Paper
RSC Advances
2 R. Renner, Environ. Sci. Technol., 2001, 35, 410A.
3 Q. Yang and D. D. Dioonysious, J. Photochem. Photobiol., A,
2004, 165, 229.
University Press, New York, 1998; (b) I. Horvath and
P. T. Anastas, Chem. Rev., 2007, 107, 2167; (c) P. Anastas
and N. Eghbali, Chem. Soc. Rev., 2010, 39, 301; (d)
R. D. MacFarlane and K. Seddon, Aust. J. Chem., 2007, 60, 3.
4 N. Ferlin, M. Courty, S. Gatard, M. Spulak, B. Quilty,
I. Beadham, M. Ghavre, A. H. K. Kummerer, N. Gathergood 25 R. S. Varma and V. V. Namboodiri, Pure Appl. Chem., 2001,
and S. Bouquillon, Tetrahedron, 2013, 69, 6150.
5 K. R. Seddon, Kinet. Catal., 1996, 37, 693.
6 P. Walden, Bull. Acad. Imp. Sci. St.-Petersbourg, 1914, 8, 405.
7 M. Deetlefs and K. R. Seddon, Chim. Oggi, 2006, 24, 16.
73, 1309.
26 A. Negrea, L. Lupa, M. Ciopec, P. Negrea and I. Hulka, Int. J.
Chem. Kinet., 2014, 5, 424.
27 M. Deetlefs and K. R. Seddon, Green Chem., 2003, 5, 181.
8 S. Keskin, D. Kayrak-Talay, U. Akman and O. Hortacsu, J. 28 (a) A. de Fatima, S. Barreto, O. E. Vercillo, C. Kleber,
Supercrit. Fluids, 2007, 43, 150.
Z. Andrade and J. Braz, Chem. Soc., 2011, 22, 462; (b)
Y. Zhu, W. Wang, R. Qi and X. Hu, Angew. Chem., 2004,
116, 1434; (c) A. Aupoix, B. Pegot and G. Vo-Thanh,
Tetrahedron, 2010, 66, 1352; (d) H. Hu, H. Yang, P. Huang,
D. Cui, Y. Peng, J. Zhang, F. Lu, J. Lian and D. Shi, Chem.
Commun., 2010, 46, 3866; (e) J. Pan, J. Fu, S. Deng and
X. Lu, Energy Fuels, 2014, 28, 1380.
9 A. E. Visser, R. P. Swatloski, W. M. Reichert, R. Mayton,
S. Sheff, A. Wierzbicki, J. J. H. Davis and R. D. Rogers,
Chem. Commun., 2001, 1, 135.
10 Y. Nie, C. X. Li and Z. H. Wang, Ind. Eng. Chem. Res., 2007, 46,
5108.
11 N. V. Plechkova and K. R. Seddon, Ionic liquids: ‘Designer’
solvents for green chemistry, in Methods and Reagents for 29 K. M. Docherty and C. F. Kulpa, Green Chem., 2005, 7, 185.
Green Chemistry: An Introduction, ed. P. Tundo, A. Perosa 30 (a) L. H. Dong, D. D. Liang and R. C. Gong, Eur. J. Inorg.
and F. Zecchini, John Wiley, New York, 2007, pp. 105–130.
12 (a) L. Carson, P. K. W. Chau, M. J. Earle, M. A. Gilea,
B. F. Gilmore, S. P. Gorman, M. T. McCanna and
K. R. Seddonb, Green Chem., 2009, 11, 492; (b) C. Lagrost,
D. Carriei, M. Vaultier and P. Hapiot, J. Phys. Chem. A,
2005, 51, 745.
13 A. Shariati and C. J. Peters, J. Supercrit. Fluids, 2005, 34, 171.
14 A. Zarrouk, M. Messali, H. Zarrok, R. Salghi, A. A. Ali,
B. Hammouti, S. S. Al-Deyab and F. Bentiss, Int. J.
Electrochem. Sci., 2012, 7, 6998.
Chem., 2012, 3200; (b) P. Skehan, R. Storeng, D. Scudiero,
A. Monks, J. McMahon, D. Vistica, J. T. Warren,
H. Bokesch, S. Kenney and M. R. Boyd, J. Natl. Cancer Inst.,
1990, 82, 1107; (c) T. Satyavani, Y. Mohini, M. S. L. Karuna,
R. B. N. Prasad, C. G. Kumar, M. Poornima and P. Sujitha,
Med. Chem. Res., 2014, 23, 3617; (d) G. C. Ramaprasad,
B. Kalluraya and B. S. Kumar, Med. Chem. Res., 2014, 23,
3644; (e) B. Umesha and Y. B. Basavaraju, Med. Chem. Res.,
2014, 23, 3744; (f) R. Raj, V. Sharma, M. J. Hopper,
N. Patel, D. Hall, L. A. Wrischnik, K. M. Land and
V. Kumar, Med. Chem. Res., 2014, 23, 3671; (g) S. Eriskin,
N. Sener, S. Yavuz and I. Sener, Med. Chem. Res., 2014, 23,
3733; (h) M. Pamerla, D. R. S. Reddy, B. S. Rao, N. Bodipati
and Y. L. N. Murthy, Med. Chem. Res., 2014, DOI: 10.1007/
s00044-014-1159-x.
