Chemistry:Polyene
In organic chemistry, polyenes are poly-unsaturated, organic compounds that contain at least three alternating double (C=C) and single (C–C) carbon–carbon bonds. These carbon–carbon double bonds interact in a process known as conjugation, resulting in some unusual optical properties. Related to polyenes are dienes, where there are only two alternating double and single bonds.
The following polyenes are used as antimycotics for humans: amphotericin B, nystatin, candicidin, pimaricin, methyl partricin, and trichomycin.[1]
Optical properties
Some polyenes are brightly colored, an otherwise rare property for a hydrocarbon. Normally alkenes absorb in the ultraviolet region of a spectrum, but the absorption energy state of polyenes with numerous conjugated double bonds can be lowered such that they enter the visible region of the spectrum, resulting in compounds which are coloured (because they contain a chromophore). Thus many natural dyes contain linear polyenes.
Chemical and electrical properties
Polyenes tend to be more reactive than simpler alkenes. For example, polyene-containing triglycerides are reactive towards atmospheric oxygen. Polyacetylene, which partially oxidized or reduced, exhibits high electrical conductivity. Most conductive polymers are polyenes, and many have conjugated structures. Poly(aza)acetylenes are readily prepared from pyridine precursors without the necessity of a controlled atmosphere, simply by ultraviolet irradiation of a mixture of pyridine and poly(4-vinyl) pyridine. Recent research at the Weizmann Institute and Aix-Marseille University showed a clear transition between ionic and electronic conductivity with increasing UV dose over 30 hours.[2]
Occurrence
A few fatty acids are polyenes. Another class of important polyenes are polyene antimycotics,[3]
- Representative Polyenes
Amphotericin B is an example of a polyene antifungal (antimycotic) agent.[4]
Leukotriene A4 is a regulator of the immune response.
Polyacetylenes are a synthetic polymer of theoretical interest because they exhibit metallic properties upon oxidation.[5]
References
- ↑ Zotchev, Sergey B. (2003). "Polyene macrolide antibiotics and their applications in human therapy". Current Medicinal Chemistry 10 (3): 211–223. doi:10.2174/0929867033368448. PMID 12570708.
- ↑ Vaganova, Evgenia; Eliaz, Dror; Shimanovich, Ulyana; Leitus, Gregory; Aqad, Emad; Lokshin, Vladimir; Khodorkovsky, Vladimir (January 2021). "Light-Induced Reactions within Poly(4-vinyl pyridine)/Pyridine Gels: The 1,6-Polyazaacetylene Oligomers Formation" (in en). Molecules 26 (22): 6925. doi:10.3390/molecules26226925. ISSN 1420-3049. PMID 34834017.
- ↑ NCBI Bookshelf (1996). "Polyene Antifungal Drugs". The University of Texas Medical Branch at Galveston. https://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=mmed&part=A4050.
- ↑ Torrado, J. J.; Espada, R.; Ballesteros, M. P.; Torrado-Santiago, S. "Amphotericin B formulations and drug targeting" Journal of Pharmaceutical Sciences 2008, volume 97, pp. 2405-2425. doi:10.1002/jps.21179
- ↑ Lam, Jacky W. Y.; Tang, Ben Zhong "Functional Polyacetylenes" Accounts of Chemical Research 2005, volume 38, pp. 745-754. doi:10.1021/ar040012f
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