Transition metal alkyne complex: Difference between revisions
m Checkwiki error fix #72. ISBN-10 with wrong checksum |
ref to cyclooctyne chem |
||
| Line 11: | Line 11: | ||
==Structure and Bonding== |
==Structure and Bonding== |
||
[[File:VarietyPackAlkyneCmpx.svg|thumb|center|620px|Structures of various metal-alkyne complexes.]] |
[[File:VarietyPackAlkyneCmpx.svg|thumb|center|620px|Structures of various metal-alkyne complexes.]] |
||
The coordination of alkynes to transition metals is similar to that of alkenes. The bonding is described by the [[Dewar-Chatt-Duncanson model]]. Upon complexation the C-C bond elogates and the alkynyl carbon bends. For example in the phenylpropyne complex Pt(PPh<sub>3</sub>)<sub>2</sub>(C<sub>2</sub>)Ph(Me), the C-C distance is 1.277(25) |
The coordination of alkynes to transition metals is similar to that of alkenes. The bonding is described by the [[Dewar-Chatt-Duncanson model]]. Upon complexation the C-C bond elogates and the alkynyl carbon bends away from 180º. For example in the phenylpropyne complex Pt(PPh<sub>3</sub>)<sub>2</sub>(C<sub>2</sub>)Ph(Me), the C-C distance is 1.277(25) vs 1.20 Å for a typical alkyne. The C-C-C angle distorts 40° from linearity.<ref>William Davies, B.; C. Payne, N., "Studies on metal-acetylene complexes: V. Crystal and molecular structure of bis(triphenylphosphine)(1-phenylpropyne)platinum(0), [P(C<sub>6</sub>H<sub>5</sub>)<sub>3</sub>]<sub>2</sub>(C<sub>6</sub>H<sub>5</sub>CCCH<sub>3</sub>)Pt<sup>0</sup>" J. Organomet. Chem. 1975, volume 99, pp. 315. {{doi|10.1016/S0022-328X(00)88462-4}}</ref> Because the bending induced by complexation, strained alkynes such as cycloheptyne and cyclooctyne are stabilized by complexation.<ref>{{cite journal|title=Metal Complexes of Small Cycloalkynes and Arynes |first1=Martin A. |last1=Bennett |first2=Heinz P. |last2=Schwemlein |journal=[[Angew. Chem. Int. Ed. Engl.]] |date=1989 |volume=28|issue=10 |pages=1296–1320|doi=10.1002/anie.198912961}}</ref> |
||
In the IR spectra, the C-C vibration of alkynes, which occurs near 2300 cm<sup>−1</sup>, shifts upon complexation to around 1800 cm<sup>−1</sup>, indicating a weakening of the C-C bond. |
|||
===η<sup>2</sup>-coordination to a single metal center=== |
===η<sup>2</sup>-coordination to a single metal center=== |
||
When bonded side-on to a single metal atom, an alkyne serves as a dihapto usually two-electron donor. For early metal complexes, e.g., Cp<sub>2</sub>Ti(C<sub>2</sub>R<sub>2</sub>), strong π-backbonding into one of the π* antibonding orbitals of the alkyne is indicated. This complex is described as a metallacyclopropene derivative of Ti(IV). For late transition metal complexes, e.g., Pt(PPh<sub>3</sub>)<sub>2</sub>(MeC<sub>2</sub>Ph), the π-backbonding is less prominent, and the complex is assigned oxidation state (0).<ref>Hill, A.F. ''Organotransition Metal Chemistry'', 2002, Royal Society of Chemistry, ISBN 0-471-28163-8.</ref><ref name=Crabtree>Crabtree, R. H. ''Comprehensive Organometallic Chemistry V'', 2009, John Wiley & Sons, Inc. ISBN 978-0-470-25762-3 {{Verify source|date=May 2015}}</ref> |
When bonded side-on to a single metal atom, an alkyne serves as a dihapto usually two-electron donor. For early metal complexes, e.g., Cp<sub>2</sub>Ti(C<sub>2</sub>R<sub>2</sub>), strong π-backbonding into one of the π* antibonding orbitals of the alkyne is indicated. This complex is described as a metallacyclopropene derivative of Ti(IV). For late transition metal complexes, e.g., Pt(PPh<sub>3</sub>)<sub>2</sub>(MeC<sub>2</sub>Ph), the π-backbonding is less prominent, and the complex is assigned oxidation state (0).<ref>Hill, A.F. ''Organotransition Metal Chemistry'', 2002, Royal Society of Chemistry, ISBN 0-471-28163-8.</ref><ref name=Crabtree>Crabtree, R. H. ''Comprehensive Organometallic Chemistry V'', 2009, John Wiley & Sons, Inc. ISBN 978-0-470-25762-3 {{Verify source|date=May 2015}}</ref> |
||
In some complexes, the alkyne is classified as a four-electron donor. In these cases, both pairs of pi-electrons donate to the metal. This kind of bonding was first implicated in complexes of the type W(CO)(R<sub>2</sub>C<sub>2</sub>)<sub>3</sub>.<ref>Joseph L. Templeton "Four-Electron Alkyne Ligands in Molybdenum(II) and Tungsten(II) Complexes" Advances in Organometallic Chemistry Volume 29 |
In some complexes, the alkyne is classified as a four-electron donor. In these cases, both pairs of pi-electrons donate to the metal. This kind of bonding was first implicated in complexes of the type W(CO)(R<sub>2</sub>C<sub>2</sub>)<sub>3</sub>.<ref>Joseph L. Templeton "Four-Electron Alkyne Ligands in Molybdenum(II) and Tungsten(II) Complexes" Advances in Organometallic Chemistry 1989, Volume 29, Pages 1–100.{{doi|10.1016/S0065-3055(08)60352-4}}</ref> |
||
===η<sup>2</sup>, η<sup>2</sup>-coordination bridging two metal centers=== |
===η<sup>2</sup>, η<sup>2</sup>-coordination bridging two metal centers=== |
