PHOTOLYSIS OF DIMEPIPERATE IN AQUEOUS-SOLUTION

被引:1
作者
PUSINO, A [1 ]
GESSA, C [1 ]
LIU, WP [1 ]
机构
[1] ZHEJIANG UNIV,DEPT CHEM,HANGZHOU 310027,PEOPLES R CHINA
来源
PESTICIDE SCIENCE | 1992年 / 34卷 / 03期
关键词
D O I
10.1002/ps.2780340313
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Dimepiperate, S-(1-methyl-1-phenylethyl) piperidine-1-carbothioate (I) was degraded in aqueous solution by ultraviolet irradiation into piperidine (II), alpha-methylstyrene (III), acetophenone (IV), and formaldehyde (V). The reaction followed first-order kinetics. In sunlight the reaction occurred only in the presence of a sensitiser and afforded the same four photolytic degradation products. In the absence of oxygen the herbicide was converted much more rapidly, but yielded only (II) and (III) as products. A mechanism which accounts for the formation of the photoproducts is proposed.
引用
收藏
页码:269 / 271
页数:3
相关论文
共 8 条
[1]   1,2-DIOXETANE - SYNTHESIS, CHARACTERIZATION, STABILITY, AND CHEMI-LUMINESCENCE [J].
ADAM, W ;
BAADER, WJ .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1984, 23 (02) :166-167
[2]   4-MEMBERED RING PEROXIDES AS EXCITED-STATE EQUIVALENTS - A NEW DIMENSION IN BIOORGANIC CHEMISTRY [J].
ADAM, W ;
CILENTO, G .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1983, 22 (07) :529-542
[3]  
ANTONELLI C, 1986, ATTI GIORNATE FITOPA, V3, P327
[4]   REACTION OF SINGLET OXYGEN WITH OLEFINS - QUESTION OF MECHANISM [J].
FRIMER, AA .
CHEMICAL REVIEWS, 1979, 79 (05) :359-387
[5]  
IKEDA K, 1982, SHOKUBUTSU NO KAGAKU, V17, P163
[6]  
LOVERIDG.EL, 1971, J ORG CHEM, V36, P221
[7]  
TANAKA M, 1984, JPN PESTIC INF, V45, P18
[8]  
Vogel A., 1978, TXB PRACTICAL ORGANI, p[1130, 1228]