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Catalysis Science & Technology
Page 11 of 12
Journal Name
DOI: 10.1039/C7CY01687E
ARTICLE
11 S. Menuel, B. Léger, A. Addad, E. Monflier and F. Hapiot,
Green Chem., 2016, 18, 5500.
12 R. Herbois, S. Noël, B. Leger, L. Bai, A. Roucoux, E. Monflier
and A. Ponchel, Chem. Commun., 2012, 48, 3451.
13 S. Kuklin, A. Maximov, A. Zolotukhina and E. Karakhanov,
Catal. Commun., 2016, 73, 63.
14 A. Denicourt-Nowicki, A. Ponchel, E. Monflier and A.
Roucoux, Dalton Trans., 2007, 43, 5714.
15 R. Herbois, S. Noël, B. Léger, S. Tilloy, S. Menuel, A. Addad, B.
distributions. The physical features of the colloidal suspensions
remained practically unaffected by the pH change (from pH 10
down to pH 4). The beneficial impact of the different
interactions (steric-type, electrostatic-type and host-guest-
type) within this novel polymer of
the model reaction of 1-
β-CD was demonstrated in
tetradecene. The positive results were successfully extended
to a wide range of substrates (long-alkyl chain olefins,
aromatics and FAMEs) as well as derivatives bearing carboxylic
acid substituents. This catalytic system could be readily
recycled and reused for several runs, demonstrating its high
resistance against aggregation and deactivation during
catalysis. These results open up promising perspectives for the
hydrogenation of even more sophisticated substrates, such as
lignin derivatives or bio-oils.
Martel, A. Ponchel and E. Monflier, Green Chem., 2015, 17
2444.
,
16 J. Schulz, S. Levigne, A. Roucoux and H. Patin, Adv. Synth.
Catal., 2002, 344, 266.
17 J. Junthip, N. Tabary, L. Leclercq and B. Martel, Carbohydr.
Polym., 2015, 126, 156.
18 O. Egyed, Vib. Spectrosc., 1990, 1, 225.
19 A. Ponchel, S. Abramson, J. Quartararo, D. Bormann, Y.
Barbaux and E. Monflier, Microporous Mesoporous Mater.,
2004, 75, 261.
20 P. Swain, C. Mallika, C. Jagadeeswara Rao, U. Kamachi
Mudali and R. Natarajan, J. Appl. Electrochem., 2015, 45,
Conflicts of interest
209.
21 K. Q. Ferreira and E. Tfouni, J. Braz. Chem. Soc., 2010, 21
There are no conflicts to declare.
,
1349.
22 M. Askari, Y. Xiao, P. Li and T.-S. Chung, J. Memb. Sci., 2012,
390–391, 141.
23 H. Madhavaram, H. Idriss, S. Wendt, Y. D. Kim, M. Knapp, H.
Over, J. Aßmann, E. Löffler and M. Muhlerz, J. Catal., 2001,
202, 296.
Acknowledgements
Chevreul Institute (FR 2638), Ministère de l’Enseignement
Supérieur et de la Recherche, Région Nord – Pas de Calais and
FEDER are acknowledged for supporting and funding partially
this work. The TEM and XPS facilities in Lille (France) are
supported by the Conseil Régional du Nord-Pas de Calais, and
the European Regional Development Fund (ERDF). The authors
are grateful to Dr. Nicolas Kania (UCCS, University of Artois) for
technical assistance in FTIR and TGA measurements. The
authors are grateful to Dr. Ahmed Addad (UMET, University of
Lille 1) for technical assistance in TEM measurements and to
M. Trentesaux ans Dr. P. Simon for XPS analysis.
24 G. W. Morey and H. E. Merwin, J. Am. Chem. Soc., 1936, 58
2248.
,
25 J. Potier, S. Menuel, D. Fournier, S. Fourmentin, P. Woisel, E.
Monflier and F. Hapiot, ACS Catal., 2012, , 1417.
2
26 S. Noel, B. Leger, R. Herbois, A. Ponchel, S. Tilloy, G. Wenz
and E. Monflier, Dalton Trans., 2012, 41, 13359.
27 K. Sadrerafi, E. E. Moore and M. W. Lee, J. Incl. Phenom.
Macrocycl. Chem., 2015, 83, 159.
28 Y.-H. Wang, M.-Z. Zhu, X.-Y. Ding, J.-P. Ye, L. Liu and Q.-X.
Guo, J. Phys. Chem. B, 2003, 107, 14087.
29 F. Hapiot, L. Leclercq, N. Azaroual, S. Fourmentin, S. Tilloy
and E. Monflier, Curr. Org. Synth., 2008, 5, 162.
30 M. Besson, P. Gallezot and C. Pinel, Chem. Rev., 2014, 114
,
1827.
31 M. Niu, Y. Wang, W. Li, J. Jiang, Z. Jin, Catal. Commun., 2016,
38, 77.
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