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Special direction

Figure 1. Relativistic KKR-CPA D.O.S. for Cuo.73Pto.23 as calculated by a) special directions method (continuos line) b) Zeno s method (long dashed line) c) Zeno s method but in a fet lattice with c/a l (dotted line). The site potentials are in the ASA fonn. Figure 1. Relativistic KKR-CPA D.O.S. for Cuo.73Pto.23 as calculated by a) special directions method (continuos line) b) Zeno s method (long dashed line) c) Zeno s method but in a fet lattice with c/a l (dotted line). The site potentials are in the ASA fonn.
Special directions for administration, stated by either the primary health care provider or manufacturer, are also important. For example, cisplatin cannot be prepared or administered with needles or IV administration sets containing aluminum because aluminum reacts with cisplatin, causing formation of a precipitate and loss of potency. [Pg.596]

PbS has attracted much attention due to its special direct band gap energy (0.4 eV) and a relatively large exciton Bohr radius (18 nm) and their nanoclusters have potential applications in electroluminescent devices such as light-emitting diodes. PbS nanocrystals with rod like structures with diameters of 20-60 nm and lengths of 1-2 pm have been obtained using the sonochemical method and by using PEG-6000 [66]. Addition of PEG and the time of sonication have been found to play a key role in the formation of these rods. [Pg.206]

Because of translational symmetry special directions occur in crystals and it often happens that the electric fields associated with light rays transmitted through a crystal are channeled to vibrate in a special direction that provides an easy passage. This means that the light becomes polarized. [Pg.178]

This has been looked for previously but without success. The structure of the diamond cannot be explained on the hypothesis that the field of force around the carbon atom is the same in all directions or in other words, that the force between the two atoms can be expressed simply by a function of the distance between the centres. If this were so, the sphere, which would then represent the carbon atoms appropriately, would adopt the closed-packed arrangement. As a matter of fact, each atom is surrounded by four neighbours only. It is necessary, therefore, to suppose that the attachment of one atom to the next is due to some directed property, and the carbon atom has four such special directions as indeed the tetra-valency of the atom might suggest. In that case the properties of the atom in diamond are based upon a tetrahedral not a spherical form. The tetrahedra point away from any (111) plane in case of half the atoms in diamond and towards it in case of the other half. Consecutive (111) sheets are not exactly of the same nature and it might reasonably be expected that they would not entirely destroy each other s effects in the second order reflection from the tetrahedral plane. It is this effect which is now found to be quite distinct, though small. ... [Pg.50]

Some special directing effects have been observed in these reductions. For example, RjSnH is directed by an OAc or Cl substituent on the allyl terminus to deliver hydride to the remote terminus,297 but a CN directs delivery to the proximal terminus (equations 326-328).287 Electrochemical reduction307 also results in formation of an a, 3-unsaturated organo product (equation 329). A remote OH functionality appears to direct NaBHt reduction to the proximal allyl terminus (equation 330).288... [Pg.647]

A spatial or three-dimensional formula for nitrogen, analogous to the carbon tetrahedron, is not possible because there is no symmetrical solid figure with five corners. Hence it was assumed that certain valencies of the nitrogen atom are directed in special directions. Thus were obtained J. H. van t Hoff s cubic or tetrahedral formula, C. Willgerodt s double tetrahedron, C. A. Bischoff s square pyramid, and the modifications suggested by W. Vaubel, and A. von Baeyer. The tetrahedral and the pyramidal or square formula can be graphically symbolized . ... [Pg.91]

If one considers theory to be at the opposite side of experiment, then Barriol was not a theoretical chemist. Was he, in these conditions, a physical chemist It is within the area of physical chemistry that our laboratory took the occasion to perform the most significant advances said Barriol, modestly. As a matter of fact, most papers were published in the Journal de Chimie Physique and the notes in the Academie des Sciences were mostly read in the physical chemistry section. Like Bauer, Barriol was interested in the theoretical aspects of physical chemistry. But, more generally, he can be considered as a kind of generalist, working at the center of the chemist s preoccupations - the structure of molecules and the nature of their interactions -who dominated general questions of fundamental chemistry, who could go ahead, rather far, in specialized directions of high interest, who was able to distribute problems to more specialized disciplines and, vice versa, to think about the responses. [Pg.115]

