Green Chemistry References

1. Bush, G. W. The White House, 2005; whitehouse.gov/news/releases/2005/05/ 20050518-4.html

2. Moore, M. Stupid White Men, Penguin, London, 2002.

3. BBC, BBC News Online, 2005; http://news.bbc.co.uk/1/hi/sci/tech/3143798.stm

4. United Nations Framework Convention on Climate Change, Kyoto Protocol, 1997; http://unfccc.int/resource / docs / convkp /kpeng.html

5. U.S. Environmental Protection Agency, Global Warming—Climate, 2000; http://yose-mite.epa.gov / oar/globalwarming.nsf / content/climate.html

6. U.S. Environmental Protection Agency, The Potential Effects of Global Climate Change on The United States, 1989; http://yosemite.epa.gov/oar/globalwarming.nsf/ UniqueKeyLookup/RAMR5CKNNG/$File/potential_effects.pdf

7. Anastas, P. T.; Warner, J. Green Chemistry: Theory and Practice, Oxford University Press, Oxford, 1998.

8. Environment Agency (UK), Greenhouse Gas Emissions, 2005; environment-agency.gov.uk/yourenv /432430/432434/432446/435321 / ?lang = _e

9. U.S. Environmental Protection Agency, High Global Warming Potential (GWP) Gases, 2004; epa.gov/highgwp/

10. Seddon, K. R., Room-temperature ionic liquids—neoteric solvents for clean catalysis, Kinet. Catal., 1996, 37(5), 693-697; Seddon, K. R. Room-temperature ionic liquids— neoteric solvents for clean catalysis, Kinet. Katal., 1996, 37(5), 743-748.

11. Seddon, K. R. Ionic liquids for clean technology, J. Chem. Technol. Biotechnol., 1997, 68(4), 351-356; Seddon, K. R. Ionic liquids for clean technology: an update, in Molten Salt Forum: Proceedings of the 5th International Conference on Molten Salt Chemistry and Technology, Wendt, H. (Ed.), Vol. 5-6, 1998, pp. 53-62.

12. Ertl, G.; Knozinger, H.; Weitkamp, J. (Eds.) Handbook of Heterogeneous Catalysis, 5 Volume Set VCH, Weinheim, 1997.

13. Sheldon, R. A., Consider the environmental quotient, Chemtech, 1994, 24(3), 38-47; Sheldon, R. A., The role of catalysis in waste minimization, in Precision Process

Technology: Perspectives for Pollution Prevention, Weijnen M. P. C.; Drinkenburg A. A. H. (Eds.), Kluwer, Dordrecht, The Netherlands, 1993, pp. 125-138.

14. Kolb, H. C.; Finn, M. G.; Sharpless, K. B. Click chemistry: diverse chemical function from a few good reactions, Angew. Chem., Int. Ed., 2001, 40, 2004-2021; Klijn, J. E. Engberts, J. B. F. N., Organic chemistry: fast reactions "on water", Nature, 2005, 435, 746-747, 900; Narayan, S.; Muldoon, J.; Finn, M. G.; et al. "On water": unique reactivity of organic compounds in aqueous suspension, Angew. Chem., Int. Ed., 2005, 44(21), 3275-3279; Li, C.-J.; Chan, T.-H. Organic Reactions in Aqueous Media, Wiley, New York, 1997; Grieco, P. A. (Ed.) Organic Synthesis in Water, Blackie, London, 1998.

15. Poliakoff, M.; Fitzpatrick, J. M.; Farren, T. R.; Anastas, P. T. Green chemistry: science and politics of change, Science, 2002, 297, 807-810; Freemantle, M. Green process uses ionic liquid and CO2, Chem. Eng. News, 1999, 77(19), 9.

16. Thomas Swan & Co., 2005, thomas-swan.co.uk/

17. Ohno, H. (Ed.) Electrochemical Aspects of Ionic Liquids, Wiley-Interscience, Hoboken, NJ, 2005; Ohno, H. (Ed.) Ionic Liquids: The Front and Future of Material Development, CMC Press, Tokyo, 2003.

18. Rogers, R. D., Seddon, K. R. (Eds.) Ionic Liquids as Green Solvents: Progress and Prospects, ACS Symposium Series, No. 856, American Chemical Society, Washington D.C., 2003.

