Carboxylic acid functionalized imidazolium-based ionic liquids: Efficient catalysts for cycloaddition of CO 2 and epoxides

Reaction Kinetics, Mechanisms and Catalysis

Volumn 106, Issue 1, 2012, Pages 25-35

  Han, Lina ^a   Choi, Soo Jin ^a   Park, Moon Seok ^a   Lee, Seon Myong ^a   Kim, Yu Jin ^a   Kim, Moon Il ^a   Liu, Binyuan ^b   Park, Dae Won ^a  

^a Pusan National University   (South Korea)

^b HEBEI UNIVERSITY OF TECHNOLOGY   (China)

Author keywords

Catalyst; CO 2; Cyclic carbonate; Ionic liquids

Indexed keywords

ALKYL CHAIN LENGTHS; COCATALYST; COUPLING REACTION; CYCLIC CARBONATES; CYCLOADDITION REACTION; EFFICIENT CATALYSTS; FUNCTIONAL MOIETIES; FUNCTIONALIZED; HALIDE IONS; HOMOGENEOUS CATALYST; IMIDAZOLIUM-BASED IONIC LIQUID; MOLECULAR COMPOSITIONS; REACTION PARAMETERS; STYRENE CARBONATES; STYRENE OXIDE;

CARBOXYLIC ACIDS; CATALYSTS; CYCLOADDITION; IONIC LIQUIDS; ORGANIC SOLVENTS; STYRENE;

CARBON DIOXIDE;

EID: 84860509080     PISSN: 18785190     EISSN: 18785204     Source Type: Journal    
DOI: 10.1007/s11144-011-0399-8     Document Type: Article

References (47)