Free atoms are spherically symmetrical, which implies conservation of their angular momenta. Quantum-mechanically this means that both Lz and L2 are constants of the motion when V = V(r). The special direction, denoted Z, only becomes meaningful in an orienting field. During a chemical reaction such as the formation of a homonuclear diatomic molecule, which occurs on collisional activation, a local held is induced along the axis of approach. Polarization also happens in reactions between radicals, in which case it is directed along the principal symmetry axes of the activated reactants. When two radicals interact they do so by anti-parallel line-up of their symmetry axes, which ensures that any residual angular momentum is optimally quenched. The proposed sequence of events is conveniently demonstrated by consideration of the interactions between simple hydrocarbon molecules. [Pg.207]

In CARS two ultrashort pulses of laser light (from femtoseconds to picoseconds in duration) arrive simultaneously at the sample of interest (Mukamel, 2000 Fourkas, 2001 and references herein). The difference between the frequencies (W) - w2) matches the frequency of a Raman active vibrational mode in the sample. A probe pulse (w3) emits a signal pulse of frequency Wj - w2 + w3 in a unique special direction. By scanning the delay time between the pump and probe pulses, the delay of the vibrational coherence can be measured. The distinct advantage of CARS is that it is a background free technique, since the signal propagates in a unique direction. [Pg.4]

In the manufacture of tablets it is important to define and appreciate the physical properties of the active substance, in particular particle size and flowability. The technology involved in direct compression assumes great importance in tablet formulations because it is often the least expensive, particularly in the production of generics that the active substance permits. The limiting factors are the physical properties of the active substance and its concentration in the tablets. Even substances such as ascorbic acid, which are not generally suitable for direct compression owing to the friability of the crystals, can normally be directly pressed into tablets at concentrations of 30-40%. Ffowever, this technique is not as suitable if the content of ascorbic acid is higher. This limit may be shifted upward by special direct-compression auxiliaries, for example, Ludipress (BASF). [Pg.985]

The number of rotating planes corresponds to mi. For m = 0 the wave function (16) is real. In a spherically symmetrical environment there is no special direction in space and the wave function (18) acquires geometrical meaning only when an external magnetic field is switched on. Any of the... [Pg.82]

Once the special direction has been fixed, the two remaining eigenfunctions always constitute a complex pair with rotational symmetry in the xy-plane. A geometrical representation related to such functions is shown in figure 8. The familiar drawings of a set of three orthogonal px, py and pz... [Pg.84]

Ethylene C2H4 is the simplest molecule to exhibit an electronic (non-steric) barrier to rotation. If this molecule is assumed to contain a C-C linkage, a special direction may occur in one of two possible ways... [Pg.201]

When k is in a special direction such as along the z-axis, cancellation among terms in the sum in fiq. (20-2) will cause many of the H i, values to vanish. Which ones vanish can be learned readily by symmetry, using group theory, or by direct evaluation. It is found in fact that there arc matrix elements between Bloch sums based upon the s state and upon the d state of symmetry 3z — but all other for P a. vanish. For these others, Eq. (20-3) becomes a set of independent equations E. = // , and we evaluate them directly. [Pg.482]

Ether vapor is easily ignited, and should never be brought near a flame, unless special directions are so given. [Pg.242]

In the simplest liquid-crystalline phase, namely the uniaxial nematic, there is at rest a special direction designated by a unit vector n called the director (see Fig. 10-2). In the plane transverse to the director, the fluid is isotropic. The most common nematics are composed of oblong molecules that tend to point in a common direction, which defines the director orientation. Oblate, or disc-like, molecules can also form uniaxial nematics for these discotic nematics, the director is defined by the average orientation of the short axis of the molecule. Lath-like molecules or micelles (shaped like rectangular slabs), in which all three dimensions of the molecule are significantly different from each other, can form biaxial nematics (Praefcke et al. 1991 Chandrasekhar 1992 Fialtkowski 1997). A biaxial... [Pg.446]

Follow the special directions and warnings given by the instructor. If in doubt, ask the instructor or assistant. [Pg.3]


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See also in sourсe #XX -- [ Pg.207 , Pg.281 ]




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