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Primitive cells

The FCC structure is illustrated in figure Al.3.2. Metallic elements such as calcium, nickel, and copper fonu in the FCC structure, as well as some of the inert gases. The conventional unit cell of the FCC structure is cubic with the lengdi of the edge given by the lattice parameter, a. There are four atoms in the conventional cell. In the primitive unit cell, there is only one atom. This atom coincides with the lattice pomts. The lattice vectors for the primitive cell are given by... [Pg.98]

The empirical pseiidopotential method can be illustrated by considering a specific semiconductor such as silicon. The crystal structure of Si is diamond. The structure is shown in figure Al.3.4. The lattice vectors and basis for a primitive cell have been defined in the section on crystal structures (ATS.4.1). In Cartesian coordinates, one can write G for the diamond structure as... [Pg.110]

Fig. 3. Translation vectors used to define the symmetry of a carbon nanotube (see text). The vectors a, and 82 define the 2D primitive cell. Fig. 3. Translation vectors used to define the symmetry of a carbon nanotube (see text). The vectors a, and 82 define the 2D primitive cell.
In the crystal, the total number of vibrations is determined by the number of atoms per molecule, N, and the nmnber of molecules per primitive cell, Z, multiplied by the degrees of freedom of each atom 3ZN. In the case of a-Sg (Z =4, N =8) this gives a total of 96 vibrations ( ) which can be separated in (3N-6)—Z = 72 intramolecular or "internal" vibrations and 6Z = 24 intermo-lecular vibrations or lattice phonons ("external" vibrations). The total of the external vibrations consists of 3Z = 12 librational modes due to the molecular rotations, 3Z-3 = 9 translational modes, and 3 acoustic phonons, respectively. [Pg.45]

From an energetic point of view, the bands at higher wavenumbers can be assigned to the Ss rings. However, the intensities were found as ca. 0.65 1 (pure infected) instead of 2.8 1 which would be expected from the natural abundance of the isotopomers. These discrepancies were solved by applying the mathematical formalism utilized in the treatment of intramolecular Fermi resonance (see, e.g., [132]). Accordingly, in the natural crystal we have to deal with vibrational coupling between isotopomers in the primitive cell of the crystal [109]. [Pg.61]

The resonance splitting of intramolecular modes in the crystalline state is often called Davydov splitting or factor group splitting . In contrast to the static field effects of the crystal, this splitting is due to the dynamical interaction of the constituents in the primitive cell... [Pg.94]

Ni [182], V [183], and A1 [184]. SU-M [185] is a mesoporous germanium oxide with crystalline pore walls, possessing one of the largest primitive cells and the lowest framework density of any inorganic material. The channels are defined by 30-rings. Structural and thermal information show that there exists a mismatch between framework stability and template decomposition. The latter requires temperatures higher than 450 °C, while the structure is preserved only until 300 °C. [Pg.133]

A unit cell having the smallest possible volume is called a primitive cell. For reasons of symmetry according to rule 1 and contrary to rule 3, a primitive cell is not always chosen, but instead a centered cell, which is double, triple or fourfold primitive, i.e. its volume is larger by a corresponding factor. The centered cells to be considered are shown in Fig. 2.6. [Pg.8]

The conclusion to be drawn from Eq. (37) is thfit the volume of the first Brillouin zone is equal to the reciprocal of file volume of the primitive cell. It should be noted that the scalar product... [Pg.42]

An infinite three-dimensional crystal lattice is described by a primitive unit cell which generates the lattice by simple translations. The primitive cell can be represented by three basic lattice vectors such as and h defined above. They may or may not be mutually perpendicular, depending on the crystal... [Pg.251]

Unfortunately, the analytical composition of what we take to be the simplest cells we know is based on existing anaerobic (archaeic) bacteria. There may well have been many types of such cells existing together. The clearest statements that can be made are the essential ingredients of the most primitive cells ... [Pg.21]

As far as I can judge, all primitive cells had a basic reducing cell metabolism glycolysis, a citric acid cycle or its reverse, amino acid and base synthesis, while all maintained high K+, low Na+ and Cl-, moderate Mg2+, and very low Ca2+ (see Figure 2.3) by input and output pumps. Chemical... [Pg.23]

