Principles for regulatory testing and interpretation of semi-field and field studies with non-target arthropods

This paper is a guidance document for side-effect testing with plant protection products on non-target arthropods under semi-field and field conditions. The principles, methods, endpoints and interpretation of non-target arthropod semi-field and field trials which should be conducted for registration of plant protection products in the European Union are presented and discussed. The recommendations presented reflect the opinions of the experts from authority, academia, industry and consulting which participated at the IOBC (International Organisation of Biological Control), BART (Beneficial Arthropod Regulatory Testing) group and EPPO (European Plant Protection Organisation) Joint Initiative workshop held in Versailles (France) on the 25–26 October, 1999.     

The (Me5C5)Si+ cation: a stable derivative of HSi+

The reaction of decamethylsilicocene, (Me5C5)2Si, with the proton-transfer reagent Me5C5H2+B(C6F5)4- produces the salt (Me5C5)Si+ B(C6F5)4(2), which can be isolated as a colorless solid that is stable in the absence of air and moisture. The crystal structure reveals the presence of a cationic pi complex with an eta5-pentamethylcyclopentadienyl ligand bound to a bare silicon center. The 29Si nuclear magnetic resonance at very high field (delta = - 400.2 parts per million) is typical of a pi complex of divalent silicon. The (eta5-Me5C5)Si+ cation in 2 can be regarded as the "resting state" of a silyliumylidene-type (eta1-Me5C5)Si+ cation. The availability of 2 opens new synthetic avenues in organosilicon chemistry. For example, 2 reacted with lithium bis(trimethylsilyl)amide to give the disilene E-[(eta1-Me5C5)[N(SiMe3)2]Si]2(3).