Molecular orbital theory elements

To illustrate molecular orbital theory, we apply it to the diatomic molecules of the elements in the first two periods of the periodic table. [Pg.650]

Among the diatomic molecules of the second period elements are three familiar ones, N2,02, and F2. The molecules Li2, B2, and C2 are less common but have been observed and studied in the gas phase. In contrast, the molecules Be2 and Ne2 are either highly unstable or nonexistent. Let us see what molecular orbital theory predicts about the structure and stability of these molecules. We start by considering how the atomic orbitals containing the valence electrons (2s and 2p) are used to form molecular orbitals. [Pg.651]

Finally, the present guide is much less academic and much more practical than ""Ab Initio Molecular Orbital Theory . Focus is not on the underlying elements of the theory or in the details of how the theory is actually implemented, but rather on providing an overview of how different theoretical models fit into the overall scheme. Mathematics has been kept to a minimum and for the most part, references are to monographs and reviews rather than to the primary literature. [Pg.807]

The VSEPR approach is largely restricted to Main Group species (as is Lewis theory). It can be applied to compounds of the transition elements where the nd subshell is either empty or filled, but a partly-filled nd subshell exerts an influence on stereochemistry which can often be interpreted satisfactorily by means of crystal field theory. Even in Main Group chemistry, VSEPR is by no means infallible. It remains, however, the simplest means of rationalising molecular shapes. In the absence of experimental data, it makes a reasonably reliable prediction of molecular geometry, an essential preliminary to a detailed description of bonding within a more elaborate, quantum-mechanical model such as valence bond or molecular orbital theory. [Pg.12]

Offenhartz PO D (1970) Atomic and molecular orbital theory. McGraw-Hill, New York, p 325 (these matrix elements are zero because the AO functions belong to different symmetry species, while the operator (kinetic plus potential energy) is spherically symmetric... [Pg.439]

However, in sulphides and related minerals, the effects of covalent bonding predominate and orbital overlap must be taken into account. Thus, concepts of molecular orbital theory are described in chapter 11 and applied to aspects of the sulfide mineralogy of transition elements. Examples of computed energy diagrams for molecular clusters are also presented in chapter 11. There, it is noted that the fundamental 3d orbital energy splitting parameter of crystal field theory, A, receives a similar interpretation in the molecular orbital theory. [Pg.5]

Covalency of ligands clearly influences the positions and intensities of absorption bands in crystal field spectra of oxides and silicates, so that it is pertinent to discuss the types of covalent bonds that exist when transition elements are present in mineral structures. In this section, the more qualitative aspects of molecular orbital theory are described. [Pg.435]

The choice of topics is largely governed by the author s interests. Following a brief introduction the crystal field model is described non-mathematically in chapter 2. This treatment is extended to chapter 3, which outlines the theory of crystal field spectra of transition elements. Chapter 4 describes the information that can be obtained from measurements of absorption spectra of minerals, and chapter 5 describes the electronic spectra of suites of common, rock-forming silicates. The crystal chemistry of transition metal compounds and minerals is reviewed in chapter 6, while chapter 7 discusses thermodynamic properties of minerals using data derived from the spectra in chapter 5. Applications of crystal field theory to the distribution of transition elements in the crust are described in chapter 8, and properties of the mantle are considered in chapter 9. The final chapter is devoted to a brief outline of the molecular orbital theory, which is used to interpret some aspects of the sulphide mineralogy of transition elements. [Pg.571]

To finish up this section on molecular orbital theory, let s look at the configurations for the elements from lithium to neon. (See Table 7.4.) These should provide you with sufficient examples to see the main principles behind molecular orbital theory. [Pg.144]

As it is well known (see, for example, [16,17]), the Hiickel molecular orbital theory is based on a Hamiltonian operator, ff defined by means of the matrix elements... [Pg.33]

Three levels of explanation have been advanced to account for the patterns of reactivity encompassed by the Woodward-Hoffmann rules. The first draws attention to the frequency with which pericyclic reactions have a transition structure with (An + 2) electrons in a cyclic conjugated system, which can be seen as being aromatic. The second makes the point that the interaction of the appropriate frontier orbitals matches the observed stereochemistry. The third is to use orbital and state correlation diagrams in a compellingly satisfying treatment for those cases with identifiable elements of symmetry. Molecular orbital theory is the basis for all these related explanations. [Pg.214]

The VSEPR model works at its best in rationalizing ground state stereochemistry but does not attempt to indicate a more precise electron distribution. The molecular orbital theory based on 3s and 3p orbitals only is also compatible with a relative weakening of the axial bonds. Use of a simple Hiickel MO model, which considers only CT orbitals in the valence shell and totally neglects explicit electron repulsions can be invoked to interpret the same experimental results. It was demonstrated that the electron-rich three-center bonding model could explain the trends observed in five-coordinate speciesVarious MO models of electronic structure have been proposed to predict the shapes and other properties of non-transition element... [Pg.117]

Cluster Compounds Inorganometalhc Compounds Containing Transition Metal Main Group Elements Electronic Stmcture of Main-group Compounds Molecular Orbital Theory Phosphorus Inorganic Chemistry. [Pg.3759]

B. Wang and G. P. Ford, J. Chem. Phys., 97, 4162 (1992). Molecular-Orbital Theory of a Solute in a Continuum with an Arbitrarily Shaped Boundary Represented by Finite Surface Elements. [Pg.70]

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