19. Rogers, R. D.; Seddon, K. R. (Eds.) Ionic Liquids: Industrial Applications for Green Chemistry, ACS Symposium Series, No. 818, American Chemical Society, Washington D.C., 2002.

20. Rogers, R. D.; Seddon, K. R.; Volkov, S. (Eds.) Green Industrial Applications of Ionic Liquids, NATO Science Series II: Mathematics, Physics and Chemistry, Vol. 92, Kluwer, Dordrecht, The Netherlands, 2002.

21. Wasserscheid, P.; Welton, T. (Eds.) Ionic Liquids in Synthesis, Wiley-VCH, Weinheim, 2003.

22. Rogers, R. D.; Seddon, K. R. (Eds.) Ionic Liquids IIIB: Fundamentals, Progress, Challenges, and Opportunities—Transformations and Processes, ACS Symposium Series, No. 902, American Chemical Society, Washington D.C., 2005; Rogers, R. D.; Seddon, K. R. (Eds.) Ionic Liquids IIIA: Fundamentals, Progress, Challenges, and Opportunities—Properties and Structure, ACS Symposium Series, No. 901, American Chemical Society, Washington D.C., 2005.

23. Earle, M. J.; Seddon, K. R.; McCormac, P. B. The first high yield green route to a pharmaceutical in a room temperature ionic liquid, Green Chem., 2000, 2(6), 261-262.

24. Allen, D.; Baston, G.; Bradley, A. E.; et al. An investigation of the radiochemical stability of ionic liquids, Green Chem., 2002, 4(2), 152-158.

25. Gratzel, M. Highly efficient nanocrystalline photovoltaic devices, Plat. Met. Rev., 1994, 38, 151-159; Gratzel, M. Dye-sensitized solar cells, J. Photochem. Photobiol. C-Photochem. Rev., 2003, 4(2), 145-153.

26. Kitazume, T. Organic synthesis in ionic liquids, Kagaku Kogyo, 2000, 51(6), 437-444.

27. Hagiwara, R., Ito, Y. Room temperature ionic liquids of alkylimidazolium cations and fluoroanions, J. Fluorine Chem., 105(2), 2000, 221-227; Welton, T. Room-temperature Ionic Liquids. Solvents for Synthesis and Catalysis, Chem. Rev., 1999, 99, 2071-2084;

Olivier, H. Recent developments in the use of non-aqueous ionic liquids for two-phase catalysis, J. Mol. Catal. A: Chem., 1999,146(1-2), 285-289.

28. Earle, M. J., Seddon, K. R. Ionic liquids. Green solvents for the future, Pure Appl. Chem., 2000 72(7), 1391-1398; Earle, M. J.; Seddon, K. R. Ionic liquids: green solvents for the future, in Clean Solvents: Alternative Media for Chemical Reactions and Processing, Abraham M.; Moens, L. (Eds.) ACS Symposium Series, No. 819, American Chemical Society, Washington, D.C., 2002), pp. 10-25; Earle, M. J. Ionic liquids: solvents for the twenty-first century, in Ionic Liquids: Industrial Applications for Green Chemistry, Rogers R. D., Seddon, K. R. (Eds) ACS Symposium Series, No. 818, American Chemical Society, Washington D.C., 2002, pp. 90-105.

29. Rooney, D. W., Seddon, K. R. Ionic liquids, in Handbook of Solvents, G. Wypych (Ed.), ChemTech Publishing, Toronto, 2001, pp. 1459-1484.

30. Ott, L. S.; Cline, M. L.; Deetlefs, M. et al. Nanoclusters in ionic liquids: evidence for N-heterocyclic carbene formation from imidazolium-based ionic liquids detected by H-2 NMR, J. Am. Chem. Soc., 2005, 127(16), 5758-5759; Hamill, N. A., Hardacre, C.; McMath, S. E. J. In situ XAFS investigation of palladium species present during the Heck reaction in room temperature ionic liquids, Green Chem., 2002, 4(2), 139-142.

31. Rogers, R. D.; Seddon, K. R. Ionic liquids—solvents of the future? Science, 2003, 302, 792-793; Seddon, K. R. Ionic liquids: a taste of the future, Nature Mater., 2003, 2, 363-364.

32. American Chemical Society, ACS Green Chemistry Institute, 2005; chemistry.org/ greenchemistryinstitute

33. Freemantle, M. Designer solvents—ionic liquids may boost clean technology development, Chem. Eng. News, 1998, 76(13), 32-37.

