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Neutral groups

For these calculations, switching based on neutral groups and over a long range is probably best. [Pg.137]

Patel et al., 1974), but no effect is observed for neutral (Group IV) impurities in Ge or Si. Also, impurities that are electron-donors soften both Ge and Si at temperatures above about 450 °C whereas accepter type impurities soften Ge, but not Si. Another important point is that small impurity concentrations have little effect. The effects begin at concentrations of about 1018/cc. Since the atomic volume of Si is 20 A3, the critical ratio of impurity to Si atom is about 2 x 10 5. Therefore, the average lineal distance between impurity atoms is about one every 270 A. [Pg.81]

Terminal methylene complexes are relatively rare—less than 10 such compounds have been isolated and about as many again have been characterized by spectroscopic techniques only. The methylene complexes previously reported fall into two groups, (i) neutral complexes of the early transition metals (e.g., Ti, Ta) and (ii) cationic complexes of the later transition metals (e.g., Re, Fe). The osmium complex 47 is important, then, as it is a new example extending the neutral group to the later transition metals. Compound 47 is the prototype for the series Os(=CHR)Cl(NO)(PPh3)2 and is one of only three terminal methylene complexes to be structurally characterized by X-ray crystallography (see Section IV,B). [Pg.157]

Neutral Group 3 Metallocene Complexes as Catalysts of Polymerization... [Pg.16]

At present, the difficulties described in 7-9 can be solved. The use of MAO can be avoided by the use of non-MAO catalysts such as cationic Group 4 metallocenes or neutral Group 3 metallocenes. It has been found that the molecular weight of the resulting polymer can be increased by introducing substituents at the 2,5-position in the cyclopentadienyl group of the... [Pg.44]

Neutral loss scan3 Scan with constant loss of neutral group identification of functional groups High Medium... [Pg.149]

Figure 7. Molecular orbitals diagram of the mixing process involved in the insertion of ethene into a Mt-C(alkyl) bond for a generic d° neutral group 3 or cationic group 4 catalyst. Figure 7. Molecular orbitals diagram of the mixing process involved in the insertion of ethene into a Mt-C(alkyl) bond for a generic d° neutral group 3 or cationic group 4 catalyst.
A clear experimental estimate of the intrinsic reaction barrier to olefin insertion is still missing. The NMR analysis of Erker and co-workers estimated the intrinsic activation barrier for 1-olefin insertion into the Zr-C bond of the (MeCp)2Zr( j.-C4H6-borate betaine) to be about 10-11 kcal/mol [69, 77]. Very recent NMR experiments of Casey and co-workers on the propene insertion into the Y-C c-bond of the neutral group 3 (C5Me5)YCH2CH2CH(CH3)2 system resulted in a AG of 11.5 kcal/mol [70],... [Pg.43]

The limitations of the simple Zintl-Klemm concept can be illustrated by differences in the two [MT1] intermetallics (M = Na [79] and Cs [80]). Complete electron transfer from M to T1 leads to [ M TI, where the Tl anion with four valence electrons is isoelectronic with a neutral group 14 atom and four bonds and needed to attain the octet configuration. Hence, the Tl- anion should form structures similar to allotropes of carbon or heavier group 14 elements. Indeed, [NaTl] has a stuffed diamond structure [79] with internal Na and an anionic (Tl-) lattice similar to diamond. However, the Tl- anions in [CsTl] form tetragonally compressed octahedra [80] unlike any structures of the allotropes of carbon or its heavier congeners. [Pg.19]

Neutral Groups Negative Charged Positive Charged... [Pg.26]

Maignan, S., Guilloteau, J.-P., Choi-Sledeski, Y.M., Becker, M.R., and Ewing, W.R. Molecular stmctures of human factor xa complexed with ketopiperazine inhibitors preference for a neutral group in the SI pocket./. Med. Chem. 2003, 46, 685-690. [Pg.102]

The theoretical section introduced divalent carbon(O) compounds as molecules CL2 where the ligand L is a ct donor. In principle this task can be fulfilled by various neutral group 15 compounds (N2, nitriles, amines, phosphanes, arsanes, etc.), neutral group 16 compounds (sulfides, selenides, etc.) as well as by divalent C(II) with a free pair of electrons at a carbon atom, such as isonitriles, NHCs, carbenes, CO, ylides, etc. The neutral and isolable compound C2PPh3 [14,15] may also serve as a donor L to stabilize a carbon atom. [Pg.56]

The valency of the complex radicle is the same as that of the central metallic atom when the complex contains only ammonia, substituted ammonia, water, or other neutral group. For example, cobalt in eobaltie. salts is trivalent, and the cobalt complex with ammonia, Co(NI13)8 ", is likewise trivalent copper in cupric sulphate is divalent, and the copper complex, [Cu(NH3)4] , is also divalent. In the same wn.y [Co(NH3)5.H30] " and [Co(NII3)4.(II20)2] " are trivalent, as also [Co(NH3)2.en2]" and [Co.en3] ", where en represents cthyleucdiamine, CH NH2... [Pg.18]


See other pages where Neutral groups is mentioned: [Pg.202]    [Pg.343]    [Pg.348]    [Pg.543]    [Pg.104]    [Pg.447]    [Pg.540]    [Pg.958]    [Pg.214]    [Pg.4]    [Pg.1316]    [Pg.137]    [Pg.209]    [Pg.50]    [Pg.164]    [Pg.324]    [Pg.331]    [Pg.35]    [Pg.299]    [Pg.257]    [Pg.36]    [Pg.209]    [Pg.231]    [Pg.333]    [Pg.1056]    [Pg.1060]    [Pg.546]    [Pg.120]    [Pg.126]    [Pg.251]    [Pg.314]    [Pg.137]    [Pg.217]    [Pg.18]    [Pg.19]   
See also in sourсe #XX -- [ Pg.88 ]




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