Related Experiment Video
Updated: May 9, 2026

Combining Solid-state and Solution-based Techniques: Synthesis and Reactivity of Chalcogenidoplumbates(II or IV)
Published on: December 29, 2016
Synthesis of cationic R2P5(+) cages and subsequent chalcogenation reactions
Michael H Holthausen1, Alexander Hepp, Jan J Weigand
1Institut für Anorganische und Analytische Chemie, Westfälische Wilhelms-Universität Münster, Corrensstrasse 30, 48149 Münster, Germany.
Abstract:
Cationic R2P5(+) cage compounds (1(+)) have been synthesized by the stoichiometric reaction of R2PCl, GaCl3 and P4. The reaction conditions depend on the substituent R. Alkyl-substituted derivatives (1 a-1 d[GaCl4]) are best synthesized under solvent-free conditions, whereas aryl-substituted derivatives (1 e-1 h[GaCl4]) are formed in C6H5F. All compounds have been prepared on a multi-gram scale in good to excellent yields and have been fully characterized with an emphasis on (31P NMR spectroscopy in solution and single-crystal structure determination. Subsequent chalcogenation reactions of cations R2P5(+) (1 a(+), 1 e(+)) and trication Ph6P7(3+) (3(3+)) with elemental sulfur (α-S8) or grey selenium (Se(grey)) yielded a series of unique polyphosphorus-chalcogen cations (4 a(+), 4 e(+), 5 a(+), 6(2+) and 7(2+)), possessing nortricyclane-type molecular structures. An in-depth study of the (31)P{(1)H} and (77)Se NMR spectroscopic parameters is presented, and correlations between the substitution pattern and the observed structural features have been investigated in detail.
More Related Videos
Related Concept Videos
Preparation and Reactions of Sulfides
Carboxylic Acids to Acid Chlorides
Electrophilic Aromatic Substitution: Chlorination and Bromination of Benzene
Chirality at Nitrogen, Phosphorus, and Sulfur
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
[3,3] Sigmatropic Rearrangement of 1,5-Dienes: Cope Rearrangement
α-Bromination of Carboxylic Acids: Hell–Volhard–Zelinski Reaction