34. Seddon, K. R.; Hardacre, C.; McCauley, B. J. Catalyst comprising indium salt and organic ionic liquid and process for Friedel-Crafts reactions, World Patent WO 03, 028883 (2003); Earle, M. J.; McAuley, B. J.; Ramani, A.; et al. Chemical reactions catalyzed by fluoroalkylsulfonated compounds, preferably bis-triflimide compounds, World Patent WO 02, 072519 (2002); Csihony, S.; Mehdi, H.; Homonnay, Z.; et al. In situ spectroscopic studies related to the mechanism of the Friedel-Crafts acetylation of benzene in ionic liquids using AlCl3 and FeCl3, J. Chem. Soc., Dalton Trans., 680685; 2002, Valkenberg, M. H.; Sauvage, E.; De Castro-Moreira, C. P.; Hoelderich, W. F. Immobilized ionic liquids, World Patent WO 0132308 (2001); Adams, C. J.; Earle, M. J.; Roberts, G.; Seddon, K. R. Friedel-Crafts reactions in room temperature ionic liquids, Chem. Commun., 1998, 2097-2098; Boon, J. A., Levisky, J. A., Pflug, J. L.; Wilkes, J. S. Friedel-Crafts reactions in ambient-temperature molten salts, J. Org. Chem., 1986, 51(4), 480-483; Earle, M. J.; Hakala, U.; Hardacre, C.; et al. Chloroindate(III) ionic liquids: recyclable media for Friedel-Crafts acylation reactions, Chem. Commun., 2005, 903-905; Earle, M. J.; Hakala, U.; McAuley, B. J.; et al. Metal bis{(trifluoromethyl)sulfonyl}amide complexes: highly efficient Friedel-Crafts acylation catalysts, Chem. Commun., 2004, 1368-1369.

35. Earle, M. J., McCormac, P. B.; Seddon, K. R. Diels-Alder reactions in ionic liquids: a safe recyclable green alternative to lithium perchlorate-diethyl ether mixtures, Green Chem., 1999, 1(1), 23-25; Doherty, S.; Goodrich, P.; Hardacre, C.; et al. Marked enantioselectivity enhancements for Diels-Alder reactions in ionic liquids catalysed by platinum diphosphine complexes, Green Chem., 2004, 6(1), 63-67.

36. Kobayashi, S.; J0rgensen, K. A. (Eds.) Cycloaddition Reactions in Organic Synthesis, Wiley-VCH, Weinheim, Germany, 2002; Carmichael, A. J., Earle, M. J., Holbrey, J. D.; et al. The Heck reaction in ionic liquids: a multiphasic catalyst system, Org. Lett., 1999, 1, 997-1000; Forsyth, S. A., Gunaratne, H. Q. N.; Hardacre, C.; et al. Utilisation of ionic liquid solvents for the synthesis of Lily-of-the-Valley fragrance {beta-Lilial (R), 3-(4-t-butylphenyl)- 2-methylpropanal}, J. Mol. Catal. A-Chem., 2005, 231(1-2), 61-66.

37. Winterton, N.; Seddon, K. R.; Patell, Y. Halogenation of unsaturated hydrocarbons in ionic liquids, World Patent WO 0037400 (2000).

38. Van Rantwijk, F.; Lau, R. M., Sheldon, R. A. Biocatalytic transformations in ionic liquids, Trends Biotechnol., 2003, 21(3), 131-138; Sheldon, R. A.; Lau, R. M.; Sorge-drager, M. J.; et al., Biocatalysis in ionic liquids, Green Chem., 2002, 4(2), 147-151; Sheldon, R. A. Catalytic reactions in ionic liquids, Chem. Commun., 2001, 23992407.

39. Cull, S. G.; Holbrey, J. D.; Vargas-Mora, V.; et al. Room-temperature ionic liquids as replacements for organic solvents in multiphase bioprocess operations, Biotechnol. Bioeng., 2000, 69(2), 227-233; Lau, R. M.; van Rantwijk, F.; Seddon, K. R.; Sheldon, R. A. Lipase-catalyzed reactions in ionic liquids, Org. Lett., 2000, 2(26), 4189-4191.

