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Tetrahedrally bonded carbon atoms

It is important to stress that nitrogen incorporation in a-C H films always result, at least above a certain level, in a strong decrease in the tetrahedrally bonded carbon atom fraction. Raman spectroscopy also gives support to this observation, because the increase in the size of graphitic clusters only can proceed with also increasing sp fraction. [Pg.255]

Figure 4 Sketch of two possible stereochemical arrangements for a chiral monomer. P represents the polymer chain, R represents a vinyl substitutent on a carbon, H represents hydrogen, (a) Linear sketch showing one conformation and two configurations (bracketed and unbracketed). The apex of bonds is a tetrahedrally bonded carbon atom (solid and dashed circles), (b) Newman projection of the same monomer showing the free rotation about the C-C bond. Figure 4 Sketch of two possible stereochemical arrangements for a chiral monomer. P represents the polymer chain, R represents a vinyl substitutent on a carbon, H represents hydrogen, (a) Linear sketch showing one conformation and two configurations (bracketed and unbracketed). The apex of bonds is a tetrahedrally bonded carbon atom (solid and dashed circles), (b) Newman projection of the same monomer showing the free rotation about the C-C bond.
In this section, we review the effects of structure modifications for PFs with alkyl and aryl side chains or with charge-transport moieties on device performance. Spiropolyfluorenes (SPFs) having the structure of two phenylene units perpendicularly connected by a tetrahedrally bonded carbon atom are also discussed. [Pg.54]

A chiral molecule and its non-superimposable image are called enantiomers. So isomers that are mirror images of each other are enantiomers. For molecules to have enantiomers, their structure must be asymmetrical. The simplest asymmetrical molecule is the tetrahedrally bonded carbon atom with four different types of atoms or groups attached to it. These kinds of carbon atoms are called asymmetric or chiral carbon atoms and the molecules are called chiral molecules. Some compounds may occur in nature with both enantiomers present. For example, lactic acid can be found in nature this way. [Pg.138]

The role of the aromatic centers in coal structure has also been questioned insofar as clusters of tetrahedrally bonded carbon atoms give rise to x-ray diffraction bands in approximately the same angular region where the two-dimensional reflections of graphite-like layers occur. In fact. [Pg.325]

Fig. 4.17 Unit cells of PAFs, a PAF-301, b PAF-302, c PAF-303, and d PAF-304, derived from topology design and geometry optimization with the force field method. Here, gray and pink spheres represent carbon and hydrogen atoms, respectively, while the blue polyhedron represents the tetrahedrally bonded carbon atoms. In addition, the yellow sphere denotes the pores in 3D PAFs. Reproduced from Ref. [103] with permission from the American Chemical Society... Fig. 4.17 Unit cells of PAFs, a PAF-301, b PAF-302, c PAF-303, and d PAF-304, derived from topology design and geometry optimization with the force field method. Here, gray and pink spheres represent carbon and hydrogen atoms, respectively, while the blue polyhedron represents the tetrahedrally bonded carbon atoms. In addition, the yellow sphere denotes the pores in 3D PAFs. Reproduced from Ref. [103] with permission from the American Chemical Society...
The chemistry of propylene is characterized both by the double bond and by the aHyUc hydrogen atoms. Propylene is the smallest stable unsaturated hydrocarbon molecule that exhibits low order symmetry, ie, only reflection along the main plane. This loss of symmetry, which implies the possibiUty of different types of chemical reactions, is also responsible for the existence of the propylene dipole moment of 0.35 D. Carbon atoms 1 and 2 have trigonal planar geometry identical to that of ethylene. Generally, these carbons are not free to rotate, because of the double bond. Carbon atom 3 is tetrahedral, like methane, and is free to rotate. The hydrogen atoms attached to this carbon are aUyflc. [Pg.124]

Like a single carbon atom capped with tetrahedrically coordinated hydrogen atoms, Fig. 4.4, a cluster of sp -bonded carbon atoms can also be capped with hydrogen to form hydrogenated fragments of a diamond structure diamondoids. [Pg.293]

