The Thorpe–Ingold effect, gem-dimethyl effect, or angle compression is an effect observed in chemistry where increasing steric hindrance favours ring closure and intramolecular reactions. The effect was first reported by Beesley, Thorpe, and Ingold in 1915 as part of a study of cyclization reactions.[1] It has since been generalized to many areas of chemistry.[2]

The comparative rates of lactone formation (lactonization) of various 2-hydroxybenzenepropionic acids illustrate the effect. The placement of an increasing number of methyl groups accelerates the cyclization process.[3]

One application of this effect is addition of a quaternary carbon (e.g., a gem-dimethyl group) in an alkyl chain to increase the reaction rate and/or equilibrium constant of cyclization reactions. An example of this is an olefin metathesis reaction:[4] In the field of peptide foldamers, amino acid residues containing quaternary carbons such as 2-aminoisobutyric acid are used to promote formation of certain types of helices.[5]

One proposed explanation for this effect is that the increased size of the substituents increases the angle between them. As a result, the angle between the other two substituents decreases. By moving them closer together, reactions between them are accelerated. It is thus a kinetic effect.

The effect also has some thermodynamic contribution as the in silico strain energy decreases on going from cyclobutane to 1-methylcyclobutane and 1,1-dimethylcyclobutane by a value between 8 kcal/mole[6] and 1.5 kcal/mole.[7] A noteworthy example of the Thorpe-Ingold effect in supramolecular catalysis is given by diphenylmethane derivatives provided with guanidinium groups.[8] These compounds are active in the cleavage of the RNA model compound HPNP. Substitution of the methylene group of the parent diphenylmethane spacer with cyclohexylidene and adamantylidene moieties enhances catalytic efficiency, with gem dialkyl effect accelerations of 4.5 and 9.1, respectively.

See also

References

  1. ↑ Beesley, Richard Moore; Ingold, Christopher Kelk; Thorpe, Jocelyn Field (1915). "CXIX.–The formation and stability of spiro-compounds. Part I. Spiro-Compounds from cyclohexane". J. Chem. Soc., Trans. 107: 1080–1106. doi:10.1039/CT9150701080.
  2. ↑ Shaw, B. L. (1975). "Formation of Large Rings, Internal Metalation Reactions, and Internal Entropy Effects". Journal of the American Chemical Society. 97 (13): 3856–3857. doi:10.1021/ja00846a072.
  3. ↑ Michael N. Levine, Ronald T. Raines "Trimethyl lock: a trigger for molecular release in chemistry, biology, and pharmacology (perspective)" Chem. Sci., 2012, volume 3, 2412–2420. doi:10.1039/C2SC20536J
  4. ↑ Fürstner, A; Langemann, K. (1996). "A Concise Total Synthesis of Dactylol via Ring Closing Metathesis" (PDF). J. Org. Chem. 61 (25): 8746–8749. doi:10.1021/jo961600c. hdl:11858/00-001M-0000-0024-07AC-2. PMID 11667847.
  5. ↑ Misra, Rajkumar; George, Gijo; Reja, Rahi M.; Dey, Sanjit; Raghothama, Srinivasarao; Gopi, Hosahudya N. (2020). "Structural insight into hybrid peptide ε-helices". Chemical Communications. 56 (14): 2171–2173. doi:10.1039/C9CC07413A. ISSN 1359-7345. PMID 31970340. S2CID 210872237.
  6. ↑ Ringer, Ashley L.; Magers, David H. (1 March 2007). "Conventional Strain Energy in Dimethyl-Substituted Cyclobutane and the gem -Dimethyl Effect". The Journal of Organic Chemistry. 72 (7): 2533–2537. doi:10.1021/jo0624647. PMID 17341119.
  7. ↑ Bachrach, Steven M. (1 March 2008). "The gem -Dimethyl Effect Revisited". The Journal of Organic Chemistry. 73 (6): 2466–2468. doi:10.1021/jo702665r. PMID 18278945.
  8. ↑ Salvio, Riccardo; Mandolini, Luigi; Savelli, Claudia (19 July 2013). "Guanidine–Guanidinium Cooperation in Bifunctional Artificial Phosphodiesterases Based on Diphenylmethane Spacers; gem -Dialkyl Effect on Catalytic Efficiency". The Journal of Organic Chemistry. 78 (14): 7259–7263. doi:10.1021/jo401085z. PMID 23772969.
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