Results 231 to 240 of about 15,838,839 (288)
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Phospha-S-triazines. VIII. Chloro-substituted diphospha-S-triazines
Journal of Fluorine Chemistry, 1985Abstract 1,3-Bis(phenylchlorophospha)-5-perfluoroalkyl-2,4,6- triazine and the corresponding perfluoroalkylether analogue were synthesized by interaction of equimolar amounts of the respective amidines and imido-diphenyl-diphosphinic acid pentachloride.
K.J.L. Paciorek +4 more
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The vibrational spectra of s-triazine and s-triazine-d3
Spectrochimica Acta, 1961Abstract The infrared and Raman spectra of s-triazine and s-triazine-d3 have been taken and an assignment of the fundamental vibrational modes has been made. Nearly all the remaining observed bands are accounted for as combinations or overtones. A simple valence force field normal co-ordinate analysis was made, and the values of some force constants ...
J.E. Lancaster, R.F. Stamm, N.B. Colthup
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S-triazine residues in groundwater
Chemosphere, 1997In the last years, the occurrence of pesticides and other chemicals in groundwater has been confirmed. The herbicide atrazine is among the pesticides most frequently detected in groundwater. In groundwater samples from the United States atrazine concentrations reached levels up to 10 micrograms/1.
U, Dörfler, E A, Feicht, I, Scheunert
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Phospa-s-triazines. X. Thiophenyl-substituted phospha-s-triazines
Journal of Fluorine Chemistry, 1985Abstract A series of thiophenyl-substituted mono- and diphosphas-triazines was prepared. These materials exhibited physical characteristics similar to those of the corresponding phenyl analogues, but the mass spectral breakdown patterns were dominated by the loss of the thiophenyl group and differed signficantly from that of the other phospha-s ...
K.J.L. Paciorek +4 more
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Journal of Molecular Structure, 1996
The vibrational spectra of s-triazine, trifluoro-s-triazine and trichloro-s-triazinc were calculated by using the 3-21G basis set and the program system GAUSSIAN 90. The ab initio force fields were scaled to try to reproduce the best values assigned for experimental frequencies for the above-mentioned molecules. The transferability of the scale factors
A. Navarro +4 more
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The vibrational spectra of s-triazine, trifluoro-s-triazine and trichloro-s-triazinc were calculated by using the 3-21G basis set and the program system GAUSSIAN 90. The ab initio force fields were scaled to try to reproduce the best values assigned for experimental frequencies for the above-mentioned molecules. The transferability of the scale factors
A. Navarro +4 more
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Phospha-s-triazines. VII. Phenyl-bridged phospha-s-triazines
Journal of Fluorine Chemistry, 1983Abstract 1,4-Bis (phenyltrichlorophosphino)benzene was synthesized by a 4-step process in an overall 58% yield. Interaction of the bis(trichlorophosphorane) with the appropriate imidoylamidines afforded the novel 1,4-bis[1-phenylphospha-3,5-bis(perfluoro-n-heptyl)-2,4,6-triazino]benzene and 1,4-bis[1-phenylphospha-3,5-bis(perfluoroalkylether)-2,4,6 ...
K.J.L. Paciorek +4 more
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Capillary gas chromatography of s-triazines
Journal of Chromatography A, 1977In order to achieve better resolution and lower detection limits for s-triazines, glass capillary columns made of soft soda-lime glass and etched with gaseous hydrogen chloride have been introduced. Columns with non-polar (OV-101, SE-30) mixed (Carbowax 20M + SE-30) and polar stationary liquids (Carbowax 20M) were used.
E, Matisová, J, Krupcik
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s-Triazines. Part I. Synthesis and reactions of dihalogeno-heteroaryl-s-triazines
Journal of the Chemical Society, Perkin Transactions 1, 1973Metallated derivatives of substituted or unsubstituted furans, thiophens, and pyrroles react with 2,4,6-trichloro-s-triazine (cyanuric chloride) to produce the corresponding 2,4-dichloro-6-(heteroaryl)-s-triazines. The effect of electrophilic substitution (nitration and bromination) on such ring systems is described.
Jiban K. Chakrabarti +2 more
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Chemischer Informationsdienst, 1974
AbstractAus Cyanurchlorid (I) und verschiedenen Pyrrol‐, Thiophen‐ oder Furan‐Derivaten (II) entstehen die Monosubstitutionsprodukte (III), die z.Tl. einer nachträglichen Modifizierung unterworfen werden.
J. K. CHAKRABARTI, D. E. TUPPER
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AbstractAus Cyanurchlorid (I) und verschiedenen Pyrrol‐, Thiophen‐ oder Furan‐Derivaten (II) entstehen die Monosubstitutionsprodukte (III), die z.Tl. einer nachträglichen Modifizierung unterworfen werden.
J. K. CHAKRABARTI, D. E. TUPPER
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Microbial degradation of s-triazine herbicides
1970Biodegradation is a significant factor affecting the residual life and toxicity of many pesticides1 in soils. Soil microorganisms may act upon a pesticide in several ways. One mechanism may involve degradation with ultimate detoxication and/or metabolism of the pesticide, whereas another mechanism may involve the activation or toxication of an ...
D D, Kaufman, P C, Kearney
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