||
Revision as of 18:27, 25 July 2016
In organometallic chemistry, a transition metal alkyne complex is a coordination compound containing one or more alkyne ligands. Such compounds are intermediates in many catalytic reactions that convert alkynes to other organic products, e.g. hydrogenation and trimerization.[1]
Synthesis
Transition metal alkyne complexes are often formed by the displacement of labile ligands by the alkyne. For example, a variety of cobalt-alkyne complexes may be formed by reaction of the alkyne with dicobalt octacarbonyl.[2]
- Co2(CO)8 + R2C2 → Co2(C2R2)(CO)6 + 2 CO
Many alkyne complexes are produced by reduction of metal halides, e.g. titanocene dichloride and bis(triphenylphosphine)platinum dichloride in the presence of the alkyne:
- Cp2TiCl2 + C2R2 + Mg → Cp2Ti(C2R2) + MgCl2
Structure and Bonding
The coordination of alkynes to transition metals is similar to that of alkenes. The bonding is described by the Dewar-Chatt-Duncanson model. Upon complexation the C-C bond elogates and the alkynyl carbon bends away from 180º. For example in the phenylpropyne complex Pt(PPh3)2(C2)Ph(Me), the C-C distance is 1.277(25) vs 1.20 Å for a typical alkyne. The C-C-C angle distorts 40° from linearity.[3] Because the bending induced by complexation, strained alkynes such as cycloheptyne and cyclooctyne are stabilized by complexation.[4]
In the IR spectra, the C-C vibration of alkynes, which occurs near 2300 cm−1, shifts upon complexation to around 1800 cm−1, indicating a weakening of the C-C bond.
η2-coordination to a single metal center
When bonded side-on to a single metal atom, an alkyne serves as a dihapto usually two-electron donor. For early metal complexes, e.g., Cp2Ti(C2R2), strong π-backbonding into one of the π* antibonding orbitals of the alkyne is indicated. This complex is described as a metallacyclopropene derivative of Ti(IV). For late transition metal complexes, e.g., Pt(PPh3)2(MeC2Ph), the π-backbonding is less prominent, and the complex is assigned oxidation state (0).[5][6]
In some complexes, the alkyne is classified as a four-electron donor. In these cases, both pairs of pi-electrons donate to the metal. This kind of bonding was first implicated in complexes of the type W(CO)(R2C2)3.[7]
η2, η2-coordination bridging two metal centers
Because alkynes have two π bonds, alkynes can form stable complexes in which they bridge two metal centers. The alkyne donates a total of four electrons, with two electrons donated to each of the metals. And example of a complex with this bonding scheme is η2-diphenylacetylene-(hexacarbonyl)dicobalt(0).[6]
Benzyne complexes
Transition metal benzyne complexes represent a special case of alkyne complexes since the free benzynes are not stable in the absence of the metal.[8]
Applications
Metal alkyne species are implicated as intermediates in the hydrogenation of alkynes, e.g. to alkenes.
Metal-alkyne complexes are intermediates in the metal-catalyzed alkyne trimerisation. With the shift away from coal-based (acetylene) to petroleum-based feedstocks (olefins), catalytic reactions with alkynes are not widely practiced industrially. Specialized variants are still exploited for certain niche uses, e.g. synthesis of substituted pyridines. Cyclooctatetraene is produced from acetylene via the intermediacy of metal alkyne complexes. The Pauson-Khand reaction provides a route to cyclopentenones via the intermediacy of cobalt-alkyne complexes.
References
- ^ Elschenbroich, C. ”Organometallics” 2006 Wiley-VCH: Weinheim. ISBN 3-527-29390-6.
- ^ Kemmitt, R. D. W.; Russell, D. R.; "Cobalt" in Comprehensive Organometallic Chemistry I; Abel, E.W.; Stone, F.G.A.; Wilkinson, G. eds., 1982, Pergamon Press, Oxford. ISBN 0-08-025269-9
- ^ William Davies, B.; C. Payne, N., "Studies on metal-acetylene complexes: V. Crystal and molecular structure of bis(triphenylphosphine)(1-phenylpropyne)platinum(0), [P(C6H5)3]2(C6H5CCCH3)Pt0" J. Organomet. Chem. 1975, volume 99, pp. 315. doi:10.1016/S0022-328X(00)88462-4
- ^ Bennett, Martin A.; Schwemlein, Heinz P. (1989). "Metal Complexes of Small Cycloalkynes and Arynes". Angew. Chem. Int. Ed. Engl. 28 (10): 1296–1320. doi:10.1002/anie.198912961.
- ^ Hill, A.F. Organotransition Metal Chemistry, 2002, Royal Society of Chemistry, ISBN 0-471-28163-8.
- ^ a b Crabtree, R. H. Comprehensive Organometallic Chemistry V, 2009, John Wiley & Sons, Inc. ISBN 978-0-470-25762-3 [verification needed]
- ^ Joseph L. Templeton "Four-Electron Alkyne Ligands in Molybdenum(II) and Tungsten(II) Complexes" Advances in Organometallic Chemistry 1989, Volume 29, Pages 1–100.doi:10.1016/S0065-3055(08)60352-4
- ^ William M. Jones, Jerzy Klosin "Transition-Metal Complexes of Arynes, Strained Cyclic Alkynes, and Strained Cyclic Cumulenes" Advances in Organometallic Chemistry 1998, Volume 42, Pages 147–221. doi:10.1016/S0065-3055(08)60543-2