It is interesting to note that the fluoride ion-promoted Si-C bond cleavage of vinyl silanes is greatly facilitated by the presence of a hydroxyl group at the tetrahedral P-carbon atom [67]. [Pg.97]

Because of the tetrahedral arrangement of the four bonds around single-bonded carbon atoms and most phosphorus atoms, all six of the bond angles about the central atom have nearly the same tetrahedral angle of 109.5°. [Pg.39]

We turn now to compounds that provide the most intimate views of the catalytic process itself Linus Pauling proposed in 1948 that compounds resembling the transition state of a catalyzed reaction should be very effective inhibitors of enzymes. These mimics are called transition-state analogs. The inhibition of proline racemase is an instructive example. The racemization of proline proceeds through a transition state in which the tetrahedral a- carbon atom has become trigonal by loss of a proton (Figure 8.24). In the trigonal form, all three bonds are in the same plane C also carries a... [Pg.331]

Fig. 22. (a) Franklin s model for pregra-phitic carbon stacked graphene layers are represented by straight lines. Bent or 2.45 A curved lines represent tetrahedrally bonded carbon chains or buckled graphene layers. Tbe nanodispersed silicon atoms are represented as shaded dots. After Wilson and Dahn [194]. (b) Schematic drawing of the lithium sites on a single layer of boron-substituted carbon. The broken circle represents tbe site for additional lithium beyond jc = 1 in Lij((B2Ci z)6. After Dahn et al. [195]. [Pg.346]

Microstructural changes of amorphous cartwn (a-C) and tetrahedrally amorphous carbon (ta-C) upon laser irradiation is studied in this paper. As it is shown, ta-C films with higher ratio of sp bonded carbon atoms are more stable compare to low density a-C films. The sjf bonded atoms in a-C films start clustering at laser energies lower than the energy needed for clustering of sp bonded atoms in ta-C films. [Pg.451]

Figure 2.1. (A) The tetrahedral model for methane. The small black spheres represent the positions of the hydrogen atoms surrounding the tetrahedron of carbon. (B) Ethane, C2H6, with a pair of singly bonded carbon atoms. (C) Ethylene, C2H4, with a pair of doubly bonded carbon atoms. (D) Acetylene, C2H2, with a pair of triply bonded carbon atoms. Figure 2.1. (A) The tetrahedral model for methane. The small black spheres represent the positions of the hydrogen atoms surrounding the tetrahedron of carbon. (B) Ethane, C2H6, with a pair of singly bonded carbon atoms. (C) Ethylene, C2H4, with a pair of doubly bonded carbon atoms. (D) Acetylene, C2H2, with a pair of triply bonded carbon atoms.

See other pages where Tetrahedrally bonded carbon atoms is mentioned: [Pg.181]    [Pg.479]    [Pg.183]    [Pg.381]    [Pg.479]    [Pg.31]    [Pg.627]    [Pg.18]    [Pg.319]    [Pg.11]    [Pg.181]    [Pg.479]    [Pg.183]    [Pg.381]    [Pg.479]    [Pg.31]    [Pg.627]    [Pg.18]    [Pg.319]    [Pg.11]    [Pg.10]    [Pg.10]    [Pg.648]    [Pg.96]    [Pg.7]    [Pg.179]    [Pg.71]    [Pg.38]    [Pg.78]    [Pg.92]    [Pg.94]    [Pg.180]    [Pg.110]    [Pg.322]    [Pg.115]    [Pg.110]    [Pg.110]    [Pg.56]    [Pg.265]    [Pg.232]    [Pg.291]    [Pg.284]    [Pg.39]   
See also in sourсe #XX -- [ Pg.381 ]




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Atomic bonding

Atoms bonds

Bonds atomic

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Carbon, bonding tetrahedral

Oxygen Bonded to Activated Tetrahedral Carbon Atoms

Tetrahedral atom

Tetrahedral bonding

Tetrahedral bonds

Tetrahedral carbon

Tetrahedral carbon atom

Tetrahedrally bonded

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