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Atomic chains

Finally, in 1985, the results of an extensive investigation in which adsorjDtion took place onto an aluminium oxide layer fonned on a film of aluminium deposited in vacuo onto a silicon wafer was published by Allara and Nuzzo 1127, 1281. Various carboxylic acids were dissolved in high-purity hexadecane and allowed to adsorb from this solution onto the prepared aluminium oxide surface. It was found that for chains with more than 12 carbon atoms, chains are nearly in a vertical orientation and are tightly packed. For shorter chains, however, no stable monolayers were found. The kinetic processes involved in layer fonnation can take up to several days. [Pg.2623]

This compound permits the introduction (in moderate yield) of a four carbon atom chain at the site of the carbonyl group by the use of the Reformatsky reaction (compare Section VI,8) ... [Pg.926]

The reverse reaction (ion formation) can occur in two ways internally, by attack of the penultimate polymer oxygen atom, or externally, by attack of a monomer oxygen atom (chain growth). The external process is about 10 times slower than the internal process in bulk THF (1). Since ion formation is a slow process compared to ion chain growth, chain growth by external attack of monomer on covalent ester makes a negligible contribution to the polymerization process. [Pg.362]

In recent years, especially in the USSR and Europe, synthetic fatty acids, prepared via hydrocarbon oxidation, have been used to prepare fatty amines (2,9). In 1978 Eastern Europeans produced an estimated 0.55 biUion kg of synthetic fatty acids with odd and even numbers of carbon atoms, whereas in the United States, production of natural fatty acids with even carbon atom chain-length acids was 435 million kg. To date, there has been no significant production of synthetic fatty acids in the United States. [Pg.218]

FIGURE 18.32 Biotin is covalently linked to a protein via the e-amino group of a lysine residue. The biotin ring is thus tethered to the protein by a 10-atom chain. It functions by carrying carboxyl groups between distant sites on biotin-dependent enzymes. [Pg.601]

Atom-kem, m. atomic nucleus, -kette,/. chain of atoms, atomic chain, -lage, /. atomic layer atomic position, -lehre, /, doctrine of atoms, atomic theory, -mechanik, /. mechanics of the atom, -modell, n, atomic model, -nummer, /, atomic number, -ord-nung, /. atomic arrangement, -refraktion, /. atomic refraction, -rest, m. atomic residue (= Atomrumpf). -ring, m. ring of atoms, -rumpf, m. atomic residue or core (remainder of an atom, as after removal of some electrons), -schale, /, atomic shell, -strabl, m. atomic ray, -tafel, /, atomic table, atomtbeoretisch, a. of or according to the atomic theory,... [Pg.37]

For polymer containing labile hydrogen atoms, chain peroxidation can lead to hydroperoxide formation. The following reactions are expected to take place. [Pg.491]

The most popular bonded phases are, without doubt, the reverse phases which consist solely of aliphatic hydrocarbon chains bonded to the silica. Reverse phases interact dispersively with solvent and solute molecules and, as a consequence, are employed with very polar solvents or aqueous solvent mixtures such as methanol/water and acetonitrile/water mixtures. The most commonly used reverse phase appears to be the brush type phase with aliphatic chains having four, eight or eighteen carbon atom chains attached. These types of reverse phase have been termed C4, C8 and Cl8 phases respectively. The C8... [Pg.76]

Figure 1. The torsional angle, 4>, and bond angle, S, are shown as a function of dj for the four atom chain with values of 7. equal to 5.0 x 10, 5.0 x 10, and 5.0 x 10 kg/mol-ns. (Reproduced with permission from ref. 13. Copyright 1988 Wiley.)... Figure 1. The torsional angle, 4>, and bond angle, S, are shown as a function of dj for the four atom chain with values of 7. equal to 5.0 x 10, 5.0 x 10, and 5.0 x 10 kg/mol-ns. (Reproduced with permission from ref. 13. Copyright 1988 Wiley.)...
Fig. 5.5. Illustration of the coarse-graining procedure for a united atom chain. The chain is a segment of PE at 509 K from molecular dynamics simulations with the united atom model [Eqs. (5.7)—(5.11)]. One coarse-grained bond represents the end-to-end distance of n = 5 consecutive united atom bonds. From [32]... Fig. 5.5. Illustration of the coarse-graining procedure for a united atom chain. The chain is a segment of PE at 509 K from molecular dynamics simulations with the united atom model [Eqs. (5.7)—(5.11)]. One coarse-grained bond represents the end-to-end distance of n = 5 consecutive united atom bonds. From [32]...
Up to now we have assumed evenly spaced H atoms. If we now allow the H atoms to approach each other in pairs, a change in the band structure takes place. The corresponding movements of the atoms are marked by arrows in Fig. 10.6. At k = 0 this has no consequences at the lower (or upper) end of the band an energy gain (or loss) occurs for the atoms that approach each other it is compensated by the energy loss (or gain) of the atoms moving apart. However, in the central part of the band, where the H atom chain has... [Pg.94]

In the early stage of the development of molecular conductors based on metal complexes, partially oxidized tetracyanoplatinate salts (for example, KCP K2 [Pt(CN)4]Br0.30-3H2O) and related materials were intensively studied [6], In this system, the square-planar platinum complexes are stacked to form a linear Pt-atom chain. The conduction band originates from the overlap of 5dz2 orbitals of the central platinum atom and exhibits the one-dimensional character. [Pg.39]