40. Hardacre, C.; Holbrey, J. D.; Katdare, S. P.; Seddon, K. R. Alternating copolymerisa-tion of styrene and carbon monoxide in ionic liquids, Green Chem., 2002, 4(2), 143146; Carmichael, A. J.; Haddleton, D. M.; Bon, S. A. F.; Seddon, K. R. Copper(I) mediated living radical polymerisation in an ionic liquid, Chem. Commun., 2000, 1237-1238.

41. Adams, C. J.; Earle, M. J.; Seddon, K. R. Catalytic cracking reactions of polyethylene to light alkanes, Green Chem., 2000, 2(1), 21-24.

42. Seddon, K. R.; Stark, A. Selective catalytic oxidation of benzyl alcohol and alkylben-zenes in ionic liquids, Green Chem., 2002, 4(2), 119-123.

43. Anderson, K.; Goodrich, P.; Hardacre, C.; McCath, S. E. J. Hydrogenation processes performed in ionic liquids, World Patent, WO 02, 094740 (2002); Dyson, P. J.; Ellis, D. J.; Parker, D. G.; Welton, T. Arene hydrogenation in a room-temperature ionic liquid using a ruthenium cluster catalyst, Chem. Commun., 1999, 25-26; Adams, C. J.; Earle, M. J.; Seddon, K. R. Stereoselective hydrogenation reactions in chloroalumina-te(III) ionic liquids: a new method for the reduction of aromatic compounds, Chem. Commun., 1999, 1043-1044.

44. Beletskaya, I. P.; Cheprakov, A. V. The Heck reaction as a sharpening stone of palladium catalysis, Chem. Rev., 2000, 100, 3009-3066.

45. Von Walden, P. Uber die Molekulargrosse und elektrische Leitfahigkeit einiger geseh-molzenen Salze, Bull. Acad. Imp. Sci. St. Petersburg, 1914, 8, 405 -422.

46. Wier, T. P. Jr., U.S. Patent 4,446,350 (1948); Wier, T. P. Jr., Hurley, F. H. U.S. Patent 4,446,349, 1948; Hurley, F. H. U.S. Patent 4,446,331 (1948).

47. Hurley, F. H.; Wier, T. P. The electrodeposition of aluminium from nonaqueous solutions at room temperature, J. Electrochem. Soc., 1951, 98, 207 -212; Hurley, F. H.; Wier, T. P. J. Electrochem. Soc., 1951, 98, 203-206.

48. Chum, H. L.; Koch, V. R.; Miller, L. L.; Osteryoung, R. A. An electrochemical scrutiny of organometallic iron complexes and hexamethylbenzene in a room temperature molten salt, J. Am. Chem. Soc., 1975, 97, 3264-3265.

49. Wilkes, J. S.; Levisky, J. A.; Wilson, R. A.; Hussey, C. L. Dialkylimidazolium chlor-oaluminate melts—A new class of room-temperature ionic liquids for electrochemistry, spectroscopy, and synthesis, Inorg. Chem., 1982, 21(3), 1263-1264.

50. Wilkes, J. S.; Zaworotko, M. J. Air and water stable 1-ethyl-3-methylimidazolium based ionic liquids, J. Chem. Soc., Chem. Commun., 1992, 965-967.

51. Abdul-Sada, A. K.; Atkins, M. P.; Ellis, B.; et al. Process and catalysts for the alky-lation of aromatic hydrocarbons, World Patent WO 95, 21806 (1995); Abdul-Sada, A. K.; Ambler, P. W.; Hodgson, P. K. G.; et al. Ionic liquids of imidazolium halide for oligomerization or polymerization of olefins, World Patent WO 95, 21871 (1995); Bowlas, C. J.; Bruce, D. W.; Seddon, K. R. Liquid-crystalline ionic liquids, Chem. Commun., 1996, 1625-1626.

52. Gordon, C. M., Holbrey, J. D., Kennedy, A. R.; Seddon, K. R. Ionic liquid crystals: hexafluorophosphate salts, J. Mater. Chem., 1998, 8(12), 2627-2636.

53. Holbrey, J. D.; Seddon, K. R. The phase behaviour of 1-alkyl-3-methylimidazolium tetrafluoroborates: ionic liquids and ionic liquid crystals, J. Chem. Soc., Dalton Trans., 1999, 2133-2139.

