In organic chemistry, a pericyclic reaction is a type of organic reaction wherein the transition state of the molecule has a cyclic geometry, the reaction progresses in a concerted fashion, and the bond orbitals involved in the reaction overlap in a continuous cycle at the transition state. Pericyclic reactions stand in contrast to linear reactions, encompassing most organic transformations and proceeding through an acyclic transition state, on the one hand and coarctate reactions, which proceed through a doubly cyclic, concerted transition state on the other hand. Pericyclic reactions are usually rearrangement or addition reactions. The major classes of pericyclic reactions are given in the table below (the three most important classes are shown in bold). Ene reactions and cheletropic reactions are often classed as group transfer reactions and cycloadditions/reversions, respectively, while dyotropic reactions and group transfer reactions (if ene reactions are excluded) are rarely encountered.
|Electrocyclic reaction||+ 1||− 1|
|Cycloaddition (and cycloreversion)||+ 2||− 2|
|Group transfer reaction||0||0|
|Ene reaction||+ 1||− 1|
|Cheletropic reaction||+ 2||− 2|
In general, these are considered to be equilibrium processes, although it is possible to push the reaction in one direction by designing a reaction by which the product is at a significantly lower energy level; this is due to a unimolecular interpretation of Le Chatelier's principle. There is thus a set of "retro" pericyclic reactions.
By definition, pericyclic reactions proceed through a concerted mechanism involving a single, cyclic transition state. Because of this, prior to a systematic understanding of pericyclic processes through the principle of orbital symmetry conservation, they were facetiously referred to as 'no-mechanism reactions'. However, reactions for which pericyclic mechanisms can be drawn often have related stepwise mechanisms proceeding through radical or dipolar intermediates that are also viable. Some classes of pericyclic reactions, such as the [2+2] ketene cycloaddition reactions, can be 'controversial' because their mechanism is sometimes not definitively known to be concerted (or may depend on the reactive system). Moreover, pericyclic reactions also often have metal-catalyzed analogs, although usually these are also not technically pericyclic, since they proceed via metal-stabilized intermediates, and therefore are not concerted.
Despite these caveats, the theoretical understanding of pericyclic reactions is probably among the most sophisticated and well-developed in all of organic chemistry. The understanding of how orbitals interact in the course of a pericyclic process has led to the Woodward-Hoffmann rules, a simple set of criteria to predict whether a pericyclic mechanism for a reaction is likely or favorable. For instance, these rules predict that the [4+2] cycloaddition of butadiene and ethylene under thermal conditions is likely a pericyclic process, while the [2+2] cycloaddition of two ethylene molecules is not. These are consistent with experimental data, supporting an ordered, concerted transition state for the former and a multistep radical process for the latter. Several equivalent approaches, outlined below, lead to the same predictions.
The aromatic transition state theory assumes that the minimum energy transition state for a pericyclic process is aromatic. For reactions involving (4n + 2)-electron systems (2, 6, 10, ... electrons), Hückel topology transition states are proposed, in which the reactive portion of molecule has orbitals interacting in a continuous cycle without a node. In 4n-electron systems (4, 8, 12, ... electrons) Möbius topology transition states are proposed, in which the reactive portion of the molecule has orbitals interacting in a twisted continuous cycle containing one node. The corresponding (4n + 2)-electron Möbius and 4n-electron Hückel transition states are antiaromatic and are thus strongly disfavored.
Equivalently, pericyclic reactions have been analyzed with correlation diagrams, which track the evolution of the molecular orbitals (known as 'correlating' the molecular orbitals) of the reacting molecules as they progress from reactants to products via a transition state, based on their symmetry properties. Reactions are favorable ('allowed') if the ground state of the reactants correlate with the ground state of the products, while they are unfavorable ('forbidden') if the ground state of the reactants correlate with an excited state of the products. This idea is known as the conservation of orbital symmetry. Consideration of the interactions of the highest occupied and lowest unoccupied molecular orbitals (frontier orbital analysis) is another approach to analyzing the transition state of a pericyclic reaction.
Closely related to pericyclic processes are reactions that are pseudopericyclic. Although a pseudopericyclic reaction proceeds through a cyclic transition state, two of the orbitals involved are constrained to be orthogonal and cannot interact. Perhaps the most famous example is the hydroboration of an olefin. Although this appears to be a 4-electron Hückel topology forbidden group transfer process, the empty p orbital and sp2 hybridized B–H bond are orthogonal and do not interact. Hence, the Woodward-Hoffmann rules do not apply. (The fact that hydroboration is believed to proceed through initial π complexation may also be relevant.)
Pericyclic reactions also occur in several biological processes:
- Claisen rearrangement of chorismate to prephenate in almost all prototrophic organisms
- [1,5]-sigmatropic shift in the transformation of precorrin-8x to hydrogenobyrinic acid
- non-enzymatic, photochemical electrocyclic ring opening and a (1,7) sigmatropic hydride shift in vitamin D synthesis
- Isochorismate pyruvate lyase catalyzed conversion of isochorismate into salicylate and pyruvate