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Molecular lattices

In the present book, we aim at the unified description of ground states and collective excitations in orientationally structured adsorbates based on the theory of two-dimensional dipole systems. Chapter 2 is concerned with the discussion of orientation ordering in the systems of adsorbed molecules. In Section 2.1, we present a concise review on basic experimental evidence to date which demonstrate a variety of structures occurring in two-dimensional molecular lattices on crystalline dielectric substrates and interactions governing this occurrence. [Pg.3]

Substrate Molecule So Molecular lattice (Distances in A) a b a Orientational structure (Angles in degrees) 6 q> Method and Refs. [Pg.8]

As a rule, the density of states for molecular lattice vibrations is negligible as compared to that for crystal phonons. Therefore, the K-mode of a molecular lattice is coupled with the crystal phonons specified by the same wave vector K. Besides, the low-frequency collective mode m of adsorbed molecules can be considered as a... [Pg.175]

Thermal destabilization of the molecular lattice of aromatlc-rlch macerals In bituminous coals at temperatures above 600 K Is associated with their characteristic thermoplasticity (10). The relationship between the extent of this fusion and the molecular properties of the vltrlnlte and Inertlnlte macerals, however. Is not well understood. [Pg.112]

Interaction In the stabilization of the molecular lattice of these coals. This process no doubt gives rise to the formation of the ordered graphlte-llke structures detectable by X-ray diffraction (e.g. and apparently not disrupted by exposure of the coals to pyridine and their resultant swelling (20,21). Also the microscopic conformal and reversible nature of the swelling of coals by pyridine established by Brenner ( ) points to these ordered structures existing In mlcrodomalns of dimension less than 10 m. [Pg.113]

The van der Waals-London forces play a particularly important part in the formation of molecular lattices even when the molecules still have an ionic structure screening and polarization diminish the effect of electrostatic forces to a great extent, and the van der Waals forces are therefore preponderant. Examples of substances which form molecular lattices are those of the type XY4, such as CC14, CI4, SnCl4, etc. In these a small positive ion is surrounded by four large halogen ions in the form of a tetrahedron, with the result that the external electric field of the positive ion is very weak. Mutual attraction of molecules is often exclusively the result of the van der... [Pg.189]

Chiral compounds (Continued) epoxy alcohols, 141 formulas, xiii xvii hydroxystannanes, 318 liquid crystals, 350 molecular lattics, 347 natural, 1 NMR spectra, 282 olefins, 173 oxetanones, 326 phenols, 287 see also Binaphthol phenylbutenes, 172 protonating agents, 324 sulfoxides, 159 sulfur ylides, 328 synthesis, I... [Pg.193]

Certain chiral organic compounds create crystalline environments and act as enantio-controlling media (7) even though they do not function as true catalysts. Natta s asymmetric reaction of prochiral trans-1,3-pentadiene, which was included in the crystal lattice of chiral perhydro-triphenylene as a host compound, to form an optically active, isotactic polymer on 7-ray irradiation, is a classic example of such a chiral molecular lattice (Scheme 1) (2). Weak van der Waals forces cause a geometric arrangement of the diene monomer that favors one of the possible enantiomeric sequences. [Pg.377]

There is some evidence that the strength of intermolecular forces determines the degree of cooperativity and the rate of spin state interconversion in the lattice (154,155). This is a reasonable hypothesis, for it assumes a continuum of behavior, from very weak interactions, which reflect intramolecular properties, to strong intermolecular forces, which cause cooperative phase transitions and abrupt spin state changes. Neutral complexes with a molecular lattice and little or no hydrogen bonding between the molecules, such as some iron(III)... [Pg.37]

The components of a thermoelectric cooler are indicated by the cross section of a typical unit shown in Fig. 1. Therm oelectiic coolers such as this are actually small heat pumps that operate on the physical principles well established over a century ago. Semiconductor materials with dissimilar characteristics are connected electrically in senes and thermally in parallel, so that two junctions are created. The semiconductor materials are n- and /i-type and are so named because either they have more electrons than necessary to complete a perfect molecular lattice structure (ri-type), or not enough electrons to complete a lattice structure (/7-type). The extra electrons in the -type material and the holes left in the /7-type material are called carriers and they are the agents that move the heat energy from the cold to the hot junction. [Pg.1608]

