1950
DOI: 10.1007/bf01525622
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�ber lonotropie

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Cited by 3 publications
(3 citation statements)
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“…Topchiev et al (2) prepared poly-P-nitrostyrene by the action of sodium methylate on the monomer, but did not succeed with BF3.Et20, BF3.H3P0, or benzoylperoxyde a s initiator. Worrall zaldehyde and nitromethane by the method of Thiele (9), melted at 56- (2) Copolymerization. Preliminary experiments showed that the addition of 10% w/w of P-nitrostyrene to styrene inhibits its polymerization, even when heating for several days at 8OoC.…”
Section: Introductionmentioning
confidence: 99%
“…Topchiev et al (2) prepared poly-P-nitrostyrene by the action of sodium methylate on the monomer, but did not succeed with BF3.Et20, BF3.H3P0, or benzoylperoxyde a s initiator. Worrall zaldehyde and nitromethane by the method of Thiele (9), melted at 56- (2) Copolymerization. Preliminary experiments showed that the addition of 10% w/w of P-nitrostyrene to styrene inhibits its polymerization, even when heating for several days at 8OoC.…”
Section: Introductionmentioning
confidence: 99%
“…With the exception of the value for run 11 the k^ values for both the electron exchange (runs [1][2][3][4][5][6][7][8][9][10][11][12][13] and the £(G^.^)…”
Section: Analysis Of These Solutions Indicates the Presencementioning
confidence: 99%
“…Extraction of these solutions with water yields basic solutions (pEf?). The compound does not cause the liberation of iodine from potassium iodide and cannot be hydrogenated with the usual catalysts 7…”
mentioning
confidence: 99%