Investigations on fungicides

A number of bis-[(i-formamido-2,2,2-trichloro)ethylamino]-alkanes and their dioxy and dithio analogues were examined for direct and systemic antifungal activity. All compounds showed very low in vitro fungitoxicity and only slight protectant anti-mildew activity when applied as a foliar spray. Certain diamino and dioxy derivatives were, however, systemically active against powdery mildew fungi when applied as a root drench to seedlings of wheat or cucumber; the dithio analogues were inactive. The level of systemic activity shown by these compounds was markedly influenced by the nature of the hydrocarbon ‘bridging’ group.     

Substituted benzoic and picolinic acids as foliar sprays against potato common scab

Glasshouse tests on potato cv. Arran Banner measured the effects of single early foliar sprays of 18 substituted benzoic and two dichloropicolinic acids on the severity of common scab, caused by soil-borne Streptomyces scabies. The monosubstituted benzoic acids tested (25 mM) did not affect scab. However, anti-scab action was shown by some 2,5-disubstituted acids. Decreases in scab severity were about 35% from 1·6 mM 5-bromo-2-chloro- and 2,5-dimethylbenzoic acids, and over 50% from 1·6 mM 2,5-dichloro-, 2,5-dibromo- and 5-chloro-2-nitrobenzoic acids and from 0·05 mM 3,6-dichloropicolinic acid (clopyralid), which is structurally similar to 2,5-dichlorobenzoic acid. None of the spray treatments affected yield or shape of tubers. No visible effects on foliage were caused by two of the benzoic acids active against scab (5-chloro-2-nitro- and 2,5-dimethyl-), but the other active acids caused some distortion. In tests of the six dichlorobenzoic acids against S. scabies in culture, the 2,5-isomer (which was the most effective against the disease in plants) was one of the least toxic. With other 2,5-disubstituted benzoic acids, it probably decreased scab indirectly by altering the response of the host to infection.