Crown ether

Crown ethers are cyclic chemical compounds that consist of a ring containing several ether groups. The most common crown ethers are cyclic oligomers of ethylene oxide, the repeating unit being ethyleneoxy, i.e., –CH2CH2O–. Important members of this series are the tetramer (n = 4), the pentamer (n = 5), and the hexamer (n = 6). The term "crown" refers to the resemblance between the structure of a crown ether bound to a cation, and a crown sitting on a person's head. The first number in a crown ether's name refers to the number of atoms in the cycle, and the second number refers to the number of those atoms that are oxygen. Crown ethers are much broader than the oligomers of ethylene oxide; an important group are derived from catechol.

Crown ethers strongly bind certain cations, forming complexes. The oxygen atoms are well situated to coordinate with a cation located at the interior of the ring, whereas the exterior of the ring is hydrophobic. The resulting cations often form salts that are soluble in nonpolar solvents, and for this reason crown ethers are useful in phase transfer catalysis. The denticity of the polyether influences the affinity of the crown ether for various cations. For example, 18-crown-6 has high affinity for potassium cation, 15-crown-5 for sodium cation, and 12-crown-4 for lithium cation.[1] The high affinity of 18-crown-6 for potassium ions contributes to its toxicity. Crown ethers are not the only macrocyclic ligands that have affinity for the potassium cation. Ionophores such as valinomycin also display a marked preference for the potassium cation over other cations.

Crown ethers have been shown to coordinate to Lewis acids through electrostatic, σ-hole (see halogen bond) interactions, between the Lewis basic oxygen atoms of the crown ether and the electrophilic Lewis acid center.[2][3]


In 1967, Charles Pedersen, who was a chemist working at DuPont, discovered a simple method of synthesizing a crown ether when he was trying to prepare a complexing agent for divalent cations.[4][5] His strategy entailed linking two catecholate groups through one hydroxyl on each molecule. This linking defines a polydentate ligand that could partially envelop the cation and, by ionization of the phenolic hydroxyls, neutralize the bound dication. He was surprised to isolate a by-product that strongly complexed potassium cations. Citing earlier work on the dissolution of potassium in 16-crown-4,[6][7] he realized that the cyclic polyethers represented a new class of complexing agents that were capable of binding alkali metal cations. He proceeded to report systematic studies of the synthesis and binding properties of crown ethers in a seminal series of papers. The fields of organic synthesis, phase transfer catalysts, and other emerging disciplines benefited from the discovery of crown ethers. Pedersen particularly popularized the dibenzo crown ethers.[8]

Pedersen shared the 1987 Nobel Prize in Chemistry for the discovery of the synthetic routes to, and binding properties of, crown ethers.

Affinity for cations

Apart from its high affinity for potassium cations, 18-crown-6 can also bind to protonated amines and form very stable complexes in both solution and the gas phase. Some amino acids, such as lysine, contain a primary amine on their side chains. Those protonated amino groups can bind to the cavity of 18-crown-6 and form stable complexes in the gas phase. Hydrogen-bonds are formed between the three hydrogen atoms of protonated amines and three oxygen atoms of 18-crown-6. These hydrogen-bonds make the complex a stable adduct. By incorporating luminescent substituents into their backbone, these compounds have proved to be sensitive ion probes, as changes in the absorption or fluorescence of the photoactive groups can be measured for very low concentrations of metal present.[10] Some attractive examples include macrocycles, incorporating oxygen and/or nitrogen donors, that are attached to polyaromatic species such as anthracenes (via the 9 and/or 10 positions)[11] or naphthalenes (via the 2 and 3 positions).[12]


21- and 18-membered diazacrown ether derivatives exhibit excellent calcium and magnesium selectivities and are widely used in ion-selective electrodes.[13] Some or all of the oxygen atoms in crown ethers can be replaced by nitrogens to form cryptands. A well-known tetrazacrown is cyclen in which there are no oxygens.[14]

Lariat crown ethers have sidearms that can augment complexation of cation. The lariat is typically attached to an amine centre in an azacrown.[15]

