Patents Alert /Journal
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surface energy, high hydrophobicity, low glass transition temperature and low coefficient of friction. The polyurethanes derived from the prepolymers of this invention are elastomeric and, in addition to the above characteristics, exhibit high moisture resistance, high tear strength and excellent adhesion to a variety of substrates.
Chemisty
87 (1998)
123-132
127
5659088 PROCESS FOR THE PREPARATION 4-FLUOROTHIOPHENOL
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Fiege Helmu; Hagedorn Ferdinand; Eymann Wolfgang; Neuner Otto; Mum1 uller Herbert Leverkusen, GERMANY assigned to Bayer Aktiengesellschaft
5458689 RECHARGEABLE LITHIUM BATTERY HAVING A SPECIFIC ELECTROLYTE Kawakami Soichiro; Kobayashi Naoya; Asao Masaya Nara, JAPAN assigned to Canon Kabushiki Kaisha A rechargeable lithium battery comprising at least an anode, a separator,a cathode, and an electrolyte integrated in a battery housing, characterized in that said electrolyte comprises a salt ‘of an organic fluorine-silicon compound containing at least fluorine, silicon and carbon elements as the constituents.
5659046 METHOD FOR THE PREPARATION Z-PERFLUOROALKYL-3-OXA.ZOLIN-5-O NE
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Kameswaran Venkataraman Princeton Junction, NJ, UNITED STATES assigned to American Cyanamid Company There is provided a method for the preparation of a 2-peffluoroalkyl-3-oxazolin-5-one compound comprising reacting an aminonitrile with a perfluoroacylating agent in the presence of a solvent to form a perfluoroalkanoyl aminonitrile intermediate and cyclizing the intermediate in the presence of an acid and at least one molar equivalent of water.
4-Fluorothiophenol is obtained in outstanding purifies and yields if 4-fluorobenzenesulphonyl chloride is reacted with sodium hydrogen sulphite solution to give a solution of sodium 4-fluorobenzenesulphinate,this solution is reduced with sulphur dioxide to give 4,4’-difluorodiphenyl disulphide and finally this is reacted with sodium borohydride in a water-miscible inert organic solvent to give 4-fluorothiophenol (sodium salt). Free 4-fluorothiophenol can be isolated from the sodium salt solution by acidification.
5659093 METHOD OF PRODUCING 1,1,1,3,3-PENTAFLUOROPROPANE, A METHOD OF PRODUCING 1,1,1,3,3-PENTAFLUORO-ZHALOGENO-3CHLOROPROPANE, AND A METHOD OF PRODUCING 1,1,1,2,3,3-HEXACHLOROPROPENE Takubo Seij; Aoyama Hirokazu; Nakada Tatsuo Settsu, JAPAN assigned to Daikin Industries Ltd PCT No. PCT/JP93/01887 Sec. 37 1 Date Jun. 27, 1995 Sec. 102(e) Date Jun. 27, 1995 PCT Filed Dec. 24, 1993 PCT Pub. No. WO94/14736 PCT Pub. Date Jul. 7, 1994. There are provided production methods of 1,l, 1,3,3-pentafluoropropane characterized in that 1,l ,1,3,3-pentafluoro-2,3-dichloropropane is reacted with hydrogen fluoride in the presence of metal catalyst; of a noble 1,I ,1,3,3-pentafluoro-2-halogeno-3-chloropropane characterized in that the halogenated propene