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Chemistry covalent bond

In the first monolayer of conjugated model material, a model molecular solid or a polymer adsorbate, assume that no chemistry (covalent bonding) occurs, since, in the absence of, for example, mechanical rupturing, the bonds at the surface of the molecular film are completely satisfied. This assumption is supported by the fact that, at least for condensed molecular solids, vapor-deposited films may be re-evaporated (removed) from the surface by gentle heating in UHV. [Pg.143]

In chemistry, covalent bonds in which two electrons are shared are represented by a single straight line, denoting a single covalent bond. Figure 22-2 shows four different ways to represent a methane molecule. [Pg.699]

In terms of attachment chemistry, covalent bond formation between the protein and the glass slide or affinity interactions are exploited... [Pg.2881]

The most important interatomic bond in polymers, and indeed in organic chemistry, is the covalent bond. This is formed by the sharing of one or more pairs of electrons between two atoms. An example is the bonding of carbon and hydrogen to form methane Figure 5.2). [Pg.77]

The concepts of directed valence and orbital hybridization were developed by Linus Pauling soon after the description of the hydrogen molecule by the valence bond theory. These concepts were applied to an issue of specific concern to organic chemistry, the tetrahedral orientation of the bonds to tetracoordinate carbon. Pauling reasoned that because covalent bonds require mutual overlap of orbitals, stronger bonds would result from better overlap. Orbitals that possess directional properties, such as p orbitals, should therefore be more effective than spherically symmetric 5 orbitals. [Pg.4]

The polarity of covalent bonds between carbon and substituents is the basis of important structure-reactivity relationships in organic chemistry. The effects of polar bonds are generally considered to be transmitted in two ways. Successive polarization through bonds is called the inductive fect. It is expected that such an effect would diminish as the number of intervening bonds increases. [Pg.18]

As is true for macroscopic adhesion and mechanical testing experiments, nanoscale measurements do not a priori sense the intrinsic properties of surfaces or adhesive junctions. Instead, the measurements reflect a combination of interfacial chemistry (surface energy, covalent bonding), mechanics (elastic modulus, Poisson s ratio), and contact geometry (probe shape, radius). Furthermore, the probe/sample interaction may not only consist of elastic deformations, but may also include energy dissipation at the surface and/or in the bulk of the sample (or even within the measurement apparatus). Study of rate-dependent adhesion and mechanical properties is possible with both nanoindentation and... [Pg.193]

Electronic characteristics and their effects on the ability of side chains to engage in ionic bonding, covalent bonding, hydrogen bonding, van der Waals forces, and acid-base chemistry... [Pg.1110]

Chemical compounds that contain methylol groups (-CH2 OH) form stable, covalent bonds with cellulose fibers. Those compounds are well known and widely used in textile chemistry. Hydrogen bonds with cellulose can be formed in this reaction as well. The treatment of cellulose with methylolmelamine compounds before forming cellulose unsaturated polyesters (UP) composites decreases the moisture pickup and increases the wet strength of reinforced plastic [48,49]. [Pg.797]

Organic chemistry, then, is the study of carbon compounds. But why is carbon special Why, of the more than 30 million presently known chemical compounds, do more than 99% of them contain carbon The answers to these questions come from carbon s electronic structure and its consequent position in the periodic table (Figure 1.1). As a group 4A element, carbon can share four valence electrons and form four strong covalent bonds. Furthermore, carbon atoms can bond to one another, forming long chains and rings. Carbon, alone of all elements, is able to form an immense diversity of compounds, from the... [Pg.3]

We saw in the last chapter how covalent bonds between atoms are described, and we looked at the valence bond model, which uses hybrid orbitals to account for the observed shapes of organic molecules. Before going on to a systematic study of organic chemistry, however, we still need to review a few fundamental topics. In particular, we need to look more closely at how electrons are distributed in covalent bonds and at some of the consequences that arise when the electrons in a bond are not shared equally between atoms. [Pg.35]

The ions dealt with to this point (e.g., Na+, Cl-) are monatomic that is, they are derived from a single atom by the loss or gain of electrons. Many of the most important ions in chemistry are polyatomic, containing more than one atom. Examples include the hydroxide ion (OH-) and the ammonium ion (NH ). In these and other polyatomic ions, the atoms are held together by covalent bonds, for example,... [Pg.36]

In 1923. Lewis published a classic book (later reprinted by Dover Publications) titled Valence and the Structure of Atoms and Molecules. Here, in Lewis s characteristically lucid style, we find many of the basic principles of covalent bonding discussed in this chapter. Included are electron-dot structures, the octet rule, and the concept of electronegativity. Here too is the Lewis definition of acids and bases (Chapter 15). That same year, Lewis published with Merle Randall a text called Thermodynamics and the Free Energy of Chemical Substances. Today, a revised edition of that text is still used in graduate courses in chemistry. [Pg.174]

In the 1930s a theoretical treatment of the covalent bond was developed by, among others, Linus Pauling (1901-1994), then at the California Institute of Technology. The atomic orbital or valence bond model won him the Nobel Prize in chemistry in 1954. Eight years later, Pauling won the Nobel Peace Prize for his efforts to stop nuclear testing. [Pg.185]

In principle, any molecule or anion with an unshared pair of electrons can act as a Lewis base. In other words, it can donate a lone pair to a metal cation to form a coordinate covalent bond. In practice, a ligand usually contains an atom of one of die more electronegative elements (C, N, O, S, F, Cl, Br, I). Several hundred different ligands are known. Those most commonly encountered in general chemistry are NH3 and HzO molecules and CN , Cl-, and OH- ions. [Pg.411]

The transition metals, unlike those in Groups 1 and 2, typically show several different oxidation numbers in their compounds. This tends to make their redox chemistry more complex (and more colorful). Only in the lower oxidation states (+1, +2, +3) are the transition metals present as cations (e.g., Ag+, Zn2+, Fe3+). In higher oxidation states (+4 to +7) a transition metal is covalently bonded to a nonmetal atom, most often oxygen. [Pg.544]


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