54. Abdul-Sada, A. K.; Greenway, A. M.; Hitchcock, P. B.; et al. Structure of room temperature haloaluminate ionic liquids, J. Chem. Soc., Chem. Commun., 1986, 17531754; Abdul-Sada, A. K.; Al-Juaid, S.; Greenway, A. M.; et al. Upon the hydrogen-bonding ability of the H(4) and H(5) protons of the imidazolium cation, Struct. Chem., 1990, 1, 391-394; Abdul-Sada, A. K.; Elaiwi, A. E.; Greenway, A. M.; Seddon, K. R. Evidence for the clustering of substituted imidazolium salts via hydrogen bonding under the conditions of fast atom bombardment mass spectrometry, Eur. Mass Spectrom., 1997, 3(3), 245-247; Hitchcock, P. B.; Seddon, K. R.; Welton, T. Hydrogen-bond acceptor abilities of tetrachlorometallate(II) complexes in ionic liquids, J. Chem. Soc., Dalton Trans., 1993, 2639-2643; Avent, A. G.; Chaloner, P. A.; Day, M. P.; et al. Evidence for hydrogen-bonding in solutions of 1-ethyl-3-methylimidazolium halides, and its implications for room-temperature halo-genoaluminate(III) ionic liquids, J. Chem. Soc., Dalton Trans., 1994, 3405-3413; Elaiwi, A.; Hitchcock, P. B.; Seddon, K. R.; et al. Hydrogen bonding in imidazolium salts and its implications for ambient-temperature halogenoaluminate(III) ionic liquids, J. Chem. Soc., Dalton Trans., 1995, 3467-3472; Avent, A. G.; Chaloner, P. A.; Day, M. P.; et al. Evidence for hydrogen-bonding in solutions of 1-methyl-3-ethyl-imidazolium halides, as determined by 1H, 35Cl and 127I N.M.R. spectroscopy, and its implications for room- temperature halogenoaluminate(III) ionic liquids, in Proceedings of the Seventh International Symposium on Molten Salts, vol. PV 90-17. Hussey, C. L.; Wilkes, J. S.; Flengas, S. N.; Ito, Y. (Eds.) The Electrochemical Society Inc., Pennington, N.J., 1990, pp. 98-133.

55. Abdul-Sada, A. K.; Avent, A. G.; Parkington, M. J.; et al. The removal of oxide impurities from room-temperature halogenoaluminate ionic liquids, J. Chem. Soc., Chem. Commun., 1987, 1643-1644; Abdul-Sada, A. K.; Avent, A. G.; Parkington, M. J.; et al. Removal of oxide contamination from ambient-temperature chloroaluminate(III) ionic liquids, J. Chem. Soc., Dalton Trans., 1993, 3283-3286.

56. Abdul-Sada, A. K.; Greenway, A. M.; Seddon, K. R.; Welton, T. Upon the existence of [Al3Cl10]_ in room-temperature chloroaluminate ionic liquids, Org. Mass Spectrom., 1989, 24(10), 917-918; Dent, A. J.; Seddon, K. R.; Welton, T. The structure of halo-genometallate complexes dissolved in both basic and acidic room-temperature halogenoaluminate(III) ionic liquids, as determined by EXAFS, J. Chem. Soc., Chem. Commun., 1990, 315-316.

57. Abdul-Sada, A. K.; Seddon, K. R.; Stewart, N. J. Ionic liquids of ternary melts, World Patient WO 95 21872 (1995).

58. Seddon, K. R.; Stark, A.; Torres, M.-J. Influence of chloride, water, and organic solvents on the physical properties of ionic liquids, Pure Appl. Chem., 2000, 72(12), 2275-2287; Seddon, K. R.; Stark, A.; Torres, M. J. Viscosity and density of 1-alkyl-3-methylimidazolium ionic liquids, in Clean Solvents: Alternative Media for Chemical Reactions and Processing, Eds. Abraham, M.; Moens, L. ACS Symposium Series, Vol. 819, American Chemical Society, Washington D.C., 2002, pp. 34-49.

59. Seddon, K. R. Ionic liquids: designer solvents? in The International George Papatheo-dorou Symposium: Proceedings, Boghosian, S.; Dracopoulos, V.; Kontoyannis, C. G.; and Voyiatzis, G. A. (Eds). Institute of Chemical Engineering and High Temperature Chemical Processes, Patras, Greece, 1999, pp. 131-135.

