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Obitals

Figure 2.3 The shapes of orbitals for the s electron pair, the three pairs of p electrons with obitals mutally at right angles, and the sp orbitals which have the major lobes pointing towards the apices of a regular tetrahedron. Figure 2.3 The shapes of orbitals for the s electron pair, the three pairs of p electrons with obitals mutally at right angles, and the sp orbitals which have the major lobes pointing towards the apices of a regular tetrahedron.
Fig. 23 AFM images of examples of calculations by DNA self-assembly, a Section of patterned DNA lattice containing barcode information of 01101 the 1 and Obit values are clearly visible as lighter and darker stripes, respectively (from [151] reprinted with permission), b Branched tiled DNA nanostructures, mimicking the solution of a Pascal triangle [152]. Reprinted with permission... Fig. 23 AFM images of examples of calculations by DNA self-assembly, a Section of patterned DNA lattice containing barcode information of 01101 the 1 and Obit values are clearly visible as lighter and darker stripes, respectively (from [151] reprinted with permission), b Branched tiled DNA nanostructures, mimicking the solution of a Pascal triangle [152]. Reprinted with permission...
Fig. 520 Enragy level diagram for the molecular orbitals of carbon monoxide. Note that Upon bond Formation electrons occtjjy obitals that are more oxygen-likc than carbon-like. Note carefuBy the bond order The Icr and 3 r MOs arc essentially nonbonding. The bond order, as in the N-. molecule is three. Fig. 520 Enragy level diagram for the molecular orbitals of carbon monoxide. Note that Upon bond Formation electrons occtjjy obitals that are more oxygen-likc than carbon-like. Note carefuBy the bond order The Icr and 3 r MOs arc essentially nonbonding. The bond order, as in the N-. molecule is three.
However, for this structure, there is a small occupancy of the jt-antibonding obitals near the T-point. Presumably, it is the occupation of these antibonding orbitals which drives the WC to adopt the hexagonal structure. Figure 5.10 shows the calculated bands for this structure. Here the bands near the Fermi energy show a greater degree of jt-character than in the carbides with the NaCl structure. [Pg.72]

The value of KM decreases with increasing electronwithdrawing capability of the aluminum component, i.e. with decreasing electron density at the vanadium induced by the aluminum component bonded to the vanadium in the bimetallic structure of the active center. This result seems to suggest that electron back-donation from a filled vanadium d orbital to the empty propylene jc obital (it-bonding) is the main factor in determining the vanadium-propylene interaction. [Pg.221]

The electrical properties of any material are a result of the material s electronic structure. The presumption that CPs form bands through extensive molecular obital overlap leads to the assumption that their electronic properties can be explained by band theory. With such an approach, the bands and their electronic population are the chief determinants of whether or not a material is conductive. Here, materials are classified as one of three types shown in Scheme 2, being metals, semiconductors, or insulators. Metals are materials that possess partially-filled bands, and this characteristic is the key factor leading to the conductive nature of this class of materials. Semiconductors, on the other hand, have filled (valence bands) and unfilled (conduction bands) bands that are separated by a range of forbidden energies (known as the band gap ). The conduction band can be populated, at the expense of the valence band, by exciting electrons (thermally and/or photochemically) across this band gap. Insulators possess a band structure similar to semiconductors except here the band gap is much larger and inaccessible under the environmental conditions employed. [Pg.63]

Sayre, Anne. Remembering Dorothy Hodgkin. Available from . [Pg.209]

In practice hydroxylamine and hydrazine are very reactive nucleophiles, far more so than might be expected from consideration of simple physical parameters. The inceased nucleophilicity of a heteroatom when bonded to a second hereoatom is known as the a effect. For a theoretical rationalisation of the a effect in terms of frontier obitals see Fleming, 1976. [Pg.29]

The calculation of fixed points and periodic obits for the shift map is straightforward. There are exactly two fixed points. Since for a fixed point of period 1 a single shift of the binary point to the right has to reproduce the seed, there are only two possibilities ... [Pg.43]

The one-electron molecular orbitals thus formed consist erf a bonding molecular obital ( and an aniibonding molecular orbital ( ). If we allow a single electron to occupy the bonding molecular orbital (as in Hj. for example), the approximate wave function for the molecule is... [Pg.89]

MARSTON AND WYATT Resonant Quasi-periodic Periodic Obits... [Pg.445]

The SACHE web site has a great discussion on reactor safety with exan (wiviv.j ache.orgi. You will need a user name and password both can be obit froin your department chair. Hit 2003 Tab. Go to K Problems. [Pg.644]

ObtG - Oo transporters OhiiD - components of Oo cheiatase OobN ObiT, ObiS - components of aipha-ribazole-5P synthesis... [Pg.147]

P. Fossman, Green Light for Extraction in Germany, Fhtssiges Obit, 9, 534-540 (1982). [Pg.574]


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See also in sourсe #XX -- [ Pg.7 , Pg.15 , Pg.18 , Pg.19 ]




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