ARTHROPODICIDAL OXAZOLINES AND THIAZOLINES

Compounds of formula (I), and their N-oxides and agriculturally suitable salts, are disclosed which are useful as arthropodicides, wherein R is selected from the group Si(R )(R )(R ); Ge(R )(R )(R ); 2,8,9-trioxa-5-aza-1-silabicyclo[3.3.3]undecan-1-yl optionally substituted with 1-6 C1-C3 alkyl; C1-C3 alkylthio; C1-C3 haloalkylthio; C1-C3 alkylsulfinyl; C1-C3 haloalkylsulfinyl; C1-C3 alkylsulfonyl; C1-C3 haloalkylsulfonyl; phenyl substituted with C1-C3 haloalkylthio, C1-C3 haloalkylsulfinyl; C1-C3 haloalkylsulfonyl or C1-C3 haloalkylsulfonyloxy and optionally substituted with 1-2 W; hydroxymethyl substituted on the carbon atom with 1-2 J; and C1-C6 alkyl substituted with 1-3 members independently selected from the group cyano, hydroxy, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, formyl, C2-C4 alkoxycarbonyl,, C2-C4 alkylcarbonyloxy, C2-C4 alkoxycarbonyloxy, phenoxy optionally substituted with 1-3 W, phenylthio optionally substituted with 1-3 W, phenylsulfinyl optionally substituted with 1-3 W, and phenylsulfonyl optionally substituted with 1-3 W, or, when two members are attached to the same carbon atom, said members can be taken together as -OCH2CH2O-, -OCH2CH2CH2O-, -SCH2CH2S-, or -SCH2CH2CH2S-, each CH2 of said taken together members optionally substituted with 1-2 C1-C3 alkyl; and A, E, Y, Z, R , R , R -R , R , and q are as defined in the disclosure. Also disclosed are compositions containing the compounds of formula (I) and a method for controlling arthropods which involves contacting the arthropods or their environment with an effective amount of a compound of formula (I). L'invention concerne les composés de la formule (I), ainsi que leurs oxydes-N et leurs sels adaptés pour l'agriculture, qui sont utilisés comme arthropodicides. Dans la formule (I), R est sélectionné dans le groupe Si(R )(R )(R ); Ge(R )(R )(R ); 2,8,9-trioxa-5-aza-1-silabicyclo[3.3.3]undécane-1-yle éventuellement remplacé par un alcoyle en 1-6 C1-C3; thioalcoyle en C1-C3; halothioalcoyle en C1-C3; alcoylsulfinyle en C1-C3; haloalcoylsulfinyle en C1-C3; alcoylsulfonyle en C1-C3; haloalcoylsulfonyle en C1-C3; phényle remplacé par un halothioalcoyle en C1-C3, haloalcoylsulfinyle en C1-C3; haloalcoylsulfonyle en C1-C3 ou haloalcoylsulfoniloxy en C1-C3 et éventuellement remplacé par 1-2 W; hydroxyméthyle remplacé sur l'atome de carbone par 1-2J; et alcoyle en C1-C6 remp