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Centre, 427 Silicon

Figure 5. Possible tetrahedral environments of a silicon atom (marked with a cross) in the faujasite framework. First-order tetrahedral neighbours are separated from the second-order neighbours by the dotted line. Open circles denote silicon, closed circle aluminium arrows indicate Si(OAl) sites. The number of such sites eliminated by substituting the centred silicon by an aluminium is indicated under each diagram. Figure 5. Possible tetrahedral environments of a silicon atom (marked with a cross) in the faujasite framework. First-order tetrahedral neighbours are separated from the second-order neighbours by the dotted line. Open circles denote silicon, closed circle aluminium arrows indicate Si(OAl) sites. The number of such sites eliminated by substituting the centred silicon by an aluminium is indicated under each diagram.
Figure Al.3.23. Phase diagram of silicon in various polymorphs from an ab initio pseudopotential calculation [34], The volume is nonnalized to the experimental volume. The binding energy is the total electronic energy of the valence electrons. The slope of the dashed curve gives the pressure to transfomi silicon in the diamond structure to the p-Sn structure. Otlier polymorphs listed include face-centred cubic (fee), body-centred cubic (bee), simple hexagonal (sh), simple cubic (sc) and hexagonal close-packed (licp) structures. Figure Al.3.23. Phase diagram of silicon in various polymorphs from an ab initio pseudopotential calculation [34], The volume is nonnalized to the experimental volume. The binding energy is the total electronic energy of the valence electrons. The slope of the dashed curve gives the pressure to transfomi silicon in the diamond structure to the p-Sn structure. Otlier polymorphs listed include face-centred cubic (fee), body-centred cubic (bee), simple hexagonal (sh), simple cubic (sc) and hexagonal close-packed (licp) structures.
More recent developments are based on the finding, that the d-orbitals of silicon, sulfur, phosphorus and certain transition metals may also stabilize a negative charge on a carbon atom. This is probably caused by a partial transfer of electron density from the carbanion into empty low-energy d-orbitals of the hetero atom ( backbonding ) or by the formation of ylides , in which a positively charged onium centre is adjacent to the carbanion and stabilization occurs by ylene formation. [Pg.6]

Some Bell employees had been trying to focus attention on germanium, the sister element to silicon, but had been discouraged, just as Wilson had been discouraged across the Atlantic a decade earlier. It was Bardeen who eventually focused on the merits of germanium and the research which led to the transistor in 1947 was centred on this element the fact that on germanium, surface oxide could be washed off with water played a major role. [Pg.258]

Silicon-iron and Graphite Anodes of these materials are now frequently manufactured with the anode cable tail connected at the centre of the rod... [Pg.224]

The nature of the transition state in bromodesilylation is problematical, since the reaction appears to take place in the non-polar solvents benzene and carbon tetrachloride with inversion of configuration at silicon, and, therefore, cannot proceed through a 4-centre intermediate (LVII) as this would lead to retention of configuration746,747. The results are, however, consistent with a six-centre transition state (LVIII), which could follow from the high kinetic order in bromine... [Pg.381]

Additionally, organotin-catalysed silicones have been used in products such as coatings on baking paper (for use in food preparation), and this use is considered in more detail in the consumer exposure assessment (section 6). Information provided by the Centre Europeen des Silicones (CES, 2002b) indicated that organotin-catalysed silicones are used in only a small proportion of baking paper produced in the EU ... [Pg.11]

CES (2002a) Silioones industry information. Brussels, Centre Europeen des Silioones (http //wvwv.silicones-europe.eom downloaded 2003). [Pg.44]

CES (2002b) Comments on near final risk assessment report. Letter from Centre Europeen des Silicones, Brussels, 9 July. [Pg.44]

