{{short description|Hydrocarbon compound made of a 5-carbon chain with two single and two double bonds}} thumb|150px|1,2-Pentadiene thumb|150px|1,3-Pentadiene thumb|150px|1,4-Pentadiene thumb|150px|(''R'')-2,3-Pentadiene In organic chemistry, '''pentadiene''' is any hydrocarbon with an open chain of five carbons, connected by two single bonds and two double bonds. All those compounds have the same molecular formula {{chem2|C5H8}}. The inventory of pentadienes include: * 1,2-pentadiene, or ethyl allene, {{chem2|H2C\dC\dCH\sCH2\sCH3}}.<ref name=durig1996>James R. Durig, Stephen Bell, Gamil A. Guirgis (1996): "Infrared and Raman spectra, conformational stability, ab initio calculations and vibrational assignment for 1,2-pentadiene (ethyl allene)". ''Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy'', volume 52, issue 14, pages 1843-1859.{{doi|10.1016/S0584-8539(96)01740-0}}</ref> It and 2,3-pentadiene are the least common isomers of pentadiene. * 1,3-pentadiene, {{chem2|H2C\dCH\sCH\dCH\sCH3}} with two isomers:<ref name=prio1975>Aldo Priola, Sebastiano Cesca, Giuseppe Ferraris, and Mario Bruzzone (1975): "Relative reactivity of cis‐ and trans‐1,3‐pentadiene in the cationic copolymerization with isobutene". ''Die Makromolekulare Chemie'', volume 176, issue 7, pages 1969-1981. {{doi|10.1002/macp.1975.021760707}}</ref><ref name=boue1970>S. Boue and Rangaswamy Srinivasan (1970): "Differences in reactivity between excited states of cis- and trans-1,3-pentadiene". ''Journal of the American Chemical Association'', volume 92, issue 10, pages 3226–3227. {{doi|10.1021/ja00713a074}}</ref> ** ''cis''-1,3-pentadiene. ** ''trans''-1,3-pentadiene, also known as piperylene. * 1,4-pentadiene, {{chem2|H2C\dCH\sCH2\sCH\dCH2}}.<ref name=koge1930>Paul N. Kogerman (1930): "Synthesis of 1,4-pentadiene". ''Journal of the American Chemical Association'', volume 52, issue 12, pages 5060–5065. {{doi|10.1021/ja01375a064}}</ref> * 2,3-pentadiene, {{chem2|H3C\sCH\dC\dCH\sCH3}}, with two enantiomers (''R'' and ''S'').<ref name=wibe2008>Kenneth B. Wiberg, Yi-gui Wang, Shaun M. Wilson, Patrick H. Vaccaro, William L. Jorgensen, T. Daniel Crawford, Micah L. Abrams, James R. Cheeseman, and Mark Luderer (2008): "Optical Rotatory Dispersion of 2,3-Hexadiene and 2,3-Pentadiene". ''Journal of Physical Chemistry A'' J. Phys. Chem. A, 112, 2415-2422. {{doi|10.1021/jp076572o}}</ref> It and 1,2-pentadiene are the least common isomers of pentadiene.
Well known derivatives containing pentadiene groups include hexadienes, cyclopentadiene, and especially three fatty acids linoleic acid, α-linolenic acid, and arachidonic acid as well as their triglyceride esters (fats).
== Preparation and basic reactions == 1,4-Pentadiene can be prepared from 1,5-pentanediol via the diacetate.<ref>{{cite journal |author=R. E. Benson, B. C. McKusick, Oliver Grummitt, E. P. Budewitz, C. C. Chudd|doi=10.15227/orgsyn.038.0078 |title=1,4-Pentadiene |journal=Organic Syntheses |date=1958 |volume=38 |page=78 }}</ref>
1,3-Pentadiene, like 1,3-butadiene, undergoes a variety of cycloaddition reactions. For example, it forms a sulfolene upon treatment with sulfur dioxide.<ref>{{cite journal |doi=10.15227/orgsyn.029.0059|title=Isoprene Cyclic Sulfone |journal=Organic Syntheses |year=1949 |volume=29 |page=59|author=Robert L. Frank, Raymond P. Seven }}</ref>
==Biochemistry== {{main|Lipid peroxidation}} Methylene-interrupted polyenes are 1,4-pentadiene groups found in polyunsaturated fatty acids linoleic acid, α-linolenic acid, and arachidonic acid. These pentadiene derivatives are susceptible to lipid peroxidation, far moreso than monounsaturated or saturated fatty acids. The basis for this reactivity is the weakness of doubly allylic C-H bonds, leading to pentadienyl radicals. A range of reactions with oxygen occur. Products include fatty acid hydroperoxides, epoxy-hydroxy polyunsaturated fatty acids, jasmonates, divinylether fatty acids, and leaf aldehydes. Some of these derivatives are signalling molecules, some are used in plant defense (antifeedants), some are precursors to other metabolites that are used by the plant.<ref name=ARPB>{{cite journal |doi=10.1146/annurev.arplant.53.100301.135248 |title=The Lipoxygenase Pathway |date=2002 |last1=Feussner |first1=Ivo |last2=Wasternack |first2=Claus |journal=Annual Review of Plant Biology |volume=53 |pages=275–297 |pmid=12221977 }}</ref>
Cyclooxygenases ("COX") are enzymes that generate prostanoids, including thromboxane and prostaglandins such as prostacyclin. Aspirin and ibuprofen exert their effects through inhibition of COX. [[File:PGG2 mechanism.png|thumb|left|390px| Mechanism of COX activation and catalysis. The tyrosyl radical can abstracts the 13-pro(''S'') hydrogen of arachidonic acid to generate a pentadienyl radical, initiating the COX cycle.]]
==Drying and rancidification== :[[image:DryOilSteps.svg|thumb|190px|right|Simplified chemical reactions associated with the formation of a hydroperoxide from a typical polyunsaturated fatty acid. In the second step, the hydroperoxide combines with another unsaturated side chain to generate a crosslink.<ref>Ned A. Porter, Sarah E. Caldwell, Karen A. Mills "Mechanisms of free radical oxidation of unsaturated lipids" Lipids 1995, volume 30, Pages 277-290. {{doi|10.1007/BF02536034}}</ref>]] Fats containing 1,4-pentadiene groups are drying oils, i.e. film-forming liquids suitable as paints. One practical consequence is that polyunsaturated fatty acids have poor shelf life owing to their tendency toward autoxidation, leading, in the case of edibles, to rancidification. Metals accelerate the degradation.
==Further reading== *Pentadienyl *Juergen Herzler, Jeffrey A. Manion, and Wing Tsang (2001): "1,2‐Pentadiene decomposition". ''International Journal of Chemical Kinetics'', volume 33, issue 11, pages 755-767. {{doi|10.1002/kin.1072}}
==References== {{Reflist}}
{{hydrocarbons}}
Category:Anions Category:Free radicals Category:Alkadienes