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Atomic interactions shared

Atoms in a molecule are joined by bonds. Bonds are formed when the valence or outermost electrons of two or more atoms interact. The nature of the bond between atoms goes a long way toward determining the properties of the molecule. Chapter 5 introduced the two common types of chemical bonds covalent and ionic. Elements with similar electronegativities share electrons and form covalent bonds. But elements with greatly different electronegativities exchange one or more electrons. This is called an ionic bond. [Pg.81]

As metal atoms interact with nearest neighbors at relatively short distance, orbital overlap results in electron density being shared. As mentioned earlier, that electron density is delocalized in orbitals that are essentially molecular orbitals encompassing all of the atoms. The number of atoms that contribute an orbital to the molecular orbital scheme approaches the number of atoms present. As two atoms... [Pg.356]

Hydrogen bonds are strongest when the bonded molecules are oriented to maximize electrostatic interaction, which occurs when the hydrogen atom and the two atoms that share it are in a straight line—that is, when the acceptor atom is in line with the covalent bond between the donor atom and H (Fig. 2-5). Hydrogen bonds are thus highly directional and capable of hold-... [Pg.50]

Metal ions having coordination number two occur in Hg(CN)2, [Ag(CN)2]- and [Au(CN)2]-, all derivatives of d ° species in each case the structure is linear. In K[Cu(CN)2] the copper atom is actually three-coordinated, the anion being an infinite chain each copper has a carbon atom of an unshared cyanide, and a carbon atom and a nitrogen atom of shared cyanides, as nearest neighbours in approximately planar coordination. Three-coordination also occurs in the [Hg(CN)3]- ion, but there are weak interactions between two of the nitrogen atoms and mercury atoms of other anions, giving rise to a loosely bonded chain structure. [Pg.10]

A chemical bond forms when atoms gain, lose, or share electrons. How electrons from two or more atoms interact determines the type of chemical bond formed. The interaction of electrons depends on the location and number of electrons in the atom. [Pg.15]

This diagram showing how the valence electrons interact is called a Lewis structure. In this case both hydrogen atoms have satisfied their need to have a full outermost principal energy level. Because both hydrogen atoms have the same electronegativity, the atoms will share the electrons equally. This will be the case with any diatomic molecule, such as chlorine gas (see Figure 5.6). [Pg.86]

The question then arises how can the two outer-shell electrons of beryllium interact with the hydrogen electrons Two electrons in the same orbital have opposite spins, and constitute a stable pair that has no tendency to interact with unpaired electrons on other atoms. Electron sharing, as we have seen so far, can only take place when UNpaired electrons on adjacent atoms interact. [Pg.37]

The sum in this equation runs over the surfaces shared with atoms bonded to n, the atoms linked to 2 by atomic interaction lines. This expression for the force acting on an atom provides the physical basis for the model in which a molecule is viewed as a set of interacting atoms. It isolates, through the definition of structure, the set of atomic interactions which determines the force acting on each atom in a molecule for any configuration of the nuclei. [Pg.175]

Fig. 7,16. Relief maps of the negative of the Laplacian distribution of p to contrast the distinguishing features of the shared and closed-shell limits of atomic interactions as represented by Nj and Arj, respectively. The map for Fj is intermediate between the two limits. While V pfr.,) is positive for F2 as found for Ar2, its value of p(r J Is three times larger than that forArj. Electronic charge is accumulated in the binding region of F2, as is typical of a shared interaction, but is concentrated in the atomic basins, as is typical of a closed-shell interaction. While V pfrJ > 0 for both Ar2 and Fj, the Laplacian distribution is a minimurn at r, for Arj, but a maximum at the same point in Fj. The charge densities are calculated using a 6-31IG (2d, 2p)... Fig. 7,16. Relief maps of the negative of the Laplacian distribution of p to contrast the distinguishing features of the shared and closed-shell limits of atomic interactions as represented by Nj and Arj, respectively. The map for Fj is intermediate between the two limits. While V pfr.,) is positive for F2 as found for Ar2, its value of p(r J Is three times larger than that forArj. Electronic charge is accumulated in the binding region of F2, as is typical of a shared interaction, but is concentrated in the atomic basins, as is typical of a closed-shell interaction. While V pfrJ > 0 for both Ar2 and Fj, the Laplacian distribution is a minimurn at r, for Arj, but a maximum at the same point in Fj. The charge densities are calculated using a 6-31IG (2d, 2p)...
Fig. 7.19. Contour maps of the Laplacian of p for second- and third-row diatomic hydrides. The intersection of the interatomic surface with the plane of the diagram is also shown. These maps illustrate the transition from closed-shell to shared atomic interactions. Fig. 7.19. Contour maps of the Laplacian of p for second- and third-row diatomic hydrides. The intersection of the interatomic surface with the plane of the diagram is also shown. These maps illustrate the transition from closed-shell to shared atomic interactions.
The requirements of binding, as viewed through the electrostatic theorem, emphasize the existence of an atomic interaction line as a necessary condition for a state to be bound, whether it be at the shared or closed-shell limit of interaction. The differing properties associated with the distributions of electronic charge at the shared and closed-shell limits of interaction are reflected in the differing mechanisms by which the forces on the nuclei are balanced to achieve electrostatic equilibrium in the two cases. [Pg.322]

As we explore the interaction of cold-atom systems with microwave and terahertz radiation, we find that they have some unique properties as detectors. A comparison with superconductor-based detectors such as SQUlDs is instractive. Because of the third law of thermodynamics, i.e., a system in a single quantum state has zero entropy, the response of a SQUID is almost free of thermal noise. But an additional properly of SQUIDs is that they exhibit the phenomenon of coherence, i.e., wave interference, which leads to entirely new effects, e.g. the AC and DC Josephson effects. Cold atom clouds share this behavior, as we will discuss below. [Pg.162]

Hydrogen bonds are noncovalent interactions in which a hydrogen atom is shared between two other atoms, as in... [Pg.56]


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