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Atomic silicon

Another view of the Si(lOO) etching mechanism has been proposed recently [28], Calculations have revealed that the most important step may actually be the escape of the bystander silicon atom, rather than SiBr2 desorption. In this way, the SiBr2 becomes trapped in a state that otherwise has a very short lifetime, pennitting many more desorption attempts. Prelimmary results suggest that indeed this vacancy-assisted desorption is the key step to etching Si(lOO) with Br2. [Pg.937]

Figure B3.3.14. Template molecule in a zeolite cage. The CFIA stmcture (periodic in the calculation but only a fragment shown here) is drawn by omitting the oxygens which are positioned approximately halfway along the lines shown coimecting the tetrahedral silicon atoms. The molecule shown is 4-piperidinopiperidine, which was generated from the dicyclohexane motif suggested by computer. Thanks are due to D W Lewis and C R A Catlow for this figure. For fiirther details see [225]. Figure B3.3.14. Template molecule in a zeolite cage. The CFIA stmcture (periodic in the calculation but only a fragment shown here) is drawn by omitting the oxygens which are positioned approximately halfway along the lines shown coimecting the tetrahedral silicon atoms. The molecule shown is 4-piperidinopiperidine, which was generated from the dicyclohexane motif suggested by computer. Thanks are due to D W Lewis and C R A Catlow for this figure. For fiirther details see [225].
The concept of oxidation states is best applied only to germanium, tin and lead, for the chemistry of carbon and silicon is almost wholly defined in terms of covalency with the carbon and silicon atoms sharing all their four outer quantum level electrons. These are often tetrahedrally arranged around the central atom. There are compounds of carbon in which the valency appears to be less than... [Pg.162]

Crystalline silicon has the tetrahedral diamond arrangement, but since the mean thermochemical bond strength between the silicon atoms is less than that found between carbon atoms (Si—Si, 226 kJmol , C—C, 356kJmol ), silicon does not possess the great hardness found in diamond. Amorphous silicon (silicon powder) is microcrystalline silicon. [Pg.166]

Note that in the compound (CH3)2Si(OH)2 the silicon atom can hold two OH groups, unlike carbon. It is this property that makes the existence of silicones possible. By variation of the compounds and conditions of hydrolysis, straight chains, rings and cross-linked polymers are obtained, for example ... [Pg.190]

Silica gel is again obtained but silicon does not form the corresponding hexachlorosilicic acid since the small silicon atom is unable to coordinate six chlorine atoms. [Pg.197]

In sorn e situation s, using this option m ay he im portan t. For exam -pic, if p orbitals on electronegative atoms irileracL with d orbitals, (as for a silicon atom bonded to an amine group), you may want to include d orbitals. [Pg.118]

Witir the correct choice of the parameters k and the ah initio data in Figure 4.50 could be reproduced very well. In this force field a Urey-Bradley term was also included between the silicon atoms in such angles to model the lengthening of the Si—O bond as the angle decreased. [Pg.255]

Without carbon, the basis for life would be impossible. While it has been thought that silicon might take the place of carbon in forming a host of similar compounds, it is now not possible to form stable compounds with very long chains of silicon atoms. The atmosphere of Mars contains 96.2% CO2. Some of the most important compounds of carbon are carbon dioxide (CO2), carbon monoxide (CO), carbon disulfide (CS2), chloroform (CHCb), carbon tetrachloride (CCk), methane (CHr), ethylene (C2H4), acetylene (C2H2), benzene (CeHe), acetic acid (CHsCOOH), and their derivatives. [Pg.16]

A silicon atom might be expected to release electrons inductively, but because of empty 7-orbitals shows the overall character ( + 7 —717). Nitration of trimethylsilylbenzene with nitric acid in acetic anhydride at —10 to o °C gives 25-5,39-8,30-2 and 6-8 %, respectively, of 0-, m-, and /)-nitro-trimethylsilylbenzene and nitrobenzene, with a rate of reaction relative to that of benzene of about 1-5. The figures give no indication of an important conjugative effect. [Pg.182]

When a chain or ring system is composed entirely of alternating silicon and oxygen atoms, the parent name siloxane is used with a multiplying affix to denote the number of silicon atoms present. The parent name silazane implies alternating silicon and nitrogen atoms multiplying affixes denote the number of silicon atoms present. [Pg.37]

Si—Aryl 1125-1090 (vs) Splits into two bands when two aryl groups are attached to one silicon atom, but has only one band when three aryl groups attached... [Pg.750]

A completely dehydroxylated surface consists essentially of an array of oxygen atoms the Si-0 linkages are essentially covalent so that the silicon atoms are almost completely screened by the much larger oxygen atoms. Such a surface represents the extreme case and, even on samples ignited at 1100°C, a minute residue of isolated hydroxyl groups will be present. [Pg.270]

