The ionic bond results from the attraction of oppositely charged ions. The atoms of metallic elements, e.g., those of sodium, lose their outer electrons easily, while the atoms of nonmetals, e.g., those of chlorine, tend to gain electrons. The highly stable ions that result retain their individual structures as they approach one another to form a stable molecule or crystal. In an ionic crystal like sodium chloride, no discrete diatomic molecules exist; rather, the crystal is composed of independent Na+ and Cl- ions, each of which is attracted to neighboring ions of the opposite charge. Thus the entire crystal is a single giant molecule.
A single covalent bond is created when two atoms share a pair of electrons. There is no net charge on either atom; the attractive force is produced by interaction of the electron pair with the nuclei of both atoms. If the atoms share more than two electrons, double and triple bonds are formed, because each shared pair produces its own bond. By sharing their electrons, both atoms are able to achieve a highly stable electron configuration corresponding to that of an inert gas. For example, in methane (CH4), carbon shares an electron pair with each hydrogen atom; the total number of electrons shared by carbon is eight, which corresponds to the number of electrons in the outer shell of neon; each hydrogen shares two electrons, which corresponds to the electron configuration of helium.
In most covalent bonds, each atom contributes one electron to the shared pair. In certain cases, however, both electrons come from the same atom. As a result, the bond has a partly ionic character and is called a coordinate link. Actually, the only purely covalent bond is that between two identical atoms.
Covalent bonds are of particular importance in organic chemistry because of the ability of the carbon atom to form four covalent bonds. These bonds are oriented in definite directions in space, giving rise to the complex geometry of organic molecules. If all four bonds are single, as in methane, the shape of the molecule is that of a tetrahedron. The importance of shared electron pairs was first realized by the American chemist G. N. Lewis (1916), who pointed out that very few stable molecules exist in which the total number of electrons is odd. His octet rule allows chemists to predict the most probable bond structure and charge distribution for molecules and ions. With the advent of quantum mechanics, it was realized that the electrons in a shared pair must have opposite spin, as required by the Pauli exclusion principle. The molecular orbital theory was developed to predict the exact distribution of the electron density in various molecular structures. The American chemist Linus Pauling introduced the concept of resonance to explain how stability is achieved when more than one reasonable molecular structure is possible: the actual molecule is a coherent mixture of the two structures.
Unlike the ionic and covalent bonds, which are found in a great variety of molecules, the metallic and hydrogen bonds are highly specialized. The metallic bond is responsible for the crystalline structure of pure metals. This bond cannot be ionic because all the atoms are identical, nor can it be covalent, in the ordinary sense, because there are too few valence electrons to be shared in pairs among neighboring atoms. Instead, the valence electrons are shared collectively by all the atoms in the crystal. The electrons behave like a free gas moving within the lattice of fixed, positive ionic cores. The extreme mobility of the electrons in a metal explains its high thermal and electrical conductivity.
Hydrogen bonding is a strong electrostatic attraction between two independent polar molecules, i.e., molecules in which the charges are unevenly distributed, usually containing nitrogen, oxygen, or fluorine. These elements have strong electron-attracting power, and the hydrogen atom serves as a bridge between them. The hydrogen bond, which plays an important role in molecular biology, is much weaker than the ionic or covalent bonds. It is responsible for the structure of ice.
See L. Pauling, The Nature of the Chemical Bond (3d ed. 1960); A. L. Companion, Chemical Bonding (2d ed. 1979).
See L. A. Jones, Bonds and Bond Securities (4th ed., 4 vol., 1935-50); T. R. Atkinson, Trends in Corporate Bond Quality (1967); A. Rabinowitz, Municipal Bond Finance and Administration (1969); H. D. Sherman and R. E. Schrager, Junk Bonds and Tender Offer Financing (1987); D. R. Nichols, The Personal Investor's Complete Book of Bonds (1988).
See his In Love and War (with his wife, Sybil Stockdale, 1984, 2d ed. 1990).
See E. S. Holden, Memorials of William Cranch Bond and of His Son George Phillips Bond (1897).
See biographies by J. Neary (1971) and R. M. Williams (1971).
See E. S. Holden, Memorials of William Cranch Bond and of His Son George Phillips Bond (1897).
See her autobiography, The Roads of Melody (1927).
Bond issued by a municipality, state, or public agency authorized to build, acquire, or improve a revenue-producing property such as a waterworks, electric generating plant, or railroad. Unlike general-obligation bonds, which are repaid through a variety of tax sources, revenue bonds are payable from specified revenues only, usually the revenues from the facility for which the bond was originally issued. Revenue bonds typically pay interest rates higher than those of general-obligation bonds. The separation of the revenue bond obligation from a municipality's other bond obligations allows the municipality to circumvent legislated debt limits.
