Pyrethroid photochemistry: decamethrin
Pyrethroid photochemistry: decamethrin
复制标题
拟除虫菊酯光化学:十氢菊酯
DOI:
10.1021/jf60214a006
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发表时间:
1977
影响因子:
6.1
通讯作者:
J. Casida
中科院分区:
文献类型:
--
作者:
L. Ruzo;R. L. Holmstead;J. Casida
MATERIALS AND METHODS Spectroscopy. Ultraviolet (UV) spectra were determined using the Bausch and Lomb Spectronic 505 double-beam UV spectrophotometer. Infrared (IR) spectra were recorded as KBr pellets unless otherwise specified with the Perkin-Elmer Model 457 grating IR spectro-photometer. Nuclear magnetic resonance(NMR) spectra were obtained with the Perkin-Elmer R32B 90 MHz spectrometer using samples dissolved in deuteriochloroform containing 1% tetramethylsilane (Me4Si) as internal standard. Chemical shifts () are reported in parts per million (ppm) downfield from Me4Si and coupling con-stants (J) are given in hertz (Hz). Mass spectra (MS) were recorded on a Finnigan Model 1015D mass spectrometer in combination with a System Industries Model 150 control system. The spectrometer was coupled to a Finnigan Model 9500 gas chromatograph operated with temperature programming (120-300 C, 10C/min) using He as carrier gas (20-25 mL/min). Methane was the reagent gas with a chemical ionization (Cl) source pressure of 0.5-1.0 Torr. Chromatography and Analyses. Gas chromatography (GC) for photoproduct quantitation utilized a Varian Aerograph Series 1400 instrument equipped with a flame ionization detector and a glass column (2 m X 3 mm id) of 3% Dexil on Varaport 30 (80-100 mesh). The column temperature was programmed (120-300 C, 10 C/min) with He as carrier gas (20-25 mL/min). Detector and injection port temperatures were 310 C. Individual peak