60. MacFarlane, D. R.; Forsyth, S. A.; Golding, J.; Deacon, G. B. Ionic liquids based on imidazolium, ammonium and pyrrolidinium salts of the dicyanamide anion, Green Chem., 2002, 4(5), 444-448; Golding, J.; Forsyth, S.; MacFarlane, D. R.; et al. Metha-nesulfonate and p-toluenesulfonate salts of the N-methyl-N-alkylpyrrolidinium and quaternary ammonium cations: novel low cost ionic liquids, Green Chem., 2002, 4(3), 223-229; Bonhote, P.; Dias, A. P.; Papageorgiou, N.; et al. Hydrophobic, highly conductive ambient-temperature molten salts, 1996, Inorg. Chem., 35(5), 1168-1178; Papageorgiou, N.; Athanassov, Y.; Armand, M.; et al. The performance and stability of ambient-temperature molten salts for solar cell applications, J. Electrochem. Soc., 1996, 143(10), 3099-3108.

61. Sun, J.; MacFarlane, D. R.; Forsyth, M. A new family of ionic liquids based on the 1-alkyl-2-methylpyrrolinium cation, Electrochim. Acta, 2003, 48(12), 1707-1711; Forsyth, S.; Golding, J.; MacFarlane, D. R.; Forsyth, M. N-methyl-N-alkylpyrrolidinium tetrafluoroborate salts: ionic solvents and solid electrolytes, Electrochim. Acta, 2001, 46(10-11), 1753-1757; Golding, J. J.; Macfarlane, D. R.; Spiccia, L.; et al. Weak intermolecular interactions in sulfonamide salts: structure of 1-ethyl-2-methyl-3-benzylimidazolium bis[(trifluoromethyl)sulfonyl]amide, Chem. Commun., 1998, 1593-1594.

62. Fukumoto, K.; Yoshizawa, M.; Ohno, H. Room temperature ionic liquids from 20 natural amino acids, J. Am. Chem. Soc., 2005, 127(8), 2398-2399.

63. Deetlefs, M.; Seddon, K. R. Improved preparations of ionic liquids using microwave irradiation, Green Chem., 2003, 5(2), 181-186.

64. Carmichael, A. J.; Deetlefs, M.; Earle, M. J.; et al. Ionic liquids: Improved syntheses and new products, in Ionic Liquids as Green Solvents: Progress and Prospects, Rogers, R. D.; Seddon, K. R. (Eds.) ACS Symposium Series, Vol. 856, American Chemical Society, Washington D.C., 2003, pp. 14-31; Holbrey, J. D.; Reichert, W. M.; Swatloski, R. P.; et al. Efficient, halide free synthesis of new, low cost ionic liquids: 1,3-dialkylimidazolium salts containing methyl- and ethyl-sulfate anions, Green Chem., 4(5), 2002, 407-413; Seddon, K. R.; Carmichael, A. J.; Earle, M. J. Process for preparing ambient temperature ionic liquids, World Patent WO 01, 40146 (2001); Earle, M. J.; Seddon, K. R. Preparation of imidazole car-benes and the use thereof for the synthesis of ionic liquids, World Patent, WO 01, 77081 (2001).

65. Jastorff, B., Störmann, R., Ranke, J.; et al. How hazardous are ionic liquids? Structure-activity relationships and biological testing as important elements for sustainabil-ity evaluation, Green Chem., 2003, 5, 136-142; Ranke, J.; Molter, K.; Stock, F.; et al. Biological effects of imidazolium ionic liquids with varying chain lengths in acute Vibrio fischeri and WST-1 cell viability assays (vol. 58, p. 396, 2004), Ecotoxicol. Environ. Saf., 2005 60(3), 350-350; Stock, F.; Hoffmann, J.; Ranke, J.; et al. Effects of ionic liquids on the acetylcholinesterase—A structure-activity relationship consideration, Green Chem., 2004, 6(6), 286-290; Stepnowski, P.; Olafsson, G.; Helgason, H.; Jastorff, B. Preliminary study on chemical and physical principles of astaxanthin sorption to fish scales towards applicability in fisheries waste management, Aquaculture, 2004, 232(1-4), 293-303; Ranke, J.; Molter, K.; Stock, F.; et al. Biological effects of imidazolium ionic liquids with varying chain lengths in acute Vibrio fischeri and WST-1 cell viability assays, Ecotoxicol. Environ. Saf., 2004, 58(3), 396-404.

66. Bernot, R. J.; Brueseke, M. A.; Evans-White, M. A.; Lamberti, G. A. Acute and chronic toxicity of imidazolium-based ionic liquids on daphnia magna, Environ. Toxicol. Chem., 2005, 24(1), 87-92.