See also


  1. van der Ham, Alex; Hansen, Thomas; Lodder, Gerrit; Codée, Jeroen D. C.; Hamlin, Trevor A.; Filippov, Dmitri V. (2019). "Computational and NMR Studies on the Complexation of Lithium Ion to 8-Crown-4". ChemPhysChem. 20 (16): 2103–2109. doi:10.1002/cphc.201900496. ISSN 1439-7641. PMC 6772996. PMID 31282054.
  2. Marczenko, K. M.; Mercier, H. P. A.; Schrobilgen, G. J. (2018). "A Stable Crown-Ether Complex with a Noble-gas Compound". Angew. Chem. Int. Ed. 57 (38): 12448–12452. doi:10.1002/anie.201806640. PMID 29953704.
  3. Lipkowski, J.; Fonari, M. S.; Kravtsov, V. C.; Simonov, Y. A.; Ganin, E. V.; Gemboldt, V. O. (1996). "Antimony(III) fluoride: Inclusion complexes with crown ethers". J. Chem. Crystallogr. 26 (12): 823. doi:10.1007/BF01670315.
  4. Pedersen, C. J. (1967). "Cyclic polyethers and their complexes with metal salts". Journal of the American Chemical Society. 89 (26): 7017–7036. doi:10.1021/ja01002a035.
  5. Pedersen, C. J. (1967). "Cyclic polyethers and their complexes with metal salts". Journal of the American Chemical Society. 89 (10): 2495–2496. doi:10.1021/ja00986a052.
  6. GB 785229, Stewart, D. G.; D. Y. Waddan & E. T. Borrows, issued 1957-10-23
  7. Down, J. L.; Lewis, J.; Moore, B.; Wilkinson, G. (1959). "761. The solubility of alkali metals in ethers". Journal of the Chemical Society: 3767. doi:10.1039/jr9590003767.
  8. Pedersen, Charles J. (1988). "Macrocyclic Polyethers: Dibenzo-18-Crown-6 Polyether and Dicyclohexyl-18-Crown-6 Polyether". Organic Syntheses.; Collective Volume, 6, p. 395
  9. Ashton, P. R.; Goodnow, T. T.; Kaifer, A. E.; Reddington, M. V.; Slawin, A. M. Z.; Spencer, N.; Stoddart, J. F.; Vicent, C.; Williams, D. J. (1989). "A [2] Catenane Made to Order". Angewandte Chemie International Edition in English. 28 (10): 1396–1399. doi:10.1002/anie.198913961.CS1 maint: uses authors parameter (link)
  10. Fabbrizzi, L.; Francese, G.; Licchelli, M.; Pallavicini, P.; Perotti, A.; Poggi, A.; Sacchi, D.; Taglietti, A. (1997). Desvergne, J. P.; Czarnik, A. W. (eds.). Chemosensors of Ion and Molecule Recognition. NATO ASI Series C. 492. Dordrecht: Kluwer Academic Publishers. p. 75.
  11. Bouas-Laurent, H.; Desvergne, J. P.; Fages, F.; Marsau, P. (1993). A. W., Czarnik (ed.). Fluorescent Chemosensors for Ion and Molecule Recognition. ACS Symposium Series 538. Washington, DC: American Chemical Society. p. 59.
  12. Sharghi, Hashem; Ebrahimpourmoghaddam, Sakineh (2008). "A Convenient and Efficient Method for the Preparation of Unique Fluorophores of Lariat Naphtho-Aza-Crown Ethers". Helvetica Chimica Acta. 91 (7): 1363–1373. doi:10.1002/hlca.200890148.
  13. Suzuki, K.; Watanabe, K.; Matsumoto, Y.; Kobayashi, M.; Sato, S.; Siswanta, D.; Hisamoto, H. (1995). "Design and Synthesis of Calcium and Magnesium Ionophores Based on Double-Armed Diazacrown Ether Compounds and Their Application to an Ion Sensing Component for an Ion-Selective Electrode". Anal. Chem. 67 (2): 324–334. doi:10.1021/ac00098a016.
  14. Gatto, Vincent J.; Miller, Steven R.; Gokel, George W. (1988). "4,13-Diaza-18-Crown-6". Organic Syntheses.; Collective Volume, 8, p. 152
  15. Gokel, G. W.; Barbour, L. J.; Ferdani, R.; Hu, J. (2002). "Lariat Ether Receptor Systems Show Experimental Evidence for Alkali Metal Cation Interactions". Acc. Chem. Res. 35 (10): 878–886. doi:10.1021/ar000093p.
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