Quantum Chemistry of the Surface Chemical Bond

Elementary Quantum Chemistry of the Surface Chemical Bond... 

Chemisoq)tion bonding to metal and metal oxide surfaces has been treated extensively by quantum-mechanical methods. Somoijai and Bent [153] give a general discussion of the surface chemical bond, and some specific theoretical treatments are found in Refs. 154-157 see also a review by Hoffman [158]. One approach uses the variation method (see physical chemistry textbooks) ... 

The characterization of the interrelations between chemical bonding and molecular shape requires a detailed analysis of the electronic density of molecules. Chemical bonding is a quantum mechanical phenomenon, and the shorthand notations of formal single, double, triple, and aromatic bonds used by chemists are a useful but rather severe oversimplification of reality. Similarly, the classical concepts of body and surface , the usual tools for the shape characterization of macroscopic objects, can be applied to molecules only indirectly. The quantum mechanical uncertainty of both electronic and nuclear positions within a molecule implies that valid descriptions of both chemical bonding and molecular shape must be based on the fuzzy, delocalize properties of electronic density distributions. These electron distributions are dominated by the nuclear arrangements and hence quantum mechanical uncertainly affects electrons on two levels by the lesser positional uncertainty of the more massive nuclei, and by the more prominent positional uncertainty of the electrons themselves. These two factors play important roles in chemistry and affect both chemical bonding and molecular shape. 

Quantum-chemical cluster models, 34 131-202 computer programs, 34 134 methods, 34 135-138 for chemisorption, 34 135 the local approach, 34 132 molecular orbital methods, 34 135 for surface structures, 34 135 valence bond method, 34 135 Quantum chemistry, heat of chemisorption determination, 37 151-154 Quantum conversion, in chloroplasts, 14 1 Quantum mechanical simulations bond activation, 42 2, 84—107 Quasi-elastic neutron scattering benzene... 

Quantum Systems in Chemistry and Physics is a broad area of science in which scientists of different extractions and aims jointly place special emphasis on quantum theory. Several topics were presented in the sessions of the symposia, namely 1 Density matrices and density functionals 2 Electron correlation effects (many-body methods and configuration interactions) 3 Relativistic formulations 4 Valence theory (chemical bonds and bond breaking) 5 Nuclear motion (vibronic effects and flexible molecules) 6 Response theory (properties and spectra atoms and molecules in strong electric and magnetic fields) 7 Condensed matter (crystals, clusters, surfaces and interfaces) 8 Reactive collisions and chemical reactions, and 9 Computational chemistry and physics. 

PHYSICAL CHEMISTRY. Application of the concepts and laws of physics to chemical phenomena in order to describe in quantitative (mathematical) terms a vast amount of empirical (observational) information. A selection of only the most important concepts of physical chemistiy would include the electron wave equation and the quantum mechanical interpretation of atomic and molecular structure, the study of the subatomic fundamental particles of matter. Application of thermodynamics to heats of formation of compounds and the heats of chemical reaction, the theory of rate processes and chemical equilibria, orbital theory and chemical bonding. surface chemistry (including catalysis and finely divided particles) die principles of electrochemistry and ionization. Although physical chemistry is closely related to both inorganic and organic chemistry, it is considered a separate discipline. See also Inorganic Chemistry and Organic Chemistry. 

Two specific approximations were developed to solve the problems of surface chemistry the periodic approximation, where quantum-chemical methods employ a periodic structure of the calculated system, and the cluster approximation, where the model of solid phase of finite size is created as a cutoff from the system of solid phase (it produces unsaturated dangling bonds at the border of cluster). The cluster approximation has been widely used for studying the interactions of molecules with all types of solids and their surfaces [24]. This approach is powerful in calculations of systems with deviations from the ideal periodic structure like doping and defects. Clay minerals are typical systems having such properties. 

Theoretical investigations of the modification phenomenon have been carried out by Roginskil and Vol kenshteln (342,418,419,420,421,423). Their work has been based upon the electronic theory of catalysis which utilizes greatly present-day knowledge of quantum chemistry and those theories of the solid state which deal with processes occurring within crystalline materials. On the basis of these concepts it is possible to treat the problems involved in the conversion of molecules adsorbed on a solid surface. The adsorbed molecule and the solid are treated as a unified system, the electrons of the lattice participating in bonding and subsequently chemical reaction. The velocity of the chemical reaction is dependent upon the electronic properties of the solid and reactants involved. 

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