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Reductive Transformations of CO$_2$ and Lignin Using Molecular Catalysts

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HAL Id: cea-02341625

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Reductive Transformations of CO_2 and Lignin Using

Molecular Catalysts

T. Cantat

To cite this version:

T. Cantat. Reductive Transformations of CO_2 and Lignin Using Molecular Catalysts. GECO 58 (Groupe d’Etudes en Chimie Organique), Aug 2017, Dinard, France. �cea-02341625�

(2)

Groupe d'Etudes en Chimie Organique

58

ème

édition

27 août – 1

er

septembre 2017, Dinard

Références

1. 1. Chauvier, C.; Cantat, T. ACS Catal., 2017, 7, 2107-2115.

2. Gomes, C. D.; Jacquet, O.; Villiers, C.; Thuery, P.; Ephritikhine, M.; Cantat, T. Angew. Chem. Int. Ed,

2012, 51, 187-190.

3. Jacquet, O.; Gomes, C. D.; Ephritikhine, M.; Cantat, T. J. Am. Chem. Soc., 2012, 134, 2934-2937. 4. Jacquet, O.; Frogneux, X.; Gomes, C. D.; Cantat, T. Chem Sci, 2013, 4, 2127-2131.

5. Jacquet, O.; Gomes, C. D.; Ephritikhine, M.; Cantat, T. ChemCatChem, 2013, 5, 117-122.

6. S. Savourey, G. Lefèvre, J.-C. Berthet, P. Thuéry, C. Genre, T. Cantat, Angew. Chem. Int. Ed., 2014, 53, 10466-10470.

7. E. Blondiaux, J. Pouessel, T. Cantat, Angew. Chem. Int. Ed, 2014, 53, 12186-12190. 8. Chauvier, C.; Tlili, A.; Gomes, C. D.; Thuéry, P. ; Cantat, T. Chem Sci, 2015, 6, 2938-2942.

9. Cantat T. et al., Patent applications n° WO 2012/137152, PCT/IB2013/054601, PCT/IB2013/054599, PCT/IB2013/059304, PCT/IB2014/060356, PCT/IB2015/054567, PCT/IB2015/054570.

10. E. Feghali, G. Carrot, P. Thuéry, C. Genre, T. Cantat, Energy Environ. Sci., 2015, 8, 2734-2743.

Reductive Transformations of CO

2

and Lignin

Using Molecular Catalysts

Thibault CANTAT

NIMBE, CEA, CNRS, Université Paris-Saclay, 91191 Gif-sur-Yvette, France

E-Mail : [email protected]

Support informatique : PC

With 95 % of organic chemical commodities deriving from fossil resources, the chemical industry is currently exploring novel and renewable carbon feedstocks for the production of both bulk and fine chemicals.1 In this context, the utilization of CO

2 or products derived from biomass wastes is an

attractive strategy to access value-added products. Because these carbon sources feature carbon atoms in an oxidized state, the development of reduction methods is needed and they call for the design of efficient catalysts able to break strong C−O and C=O bonds.

Over the last years, our group has developed novel catalytic reactions for the conversion of CO2 to

formamides, N-heterocycles, methylamines and methanol, using hydroboranes, hydrosilanes or formic acid as reductants.2-9 In parallel, we have developed an unprecedented strategy to isolate

simple aromatics, in a pure form, from natural lignin in 15 different wood species.9-10 These new

catalytic transformations rely on the use of simple organocatalysts or Zn, Fe and Ru organometallic complexes. The mechanisms at play in these transformations will be presented, based on DFT calculations and isolation of reactive catalytic intermediates.

Références

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