67. United States Senate, Green Chemistry Research and Development Act of 2005, 2005, http://frwebgate.access.gpo.gov/cgi-bin /

getdoc.cgi?dbname = 109_cong_bills&docid = f:s1270is.txt.pdf

68. Marburger, J., Green Chemistry and Homeland Security, 2003, acs.org/portal/a/ ContentMgmtService/resources?id = c373e9f7d880b6688f6a4fd8fe800100

69. Earle, M. J.; Katdare, S. P.; Seddon, K. R. Paradigm confirmed: the first use of ionic liquids to dramatically influence the outcome of chemical reactions, Org. Lett., 2004, 6(5), 707-710.

70. Dyson, P. J.; Laurenczy, G.; Ohlin, C. A.; et al. Determination of hydrogen concentration in ionic liquids and the effect (or lack of) on rates of hydrogenation, Chem. Commun., 2003, 2418-2419; Crowhurst, L., Mawdsley, P. R.; Perez-Arlandis, J. M.; et al., Solvent-solute interactions in ionic liquids, Phys. Chem. Chem. Phys., 2003, 5(13), 2790-2794; Lancaster, N. L.; Salter, P. A.; Welton, T.; Young, G. B. Nucleo-philicity in ionic liquids. 2. Cation effects on halide nucleophilicity in a series of bis(trifluoromethylsulfonyl)imide ionic liquids, J. Org. Chem., 2002, 67(25), 88558861; Anderson, J. L.; Ding, J.; Welton, T.; Armstrong, D. W. Characterizing ionic liquids on the basis of multiple solvation interactions, J. Am. Chem. Soc., 2002, 124(47), 14247-14254; Aggarwal, A.; Lancaster, N. L.; Sethi, A. R.; Welton, T. The role of hydrogen bonding in controlling the selectivity of Diels-Alder reactions in room-temperature ionic liquids, Green Chem., 2002, 4(5), 517-520; Lancaster, N. L.; Welton, T.; Young, G. B. A study of halide nucleophilicity in ionic liquids, J. Chem. Soc., Perkin Trans. II, 2001, 2267-2270; Cammarata, L., Kazarian, S. G.; Salter, P. A.; Welton, T. Molecular states of water in room temperature ionic liquids, Phys. Chem. Chem. Phys., 2001, 3(23), 5192-5200.

71. Erbeldinger, M.; Mesiano, A. J.; Russell, A. J. Enzymatic catalysis of formation of Z-aspartame in ionic liquid—An alternative to enzymatic catalysis in organic solvents, Biotechnol. Prog., 2000, 16(6), 1129-1131.

72. Freemantle, M. BASF's smart ionic liquid, Chem. Eng. News, 2003, 81(13), 9.

73. Maase, M.; Massonne, K.; Halbritter, K.; et al. Method for the separation of acids from chemical reaction mixtures by means of ionic fluids, World Patent WO 03, 062171 (2003).

74. Seddon, K. R., COIL, 2005, http://events.dechema.de/COIL.html

75. Freemantle, M. Ionic liquids make splash in industry, Chem. Eng. News, 2005, 83(31), 33-38.

76. Plechkova, N. V.; Seddon, K. R. Chem. Soc. Rev., to be submitted.

77. Atkins, M. P.; Davey, P.; Fitzwater, G.; et al. Ionic Liquids: A Map for Industrial Innovation Q001, January 2004, QUILL, Belfast, 2004.

78. Seddon, K. R. QUILL rewrites the future of industrial solvents, Green Chem., 1999, 1, G58-G59.

79. Horton, B. Green chemistry puts down roots, Nature, 1999, 400(6746), 797-799.

80. ISI Essential Science Indicators, Ionic Liquids, 2004, esi-topics.com/ionic-liquids/ index.html.

81. Leitner, W.; Seddon, K. R.; Wasserscheid, P. Green solvents for catalysis (Editorial), Green Chem., 2003, 5(2), G28.

82. Seddon, K. R. Ionic liquids (Editorial), Green Chem., 2002, 4(2), G25-G26.

83. Leitner, W.; Seddon, K. R.; Wasserscheid, P. Green solvents for synthesis meeting, Bruchsal, Germany, October 2004, Green Chem., 2005, 7(5), 253.

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