Please do not adjust margins
RSC Advances
Page 8 of 9
DOI: 10.1039/C5RA09346E
ARTICLE
Journal Name
23 N. Narkhede, S. Singh and A. Patel, Green Chem., 2015, 17
89.
,
,
MCM-41 have been found to be effective catalysts to promote
the formation of GlyC. The catalyst, 30% SiW12/MCM-41 was
found to be better amongst the two and activity was directly
correlated with the higher acidity of the catalyst confirming a
pseudo-liquid type (I) heterogeneous catalysis. The recycling
study showed that both the catalysts could be reused with
minimal loss in the activity. Further the FT-IR analysis confirms
the retention of the structure of Keggin anion in the
regenerated catalysts.
24 E. Skliri, I. N. Lykakisb and G. S. Armatas, RSC Adv., 2014,
8402.
4
25 A. Patel and N. Narkhede, Catal. Sci. Technol., 2013,
26 N. Narkhede, and A Patel, RSC Adv., 2014, , 19294.
3, 3317.
4
27 P. Ferreira, I. M. Fonseca, A. M. Ramos, J. Vital and J. E.
Castanheiro, Appl, Catal. B, 2010, 98, 94.
28 N. Narkhede and A. Patel, J. Porous. Mater., 2014, 21, 579.
29 Y. Yang, Y. Guo, C. Hu and E. Wang, Appl. Catal. A: Gen.,
2003, 252, 305.
30 G. Koyano, K. Ueno and M. Misono, Appl. Catal. A: Gen.,
1999, 181, 267.
31 R. A. Sheldon, M. Walau, I. W. C. E. Arends and U.
Schuchurdt, Acc. Chem. Res., 1998, 31, 485.
32 D-W. Kim, K-A. Park, M-J. Kim, D-H. Kang, J-G. Yang and D-W.
Park, Appl. Catal. A: Gen, 2014, 473, 31.
33 L. Wang, Y. Ma, Y. Wang, S. Liu and Y. Deng, Catal. Commun.,
2011, 12, 1458.
Acknowledgements
Mr. Nilesh Narkhede is thankful to Council of Scientific and
Industrial Research (CSIR), New Delhi, for the award of Senior
Research Fellowship.
Notes and references
1
2
3
4
M. Pagliaro, R. Ciriminna, H. Kimura, M. Rossi and C. Della
Pina, Angew. Chem., Int. Ed., 2007, 46, 4434.
C. H. C. Zhou, J. N. Beltramini, Y. X. Fan and G. Q. M. Lu,
Chem. Soc. Rev., 2008, 37, 527.
N. Dimitratos, J. A. Lopez-Sanchez and G. J. Hutchings, Top.
Catal., 2009, 52, 258.
A. C. Simao, B. Lynikaite-Pukleviciene, C. Rousseau, A.
Tatibouet, S. Cassel, A. Sackus, A. P. Rauter and P. Rollin,
Lett. Org. Chem., 2006,
G. Rokicki, P. Rakoczy, P. Parzuchowski and M. Sobiecki,
Green Chem., 2005, , 529.
L. Ubaghs, N. Fricke, H. Keul and H. Hocker, Macromol. Rapid
Commun., 2004, 25, 517.
V. Plasman and T. Caulier, Plast. Addit. Compd., 2005, 7, 30.
M. Aresta, A. Dibenedetto, F. Nocito, and C. Ferragina, J.
Catal., 2009, 268, 106.
M. A. Pacheco and C. L. Marshall, Energy & Fuels, 1997, 11,
3, 744.
5
6
7
7
8
9
2.
10 A. Dibenedetto, A. Angelini, M. Aresta, J. Ethiraj, C. Fragale,
and F. Nocito, Tetrahedron, 2011, 67, 1308.
11 B. Hammond, J. A. Lopez-sanchez, A. R. Mohd Hasbi, N.
Dimitratos, R. L. Jenkins, A. F. Carley, Q. He, C. J. Kiely, D. W.
Knight, and G. J. Hutchings, Dalton. Trans., 2011, 40, 3927.
12 J. R. Ochoa-Gomez, O. Gomez-Jimenez-Aberasturi, B.
Maestro-Madurga, A. Pesquera-Rodriguez, C. Ramirez-Lopez,
L. Lorenzo-Ibarreta, J. Torrecilla-Soria and M. C. illaran-
Velasco, Appl. Catal., A, 2009, 366, 315.
13 M. J. Climent, A. Corma, P. De Frutos, S. Iborra, M. Noy, A.
Velty and P. Concepcion, J. Catal., 2010, 269, 140.
14 J. B. Li and T. Wang, J. Chem. Thermodyn., 2011, 43, 731.
15 J. W. Yoo and Z. Mouloungui, Stud. Surf. Sci. Catal., 2003,
146, 757.
16 F. R. Marcos, V. C. Casilda, M. A. Banares and J. F. Fernandez,
J. Catal., 2010, 275, 288.
17 J. H. Park, J. S. Choi, S. K. Woo, S. D. Lee, M. Cheong, H. S.
Kim and H. Lee, Appl. Catal.: A, 2012, 433–434, 35.
18 C. R. Kumar, K. Jagadeeswaraiah, P. S. S. Prasad and N.
Lingaiah, Chem. Cat. Chem., 2012, 4, 1360.
19 K. Jagadeeswaraiah, C. R. Kumar, P. S. S. Prasad, S. Loridant
and N. Lingaiah, Appl. Catal.: A, 2014, 469, 165.
20 N. Narkhede and A. Patel, Ind. Eng. Chem. Res., 2013, 52
13637.
,
21 M. Hinoa and K. Arata, Green Chem., 2001, 3, 170.
22 B. Katryniok, S. Paul and F. Dumeignil, Green Chem., 2010,
12, 1910.
8 | J. Name., 2012, 00, 1-3
This journal is © The Royal Society of Chemistry 20xx
Please do not adjust margins