Graphene Oxide as Catalyst for the Acetalization of Aldehydes at Room Temperature

ChemCatChem

Volumn 4, Issue 12, 2012, Pages 2026-2030

  Dhakshinamoorthy, Amarajothi ^a,b   Alvaro, Mercedes ^b   Puche, Marta ^a   Fornes, Vicente ^a   Garcia, Hermenegildo ^a  

^a CSIC   (Spain)

^b UNIVERSITAT POLITÈCNICA DE VALÈNCIA   (Spain)

Author keywords

Acetalization; Acid catalysis; Graphene oxide; Heterogeneous catalysis; Sustainable processes

Indexed keywords

ACETALIZATION; ACID CATALYSIS; ACTIVE SITE; GRAPHENE OXIDES; HETEROGENEOUS CATALYST; HIGH ACTIVITY; LARGE SURFACE AREA; ROOM TEMPERATURE; SPECTROSCOPIC DATA; SULFATE GROUPS; SUSTAINABLE PROCESS; SUSTAINABLE RESOURCES;

ALDEHYDES; CATALYSIS; METHANOL; ORGANIC COMPOUNDS; TRANSITION METALS;

CATALYST ACTIVITY;

EID: 84870467166     PISSN: 18673880     EISSN: 18673899     Source Type: Journal    
DOI: 10.1002/cctc.201200461     Document Type: Article

References (24)

1. R. M. Westervelt, Science 2008, 320, 324.
2. M. Latorre-Sanchez, P. Atienzar, G. Abellan, M. Puche, V. Fornes, A. Ribera, H. Garcia, Carbon 2012, 50, 518.
3. X. Huang, X. Qi, F. Boey, H. Zhang, Chem. Soc. Rev. 2012, 41, 666.
4. X. An, J. C. Yu, RSC Adv. 2011, 1, 1426.
5. G. Liao, S. Chen, X. Quan, H. Yu, H. Zhao, J. Mater. Chem. 2012, 22, 2721.
6. V. Stengl, D. Popelkova, P. Vlacil, J. Phys. Chem. C 2011, 115, 25209.
7. Y. Zheng, J. Liu, J. Liang, M. Jaroniec, S. Z. Qiao, Energy Environ. Sci. 2012, 5, 6717.
8. G. Ning, Z. Fan, G. Wang, J. Gao, W. Qian, F. Wei, Chem. Commun. 2011, 47, 5976.
9. B. F. Machado, P. Serp, Catal. Sci. Technol. 2012, 2, 54.
10. J. Pyun, Angew. Chem. 2011, 123, 46; Angew. Chem. Int. Ed. 2011, 50, 46.
11. D. R. Dreyer, C. W. Bielawski, Chem. Sci. 2011, 2, 1233.
12. W. S. Hummers, R. E. Offeman, J. Am. Chem. Soc. 1958, 80, 1339.
13. H.-P. Jia, D. R. Dreyer, C. W. Bielawski, Adv. Synth. Catal. 2011, 353, 528.
14. D. R. Dreyer, H.-P. Jia, A. D. Todd, J. Geng, C. W. Bielawski, Org. Biomol. Chem. 2011, 9, 7292.
15. H.-P. Jia, D. R. Dreyer, C. W. Bielawski, Tetrahedron 2011, 67, 4431.
16. D. R. Dreyer, K. A. Jarvis, P. J. Ferreira, C. W. Bielawski, Macromolecules 2011, 44, 7659.
17. D. R. Dreyer, H.-P. Jia, C. W. Bielawski, Angew. Chem. 2010, 122, 6965; Angew. Chem. Int. Ed. 2010, 49, 6813.
18. F. Liu, J. Sun, L. Zhu, X. Meng, C. Qi, F.-S. Xiao, J. Mater. Chem. 2012, 22, 5495.
19. A. Dhakshinamoorthy, M. Alvaro, P. Concepcion, V. Fornes, H. Garcia, Chem. Commun. 2012, 48, 5443.
20. X. Li, Y. Jiang, L. Shuai, L. Wang, L. Meng, X. Mu, J. Mater. Chem. 2012, 22, 1283.
21. P. Bradder, S. K. Ling, S. Wang, S. Liu, J. Chem. Eng. Data 2011, 56, 138.
22. Y. Gao, D. Ma, C. Wang, J. Guan, X. Bao, Chem. Commun. 2011, 47, 2432.
23. A. Dhakshinamoorthy, M. Alvaro, H. Garcia, Adv. Synth. Catal. 2010, 352, 3022.
24. D. C. Marcano, D. V. Kosynkin, J. M. Berlin, A. Sinitskii, Z. Sun, A. Slesarev, L. B. Alemany, W. Lu, J. M. Tour, ACS Nano 2010, 4, 4806-4814.