Azalene salts 90 and 92 are obtained by quaternization of the corresponding heterocyclic bases with alkyl halides or tosylates. If the heterocyclic base contains several nitrogen atoms, alkylation can produce different quaternary salts. Quaternization, however, is surprisingly selective if certain conditions are met.205 Pyrrolo- and indolopyridines containing one pyridine-and one pyrrole-type nitrogen atom in their molecular lattice are (in aprotic solvents) almost exclusively alkylated at the nitrogen atom of the pyridine... [Pg.204]

Both methods explained above start from a molecular lattice already having the structure of the corresponding pseudoazulene system. The essential last step of a pseudoazulene synthesis, however, can also be to create... [Pg.211]

The crystals of solids are built up of ions of non-metals, ions of metals, atoms, molecules or a combination of all these particles. These possibilities result in four different crystal lattices, i.e. the ionic lattice (e.g. sodium chloride, NaCl), the atomic lattice (e.g. diamond, C), the molecular lattice (e.g. iodine, I2) and the metallic lattice (e.g. copper, Cu). The forces which hold the building blocks of a lattice together differ for each lattice and vary from the extremely strong coulombic forces in an ionic lattice to the very weak Van der Waals forces between the molecules in a molecular lattice. [Pg.59]

Low-temperature adiabatic heat capacity (Cp) measurements then were carried out on microcrystalline BABI to look for evidence of ordering below 2K 190 The expected anomaly was somewhat broad but readily seen in the right-hand chart of Fig. 25, with a maximum at 2 K the shape was consistent with expectations for a low-dimensional antiferromagnet. After subtraction of molecular lattice contributions by a Debye-type extrapolation from the higher... [Pg.143]

The big difference in melting points suggests a difference in type of crystal binding. The intermolecular forces in solid CO2 must be very low to be overcome by a low-temperature sublimation. CO2 is actually a molecular lattice held together only by the weak van der Waals forces between discrete CO2 molecules. Si02 is a covalent lattice with a three-dimensional network of bonds each silicon atom is bonded tetrahedrally to four oxygen atoms and each oxygen is bonded to two silicon atoms. [Pg.176]

Comparison of the tetramethyldipnictogens with the isoelectronic dihalogens is particularly informative. Cl2, Br2, and I2 crystallize in isostructural molecular lattices with increasing intermolecular interaction (54,59). For iodine, the atoms are connected intramolecularly at 2.72 A and inter-molecularly in a two-dimensional rectangular net at 3.50 and 3.97 A. The ratio E—E/E—E drops from 1.68 for Cl2 to 1.29 for I2. Only for I2 is there an appreciable intermolecular interaction. Again the brake occurs between the fourth and fifth periods of elements (see Table VIII) (54,59). The... [Pg.93]

F10. XV-3.—Arrangement of atoms in one-dimensional diatomic molecular lattice. [Pg.247]

Molecular dimensions, 246 Molecular lattice fitting, 159 Molecular mass, 17... [Pg.998]


See other pages where Molecular lattices is mentioned: [Pg.162]    [Pg.918]    [Pg.303]    [Pg.68]    [Pg.613]    [Pg.235]    [Pg.231]    [Pg.368]    [Pg.52]    [Pg.84]    [Pg.57]    [Pg.93]    [Pg.98]    [Pg.98]    [Pg.190]    [Pg.418]    [Pg.162]    [Pg.162]    [Pg.212]    [Pg.42]    [Pg.146]    [Pg.148]    [Pg.262]    [Pg.148]    [Pg.653]    [Pg.399]    [Pg.251]    [Pg.252]    [Pg.255]    [Pg.24]    [Pg.159]    [Pg.25]   
See also in sourсe #XX -- [ Pg.57 , Pg.93 , Pg.98 ]

See also in sourсe #XX -- [ Pg.103 ]

See also in sourсe #XX -- [ Pg.103 ]

See also in sourсe #XX -- [ Pg.15 ]




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Bravais lattice, molecular dyes in zeolite channels

Calculated lattice energies of molecular crystals

Energy minimization, molecular mechanics and lattice statics

Inverse molecular lattices

Lattice coupling in direct molecular dissociation

Lattice dynamics molecular solids

Lattice energy calculation molecular dynamics

Lattice energy calculation molecular mechanics

Lattice molecular compounds

Lattice molecular dynamics

Lattice vibrations of molecular solids

Lattice, coordination molecular

Molecular compounds, lattice energy

Molecular lattice theory

Molecular magnetic materials spin-lattice relaxation

Molecular space lattice

Polymorphism molecular lattices

Simple molecular lattice

Simple molecular lattice vibrations

Spin-lattice relaxation molecular motion

Spin-lattice relaxation molecular size

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