1. KM Kerry Yu MY Yeung Connie SC Tsang 2007 J Am Chem Soc 129 6360 10.1021/ja0706302
2. DH Gilbson 1996 Chem Rev 96 2063 10.1021/cr940212c
3. PT Anastas 2003 Green Chem 5 G29 10.1039/b211620k
4. C Song 2006 Catal Today 115 2 10.1016/j.cattod.2006.02.029 1:CAS:528:DC%2BD28XkvF2ltb4%3D
5. P Tundo A Perosa 2002 Chem Rec 2 13 10.1002/tcr.10007 1:CAS:528:DC%2BD38XhsFCnsLw%3D
6. M Shi YM Shen 2003 Curr Org Chem 7 737 10.2174/1385272033486693 1:CAS:528:DC%2BD3sXivVemurw%3D
7. PG Jessop T Ikariya R Noyori 1999 Chem Rev 99 475 10.1021/cr970037a 1:CAS:528:DyaK1MXos1el
8. S Zhang Y Chen F Li X Lu WB Dai R Mori 2006 Catal Today 115 61 10.1016/j.cattod.2006.02.021 1:CAS:528:DC%2BD28XkvF2ksrc%3D
9. N Kihara N Hara T Endo 1993 J Org Chem 58 6198 10.1021/jo00075a011 1:CAS:528:DyaK3sXmslSgsLw%3D
10. JW Huang M Shi 2003 J Org Chem 68 6705 10.1021/jo0348221 1:CAS:528:DC%2BD3sXls1egsL4%3D
11. T Zhao Y Han Y Sun 1999 Phys Chem Chem Phys 1 3047 10.1039/a901943j 1:CAS:528:DyaK1MXjsFekt7w%3D
12. Yano T, Matsui H, Kokie T, Ishiguro H, Fujihara H, Yoshihara M, Maeshima T (1997) Chem Commun 1129
13. K Yamaguchi K Ebitani T Yoshida H Yoshida K Kaneda 1999 J Am Chem Soc 121 4526 10.1021/ja9902165 1:CAS:528:DyaK1MXisFGlt74%3D
14. M Tu RJ Davis 2001 J Catal 199 85 10.1006/jcat.2000.3145 1:CAS:528:DC%2BD3MXit1aiurc%3D
15. BM Bhanage S Fujita Y Ikushima M Arai 2001 Appl Catal A 219 259 10.1016/S0926-860X(01)00698-6 1:CAS:528:DC%2BD3MXmsFWjtL4%3D
16. WN Sit SM Ng KY Kwong CP Lau 2005 J Org Chem 70 8583 10.1021/jo051077e 1:CAS:528:DC%2BD2MXpvFCnu7k%3D
17. JL Jiang F Gao R Hua X Qiu 2005 J Org Chem 70 381 10.1021/jo0485785 1:CAS:528:DC%2BD2cXhtVSmtLvI
18. HS Kim JJ Kim SD Lee MS Lah D Moon HG Jang 2003 Chem Eur J 9 678 10.1002/chem.200390076 1:CAS:528:DC%2BD3sXhtlSjs7w%3D
19. SD Allen DR Moore EB Lobkovsky GW Coates 2002 J Am Chem Soc 124 14284 10.1021/ja028071g 1:CAS:528:DC%2BD38XosFWhsbk%3D
20. T Aida S Inoue 1983 J Am Chem Soc 105 1304 10.1021/ja00343a038 1:CAS:528:DyaL3sXht1Ggsr0%3D
21. YM Shen WL Duan M Shi 2004 Eur J Org Chem 14 3080 10.1002/ejoc.200400083
22. Y Du F Cai DL Kong LN He 2005 Green Chem 7 518 10.1039/b500074b 1:CAS:528:DC%2BD2MXltl2murg%3D
23. L Han HJ Choi DK Kim SW Park B Liu DW Park 2011 J Mol Catal A 338 58 1:CAS:528:DC%2BC3MXjsFyrtrY%3D
24. WL Dai L Chen SF Yin WH Li YY Zhang SL Luo CT Au 2010 Catal Lett 137 74 10.1007/s10562-010-0346-8 1:CAS:528:DC%2BC3cXltVaktLc%3D
25. Yu JI, Choi HJ, Selvaraj M, Park DW (2011) React kinet Mech Catal 102:353
26. V Caló A Nacci A Monopoli A Fanizzi 2002 Org Lett 4 2561 10.1021/ol026189w
27. JQ Wang DL Kong JY Chen F Cai LN He 2006 J Mol Catal A 249 143 10.1016/j.molcata.2006.01.008 1:CAS:528:DC%2BD28XjslCksLg%3D
28. H Yasuda LN He T Sakakura C Hu 2005 J Catal 233 119 10.1016/j.jcat.2005. 04.030 1:CAS:528:DC%2BD2MXltlersb4%3D
29. H Kawanami A Sasaki K Matsui Y Ikushima 2003 Chem Commun 7 896 10.1039/b212823c
30. F Li L Xiao C Xia B Hu 2004 Tetrahedron Lett 45 8307 10.1016/j.tetlet. 2004.09.074 1:CAS:528:DC%2BD2cXotlSntbY%3D
31. J Sun SI Fujita F Zhao M Arai 2004 Green Chem 6 613 10.1039/b413229g 1:CAS:528:DC%2BD2cXhtVSitLbF
32. H Yasuda LN He T Sakakura 2002 J Catal 209 547 10.1006/jcat.2002.3662 1:CAS:528:DC%2BD38XltVagu7o%3D
33. LN He H Yasuda T Sakakura 2003 Green Chem 5 92 10.1039/b210007j 1:CAS:528:DC%2BD3sXhtFSgtLk%3D
34. HS Kim JJ Kim HN Kwon MJ Chung BG Lee HG Jang 2002 J Catal 205 226 10.1006/jcat.2001.3444 1:CAS:528:DC%2BD3MXpt1aquro%3D
35. GL Daniel HS Brent 2005 J Catal 232 386 10.1016/j.jcat.2005.03.015
36. YM Shen WL Duan M Shi 2003 Adv Synth Catal 345 337 10.1002/adsc.200390035 1:CAS:528:DC%2BD3sXisVCgtbk%3D
37. SS Wu XW Zhang WL Dai SF Yin WS Li YQ Ren CT Au 2008 Appl Catal A 341 106 10.1016/j.apcata.2008.02.021 1:CAS:528:DC%2BD1cXls1SjsL4%3D
38. J Sun J Ren S Zhang W Cheng 2009 Tetrahedron Lett 50 423 10.1016/j.tetlet.2008.11.034 1:CAS:528:DC%2BD1cXhsFWjurfM
39. A Zhu T Jiang BX Han J Zhang Y Xie X Ma 2007 Green Chem 9 169 10.1039/b612164k 1:CAS:528:DC%2BD2sXhsFWksLw%3D
40. SV Dzyuba RA Bartsch 2002 Tetrahedron Lett 43 4657 10.1016/S0040-4039(02) 00858-4 1:CAS:528:DC%2BD38XksFKlsr8%3D
41. LC Branco JN Rosa JJM Ramos CAM Afonso 2002 Chem Eur J 8 3671 10.1002/1521-3765(20020816)8:16<3671::AID-CHEM3671>3.0.CO;2-9 1:CAS:528:DC%2BD38Xmslequ70%3D
42. X Mi S Luo H Xu L Zhang J Cheng 2006 Tetrahedron 62 2537 10.1016/j.tet.2005.12.045 1:CAS:528:DC%2BD28XhvVSitbg%3D
43. J Sun S Zhang W Cheng J Ren 2008 Tetrahedron Lett 49 3588 10.1016/j.tetlet.2008.04.022 1:CAS:528:DC%2BD1cXlvVSrur8%3D
44. Y Zhou S Hu X Ma S Liang T Jiang B Han 2008 J Mol Catal A 284 52 10.1016/j.molcata.2008.01.010 1:CAS:528:DC%2BD1cXjtl2ht7Y%3D
45. M North R Pasquale C Young 2010 Green Chem 12 1514 10.1039/c0gc00065e 1:CAS:528:DC%2BC3cXhtFWqsbvF
46. SG Zlotin NN Makhova 2010 Russ Chem Rev 79 543 10.1070/ RC2010v079n07ABEH004156 1:CAS:528:DC%2BC3cXhsVCit7vJ
47. EH Lee JY Ahn MM Dharman DW Park SW Park I Kim 2008 Catal Today 131 130 10.1016/j.cattod.2007.10.012 1:CAS:528:DC%2BD1cXhtV2jsL8%3D