1971
DOI: 10.1021/jf60177a027
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Chlordane photoalteration products. Preparation and identification

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Cited by 33 publications
(10 citation statements)
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“…The fragment with highest mass appeared at m/e 371 which was due to loss of a chlorine from the molecular ion (M+ -Cl). The remainder of the spectra in all cases were in conformity with previous studies on similar molecules (Benson et al, 1971; Knox et al, 1973;Onuska and Comba, 1975), involving further losses of Cl, HC1, or their com- was present at m/e 373. The similarity of mass spectra in conjunction with identical retention times on GLC columns and closeness of behavior on thin-layer plates (Table II) showed that PC I and PC II were isomeric molecules.…”
Section: Resultssupporting
confidence: 88%
“…The fragment with highest mass appeared at m/e 371 which was due to loss of a chlorine from the molecular ion (M+ -Cl). The remainder of the spectra in all cases were in conformity with previous studies on similar molecules (Benson et al, 1971; Knox et al, 1973;Onuska and Comba, 1975), involving further losses of Cl, HC1, or their com- was present at m/e 373. The similarity of mass spectra in conjunction with identical retention times on GLC columns and closeness of behavior on thin-layer plates (Table II) showed that PC I and PC II were isomeric molecules.…”
Section: Resultssupporting
confidence: 88%
“…PC arises from cis-chlordane (Figure 1,1) by intramolecular rearrangement which offers several possibilities. Benson et al (1971) proposed two alternate configurations of the molecule (Figure 1, II and III) but it was not possible to decide which of the two isomeric forms was produced in their experiments. Knox et al (1973) suggested C2 to C5 bridging (Figure 1, II) in the molecule.…”
Section: Methodsmentioning
confidence: 99%
“…(Podowski et al, 1979). Exposure of cis-chlordane to UV irradiation or sunlight (Benson et al, 1971) results in the formation of the photoisomer, cis-photochlordane, which has higher acute toxicity than the parent compound to several vertebrate species (Podowski et al, 1979). Whereas the fate of photoisomers of other cyclodienes has been studied in various organisms [photodieldrin in the rat (Dailey et al, 1970(Dailey et al, ,1972; Reddy and Khan, 1974), mouse, housefly, (Reddy and Khan, 1974), rabbit (Reddy andKhan, 1975, 1977a), and rhesus monkey (Nohynek et al, 1979); photoisodrin in mouse and houseflies ( Structural formulae of cis-chlordane (I) and some of its possible photoisomers bridge; III, C2-C6;…”
mentioning
confidence: 99%
“…Shown in Figure 4-B are some of the major peaks of technical chlordane. Figure 5displays a mixture of degraded technical chlordane [22,23] and degraded toxaphene [24,25]. In this sample, toxaphene was determined by auto-integration on a packed column.…”
Section: Linearitymentioning
confidence: 99%