{{Short description|Coordination compound}} In organometallic chemistry, a '''transition metal alkene complex''' is a coordination compound containing one or more alkene ligands. The inventory is large.<ref name=Elsch>Elschenbroich, C. "Organometallics" (2006) Wiley-VCH: Weinheim. {{ISBN|3-527-29390-6}}</ref> Such compounds are intermediates in many catalytic reactions that convert alkenes to other organic products.<ref>{{cite book |title=Organotransition Metal Chemistry: From Bonding to Catalysis |author=John Hartwig |isbn=978-1-891389-53-5 |publisher=University Science Books}}</ref>
==Monoalkenes== Complexes of ethylene are particularly common. Examples include Zeise's salt (see figure), Rh<sub>2</sub>Cl<sub>2</sub>(C<sub>2</sub>H<sub>4</sub>)<sub>4</sub>, Cp*<sub>2</sub>Ti(C<sub>2</sub>H<sub>4</sub>), and {{chem2|Pt(P(C6H5)3)2(C2H4)}}.
Homoleptic alkene-complexes are well known but often are highly reactive. Examples include Ni(C<sub>2</sub>H<sub>4</sub>)<sub>3</sub>,<ref>{{cite journal |doi=10.1002/anie.197305651 |title=Tris(ethylene)nickel(0) |date=1973 |last1=Fischer |first1=Karl |last2=Jonas |first2=Klaus |last3=Wilke |first3=Günther |journal=Angewandte Chemie International Edition in English |volume=12 |issue=7 |pages=565–566 }}</ref> [Co(C<sub>2</sub>H<sub>4</sub>)<sub>4</sub>]<sup>−</sup>, and [Fe(C<sub>2</sub>H<sub>4</sub>)<sub>4</sub>]<sup>2−</sup>.<ref>{{Cite journal |last=Ellis |first=John E. |date=2006-04-17 |title=Adventures with Substances Containing Metals in Negative Oxidation States |url=https://pubs.acs.org/doi/10.1021/ic052110i |journal=Inorganic Chemistry |language=en |volume=45 |issue=8 |page=3175 |doi=10.1021/ic052110i |pmid=16602773 |issn=0020-1669|url-access=subscription }}</ref>
Substituted monoalkenes are common ligands. Cyclooctene is found in chlorobis(cyclooctene)rhodium dimer. Alkenes with electron-withdrawing groups commonly bind strongly to low-valent metals. Examples of such ligands are TCNE, tetrafluoroethylene, maleic anhydride, and esters of fumaric acid.<ref>{{cite journal |doi=10.1002/hlca.19630460128 |title=π-Olefin-eisentetracarbonyl-Komplexe mit Liganden der Malein-, Fumar-, Acryl-, Methacryl- und Zimtsäure-Reihe |date=1963 |last1=Weiss |first1=E. |last2=Stark |first2=K. |last3=Lancaster |first3=J. E. |last4=Murdoch |first4=H. D. |journal=Helvetica Chimica Acta |volume=46 |pages=288–297 }}</ref> These acceptors form adducts with many zero-valent metals.<ref name=Elsch/>
==Dienes, trienes, and related ligands== {{See also|(Diene)iron tricarbonyl}} Butadiene, cyclooctadiene, and norbornadiene are well-studied chelating agents. Trienes and even some tetraenes can bind to metals through several adjacent carbon centers. Common examples of such ligands are cycloheptatriene and cyclooctatetraene. The bonding is often denoted using the hapticity formalism. Keto-alkenes are tetrahapto ligands that stabilize highly unsaturated low valent metals as found in (benzylideneacetone)iron tricarbonyl and tris(dibenzylideneacetone)dipalladium(0). <gallery widths="160px" heights="100px" caption="Metal alkene complexes."> File:Ni(cod)2.png|Bis(cyclooctadiene)nickel(0), a catalyst and source of "naked nickel." File:Zeise'sSalt.png|The first alkene complex, the anion in Zeise's salt. File:Rh2Cl2 coe 4.svg|Chlorobis(cyclooctene)rhodium dimer, source of "RhCl". File: Crabtree.svg|Crabtree's catalyst, a very active catalyst for hydrogenation. File: (benzylideneacetone)iron-tricarbonyl-2D-skeletal.png|(Benzylideneacetone)iron tricarbonyl, source of "Fe(CO)<sub>3</sub>". File:CHTMo(CO)3.png|Mo(C<sub>7</sub>H<sub>8</sub>)(CO)<sub>3</sub>, a complex of cycloheptatriene. File:Fe(cot)2.svg|Fe(C<sub>8</sub>H<sub>8</sub>)<sub>2</sub>, a complex of cyclooctatetraene File:Mo(nbd)(CO)4.png|(Norbornadiene)molybdenum tetracarbonyl, a source of "Mo(CO)<sub>4</sub>" File:XylyleneFe(CO)3.svg|(Xylylene)Fe(CO)<sub>3</sub>, illustrating the stabilization of a labile alkene by complexation </gallery>