It is here that we hit a central feature of every organism as well as the most primitive. There has to be spatial structure, there has to be flow, and there has to be communication to co-ordinate the activities of the cell. The communication has to link the metabolic paths and consists in the primitive cell of feedback controls by small molecules (mobile coenzymes and substrates) and ions, where up to 20 elements are involved. By seeing... [Pg.24]

Of these, (2) and (3) and (1) and (5) must develop together and we see this in Table 2.1. The mixture of primitive cells from which we start our discussion all used as messengers in the cytoplasm various phosphate compounds, various substrates and the levels of minerals such as Fe2+, Mg2+ and K+. We labelled this above system as the P/Fe system of communication in the earliest life system. It may be better to view the system as diversifying at first through combination rather than as progressing. There is a part of the... [Pg.25]

The research dealing with models for the first primitive cells has had one central topic for many years the minimal cell . According to Luisi et al. (2006a), this is defined as an artificial or semi-artificial cell which contains a minimal (but sufficient) number of components to keep the cell alive . The cell is considered to be living when three conditions are fulfilled ... [Pg.264]

D. W. Deamer and J. P. Dworkin have reported in detail on the contribution of chemistry and physics to the formation of the first primitive membranes during the emergence of precursors to life the authors discussion ranges from sources of amphiphilic compounds, growth processes in protocells, self-organisation mechanisms in mixtures of prebiotic organic compounds (e.g., from extracts of the Murchison meteorite) all the way to model systems for primitive cells (Deamer and Dworkin, 2005). [Pg.273]

Fig. 10.11 The modified tree of life still has the usual tree-like structure and also confirms that the eukaryotes originally took over mitochondria and chloroplasts from bacteria. It does, however, also show a network of links between the branches. The many interconnections indicate a frequent transfer of genes between unicellular organisms. The modified tree of life is not derived, as had previously been assumed, from a single cell (the hypothetical primeval cell ). Instead, the three main kingdoms are more likely to have developed from a community of primitive cells with different genomes (Doolittle, 2000)... Fig. 10.11 The modified tree of life still has the usual tree-like structure and also confirms that the eukaryotes originally took over mitochondria and chloroplasts from bacteria. It does, however, also show a network of links between the branches. The many interconnections indicate a frequent transfer of genes between unicellular organisms. The modified tree of life is not derived, as had previously been assumed, from a single cell (the hypothetical primeval cell ). Instead, the three main kingdoms are more likely to have developed from a community of primitive cells with different genomes (Doolittle, 2000)...
Capacity to utilise catalytic Ni2+, Fe2+, W(Mo) and Mg2+ in cell metabolism (see Table 5.2). All primitive cells had to reduce CO (C02) before engaging in condensation reactions. We suppose nitrogen was available as NH3 for protein synthesis and HCN for the synthesis of nucleotide bases. [Pg.199]

The above description provides a possible starting background for the description of the beginning of cellular chemotypes, prokaryotes, but even this is less complicated than the only cells for which we have evidence since they have at least two additional groups of more sophisticated chemicals - coenzymes (see Tables 5.3 and 5.4) and certain metal cofactors, which we presume were additions to the most primitive cells. After we have described them, we shall return to the problem of cellular (cytoplasmic) organisation. Note that coenzyme novelty is not in basic pathways but in control of rates and in energy management. [Pg.202]

Fig. 5.11. A schematic picture of the roles of different elements in a primitive cell and a low redox potential environmental. 02 and S042- were introduced later. is a charge or concentration gradient. Fig. 5.11. A schematic picture of the roles of different elements in a primitive cell and a low redox potential environmental. 02 and S042- were introduced later. is a charge or concentration gradient.

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Atomic cell primitive basis orbital

Cell, unit primitive

Crystal primitive unit cell

Crystal structure primitive cell

Lattices primitive lattice cell

Primitive and nonprimitive cells

Primitive cell, defined

Primitive cubic unit cell

Primitive lattice cell

Primitives

Reciprocal lattice primitive unit cell

Unit cell cubic, simple/primitive

Wigner-Seitz primitive cell

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