Carbene radical

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]

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

Bonding interactions and Radical Reactivity

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

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]

See also

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.
  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.
  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.
  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. doi:10.1002/cctc.201601568.
  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.
  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: 1219–1224. doi:10.1039/C4SC02610A.
  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 European Journal. 19 (39): 12953–12958. doi:10.1002/chem.201301731.
  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.
  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.
  10. 1 2 3 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.
  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. PMID 21563829. doi:10.1021/ja203434c.
  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: 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.
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