Answer is (b), 2-butanol is the most appropriate name for this molecule. It has a four carbon atom chain with a hydroxyl group on the carbon second from the end. [Pg.51]

Structural (skeletal) isomers differ from each other in the length of their carbon atom chains and in the length of the side chains. The carbon skeleton differs between these isomers. Positional isomers differ in the location or position where functional groups are attached to the carbon skeleton. Geometric isomers differ in whether two substituents are on the same side of the molecule or on opposite sides of the molecule from each other usually they are on opposite sides or the same side of a double bond. [Pg.632]

Fig. 3.1. Formation of IV-atom chain from cyclic chain by breaking bond between n = 0 and N — 1 atoms. Fig. 3.1. Formation of IV-atom chain from cyclic chain by breaking bond between n = 0 and N — 1 atoms.
Fig. 3.2. Schematic representation of chemisorption, (a) Before and (b) after formation of /3a-bond between a-atom and n = 0 atom of IV-atom chain. Fig. 3.2. Schematic representation of chemisorption, (a) Before and (b) after formation of /3a-bond between a-atom and n = 0 atom of IV-atom chain.
The substrate being modelled is a metal with a semiconductor support, illustrated schematically in Fig. 5.1 (Davison et al 1988). The system has two components metal and semiconductor. The metal part consists of a finite (n+ l)-atom chain (or him), occupying atomic sites m = 0 to m = n... [Pg.75]

We consider an atomic chain of spacing a, within the TBA, having the usual site energies... [Pg.118]

The above recursive process, for the 2-atom chain, can now be repeated for the 3-atom case. The Dyson equation analogous to (7.23) is... [Pg.125]

Plots of the LDOS at the surface (n = 1) site of a 100-atom chain are presented in Fig. 7.3 for various field strengths. For no field, F = 0 (Fig. 7.3(a)), the LDOS exhibits a discretized version of the semi-elliptical shape, familiar for a surface DOS. For small field strength (Fig. 7.3(b)), an almost-linear region appears in the lower end of the quasi-band. As the field strength increases (Fig. 7.3(c) and (d)), the region spreads across the band, with increasing intensities. In addition, there is a rigid shift in the structure to... [Pg.128]

Fig. 7.3. LDOS at n = 1 site of 100-atom chain. As held increases, semi-elliptical shape is dominated by linear potential. Field strengths are as indicated. Reprinted from Davison et al (1997) with permission from the Institute of Physics. Fig. 7.3. LDOS at n = 1 site of 100-atom chain. As held increases, semi-elliptical shape is dominated by linear potential. Field strengths are as indicated. Reprinted from Davison et al (1997) with permission from the Institute of Physics.

See other pages where Atomic chains is mentioned: [Pg.497]    [Pg.5]    [Pg.33]    [Pg.282]    [Pg.665]    [Pg.267]    [Pg.33]    [Pg.34]    [Pg.627]    [Pg.717]    [Pg.69]    [Pg.179]    [Pg.1635]    [Pg.109]    [Pg.110]    [Pg.122]    [Pg.367]    [Pg.94]    [Pg.68]    [Pg.125]    [Pg.529]    [Pg.150]    [Pg.139]    [Pg.222]    [Pg.6]    [Pg.81]    [Pg.123]   
See also in sourсe #XX -- [ Pg.68 ]




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Atom transfer radical chains

Atom transfer radical polymerization chain

Atom transfer radical polymerization chain length dependence

Atom transfer radical polymerization controlled chain lengths

Atom-Transfer-Chain (ATC) Catalysis

Atom-transfer-chain

Atom-transfer-chain catalysis

Atom-transfer-chain mechanism

Atomic Structure and Polymer Chain Bonds

Atomic chain formation

Band Theory. The Linear Chain of Hydrogen Atoms

Branched chains, of carbon atoms

Carbon atoms chain selection

Chain Extensions at the Primary Carbon Atom

Chain of hydrogen atoms

Chain with a Basis of Two Identical Atoms

Chains of sp-Hybridized Carbon Atoms

Chains of three or more nitrogen atom

Chains, carbon atoms

Chains, carbon atoms hydrocarbon

Chains, carbon atoms straight

Chains, of carbon atoms

Complexes of Open-Chain Tetradenate Atoms

Compounds with Chains of Three or More Nitrogen Atoms

Core chain atoms

Evolution of Electronic Structure from Single Atom to Polymer Chain

Extended metal-atom chains

Fluorocarboxylic acids and derivatives containing an oxygen atom as a chain member

Hydrogen bond types chain atoms

Linear chain of atoms

Motion of Atoms in a Diatomic Chain

Normal Modes in a Linear Chain of Atoms

One-dimensional chain of atoms

Polynuclear chains with direct interactions between heavy atoms

Prefixes carbon-atom chain

Primary carbon atom chain extensions

Protein chain, atomic resolution

Reactions of Carbosilanes Containing Side Chains Bonded to Si-Atoms in the Molecular Skeleton

Ring-chain tautomerism atoms

Single-atom decay chains

Synthesis of Phenols with Side-chains containing Si, N or S Atoms

Unsaturated Radicals Bearing Fluorine Atoms on the Chain

Waves on a Chain of Like Atoms

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