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According to the sigma bond rule, the number of sigma bonds in a molecule is equivalent to the number of atoms plus the number of rings minus one. N σ = N atoms + N rings − 1. This rule is a special-case application of the Euler characteristic of the graph which represents the molecule. A molecule with no rings can be represented as a tree ...
The carbon–carbon single bond is a sigma bond and is formed between one hybridized orbital from each of the carbon atoms. In ethane, the orbitals are sp 3-hybridized orbitals, but single bonds formed between carbon atoms with other hybridizations do occur (e.g. sp 2 to sp 2). In fact, the carbon atoms in the single bond need not be of the ...
Sigma bonds (σ bonds) are the strongest type of covalent chemical bond. In organic chemistry , σ symbolizes the sigma constant of Hammett equation . In alchemy , Σ was sometimes used to represent sugar .
Hyperconjugation affects several properties. [6] [10]Bond length: Hyperconjugation is suggested as a key factor in shortening of sigma bonds (σ bonds). For example, the single C–C bonds in 1,3-butadiene and propyne are approximately 1.46 Å in length, much less than the value of around 1.54 Å found in saturated hydrocarbons.
The triplet and singlet excitation energies of a sigma bond can be used to determine if a bond will follow the homolytic or heterolytic pathway. [2] A metal−metal sigma bond is an exception because the bond's excitation energy is extremely high, thus cannot be used for observation purposes. [2] In some cases, bond cleavage requires catalysts.
Sigma complexes with agostic interactions represent a particularly common subgroup of sigma complexes. In these, a C-H-σ bond from one of the ligands interacts with the coordinatively unsaturated metal center, forming a chelate complex .
This allows the metal to accept the σ bonds more easily. The combination of ligand-to-metal σ-bonding and metal-to-ligand π-bonding is a synergic effect, as each enhances the other. As each of the six ligands has two orbitals of π-symmetry, there are twelve in total.
The metal ion-catalyzed σ-bond rearrangement is a collection of chemical reactions that occur with highly strained organic compounds are treated with metal ions like Ag +, Rh(I), or Pd(II) based reagents. [1] [2+2] ring openings are sometimes observed: These rearrangements proceed via oxidative addition of strained rings.