Triple Bond

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Triple Bond

 

a covalent chemical bond produced by three pairs of electrons located in the field of two atomic nuclei. A triple bond consists of one σ-bond and two π-bonds; the resultant distribution of electron density between the two bound nuclei is axially symmetrical, as in the case of a single bond.

In the structural formulas of chemical compounds, triple bonds between atoms are indicated by three bond lines—for example, N≡N, C≡C, and C≡N. If one or both π-components of a triple bond, for example, between atoms A and B, form as a result of a donor-acceptor interaction, such triple bonds (A Triple BondB or A Triple BondB) are usually called quasi-triple bonds. (In the “normal” triple bond, A≡B, the σ-component and the two π-components form as a consequence of the interaction of unpaired electrons.) Examples of quasi-triple bonds are the bond of a terminal oxygen atom with the atom of a transition metal (O Triple BondM, called an ylic bond)—for example, in K2[ReOCl5] and the bond in the BF molecule (B Triple BondF). As a result of the high bond energy of triple bonds and quasi-triple bonds, the corresponding molecules (for example, N2 and CO) or molecular fragments (N≡M or O Triple BondM) are thermodynamically stable and usually chemically inert. Thus, the fixation of molecular nitrogen—that is, the activation of nitrogen for chemical conversions—is impossible without its prior coordination as a Iigand in certain complexes of transition metals, leading to a significant reduction in the multiplicity (strength) of the nitrogen-nitrogen bond.

Whereas triple bonds between light atoms (carbon and nitrogen) were mainly studied in the past, greater attention is now being devoted to triple bonds involving heavy atoms, primarily atoms of the transition metals. Such triple bonds are found in new types of complexes. A large number of complexes of transition metals have already been studied with nitrido- (N≡), oxo-(O Triple Bond), imino- (RN Triple Bond), and carbino- (RC≡) groups as ligands with high chemical bond strength. An important feature of such ligands is their strong frans-effect (that is, the significant reduction in the metal-ligand bond strength upon transposition), which dictates the reactivity and many of the properties of these compounds. Dimeric clusters of transition metals with metal-metal triple bonds, such as Mo2[N(CH3)2]6, are also known. This molecule has a centrosymmetric inverted configuration (as in ethane, C2H6), which results from the axial symmetry of the electron density distribution in the M=M bond, where M is a metal.

REFERENCE

Shustorovich, E. M. Khimicheskaia sviaz’. Moscow, 1973.

E. M. SHUSTOROVICH

References in periodicals archive ?
The carbon-carbon triple bond FTIR band was greatly diminished following a 15 minute hold at 37500, indicating reaction was near completion and/or the remaining concentration of triple bonds was below the instrument's detection limit.
1] were also observed in the polymer spectrum, indicating that a certain amount of C[equivalent]N triple bonds remained unreacted.
This also provides strong evidence that the plasma polymerization of benzonitrile took place mainly via the opening of C[equivalent]N triple bonds under lower discharge powers.
The above results further confirm that the plasma polymerization of benzonitrile took place mainly at the unsaturated C[equivalent]N triple bonds rather than at the aromatic ring.
He was able to verify the triple bond through X-ray crystallography.