Summary
Cryptophanes are a class of organic supramolecular compounds studied and synthesized primarily for molecular encapsulation and recognition. One possible noteworthy application of cryptophanes is encapsulation and storage of hydrogen gas for potential use in fuel cell automobiles. Cryptophanes can also serve as containers in which organic chemists can carry out reactions that would otherwise be difficult to run under normal conditions. Due to their unique molecular recognition properties, cryptophanes also hold great promise as a potentially new way to study the binding of organic molecules with substrates, particularly as pertaining to biological and biochemical applications.[1]
Discovery edit
Cryptophanes were discovered by André Collet and Jacqueline Gabard in 1981[2] when these researchers created, using template-directed synthesis, the first cryptophane, now known as cryptophane-A.
Structure edit
Cryptophane cages are formed by two cup-shaped [1.1.1]–orthocyclophane units (see cyclotriveratrylene),[3] connected by three bridges (denoted Y). There are also choices of the peripheral substitutes R1 and R2 attached to the aromatic rings of the units. Most cryptophanes exhibit two diastereomeric forms (syn and anti), distinguished by their symmetry type. This general scheme offers a variety of choices (Y, R1, R2, and symmetry type) by which the shape, volume and chemical properties of the generally hydrophobic pocket inside the cage can be modified, making cryptophanes suitable for encapsulating many types of small molecules and even chemical reactions.
General classification edit
Depending on their structure, cryptophane cages are classified according to the following table.[3]
| Structure | Name | ||||
|---|---|---|---|---|---|
| Bridges Y | R1 | R2 | anti | syn | described in |
| 3 × O(CX2)2O, where X is H or D | OCX3 | OCX3 | A | Brotin et al.[4] | |
| 3 × O(CX2)2O | OCH2CO2H | OCH2CO2H | A3 | ||
| 3 × O(CX2)2O | OCH3 | H | C | D | |
| 3 × O(CH2)3O | OCH3 | OCH3 | E | F | |
| 3 × O(CH2)3O | OCH2CO2H | OCH2CO2H | E3 | ||
| 3 × O(CH2)5O | OCH3 | OCH3 | O | P | |
| 3 × O(CH2)5O | OCH2CO2H | OCH2CO2H | O3 | ||
| 3 × OCH2C≡CC≡CH2O | CH3 | CH3 | γ (gamma) | δ (delta) | |
| 2 × O(CH2)2O, 1 × O(CH2)3O | OCH3 | OCH3 | 223 | ||
| 2 × O(CH2)3O, 1 × O(CH2)2O | OCH3 | OCH3 | 233 | ||
| 2 × O(CH2)2O, 1 × O(CH2)4O | OCH3 | OCH3 | 224 | ||
Symmetry edit
The anti cryptophane isomer belongs to the D3 point group and the syn cryptophane isomer belongs to the C3h point group.[5] Both molecules therefore do not exhibit a dipole moment.
References edit
- ^ Palaniappan, K. K.; Francis, M. B.; Pines, A.; Wemmer, D. E. Molecular sensing using hyperpolarized xenon NMR spectroscopy. Isr. J. Chem. 2014, 54, 104−112.
- ^ Gabard, J.; Collet, A. (1981). "Synthesis of a (D3)-bis(cyclotriveratrylenyl) macrocage by stereospecific replication of a (C3)-subunit". Journal of the Chemical Society, Chemical Communications (21). Royal Society of Chemistry: 1137–1139. doi:10.1039/C39810001137.
- ^ a b Holman, K. Travis (2004). "Cryptophanes: Molecular Containers". In Atwood, J. L.; Steed, J. W. (eds.). Encyclopedia of Supramolecular Chemistry. CRC Press. pp. 340–348. doi:10.1081/E-ESMC. ISBN 0-8247-4723-2.
- ^ Brotin, Thierry; Devic, Thomas; Lesage, Anne; Emsley, Lyndon; Collet, André (March 2001). "Synthesis of deuterium-labeled cryptophane-A and investigation of Xe@Cryptophane complexation dynamics by 1D-EXSY NMR experiments". Chemistry: A European Journal. 7 (7): 1561–1573. doi:10.1002/1521-3765(20010401)7:7<1561::AID-CHEM1561>3.0.CO;2-9. PMID 11330913.
- ^ Peter Atkins, J. D. P., Atkins' Physical Chemistry. Oxford: 2010.