [Pg.140]    [Pg.5]    [Pg.49]    [Pg.803]    [Pg.382]    [Pg.510]    [Pg.11]    [Pg.161]    [Pg.277]    [Pg.30]    [Pg.398]    [Pg.14]    [Pg.17]    [Pg.86]    [Pg.70]    [Pg.204]    [Pg.580]    [Pg.178]    [Pg.224]    [Pg.226]    [Pg.178]    [Pg.469]    [Pg.177]    [Pg.128]    [Pg.239]    [Pg.151]    [Pg.263]    [Pg.265]    [Pg.181]   
See also in sourсe #XX -- [ Pg.3 , Pg.133 ]




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Y-Lactones via metal-catalyzed cycloaddition

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