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The Carbon and Nitrogen Atoms

A quasi-vacuum consisting of the singlet state core [Pg.57]

States of interest can be calculated from approximate wavefunctions, such as [Pg.57]

In Tables 4.3 and 4.4 the calculated exponents, total energies in Hartrees, and the ionization potential in electronvolts are given. [Pg.60]


The carbon and nitrogen atoms have steric numbers of 3, so their bonding frameworks can be... [Pg.682]

The carbon and nitrogen atoms have a p orbital left over after construction of the. s p hybrids. These two p orbitals are perpendicular to the plane that contains the five nuclei. Side-by-side overlap of the p orbitals gives a jrbond that completes the bonding description of this molecule ... [Pg.682]

The triple bond includes two itt bonds formed by the pair-wise overlap of the p orbitals that remain on the carbon and nitrogen atoms. Two figures from different perspectives help illustrate the triple bond ... [Pg.690]

Each atom in structure 3 has a closed-shell electron configuration and a formal charge of zero. We can complete the octet for the carbon and nitrogen atoms in structure 1 by converting a lone pair of electrons on each nitrogen atom into a covalent bond to the central carbon atom. [Pg.207]

To determine the number of possible compounds when R4 and R5 are cyclized, a different approach was used. The patent states, R4 and R5 when joined through the carbon and nitrogen atoms to which they are attached form a 4- to 6-membered ring . Preferred ring has the formula ... [Pg.3]

In all reported studies of isocyanides adsorbed on Ni, the isocyanide is proposed to adsorb with both the carbon and nitrogen atoms bonded to the surface. [Pg.548]

Some amines undergo direct nitration during nitrolysis nitration is then followed by partial degradation involving the cleavage of the bond between the carbon and nitrogen atoms (p. 12). [Pg.9]

Formation of S-aminolevulinic acid (ALA) All the carbon and nitrogen atoms of the porphyrin molecule are provided by two simple building blocks glycine (a nonessential amino acid) and succinyl CoA (an intermediate in the citric acid cycle). Glycine and succinyl CoA condense to form ALA in a reaction catalyzed by ALA synthase (Figure 21.3) This reaction requires pyridoxal phosphate as a coenzyme, and is the rate-controlling step in hepatic porphyrin biosynthesis. [Pg.276]

Tissues that synthesize heme, and the sources of porphyrin s carbon and nitrogen The major sites of heme biosynthesis are the liver (where the rate of synthesis is highly variable) and the erythrocyte-producing cells of the bone marrow (where the rate is generally constant). All the carbon and nitrogen atoms are provided by glycine and succinyl CoA. [Pg.493]

In the chelates of glycine, aspartic acid, and glutamic acid all the carbon and nitrogen atoms form part of the ring structure. This probably is the reason why these three acids appear to outlast all others in high rank coal. It should be pointed out that in the presence of hydrogen sulfide, copper is precipitated as the sulfide from copper-amino acid chelates. Thus, copper and perhaps other elements could be transported as amino acid chelates until sufficient hydrogen sulfide was encountered to cause precipitation. [Pg.228]

The imidazole ring of histidine (30) arises by a quite different route to that used for the formation of the imidazole ring in purine biosynthesis. The sources of the carbon and nitrogen atoms of histidine were established as a result of a series of labelling experiments with T4C and 15N substrates coupled with degradation of the labelled histidines. A summary of these results is given in Scheme 7 (59JBQ234)586). [Pg.90]

Using different approximations for the carbon and nitrogen atoms (see text). [Pg.329]

The electronic states of the CN radical have been fully characterized by Schaefer and Heil (90). Ground state CN(X2E+) has a triple bond between the carbon and nitrogen atoms, and an unpaired electron localized on the carbon atom. Collinear approach of two CN(X E+) singlet-coupled radicals leads to the... [Pg.152]

First, connect the carbon and nitrogen atoms. The only way the carbon can form four bonds and the nitrogen can form three bonds is if there is a carbon-nitrogen triple bond. [Pg.254]

When electron-withdrawing groups are present on both the carbon and nitrogen atoms of the oxime, triazoline adducts ranging in yield from 23 to 89% are obtained by reaction with diazomethane or diazoethane (Scheme 102) the aziridines formed from these triazolines are found to show unusual configurational stability.363,364... [Pg.287]

Another important consideration in the theoretical description of C-N materials is the bonding configuration for the carbon and nitrogen atoms, which make up the solid. The crystalline structures, which employ tetrahedral sp3 carbon bonding have dramatically larger calculated bulk moduli... [Pg.765]

Predict the hybridization and geometry of the carbon and nitrogen atoms in the following ions. (Hint Resonance.) O... [Pg.84]

Tungsten carbide — WC, belongs to a class of Group IV B-VIB transition metal carbides and nitrides, often referred to as interstitial alloys, in which the carbon and nitrogen atoms occupy the interstitial lattice positions of the metal [i]. These compounds possess properties known from group VIII B precious metals like platinum and palladium [ii]. Thus, they show remarkable catalytic activities, attributed to a distinct electronic structure induced by the presence of carbon or nitrogen in the metal lattice. Tungsten carbide resembles platinum in its electrocatalytic oxidation activity (- electrocatalysis) and is therefore often considered as an inexpensive anode electrocatalyst for fuel cell [iii] and -> biofuel cell [iv] application. [Pg.215]


See other pages where The Carbon and Nitrogen Atoms is mentioned: [Pg.29]    [Pg.5]    [Pg.276]    [Pg.185]    [Pg.185]    [Pg.187]    [Pg.1152]    [Pg.16]    [Pg.171]    [Pg.46]    [Pg.190]    [Pg.70]    [Pg.151]    [Pg.330]    [Pg.167]    [Pg.547]    [Pg.1004]    [Pg.1031]    [Pg.194]    [Pg.195]    [Pg.174]    [Pg.8]    [Pg.273]    [Pg.864]    [Pg.330]    [Pg.425]    [Pg.8]    [Pg.13]    [Pg.167]    [Pg.153]    [Pg.160]    [Pg.46]   


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