Cyclopropyl group

A cyclopropyl group is a chemical structure derived from cyclopropane; it is typically produced in a cyclopropanation reaction. The group has an empirical formula of C₃H₅ and chemical bonds from each of the three carbons to both of the other two.

Due to the unfavoured bond angles (60°), cyclopropyl groups are highly strained. Two orbital models were proposed to describe the bonding situation. The Coulson-Moffit model uses bent bonds. The C-C bonds are formed by overlap of two sp-hybrid orbitals. To adapt to the small bond angle, there is some rehybridization resulting in sp^~5-hybrids for the ring bonds and sp^~2 for the C-H bonds. This model resembles the banana bond model for C=C double bonds (τ bonds).

Alternatively the structure can be explained with the Walsh model. Here the two sp-hybrids forming the ring bond are separated into one sp²-hybrid and one pure p-orbital. This corresponds to the π bond description of C=C double bonds.

Cyclopropyl groups are good donors in hyperconjugation resulting in a considerable stabilization of carbocations. In contrast to double bonds, stabilization of radicals is weaker and stabilization of carbanions is negligible. This is explained by the occupation of the π system with two more electrons, making the cyclopropyl methyl cation's HOMO isolobal to the allyl anion's HOMO.^[1]

• Functional groups
• Cyclopropyl compounds

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