Diels-Alder cycloaddition of 2-methylfuran and ethylene for renewable toluene

Applied Catalysis B: Environmental

Volumn 180, Issue , 2016, Pages 487-496

  Green, Sara K ^a,e   Patet, Ryan E ^b,e   Nikbin, Nima ^b,e   Williams, C Luke ^a,e   Chang, Chun Chih ^a,e   Yu, Jingye ^d,e   Gorte, Raymond J ^d,e   Caratzoulas, Stavros ^b,e   Fan, Wei ^a,e   Vlachos, Dionisios G ^b,e   Dauenhauer, Paul J ^c,e  

^a University of Massachusetts   (United States)

^b UNIVERSITY OF DELAWARE   (United States)

^c University of Minnesota   (United States)

^d UNIVERSITY OF PENNSYLVANIA   (United States)

^e Catalysis Center for Energy Innovation   (United States)

Author keywords

Biomass; Diels Alder; Furan; Toluene; Zeolite

Indexed keywords

BIOMASS; CATALYSTS; DEHYDRATION; ETHYLENE; KINETICS; REACTION KINETICS; TOLUENE; ZEOLITES;

CATALYST LOADINGS; DIELS-ALDER; DIELS-ALDER CYCLOADDITIONS; FURAN; KINETIC ANALYSIS; REACTION CHEMISTRY; REACTION PATHWAYS; TRANSITION REGIONS;

CYCLOADDITION;

ALNUS;

EID: 84937108040     PISSN: 09263373     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.apcatb.2015.06.044     Document Type: Article

References (41)