Fig. 52 Silicon-29 CP/MAS spectrum of silica gel modified by the introduction of a phosphine linker. The signal at highest field (ca. -110 ppm) is due to unmodified Si04 centres, the other four to the structural fragments shown (clockwise)... Fig. 52 Silicon-29 CP/MAS spectrum of silica gel modified by the introduction of a phosphine linker. The signal at highest field (ca. -110 ppm) is due to unmodified Si04 centres, the other four to the structural fragments shown (clockwise)...
Silenes and saturated silicon compounds that are coordinated by donors and that thus have higher coordination numbers at the silicon centres exhibit unusual reactivities [1]. An interpretation of these experimental findings is possible when the structural features of the stable model compounds [C6H4CH2N(CH3)2]2SiCl2 (1) [2], [C6H4CH2N(CH3)2]3SiH (4), and [C6H4CH2N(CH3)2]4Si (5) are considered [3]. [Pg.165]

An additional asset of both donors in silicon and NV centres is that nuclear spins, of 31P in the former and of N and neighbouring 13C in the latter, can be employed as long-term storage quantum memories [63], or even to build multiple qubit registers [22, 67]. [Pg.194]

Silica used as a filler for rubbers is silicon dioxide, with particle sizes in the range of 10-40 nm. The silica has a chemically bound water content of 25% with an additional level of 4-6% of adsorbed water. The surface of silica is strongly polar in nature, centring around the hydroxyl groups bound to the surface of the silica particles. In a similar fashion, other chemical groups can be adsorbed onto the filler surface. This adsorption strongly influences silica s behaviour within rubber compounds. The groups found on the surface of silicas are principally siloxanes, silanol and reaction products of the latter with various hydrous oxides. It is possible to modify the surface of the silica to improve its compatibility with a variety of rubbers. [Pg.145]

The carbon atom is not the only atom which produces chiral centres in organic compounds. Silicon, germanium, tin, or N (in quaternary salts or N-oxides) whose bonds point towards the comers of a tetrahedron also form optically active compounds provided the groups are different. [Pg.128]

USA Silicone Environmental Health and Safety Council (SEHSC) Europe Centre Europeen des Silicones (CES) Japan Silicone Industry Association of Japan (SIAJ) Global Global Silicones Council (GSC). [Pg.656]

Irradiation at 77 K in trichlorofluoromethane of cyclic tertiary amines also affords radical cations that can be trapped indefinitely. In these systems there apparently is no reaction between the radical cations and free amine. The EPR spectra of the radical cations were recorded. The cations produced under these conditions can be trapped indefinitely and do not undergo proton loss to give the corresponding carbon-centred radical. Several systems (20-24) were examined in this way and all were found to be stable. In the bis amine (22, n = 1) evidence was obtained from the EPR study that there was weak N-N interaction4. The influence of silicon in 25 was also examined16. [Pg.826]

Hepplestone SP, Srivastava GP (2006) The intrinsic lifetime of low-frequency zone-centre phonon modes in silicon nanowires and carbon nanotubes. Applied Surface Science 252 7726-7729. [Pg.260]

The dendrimers containing more ferrocene units are more interesting from the electrochemical viewpoint. Scheme 6 shows the 1st and 2nd generation members of a silicon-centred series containing four and eight ferrocenyl units, respectively.48... [Pg.187]

Homolytic substitution reactions including homolytic allylation, radical [2,3]-migrations and stereochemical reactions been reviewed. The review also highlights the possible applications of homolytic substitution reactions. ni reactions at silicon (by carbon-centred radicals in the a-position of stannylated silyl ethers) are efficient UMCT reactions producing cyclized alkoxysilanes. Bimolecular reactions can also be facilitated in good yield (Schemes 32 and 33). ... [Pg.138]

The reaction of atoms, radicals or excited triplet states of some molecules with silicon hydrides is the most important way for generating silyl radicals [1,2]. Indeed, Reaction (1.1) in solution has been used for different applications. Usually radicals X are centred at carbon, nitrogen, oxygen, or sulfur atoms... [Pg.3]


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See also in sourсe #XX -- [ Pg.446 ]




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