Norbornadiene: Difference between revisions
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== Synthesis == |
== Synthesis == |
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Norbornadiene can be formed by a Diels-Alder reaction between [[cyclopentadiene]] and [[acetylene]] <ref>{{Cite journal |last=Orrego‐Hernández |first=Jessica |last2=Hölzel |first2=Helen |last3=Quant |first3=Maria |last4=Wang |first4=Zhihang |last5=Moth‐Poulsen |first5=Kasper |date=2021-10-14 |title=Scalable Synthesis of Norbornadienes via in situ Cracking of Dicyclopentadiene Using Continuous Flow Chemistry |url=https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.202100795 |journal=European Journal of Organic Chemistry |language=en |volume=2021 |issue=38 |pages=5337–5342 |doi=10.1002/ejoc.202100795 |issn=1434-193X}}</ref> |
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Norbornadiene can be formed by a Diels-Alder reaction between [[cyclopentadiene]] and [[acetylene]] {{Citation needed|date=October 2022}} |
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:[[Image:Norbornadiene synthesis.png|300px|left|Norbornadiene synthesis]] |
:[[Image:Norbornadiene synthesis.png|300px|left|Norbornadiene synthesis]] |
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Revision as of 07:32, 2 June 2024
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| Names | |||
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| Preferred IUPAC name
Bicyclo[2.2.1]hepta-2,5-diene | |||
| Other names
2,5-Norbornadiene
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| Identifiers | |||
3D model (JSmol)
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| ChemSpider | |||
| ECHA InfoCard | 100.004.066 | ||
| EC Number |
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PubChem CID
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| UNII | |||
| UN number | 2251 | ||
CompTox Dashboard (EPA)
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| Properties | |||
| C7H8 | |||
| Molar mass | 92.14 g/mol | ||
| Density | 0.906 g/cm3 | ||
| Melting point | −19 °C (−2 °F; 254 K) | ||
| Boiling point | 89 °C (192 °F; 362 K) | ||
| Insoluble | |||
| Hazards | |||
| GHS labelling: | |||
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| Danger | |||
| H225 | |||
| P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, P501 | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Norbornadiene is an organic compound and a bicyclic hydrocarbon. Norbornadiene is of interest as a metal-binding ligand, whose complexes are useful for homogeneous catalysis. It has been intensively studied owing to its high reactivity and distinctive structural property of being a diene that cannot isomerize (isomers would be anti-Bredt alkenes). Norbornadiene is also a useful dienophile in Diels-Alder reactions.
Synthesis
Norbornadiene can be formed by a Diels-Alder reaction between cyclopentadiene and acetylene [1]
Norbornadiene synthesis
Reactions
Quadricyclane, a valence isomer, can be obtained from norbornadiene by a photochemical reaction when assisted by a sensitizer such as acetophenone:[2]
The norbornadiene-quadricyclane couple is of potential interest for solar energy storage when controlled release of the strain energy stored in quadricyclane back to norbornadiene is made possible.[3]
Norbornadiene is reactive in cycloaddition reactions. Norbornadiene is also the starting material for the synthesis of diamantane[4] and sumanene and it is used as an acetylene transfer agent for instance in reaction with 3,6-di-2-pyridyl-1,2,4,5-tetrazine.[5]
As a ligand
Norbornadiene is a versatile ligand in organometallic chemistry, where it serves as a two-electron or four-electron donor. (Norbornadiene)molybdenum tetracarbonyl is used as a source of "Mo(CO)4", exploiting the lability of the diene ligand in this case.[6] which is a useful source of "chromium tetracarbonyl," e.g. in reactions with phosphine ligands.
The norbornadiene analogue of cyclooctadiene rhodium chloride dimer has been used in homogeneous catalysis. Chiral, C2-symmetric dienes derived from norbornadiene have also been described.[7][8]
See also
- Norbornane a saturated compound with the same carbon skeleton.
- Norbornene a compound with the same carbon skeleton, but with one less double bond.
References
- ^ Orrego‐Hernández, Jessica; Hölzel, Helen; Quant, Maria; Wang, Zhihang; Moth‐Poulsen, Kasper (2021-10-14). "Scalable Synthesis of Norbornadienes via in situ Cracking of Dicyclopentadiene Using Continuous Flow Chemistry". European Journal of Organic Chemistry. 2021 (38): 5337–5342. doi:10.1002/ejoc.202100795. ISSN 1434-193X.
- ^ Smith, Claiborune D. (1988). "Quadricyclane". Organic Syntheses; Collected Volumes, vol. 6, p. 962.
- ^ Gregory W. Sluggett; Nicholas J. Turro & Heinz D. Roth (1997). "Rh(III)-Photosensitized Interconversion of Norbornadiene and Quadricyclane". J. Phys. Chem. A. 101 (47): 8834–8838. Bibcode:1997JPCA..101.8834S. CiteSeerX 10.1.1.130.1791. doi:10.1021/jp972007h.
- ^ Diamantane in Organic Syntheses Coll. Vol. 6, p.378; Vol. 53, p.30 Online Article Archived 2012-07-28 at the Wayback Machine
- ^ Ronald N. Warrener & Peter A. Harrison (2001). "π-Bond Screening in Benzonorbornadienes: The Role of 7-Substituents in Governing the Facial Selectivity for the Diels-Alder Reaction of Benzonorbornadienes with 3,6-Di(2-pyridyl)-s-Tetrazine" (PDF). Molecules. 6 (4): 353–369. doi:10.3390/60400353. PMC 6236418. S2CID 53874105.
- ^ Markus Strotmann; Rudolf Wartchow & Holger Butenschön (2004). "High yield synthesis and structures of some achiral and chiral (diphosphine)tetracarbonylchromium(0) chelate complexes with tetracarbonyl(norbornadiene)chromium(0) as complexation reagent". Arkivoc: KK–1112F.
- ^ Ryo Shintani, Tamio Hayashi "Chiral Diene Ligands for Asymmetric Catalysis" Aldrich Chimica Acta 2009, vol. 42, number 2, pp. 31-38.
- ^ Huang, Yinhua; Hayashi, Tamio (2022). "Chiral Diene Ligands in Asymmetric Catalysis". Chemical Reviews. 122 (18): 14346–14404. doi:10.1021/acs.chemrev.2c00218. PMID 35972018.