Inorganic chemistry,polyenesare poly-unsaturated,organic compoundsthat contain at least three alternatingdouble(C=C) andsingle(C−C)carbon–carbon bonds.These carbon–carbon double bonds interact in a process known asconjugation,resulting in some unusualoptical properties.Related to polyenes aredienes,where there are only two alternating double and single bonds.

The following polyenes are used asantimycoticsfor humans:amphotericin B,nystatin,candicidin,pimaricin,methyl partricin, andtrichomycin.[1]

Optical properties

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Some polyenes are brightly colored, an otherwise rare property for a hydrocarbon. Normally alkenes absorb in theultravioletregion of aspectrum,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 achromophore). Thus many naturaldyescontain linear polyenes.

Chemical and electrical properties

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Polyenes tend to be more reactive than simpler alkenes. For example, polyene-containingtriglyceridesare reactive towards atmospheric oxygen.Polyacetylene,which partially oxidized or reduced, exhibits high electrical conductivity. Mostconductive polymersare polyenes, and many haveconjugatedstructures. Poly(aza)acetylenes are readily prepared frompyridineprecursors without the necessity of a controlled atmosphere, simply byultravioletirradiation of a mixture of pyridine and poly(4-vinyl) pyridine.[citation needed]Recent research at theWeizmann InstituteandAix-Marseille Universityshowed a clear transition between ionic and electronic conductivity with increasing UV dose over 30 hours.[2]

Occurrence

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A fewfatty acidsare polyenes. Another class of important polyenes arepolyene antimycotics,[3]

References

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  1. ^Zotchev, Sergey B. (2003). "Polyene macrolide antibiotics and their applications in human therapy".Current Medicinal Chemistry.10(3): 211–223.doi:10.2174/0929867033368448.PMID12570708.
  2. ^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".Molecules.26(22): 6925.doi:10.3390/molecules26226925.ISSN1420-3049.PMC8621047.PMID34834017.
  3. ^NCBI Bookshelf (1996)."Polyene Antifungal Drugs".The University of Texas Medical Branch at Galveston.Retrieved29 January2010.
  4. ^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
  5. ^Lam, Jacky W. Y.; Tang, Ben Zhong "Functional Polyacetylenes" Accounts of Chemical Research 2005, volume 38, pp. 745-754.doi:10.1021/ar040012f