Anions covalent bonds

This can be generalized to bonding in the oxides and sulfides, when each anion neighbor of a cation is considered to contribute two electrons to cr-type cation-anion covalent bond. 

The duoroborate ion has traditionally been referred to as a noncoordinating anion. It has shown Httie tendency to form a coordinate—covalent bond with transition metals as do nitrates and sulfates. A few exceptional cases have been reported (13) in which a coordinated BF was detected by infrared or visible spectroscopy. 

The reaction between a trinuclear metal carbonyl cluster and trimetbyl amine borane has been investigated (41) and here the cluster anion functions as a Lewis base toward the boron atom, forming a B—O covalent bond (see Carbonyls). Molecular orbital calculations, supported by stmctural characterization, show that coordination of the amine borane causes small changes in the trinuclear framework. 

The CC bond distances in cyclopentadienyl anion, C5H5, are all equal, because the anion is aromatic (see Chapter 12, Problem 10). Electrophiles that interact electrostaticaUy with the anion, such as Na", interact equally with all five carbons, and do not disturb the anion s aromatic character. On the other hand, electrophiles that make covalent bonds, such as H", might interact more strongly with one particular carbon and destroy the aromaticity of the ring. 

The pyrylium cation possesses, according to the substituents in positions 2, 4, and 6, a more or less pronounced electrophilic reactivity which enables it to add nucleophiles in these positions. According to the nucleophilic reactivity and the carbon basicity " of the anions, an ion pair (a substituted pyrylium cation and an anion halide, perchlorate, sulfate, fluoroborate, chloroferrate, etc.), or a covalently bonded 2H- or 4//-pyran may be formed. With the more basic anions... 

Complex ions used for electroplating are anions. The cathode tends to repel them, and their transport is entirely by diffusion. Conversely, the field near the cathode assists cation transport. Complex cyanides deserve some elaboration in view of their commercial importance. It is improbable that those used are covalent co-ordination compounds, and the covalent bond breaks too slowly to accommodate the speed of electrode reactions. The electronic structure of the cyanide ion is ... 

Diagrams of four types of substances (see text discussion). X represents a nonmetal atom, — represents a covalent bond, M+ a cation, X- an anion, and e an electron. 

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. 

Whether or not the highly electropositive alkali metals or magnesium form an ionic instead of a covalent bond to the oxygen of the enolate is less important. Even if there is a contact ion pair of the metal cation and the oxygen anion, the geometry of the six-membered chair transition state, as outlined above, will be maintained. 

In certain cases the radical-anion pairs are considered as an example of a covalent bond, close to zero 15 and an isolated pair outside a crystal was depicted17, however Shislov and coworkers16 proposed that more likely the entire potential well for the radical-anion pairs is completely the result of the action of the crystal lattice18. As a proof they used their observation that radical-anion pairs are not formed in irradiated frozen aqueous-sulfoxide glasses. 

The boron atom in BF5 can complete its octet if an additional atom or ion with a lone pair of electrons forms a bond by providing both electrons. A bond in which both electrons come from one of the atoms is called a coordinate covalent bond. For example, the tetrafluoroborate anion, BF4 (31), forms when boron trifluoride is passed over a meral fluoride. In this anion, the formation of a coordinate covalent bond with a fluoride ion gives the B atom an octet. Another example of a coordinate covalent bond is that formed when boron trifluoride reacts with ammonia ... 

Ions stack together in the regular crystalline structure corresponding to lowest energy. The structure adopted depends on the radius ratio of cation and anion. Covalent character in an ionic bond itnposes a directional character on the bonding. 

Hydrogen is unusual because it can form both a cation (1I+) and ail anion (11 ). Moreover, its intermediate electronegativity (2.2 on the Pauling scale) means that it can also form covalent bonds with all the nonmetals and metalloids. Because hydrogen forms compounds with so many elements (Table 14.2 also see Section 14.2), we shall meet more of its compounds when we study the other elements. 

B Aluminum forms an amphoteric oxide in which it has the oxidation state +3 therefore, aluminum is the element. 14.3B Hydrogen is a nonmetal and a diatomic gas at room temperature. It has an intermediate electronegativity (x — 2.2), so it forms covalent bonds with nonmetals and forms anions in combination with metals. In contrast, Group 1 elements are solid metals that have low electronegativities and form cations in combination with nonmetals. 

In addition to the ratio of concentrations olefine/HA, the donor ability, or the nucleophilicity of the anion A- is a deciding factor for the manner in which the reaction continues. This anion is formed simultaneously with the carbenium ion. When the nucleophilicity of the anion is sufficiently high, as in the case of CP, Br-, I-, for instance, the reaction proceeds as an addition by the formation of a covalent bond between A- and the carbenium ion72). 

The concept of silicates as inorganic polymers was implicit in the ideas developed by W. H. Zacheriasen in the early 1930s. He conceived of silicates as consisting of macromolecular structures held together by covalent bonds but including network-dwelling cations. These cations were not assumed to have a structural role but merely to be present in order to balance the charges on the anionic polymer network. 

Fig. 8 Reactions of various carbocations with Kuhn s anion [2 ] as compared with their reduction potentials (peak potentials measured vs. Ag/Ag in acetonitrile by cyclic voltammetry cf. Tables 1 and 8 and Okamoto et al., 1983). SALT, salt formation COV, covalent bond formation ET, single-electron transfer. 

The molecules (or atoms, for noble gases) of a molecular solid are held In place by the types of forces already discussed In this chapter dispersion forces, dipolar interactions, and/or hydrogen bonds. The atoms of a metallic solid are held in place by the delocalized bonding described in Section 10-. A network solid contains an array of covalent bonds linking every atom to its neighbors. An ionic solid contains cations and anions, attracted to one another by electrical forces as described in Section 8-. 

Sulfides play an important role in hydrotreating catalysis. Whereas oxides are ionic structures, in which cations and anions preferably surround each other to minimize the repulsion between ions of the same charge, sulfides have largely covalent bonds as a consequence there is no repulsion which prevents sulfur atoms forming mutual bonds and hence the crystal structures of sulfides differ, in general, greatly from those of oxides. 

Typical profiles for the potential response of Na -ISFETs based on the sol-gel-derived membranes modified chemically by alkoxysilylated 16-crown-5 (7) and bis(12-crown-4) (11), together with anion excluder (9) show that both of the Na -ISFETs have high sensitivity with a Nernstian response to Na activity changes in wide activity ranges of 3 x 10 to 1 M (Fig. 12). The potential response is quite fast in the Na -ISFETs in spite of the covalent bonding of the neutral carriers to the ion-sensing membranes, as exemplified in the membrane system of the bis(12-crown-4) (11). Some mobility of the chemically bonded neutral carriers can probably be maintained in the present sol-gel-derived membranes. The response time ( 9o) is several seconds for both of the Na -... 

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