Ambient-temperature molten salts and process for producing...

Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

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C546S303000

Reexamination Certificate

active

07960554

ABSTRACT:
Ambient-temperature molten salts of formula (I):wherein Y+is a cation selected from the group consisting of an ammonium ion, a sulfonium ion, a pyridinium ion, a(n) (iso)thiazolium ion, and a(n) (iso)oxazolium ion that may be optionally substituted with C1-10alkyl and/or C1-10alkyl having ether linkage, provided that the above cation has at least one substituent of —CH2Rf1or —OCH2Rf1(wherein Rf1is C1-10perfluoroalkyl); Rf2and Rf3are independently C1-10perfluoroalkyl or may together form C1-4perfluoroalkylene; and X is —SO2— or —CO—.

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Mirzaei, et al.; “Synthesis of 1-Alkyl-1,2,4-triazoles and the Formation of Quaternary 1-Alkyl-4-polyfluoroalkyl-1,2,4-triazolium Salts Leading to Ionic Liquids”; J. Org. Chem., vol. 67, No. 26; (2002); pp. 9340-9345.
Umemoto, et al.; “Synthesis of 2,2,2-Trifluoroethylated Onium Salts of Nitrogen, Sulfur, and Phosphorus with (2,2,2-Trifluoroethyl)phenyliodonium Triflate”; Bull. Chem. Soc. Jpn., vol. 64, No. 6; (1991); pp. 2008-2010.
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Umemoto, et al.; “Synthesis of 2,2,2-Trifluoroethylated Onium Salts of Nitrogen, Sulfur, and Phosphorus with (2,2,2-Trifluoroethyl)phenyliodonium Triflate”; 1991 The Chemical Society of Japan; Bull. Chem., Soc. Jpn., vol. 64, No. 6; (1991); pp. 2008-2010.
Bonhôte, et al.; “Hydrophobic, Highly Conductive Ambient-Temperature Molten Salts”; Inorg. Chem.,vol. 35, No. 5; (1996); pp. 1168-1178.
Office Action for U.S. Appl. No. 11/787,591 mailed Mar. 9, 2009.
Office Action for U.S. Appl. No. 11/787,591 mailed Sep. 11, 2009.

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