Process for preparing diorganoantimony compounds r2sboocr' and novel products so prepared
Use of cpds. RnSbX3-n (I) where R = alkyl, alkenyl, alkynyl, aryl, cycloalkyl or cycloalkenyl. X = halogen, carboxylate, alkoxide, oxide, hydroxide, sulphide or mercaptide n = 1-3 When X is divalent (e.g. oxide) cpds. of formula (II) are also included R2Sb-X-sbR2 (II) Bactericides and fungicides esp...
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| creator | LEEBRICK JOHN R REMES NATHANIEL L |
| description | Use of cpds. RnSbX3-n (I) where R = alkyl, alkenyl, alkynyl, aryl, cycloalkyl or cycloalkenyl. X = halogen, carboxylate, alkoxide, oxide, hydroxide, sulphide or mercaptide n = 1-3 When X is divalent (e.g. oxide) cpds. of formula (II) are also included R2Sb-X-sbR2 (II) Bactericides and fungicides esp. of use in the treatment of plastics, textiles, papers and paints. 27.2 g. (C4H9)2 SbCl in 500 ml. dry benzene treated with 22.5 g. sodium lauryl mercaptide. Refluxed 5 hours, filtered hot and filtrate evaporated to give di-n-butyl antimony lauryl mercaptide. |
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X = halogen, carboxylate, alkoxide, oxide, hydroxide, sulphide or mercaptide n = 1-3 When X is divalent (e.g. oxide) cpds. of formula (II) are also included R2Sb-X-sbR2 (II) Bactericides and fungicides esp. of use in the treatment of plastics, textiles, papers and paints. 27.2 g. (C4H9)2 SbCl in 500 ml. dry benzene treated with 22.5 g. sodium lauryl mercaptide. 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| subjects | ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM AGRICULTURE ANIMAL HUSBANDRY BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES, AS HERBICIDES CHEMISTRY FISHING FORESTRY HUMAN NECESSITIES HUNTING METALLURGY ORGANIC CHEMISTRY PEST REPELLANTS OR ATTRACTANTS PLANT GROWTH REGULATORS PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTSTHEREOF TRAPPING |
| title | Process for preparing diorganoantimony compounds r2sboocr' and novel products so prepared |
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