Abstract:
O,S''-dialkyl-S-hydrocarbylthioalkyl dithiophosphates can be prepared by the selective dealkylation-alkylation of the corresponding O,O''-dialkyl dithiophosphate esters. The C1 to C2 O-alkyl C3 to C4 S''-alkyl S-hydrocarbylthioalkyl dithiophosphate products show unexpectedly high effectiveness as pesticides.
Abstract:
Dithiophosphonic and dithiophosphinic acid esters can be prepared by free radical addition of the corresponding dithiophosphonic and dithiophosphinic acids to unsaturated compounds, such as olefinic and acetylene compounds, e.g. vinyl chloride, butadiene, allene, methylacetylene, etc. The unsaturated products of this novel process can be further reacted with a sulfhydryl containing compound such as methanethiol, O,O''-diethyl dithiophosphoric acid to provide SH addition thereto. Furthermore, both the dithiophosphonate adducts of the free radical addition process and also the dithiophosphonate adducts of the sulfhydryl containing compound addition step can be isomerized to form unsymmetrical dithiophosphonic acid S,S''diesters. In addition thereto the unsaturated unsymmetrical dithiophosphonic acid S,S''-diesters can also be further reacted with a sulfhydryl containing compound to provide SH addition thereto. The novel thiophosphonic and thiophosphinic compounds produced by the above described processes are useful as pesticides, particularly as insecticides, nematocides and lubricating oil additive such as antioxidants, etc.
Abstract:
Improved radiation vulcanization of elastomers is accomplished by incorporating into the elastomer composition a polythiol. The polythiol is preferably a hydrocarbon thioether thiol and is normally liquid at room temperature with a molecular weight of at least 150. Though difunctional polythiols are operative in this invention, the preferred polythiols have about three to about five thiol groups per molecule.
Abstract:
S-ALLYLIC AND S-VINYLIC O,O''-DIALKYLDITHIOPHOSPHATES CAN BE SELEVTIVELY DEALKYLATED TO FORM THEIR CORRESPONDING SALTS, WHICH THEN CAN BE REACTED WITH ALKYL HALIDES TO FORM S-ALLYLIC AND S-VINYLIC O,S''-DIALKYLDITHIOPHOSPHATES. BOTH THE DEALKYLATED PRODUCTS AND ALKYLATED PRODUCTS ARE NOVEL COMPOSITIONS, USEFUL AS PESTICIDES, ESPECIALLY AS INSECTICIDES, AND AS ANTIOXIDANTS, LUBRICATING OIL ADDITIVES, ETC.
Abstract:
UNSYMMETRICAL THIOL-ALLENE DIADDUCTS (1,3-AND 1,2-BIS (SUBSTITUTED MERCAPTO)-PROPANES) ARE PREPARED BY THE FREE RADICAL AND/OR IONIC ADDITION OF A THIOL COMPOUND TO A MONOADDUCT ALLYL SULFIDE OR THROUGH THE SEQUENTIAL ADDITION OF TWO DIFFERENT THIOL COMPOUNDS TO ALLENE. DIADDUCTS CONTAINING A DIALKYL DITHIOPHOSPHORIC ACID CONSTITUENT AND EITHER AN ALKYL OR ARYL THIOL CONSTITUENT ARE EFFECTIVE AGRICULTRUAL CHEMICALS.