Carbene radical

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Bonding Scheme of Carbene Radical Complexes as compared to Schrock and Fischer-type carbene complexes Bonding scheme carbene radical.png
Bonding Scheme of Carbene Radical Complexes as compared to Schrock and Fischer-type carbene complexes

Carbene radicals are a special class of organometallic carbenes. The carbene radical can be formed by one-electron reduction of Fischer-type carbenes using an external reducing agent, or directly upon carbene formation at an open-shell transition metal complex (in particular low-spin cobalt(II) complexes) using diazo compounds and related carbene precursors. [1] Cobalt(III)-carbene radicals have found catalytic applications in cyclopropanation reactions, [2] [3] [4] as well as in a variety of other catalytic radical-type ring-closing reactions. [5] [6] [7] [8]

Contents

Theoretical calculations and EPR studies confirmed their radical-type behaviour and explained the bonding interactions underlying the stability of the carbene radical. [9] [10] Stable carbene radicals of other metals are known, [1] but the catalytically relevant cobalt(III)-carbene radicals have thus far only been synthesized as long-lived reactive intermediates. [11] [12]

Examples of Radical-type Reactions involving Carbene Radical Complexes Radical type reactions carbene radicals.png
Examples of Radical-type Reactions involving Carbene Radical Complexes

Bonding interactions and Radical Reactivity

Example of carbene radical reaction intermediate generated by reaction of cobalt porphyrin and CHCO2Et ligand. s donation from the ligand to the "dz " orbital on the cobalt metal center occurs concurrent with p* back-donation from the t2g symmetry orbitals. Carbene radical bonding.png
Example of carbene radical reaction intermediate generated by reaction of cobalt porphyrin and CHCO2Et ligand. σ donation from the ligand to the "dz " orbital on the cobalt metal center occurs concurrent with π* back-donation from the t2g symmetry orbitals.

The chemical bond present in carbene radicals is surprising in that it possesses aspects of both Fischer and Schrock type carbenes. [1] [9] [10] As a result, the cobalt carbene radical complexes have discrete radical-character at their carbon atom, thus giving rise to interesting catalytic radical-type reaction pathways.

The mechanism of formation of a carbene radical at cobalt(II) typically involves carbene generation at the metal with simultaneous intramolecular electron transfer from the metal into the metal-carbene π* anti-bonding molecular orbital constructed from the metal d-orbital and the carbene p-orbital. As such, carbene radicals are perhaps best described as 'one-electron reduced Fischer-type carbenes'. [1]

Second Coordination Sphere Hydrogen-Bonding Effects in Controlling Carbene Radical Reactivity Carbene radical H bonding.png
Second Coordination Sphere Hydrogen-Bonding Effects in Controlling Carbene Radical Reactivity

Discrete electron transfer from a sigma-type metal d-orbital (typically the dz2 orbital) occurs, [1] [10] leads the typical radical character of the carbene carbon. This behaviour not only explains the carbon-centered radical-type reactivity of these complexes, but also their reduced electrophilicity (suppressing carbene-carbene dimerisation side reactions) as well as their enhanced reactivity to electron-deficient substrates. Furthermore, second coordination sphere hydrogen-bonding interactions give rise to faster reactions because H-bonds are stronger to the reduced carbene as compared to the precursor. [9] Such H-bonding interactions can also facilitate chirality transfer in enantioselective carbene-transfer reactions. [13]

In order for the σ bond to be stabilized (typically with a bond order slightly less than 1), a back-bonding action from the π molecular orbital to the anti-bonding π* molecular orbital is necessary and the porphyrin ring serves as an electron π-symmetry "buffer" to ensure this interaction is obtained. [10]

The back-donation to the π* orbital would result in unfavorable excess electron density on the carbene carbon but the presence of adjacent functional groups (carbonyl or sulfonyl groups have the desired electronegativity) relieve this electron build-up and yield the final radical electron, which occupies a single p atomic orbital state on the carbon. [10]