15 L. A. Blanchard, D. Hancu, E. J. Beckman and
J. F. Brennecke, Nature, 1999, 399, 28.
16 J. F. Liu, G. B. Jiang, Y. G. Chi, Y. Q. Cai, Q. X. Zhou and
J. T. Hu, J. Anal. Chem., 2003, 75, 5870.
17 J. F. Brennecke and E. J. Magin, AIChE J., 2001, 47, 2384.
18 M. Ue, M. Takeda, A. Toriumi, A. Kominato, R. Hagi-wara 31 (a) X. Hou, Q. Liu, T. J. Smith, N. Li and M. Zong, PLoS One,
ˇ
´
and Y. Ito, J. Electrochem. Soc., 2003, 150, A499.
19 A. Balducci, U. Bardi, S. Caporali, M. Mastragostino and
F. Soavi, Electrochem. Commun., 2004, 6, 566.
20 A. B. Mc-Ewen, H. L. Ngo, K. L. Compte and J. L. Goldman, J.
Electrochem. Soc., 1999, 146, 1687.
21 C. M. Gordon, J. D. Holbrey, A. R. Kennedy and K. R. Seddon,
J. Mater. Chem., 1998, 8, 2627.
22 (a) W. Chen and F. Liu, J. Organomet. Chem., 2003, 673, 5; (b)
F. Mazille, Z. Fei, D. Kuang, D. Zhao, S. M. Zakeeruddin,
M. Gratzel and P. J. Dyson, Inorg. Chem., 2006, 45, 1585; (c)
2013, 8, 59145; (b) L. Myles, R. Gore, M. Spulak,
N. Gathergood and S. J. Connon, Green Chem., 2010, 12,
1157; (c) M. Ghavre, O. Byrne, L. Altes, P. K. Surolia,
M. Spulak, B. Quilty, K. R. Thampi and N. Gathergood,
Green Chem., 2014, 16, 2252; (d) R. D. Kamble, S. V. Hese,
R. J. Meshram, J. R. Kote, R. N. Gacche and B. S. Dawane,
Med. Chem. Res., 2014, DOI: 10.1007/s00044-014-1165-z; (e)
P. N. Dube, S. S. Bule, Y. V. Ushir, M. R. Kumbhare and
P. R. Dighe, Med. Chem. Res., 2014, DOI: 10.1007/s00044-
014-1201-z.
N. Brausch, A. Metlen and P. Wasserscheid, Chem. 32 (a) Y. Zhang, L. Zhang, L. Liu, J. Guo, D. Wu, G. Xu, X. Wang
Commun., 2004, 10, 1552.
and D. Jia, Inorg. Chim. Acta, 2010, 363, 289; (b) M. Zhao,
Y. Cui, J. Yu, S. Xu and X. Guo, J. Sep. Sci., 2014, 37, 151;
(c) P. Khloya, P. Kumar, A. Mittal, N. K. Aggarwal and P. K
Sharma, Bioorg. Med. Chem. Lett., 2013, 3, 9; (d) X. Li, X. Li,
H. Liu, X. Zhou and Z. Shao, Bioorg. Med. Chem. Lett.,
2012, 2, 26.
23 (a) Z. Fei, D. Zhao, T. J. Geldbach, R. Scopelliti and
P. J. Dyson, Chem.–Eur. J., 2004, 10, 4886; (b) D. Li, F. Shi,
J. Peng, S. Guo and Y. Deng, J. Org. Chem., 2004, 69, 3582;
(c) S. Kim, Y. J. Kim, J. Y. Bae, S. J. Kim, M. S. Lah and
C. S. Chin, Organomet. Chem., 2003, 22, 2498; (d) D. Zhao,
Z. Fei, C. A. Ohlin, G. Laurenczy and P. J. Dyson, Chem. 33 (a) D. Demberelnyamba, M. Ariunaa and Y. K. Shim, Int. J.
Commun., 2004, 19, 2500; (e) K. R. Seddon, A. Stark and
M. J. Torres, Pure Appl. Chem., 2000, 72, 2275.
24 (a) P. T. Anastas and J. C. Warner, in Green Chemistry: Theory
and Practice, ISBN 0198502346, 9780198502340, Oxford
Mol. Sci., 2008, 9, 864; (b) V. Kumar and S. V. Malhotra,
Bioorg. Med. Chem. Lett., 2009, 19, 4643; (c) J. Feder-Kubis
and K. Tomczuk, Tetrahedron, 2013, 69, 4198; (d)
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