1. Christensen C.H., Rass-Hansen J., Marsden C.C., Taarning E., Egeblad K. ChemSusChem 2008, 1:283-289.
2. Huber G.W., Iborra S., Corma A. Chem. Rev. 2006, 106:4044-4098.
3. Climent M.J., Corma A., Iborra S. Green Chem. 2011, 13:520-540.
4. Carlson T.R., Cheng Y.-T., Jae J., Huber G.W. Energy Environ. Sci. 2011, 4:145-161.
5. Cheng Y., Jae J., Shi J., Fan W., Huber G.W. Angew. Chem. Int. Ed. Engl. 2012, 51:1387-1390.
6. Carlson T.R., a Tompsett G., Conner W.C., Huber G.W. Top. Catal. 2009, 52:241-252.
7. Lligadas G., Ronda J.C., Galià M., Cádiz V. Polymers (Basel) 2010, 2:440-453.
8. Fabri J., Graeser U., Simo T., Xylenes A. Ullmann's Encylopedia Inustrial. Chem. 2012, 643-663.
9. Fruscella W. Kirk-Othmer Encyclopedia of Chemical Technology Online Edition 2015, Vol. 3. John Wiley & Sons Inc.
10. Partenheimer W. Catal Today 1995, 23:69-158.
11. Raes M.C., Proulx O. J. US Patent 1985, 4506040A.
12. Raghavendrachar P., Ramachandran S. Ind Eng. Chem. Res. 1992, 31:453-462.
13. Egeblad K., Rass-hansen J., Marsden C.C., Taarning E., Christensen C.H. Catalysis 2009, 13:13-50.
14. Vennestrøm P.N.R., Osmundsen C.M., Christensen C.H., Taarning E. Angew. Chem. Int. Ed. Engl. 2011, 50:10502-10509.
15. Cheng Y.-T., Huber G.W. Green Chem. 2012, 14:3114.
16. Román-Leshkov Y., Barrett C.J., Liu Z.Y., Dumesic J.A. Nature 2007, 447:982-985.
17. Xiong K., Lee W.-S., Bhan A., Chen J.G. ChemSusChem 2014, 10027:1-5.
18. Jae J., Zheng W., Lobo R.F., Vlachos D.G. ChemSusChem 2013, 6:1158-1162.
19. Panagiotopoulou P., Vlachos D.G. Appl. Catal. A Gen. 2014, 480:17-24.
20. Williams C.L., Chang C., Do P., Nikbin N., Caratzoulas S., Vlachos D.G., Lobo R.F., Fan W., Dauenhauer P. J. ACS Catal. 2012, 935-939.
21. Green K., Williams L., Dauenhauer J., Fan W. Green Chem. 2014, 6:585-588.
22. Mahmoud E., Watson D.A., Lobo R.F. Green Chem. 2014, 16:167-175.
23. Corma A., la Torre O., de Renz M., Villandier N. Angew. Chem. Int. Ed. Engl. 2011, 50:2375-2378.
24. Li G., Li N., Wang Z., Li C., Wang A., Wang X., Cong Y., Zhang T. ChemSusChem 2012, 5:1958-1966.
25. Nikbin N., Caratzoulas S., Vlachos D.G. Appl. Catal. A Gen. 2014, 485:118-122.
26. Chang C.-C., Wang Z Dornath P., Je Cho H Fan W. RSC Adv. 2012, 2:10475-10477.
27. Zhao Y., Truhlar D.G. Theor. Chem. Acc. 2007, 120:215-241.
28. Baerlocher C., McCusker L.B. Int. Zeolite Assoc. 1996.
29. Svensson M., Froese R.D.J., Matsubara T., Sieber S., Morokuma K. J. Phys. Chem. 1996, 100:19357-19363.
30. Rappe A.K., Casewit C.J., Colwell K.S., Goddard W.A., Skiff W.M. J. Am. Chem. Soc. 1992, 114:10024-10035.
31. Frisch M.J., Trucks G.W., Schlegel H.B., Scuseria G.E., Robb M.A., Cheeseman J.R., Scalmani G., Barone V., Mennucci B., Petersson G.A., Nakatsuji H., Caricato M., Li X., Hratchian H.P., Izmaylov A.F., Bloino J., Zheng G., Sonnenberg J.L., Hada M., Ehara M., Toyota K., Fukuda R., Hasegawa J., Ishida M., Nakajima T., Honda Y., Kitao O., Nakai H., Vreven T., Montgomery J.A.J.E.P., Ogliaro F., Bearpark M., Heyd J.J., Brothers E., Kudin K.N., Staroverov V.N., Kobayashi R., Normand J., Raghavachari K., Rendell A., Burant J.C., Iyengar S.S., Tomasi J., Cossi M., Rega N., Millam J.M., Klene M., Knox J.E., Cross J.B., Bakken V., Adamo C., Jaramillo J., Gomperts R., Stratmann R.E., Yazyev O., Austin A.J., Cammi R., Pomelli C., Ochterski J.W., Martin R.L., Morokuma K., Zakrzewski V.G., Voth G.A., Salvador P., Dannenberg J.J., Dapprich S., Daniels A.D., Farkas Ö, Foresman J.B., Ortiz J.V., Cioslowski J., Fox D. J. Gaussian 2009, 09.
32. Nikbin N., Do P.T., Caratzoulas S., Lobo R.F., Dauenhauer P.J., Vlachos D.G. J. Catal. 2013, 297:35-43.
33. Corma A., la Torre O., de Renz M. ChemSusChem 2011, 4:1574-1577.
34. Corma A., la Torre O., de Renz M. Energy Environ. Sci. 2012, 5:6328-6344.
35. Li G., Li N., Yang J., Wang A., Wang X., Cong Y., Zhang T. Bioresour. Technol. 2013, 134:66-72.
36. Sims J., Duke R.E., Strozier R.W., Birge R.R., Sustmann R., Fueno T., Yamaguchi K. J. Am. Chem. Soc. 1973, 95:4094-4096.
37. Patet R.E., Nikbin N., Williams C.L., Green S.K., Chang C.-C., Fan W., Caratzoulas S., Dauenhauer P.J., Vlachos D.G. ACS Catal. 2015, 5:2367-2375.
38. Pacheco J.J., Davis M.E. Proc. Natl. Acad. Sci. U.S.A 2014, 111:1-5.
39. Loudon G. Organic Chemistry 2002, 410. Oxford University Press, New York. 4th ed.
40. Nikbin N., Caratzoulas S., Vlachos D.G. ChemSusChem 2013, 6:2066-2068.
41. Rai N., Caratzoulas S., Vlachos D.G. ACS Catal. 2013, 3:2294-2298.