1970
DOI: 10.1070/rc1970v039n01abeh001908
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Cyclodiphosphazanes

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Cited by 20 publications
(4 citation statements)
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“…Treating 2 with N , N -dimethylaminotrimethylsilane was attempted as an alternate route to 3 ; however, no reaction occurred under reasonable conditions even though formation of the aminophosphinodiazaphosphole and trimethylfluorosilane should be favored by at least 20 kJ mol -1 . The reason for the lack of reaction here is not clear as examples are known in which the reaction proceeds as expected. Cases are also known where a fluorophosphorus compound does not react with aminosilanes, and we surmise that the reduced basicity of the fluorinated phosphine 2 may inhibit reaction through kinetic constraints.…”
Section: Resultsmentioning
confidence: 83%
See 1 more Smart Citation
“…Treating 2 with N , N -dimethylaminotrimethylsilane was attempted as an alternate route to 3 ; however, no reaction occurred under reasonable conditions even though formation of the aminophosphinodiazaphosphole and trimethylfluorosilane should be favored by at least 20 kJ mol -1 . The reason for the lack of reaction here is not clear as examples are known in which the reaction proceeds as expected. Cases are also known where a fluorophosphorus compound does not react with aminosilanes, and we surmise that the reduced basicity of the fluorinated phosphine 2 may inhibit reaction through kinetic constraints.…”
Section: Resultsmentioning
confidence: 83%
“…The reason for the lack of reaction here is not clear as examples are known in which the reaction proceeds as expected. [25][26][27] Cases are also known where a fluorophosphorus compound does not react with aminosilanes, 27 and we surmise that the reduced basicity of the fluorinated phosphine 2 may inhibit reaction through kinetic constraints.…”
Section: The Dihalogenated Phosphinephospholes (A) Preparation Of The...mentioning
confidence: 99%
“…, A 8.464 (4) 8.647 (2) 8.58 (5) b, A 12.552 (4) 10.985 (3) 10.99 (5) c, A 7.345 (2) 8.440 (2) 8.50 (5) a, deg 93. 45 (2) 106.99 (2) 106.6 (10) <3, deg 113.56 (3) 113.88(2) 114.8 (10) y, deg V, A3 99.52 (3) 70.…”
Section: Introductionunclassified
“…Les phosphinimines peuvent soit exister sous la forrne monornbre, soit donner par dimtrisation, un cycle diazadiphosphacyclobutane (17). Nous n'avons obtenu une forrne monom k e stable que dans un seul cas (8A).…”
Section: Discussionunclassified