See also

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References

  1. 1 2 3 4 5 Dzik, W.I.; Zhang, X.P.; de Bruin, B. (2011). "The Redox Non-Innocence of Carbene Ligands: Carbene Radicals in (Catalytic) C-C Bond Formation". Inorganic Chemistry. 50 (20): 9896–9903. doi:10.1021/ic200043a. PMID   21520926.
  2. ↑ Ikeno, T.; Iwakura, I.; Yamada, T. (2002). "Cobalt−Carbene Complex with Single-Bond Character: Intermediate for the Cobalt Complex-Catalyzed Cyclopropanation". Journal of the American Chemical Society. 124 (51): 15152–15153. doi:10.1021/ja027713x. PMID   12487572.
  3. ↑ Huang, L.; Chen, Y.; Gao, G.-Y.; Zhang, X.P. (2003). "Diastereoselective and enantioselective cyclopropanation of alkenes catalyzed by cobalt porphyrins". Journal of Organic Chemistry. 68 (21): 8179–8184. doi:10.1021/jo035088o. PMID   14535801.
  4. ↑ Chirila, A.; Das, B.G.; Paul, N.D.; de Bruin, B. (2017). "Diastereoselective Radical-Type Cyclopropanation of Electron Deficient Alkenes mediated by the Highly Active [Co(MeTAA)] Catalyst". ChemCatChem. 9 (8): 1413–1421. doi:10.1002/cctc.201601568. PMC   5413858 . PMID   28529668.
  5. ↑ Das, B.G.; Chirila, A.; Tromp, M.; Reek, J.N.H.; de Bruin, B. (2016). "Co(III)-Carbene Radical Approach to Substituted 1H-Indenes". Journal of the American Chemical Society. 138 (28): 8968–8975. doi:10.1021/jacs.6b05434. PMID   27340837.
  6. ↑ Cui, X.; Xu, X.; Jin, L.-M.; Wojtas, L.; Zhang, X.P. (2017). "Stereoselective Radical C–H Alkylation with Acceptor/Acceptor-Substituted Diazo Reagents via Co(II)-Based Metalloradical Catalysis". Chemical Science. 6 (2): 1219–1224. doi:10.1039/C4SC02610A. PMC   4324598 . PMID   25685314.
  7. ↑ Paul, N.D.; Chirila, A.; Lu, H.; Zhang, X.P.; de Bruin, B. (2013). "Carbene Radicals in Cobalt(II) Porphyrin-Catalysed Carbene Carbonylation Reactions; A Catalytic Approach to Ketenes". Chemistry: A European Journal. 19 (39): 12953–12958. doi:10.1002/chem.201301731. PMC   4351769 . PMID   24038393.
  8. ↑ Paul, N.D.; Mandal, S.; Otte, M.; Cui, M.; Zhang, X.P.; de Bruin, B. (2014). "A Metalloradical Approach to 2H-Chromenes". Journal of the American Chemical Society. 136 (3): 1090–1096. doi:10.1021/ja4111336. PMC   3936204 . PMID   24400781.
  9. 1 2 3 Dzik, W.I.; Xu, X.; Zhang, X.P.; Reek, J.N.H.; de Bruin, B. (2010). "'Carbene Radicals' in CoII(por)-Catalyzed Olefin Cyclopropanation". Journal of the American Chemical Society. 132 (31): 10891–10902. doi:10.1021/ja103768r. PMID   20681723.
  10. 1 2 3 4 5 Belof, J.; Cioce, C.; Xu, X.; Zhang, X.P.; Space, B.; Woodcock, H.L. (2011). "Characterization of tunable radical metal–carbenes: Key intermediates in catalytic cyclopropanation". Organometallics. 30 (10): 2739–2746. doi:10.1021/om2001348. PMC   3105361 . PMID   21643517.
  11. ↑ Lu, H.; Dzik, W.; Xu, X.; Wojtas, L.; de Bruin, B.; Zhang, X.P. (2011). "Experimental evidence for cobalt(III)-carbene radicals: Key intermediates in cobalt(II)-based metalloradical cyclopropanation". Journal of the American Chemical Society. 133 (22): 8518–8521. doi:10.1021/ja203434c. PMID   21563829.
  12. ↑ Russell, S.; Hoyt, J.; Bart, S.; Milsmann, C.; Stieber, S.C.; Semproni, S.; DeBeer, S.; Chirik, P. (2014). "Synthesis, electronic structure and reactivity of bis(imino)pyridine iron carbene complexes: evidence for a carbene radical". Chemical Science. 5 (3): 1168–1174. doi:10.1039/C3SC52450G.
  13. ↑ Xu, X.; Zhu, S.; Cui, X.; Wojtas, L.; Zhang, X.P. (2013). "Cobalt(II)-Catalyzed Asymmetric Olefin Cyclopropanation with α-Ketodiazoacetates". Angewandte Chemie International Edition. 52 (45): 11857–11861. doi:10.1002/anie.201305883. PMC   3943748 . PMID   24115575.
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