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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Bauer, Tillmann
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article
Studies on the synthesis, structure and reactivity of heterocyclic metallonitridophosphinates
Abstract
<p>t-BuP(NH2)(2) reacts with base-stabilized group 13 trihydrides with adduct formation (THF-BH3), with reduction to give t-BuPH2 (Me3N-AlH3) and with elimination of H-2 and formation of a metallonitridophosphinate (Me3N-GaH3). In contrast, the reaction with Cp*TiMe3 proceeds with formation of the four-membered heterocycle [t-Bu(H)P(NH)(2)Ti(Cp*)Me-2]. The aluminonitridophosphinate [t-Bu(H)P(NH)(2)AlMe2](2), reacts with C-H acidic reagents such as ROH, H2O with protonation of the N atom and subsequent formation of t-BuP(NH,),. This general reaction sequence was used for the synthesis of the first alumino(oxo)nitridophosphinate [t-Bu(H)P(NH)OAlMe2](2). The compounds were characterized by spectroscopic methods (H-1, C-13, IR, mass spectrometry) and single crystal X-ray diffraction ([t-Bu(H)P(NH)(2)Ti(Cp*)Me-2], [t-Bu(H)P(NH)OAlMe2](2)).</p>