𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis and insecticidal activity of 4-perhaloalkoxy (or thioalkyl) benzophenonehydrazone derivatives

✍ Scribed by Dürr, Dieter; Gsell, Laurenz; Hall, Roger G; Karrer, Friedrich; Pascual, Alfons; Rindlisbacher, Alfred


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
85 KB
Volume
55
Category
Article
ISSN
1526-498X

No coin nor oath required. For personal study only.

✦ Synopsis


from both ExpF-based treatments were almost identical.

Not all xylem-mobile molecules behave in the same way and this is illustrated by a comparison between ExpF and ¯uquinconazole when both were mixed with Adj1. Fluquinconazole was recovered only in very small quantities, the single greatest recovery being 0.17% over a 24 h period. These recoveries are considerably less than those already described for ExpF when mixed with the same adjuvant. That recovery in guttation ¯uid is not solely related to the level of uptake into the plant is supported by data from other experiments (Harris RI unpublished) where the uptakes of both ¯uquinconazole and ExpF were very similar when mixed with Adj1 (60 and 69%, respectively, 24 h after application).

Using ExpF as a model compound it should be possible to investigate the behaviour of other formulation systems on target crops. A speci®c example of the use of this system is the evaluation of encapsulated formulations. It is possible to prepare capsules with a range of properties, one of these being ease of capsule breakdown, resulting in the release of the encapsulated compound. This can be monitored using arti®cial surfaces, but there is now the possibility of doing studies in vivo using the model described above.

Information about the loss of fungicide, insecticide and herbicide molecules in guttation ¯uid can also help explain biological performance against target species. For example, the activity of ExpF against Erysiphe graminis DC f sp tritici Marchal, (the causal organism of powdery mildew of wheat) was enhanced when mixed with Adj2 but not Adj1 (Moss, N A pers. comm.). From the results discussed above it is possible that a biologically signi®cant proportion of the applied dose of ExpF, when mixed with Adj1, was lost through guttation, resulting in an inferior performance compared with the mixture with Adj2. Life-cycle studies showed ExpF to be more effective as a protectant than curative fungicide and that the early stages of pathogen development were most affected. A formulation optimising surface retention rather than foliar uptake would, therefore, be more appropriate.

REFERENCES


📜 SIMILAR VOLUMES


Synthesis and insecticidal activity of n
✍ Uneme, Hideki; Iwanaga, Koichi; Higuchi, Noriko; Kando, Yasuyuki; Okauchi, Tetsu 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 202 KB 👁 2 views

## 3 Results The values (24 h) of dimethyl-and di-allyl-LD 50 thiosuünate were comparable, varying from 0.02 mg litre~1 against P. interpunctella to 0.25 mg litre~1 against C. maculatus, although those for thiosulünates were generally lower than those for disulüdes. In comparison, 24-h values for

Synthesis and insecticidal activity of n
✍ Yagi, Kazuo; Numata, Akira; Mimori, Norihiko; Miyake, Toshiro; Arai, Kazutaka; I 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 152 KB 👁 1 views

A series of novel 2-(2,4,6-trisubstituted phenyl)-1,3,4-oxadiazolin-5-one derivatives and 3-(2,4,6-trichlorophenyl)pyrazolin-5-one derivatives were synthesized and evaluated for insecticidal activity. It was found that a moderately bulky alkyl group, such as a tert-butyl group, on the heterocyclic r