0000000000988105

AUTHOR

Sabine Strobel

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Strukturanalytische Untersuchungen P-substituierter 1,3,2-Diazaphospholidine

2011

2-Diphenylphosphanyl-1,3,2-diazaphospholidines were prepared via metathesis from 2-chloro-1,3,2-diazaphospholidines and LiPPh2. For some of the products, symmetrisation to tetraphenyldiphosphane and 2,2′-bis-1,3,2-diazaphospholidinyls was observed. Most of the derivatives were characterised by single-crystal X-ray diffraction, which showed that all compounds studied feature elongated exocyclic P–Cl or P–P-bonds, respectively. The extent of this bond lengthening is in the P-phosphanyl-substituted species similar and in the P-chloro-derivatives less pronounced than in corresponding CC-unsaturated 1,3,2-diazaphospholenes. Structure correlation involving comparison of exocyclic P–X and endocycl…

Inorganic ChemistryCrystallography010405 organic chemistryStereochemistryChemistryX-ray crystallographyReactivity (chemistry)010402 general chemistryMetathesisHyperconjugation01 natural sciences0104 chemical sciencesZeitschrift für anorganische und allgemeine Chemie
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