==Bonding== thumb|Structure of (acac)Rh(C<sub>2</sub>H<sub>4</sub>)(C<sub>2</sub>F<sub>4</sub>), distances (red) in picometers.<ref name=Evans/> The bonding between alkenes and transition metals is described by the Dewar–Chatt–Duncanson model, which involves donation of electrons in the pi-orbital on the alkene to empty orbitals on the metal. This interaction is reinforced by back bonding that entails sharing of electrons in other metal orbitals into the empty pi-antibonding level on the alkene. Early metals of low oxidation state (Ti(II), Zr(II), Nb(III) etc.) are strong pi donors, and their alkene complexes are often described as metallacyclopropanes. Treatment of such species with acids gives the alkanes. Late metals (Ir(I), Pt(II)), which are poorer pi-donors, tend to engage the alkene as a Lewis acid–Lewis base interaction. Similarly, C<sub>2</sub>F<sub>4</sub> is a stronger pi-acceptor than C<sub>2</sub>H<sub>4</sub>, as reflected in metal-carbon bond distances.<ref name=Evans>{{cite journal |doi=10.1039/C29710000197 |title=The Crystal Structures of Ethylene and Tetrafluoroethylene Complexes of Rhodium(I) |year=1971 |last1=Evans |first1=J. A. |last2=Russell |first2=D. R. |journal=Journal of the Chemical Society D: Chemical Communications |issue=4 |page=197}}</ref>
<gallery class="center" caption="Bonding images" widths="180px" heights="120px"> File:DCDmodel.png|Orbital interactions in a metal-ethylene complex, as described by the Dewar–Chatt–Duncanson model File:M-C2H4.png|Two extreme depictions of M---C<sub>2</sub>H<sub>4</sub> interactions. </gallery>
===Rotational barrier=== The barrier for the rotation of the alkene about the M-centroid vector is a measure of the strength of the M-alkene pi-bond. Low symmetry complexes are suitable for analysis of these rotational barriers associated with the metal-ethylene bond.In CpRh(C<sub>2</sub>H<sub>4</sub>)(C<sub>2</sub>F<sub>4</sub>), the ethylene ligand is observed to rotate with a barrier near 12 kcal/mol but no rotation is observed for about the Rh-C<sub>2</sub>F<sub>4</sub> bond.<ref>{{cite journal |doi=10.1021/ja01038a021 |title=Bond Character and Conformational Equilibration of Ethylene- and Tetrafluoroethylenerhodium Complexes from Nuclear Magnetic Resonance Spectra |year=1969 |last1=Cramer |first1=Richard |last2=Kline |first2=Jules B. |last3=Roberts |first3=John D. |journal=Journal of the American Chemical Society |volume=91 |issue=10 |pages=2519–2524}}</ref>
==Reactions and applications== Alkene ligands lose much of their unsaturated character upon complexation. Most famously, the alkene ligand undergoes migratory insertion, wherein it is attacked intramolecularly by alkyl and hydride ligands to form new alkyl complexes. Cationic alkene complexes are susceptible to attack by nucleophiles.<ref name=Elsch/>
===Catalysis=== Metal alkene complexes are intermediates in many or most transition metal catalyzed reactions of alkenes: polymerization., hydrogenation, hydroformylation, and many other reactions.<ref name=Leeuwen>Piet W. N. M. van Leeuwen "Homogeneous Catalysis: Understanding the Art", 2004, Wiley-VCH, Weinheim. {{ISBN|1-4020-2000-7}}</ref> [[File:WackerMechWiki3.gif|center|The mechanism of the Wacker process involves Pd-alkene complex intermediates. ]]
===Separations=== Since alkenes are mainly produced as mixtures with alkanes, the separation of alkanes and alkenes is of commercial interest. Separation technologies often rely on facilitated transport membranes containing Ag<sup>+</sup> or Cu<sup>+</sup> salts that reversibly bind alkenes.<ref>{{cite journal |doi=10.1016/j.jiec.2008.04.014 |title=A Review on Olefin/Paraffin Separation Using Reversible Chemical Complexation technology |year=2008 |last1=Azhin |first1=Maryam |last2=Kaghazchi |first2=Tahereh |last3=Rahmani |first3=Mohammad |journal=Journal of Industrial and Engineering Chemistry |volume=14 |issue=5 |pages=622–638}}</ref>
In argentation chromatography, stationary phases that contain silver salts are used to analyze organic compounds on the basis of the number and type of alkene (olefin) groups. This methodology is commonly employed for the analysis of the unsaturated content in fats and fatty acids.<ref>{{cite web |url=https://lipidlibrary.aocs.org/lipid-analysis/silver-ion-chromatography-of-lipids |title=Principles of Silver Ion Complexation with Double Bonds |author=Boryana Nikolova-Damyanova}}</ref>
==Natural occurrence== Metal-alkene complexes are uncommon in nature, with one exception. Ethylene affects the ripening of fruit and flowers by complexation to a Cu(I) center in a transcription factor.<ref>Jose M. Alonso, Anna N. Stepanova "The Ethylene Signaling Pathway" ''Science'' 2004, Vol. 306, pp. 1513-1515. {{doi|10.1126/science.1104812}}</ref>
==References== {{Reflist}}
{{Organometallics}} {{Coordination complexes}}
Category:Coordination complexes Category:Organometallic chemistry Category:Transition metal compounds