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Quadruple bond

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Title: Quadruple bond  
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Subject: Chemical bond, Potassium octachlorodimolybdate, F. Albert Cotton, Dipolar bond, Stacking (chemistry)
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Quadruple bond

A quadruple bond is a type of chemical bond between two atoms involving eight electrons. This bond is an extension of the more familiar types double bonds and triple bonds.[1] Stable quadruple bonds are most common among the transition metals in the middle of the d-block, such as rhenium, tungsten, molybdenum and chromium. Typically the ligands that support quadruple bonds are π-donors, not π-acceptors.

The structure of chromium(II) acetate


Chromium(II) acetate, Cr2(μ-O2CMe)4(H2O)2, was the first chemical compound containing a quadruple bond to be synthesized. It was described in 1844 by E. Peligot, although its distinctive bonding was not recognized for more than a century.[2] The first crystallographic study of a compound with a quadruple bond was provided for salts of Re2Cl82-. The very short Re-Re distance was noted. This short distance (and the salt's diamagnetism) indicated Re-Re bonding. These researchers however misformulated the anion as a derivative of Re(II), i.e., Re2Cl84-. Soon thereafter F. A. Cotton and coworkers reported the crystal structure of potassium octachlorodirhenate or K2[Re2Cl8]·2H2O. This structural analysis indicated that the previous characterization was mistaken. Cotton and coworkers proceeded to formulate a molecular orbital rationale for the bonding that explicitly indicated a quadruple bond.[2] The rhenium–rhenium bond length in this compound is only 224 pm. In the terminology of molecular orbital theory, the bonding is described as σ2π4δ2 with one sigma bond, two pi bonds and one delta bond.

Structure and bonding

The octachlorodirhenate(III) anion, [Re2Cl8]2−, which features a quadruple Re-Re bond
Formation of a delta bond by the overlap of two d orbitals

The [Re2Cl8]2- ion adopts an eclipsed conformation as shown at left. The delta bonding orbital is then formed by overlap of the d orbitals on each rhenium which are perpendicular to the Re-Re axis and lie in between the Re-Cl bonds. The d orbitals directed along the Re-Cl bonds are stabilized by interaction with chlorine ligand orbitals and do not contribute to Re-Re bonding.[3] In contrast, the [Os2Cl8]2- ion with two more electrons (σ2π4δ2δ*2) has an Os-Os triple bond and a staggered geometry.[4]

Many other compounds with quadruple bonds between transition metal atoms have been described, often by Cotton and his coworkers. Isoelectronic with the dirhenium compound is the salt K4[Mo2Cl8] (potassium octachlorodimolybdate).[5] An example of a ditungsten compound with a quadruple bond is di-tungsten tetra(hpp).

Quadruple bonds between atoms of main group elements are unknown. Simple valence bond theory would predict a quadruple bond as the only way to satisfy the octet rule for carbon in dicarbon. However, molecular orbital theory shows that there are two sets of paired electrons in the sigma system (one bonding, one antibonding), and two sets of paired electrons in a degenerate pi bonding set of orbitals. This adds up to give a bond order of 2, meaning that there exists a double bond between the two carbons in a C2 molecule. The MO diagram of diatomic carbon would show that there are two pi bonds and no sigma bonds.


  1. ^ To Boldly Pass the Metal-Metal Quadruple Bond Radius, U.; Breher, F. Angewandte Chemie International Edition 2006, Volume 45, Issue 19 , Pages 3006 - 3010 Abstract
  2. ^ a b Cotton, F. A.; Walton, R. A. Multiple Bonds Between Metal Atoms Oxford (Oxford): 1993. ISBN 0-19-855649-7.
  3. ^ Miessler, G. L. and Tarr, D. A. Inorganic Chemistry (2nd ed., Prentice-Hall 1999), p.531
  4. ^ Miessler and Tarr p.532
  5. ^ Girolami, G. S.; Rauchfuss, T. B. and Angelici, R. J., Synthesis and Technique in Inorganic Chemistry, University Science Books: Mill Valley, CA, 1999.

Further reading

  • Cotton, F. A.; Harris, C. B. "The Crystal and Molecular Structure of Dipotassium Octachlorodirhenate(III) Dihydrate, K2[Re2Cl8]2H2O" Inorg. Chem. 1965, 4(3), 330–333. doi:10.1021/ic50025a015.

See also

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