The polycrystaUine EGS is converted to siagle-crystal silicon via the C2okralski (CZ) crystal growing process, based on the solidification of silicon atoms from the Hquid phase at a moving iaterface. Volume production of 200-mm diameter crystals is standard. Development of crystals having diameters of up to 400 mm has been predicted (3). [Pg.346]

Neutrons also transform some of the silicon atoms to phosphoms through the following reaction ... [Pg.532]

Unlike carbon, the silicon atom may utilise vacant orbitals to expand its valence beyond four, to five or six, forming additional bonds with electron donors. This is shown by isolated amine complexes. The stabiUty of the organosHane amine complexes varies over a wide range and depends on the nature of the donor and acceptor (2). [Pg.26]

Silicon atoms bond strongly with four oxygen atoms to give a tetrahedral unit (Fig. 16.4a). This stable tetrahedron is the basic unit in all silicates, including that of pure silica (Fig. 16.3c) note that it is just the diamond cubic structure with every C atom replaced by an Si04 unit. But there are a number of other, quite different, ways in which the tetrahedra can be linked together. [Pg.170]

Pure silica contains no metal ions and every oxygen becomes a bridge between two silicon atoms giving a three-dimensional network. The high-temperature form, shown in Fig. 16.3(c), is cubic the tetrahedra are stacked in the same way as the carbon atoms in the diamond-cubic structure. At room temperature the stable crystalline form of silica is more complicated but, as before, it is a three-dimensional network in which all the oxygens bridge silicons. [Pg.172]

Hydroxy derivatives of silanes in which the hydroxyl groups are attached to a silicon atom are named by adding the suffices -ol, -diol, -triol etc., to the name of the parent compound. Examples are ... [Pg.816]

The material known as bouncing putty is also a silicone polymer with the occasional Si—O—B group in the chain, in this case with 1 boron atom to about every 3-100 silicon atoms. The material flows on storage, and on slow extension shows viscous flow. However, small pieces dropped onto a hard surface show a high elastic rebound, whilst on sudden striking they may shatter. The material had some use in electrical equipment, as a children s novelty and as a useful teaching aid, but is now difficult to obtain. [Pg.834]

Polymers containing main chain silicon atoms. [Pg.842]


See other pages where Atomic silicon is mentioned: [Pg.358]    [Pg.87]    [Pg.113]    [Pg.114]    [Pg.115]    [Pg.133]    [Pg.934]    [Pg.935]    [Pg.1839]    [Pg.186]    [Pg.255]    [Pg.637]    [Pg.191]    [Pg.6]    [Pg.37]    [Pg.270]    [Pg.110]    [Pg.476]    [Pg.483]    [Pg.4]    [Pg.10]    [Pg.307]    [Pg.309]    [Pg.123]    [Pg.816]    [Pg.816]    [Pg.816]    [Pg.817]    [Pg.817]   


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ATOMIC STRUCTURE OF NITROGEN, BORON, ALUMINUM, AND SILICON

Atomic properties, carbon compared with silicon

Baeyer-Villiger reaction P-silicon atom

Carbon and Silicon Network Atomic Solids

Compounds with Hexacoordinated Silicon Atoms

Compounds with Pentacoordinated Silicon Atoms

Heavy Donor Atoms in the Silicon Coordination Sphere

Hydrogen atom with silicon hydride

Infrared Spectroscopy of Intermediates with Low Coordinated Carbon, Silicon and Germanium Atoms

Kinetic silicon atoms

Matrix infrared spectroscopy of intermediates with low coordinated carbon, silicon and germanium atoms

Network atomic solids silicon

Preparation of polyalkylsiloxanes with higher alkyl radicals at the silicon atom and varnishes based on them

Preparation of polymethylphenylsiloxanes with active hydrogen atoms and vinyl groups at the silicon atom

Pure Chemical F-Atom Etching of Silicon Flamm Formulas and Doping Effect

Pyramidalization, silicon atom

Shared oxygens, between silicon atoms

Silicon atom recoil reactions with

Silicon atom, organic group replacement

Silicon atomic properties

Silicon atomic radius

Silicon atomic size

Silicon atomic volume

Silicon atomic weight

Silicon atoms

Silicon atoms generation

Silicon atoms reaction

Silicon atoms, free

Silicon atoms, free reactions

Silicon atoms, nitrogen linked

Silicon cations, atomic, reactions with neutral

Silicon cations, atomic, reactions with neutral molecules

Silicon hydrides atomic germanium

Silicon metal atom reactions with

Silicon metal atoms

Silicon recoiling atoms

Silicon, atomic structure

Silicone atoms

Silicone atoms

Siloxane Oligomers with Functional Groups Directly Bonded to the Terminal Silicon Atoms (Si—X)

Silyl radical with silicon atom

Unstable compounds with double-bonded silicon and germanium atoms (silenes, silanones, germanones, germathiones)

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