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Electrostatic attraction between oppositely charged ions in a chemical compound. Such a bond forms when one or more electrons are transferred from one neutral atom (typically a metal, which becomes a cation) to another (typically a nonmetallic element or group, which becomes an anion). The two types of ion are held together by electrostatic forces in a solid that does not comprise neutral molecules as such; rather, each ion has neighbours of the opposite charge in an ordered overall crystalline structure. When, for example, crystals of common salt (sodium chloride, NaCl) are dissolved in water, they dissociate (see dissociation) into two kinds of ions in equal numbers, sodium cations (Na+) and chloride anions (Cl−). Seealso bonding; covalent bond.
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Force holding atoms in a molecule together as a specific, separate entity (as opposed to, e.g., colloidal aggregates; see bonding). In covalent bonds, two atoms share one or more pairs of valence electrons to give each atom the stability found in a noble gas. In single bonds (e.g., HsinglehorzbondH in molecular hydrogen), one electron pair is shared; in double bonds (e.g., OdoublehorzbondO in molecular oxygen or H2CdoublehorzbondCH2 in ethylene), two; in triple bonds (e.g., HCtriplehorzbondCH in acetylene), three. In coordinate covalent bonds, additional electron pairs are shared with another atom, usually forming a functional group, such as sulfate (SO4) or phosphate (PO4). The number of bonds and the atoms participating in each (including any additional paired electrons) give molecules their configuration; the slight negative and positive charges at the opposite ends of a covalent bond are the reason most molecules have some polarity (see electrophile; nucleophile). Carbon in organic compounds can have as many as four single bonds, each pointing to one vertex of a tetrahedron; as a result, certain molecules exist in mirror-image forms (see optical activity). Double bonds are rigid, leading to the possibility of geometric isomers (see isomerism). Some types of bonds, such as the amide linkages that join the amino acids in peptides and proteins (peptide bonds), are apparently single but have some double-bond characteristics because of the electronic structure of the participating atoms. The configurations of enzymes and their substrates, determined by their covalent bonds (particularly the peptide bonds) and hydrogen bonds, are crucial to the reactions they participate in, which are fundamental to all life. Seealso aromatic compound; compare ionic bond.
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Any of the interactions that account for the association of atoms into molecules, ions, crystals, metals, and other stable species. When atoms' nuclei and electrons interact, they tend to distribute themselves so that the total energy is lowest; if the energy of a group arrangement is lower than the sum of the components' energies, they bond. The physics and mathematics of bonding were developed as part of quantum mechanics. The number of bonds an atom can form—its valence—equals the number of electrons it contributes or receives. Covalent bonds form molecules; atoms bond to specific other atoms by sharing an electron pair between them. If the sharing is even, the molecule is not polar; if it is uneven, the molecule is an electric dipole. Ionic bonds are the extreme of uneven sharing; certain atoms give up electrons, becoming cations. Other atoms take up the electrons and become anions. All the ions are held together in a crystal by electrostatic forces. In crystalline metals, a diffuse electron sharing bonds the atoms (metallic bonding). Other types include hydrogen bonding; bonds in aromatic compounds; coordinate covalent bonds; multicentre bonds, exemplified by boranes (boron hydrides), in which more than two atoms share electron pairs; and the bonds in coordination complexes (see transition element), still poorly understood. Seealso van der Waals forces.
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In finance, loan contract issued by local, state, and national governments and by private corporations, specifying an obligation to return borrowed funds. The issuer promises to pay interest on the debt when due (usually semiannually) at a stipulated percentage of the face value and to redeem the face value of the bond at maturity in legal tender. Bonds usually indicate a debt of substantial size and are issued in more formal fashion than promissory notes, ordinarily under seal. Government bonds may be backed by taxes, or they may be revenue bonds, backed only by revenue from the specific project (toll roads, airports, etc.) to which they are committed. Bonds are rated based on the issuer's creditworthiness. The ratings, assigned by independent rating agencies, generally run from AAA to D; bonds with ratings from AAA to BBB are regarded as suitable for investment. Seealso junk bond.
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Temporary release of a prisoner in exchange for security given to guarantee the prisoner's appearance at a later hearing. It also refers to the actual security given (e.g., cash). Its main use today is to secure the freedom, pending trial, of someone arrested and charged with a criminal offense. Its use in civil (noncriminal) cases is far less common, as most do not involve imprisonment. The amount of bail is generally set in relation to the gravity of the offense, though other factors, such as the strength of the evidence, the character of the accused, and the accused's ability to secure bail may also be considered. Seealso bond, recognizance.
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(born Jan. 14, 1940, Nashville, Tenn., U.S.) U.S. politician and civil-rights leader. The son of prominent educators, Bond graduated from Morehouse College. In 1960 he helped create the Student Nonviolent Coordinating Committee (SNCC). In 1965 he was elected to the Georgia legislature, but his support of a SNCC statement accusing the U.S. of violating international law in the Vietnam War caused the legislature to deny him his seat. He was twice reelected and was twice more refused entry. The U.S. Supreme Court ruled his exclusion unconstitutional in December 1966, and he assumed his seat in January 1967. He later served in the state senate (1975–87). In 1998 he became chairman of the NAACP.
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