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Updated: May 2, 2026

Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of PhosphorusI
Published on: November 22, 2016
Cationic chains of phosphanyl- and arsanylboranes
Christian Marquardt1, Christine Thoms, Andreas Stauber
1University of Regensburg, Institut für Anorganische Chemie, 93040 Regensburg (Germany).
Researchers synthesized novel mixed Group 13/15 cationic chains, expanding known cationic chain chemistry. These new compounds exhibit high thermodynamic stability and unique structural properties.
Area of Science:
- Inorganic Chemistry
- Organometallic Chemistry
- Materials Science
Background:
- Cationic phosphorus chains have been extensively studied.
- Mixed Group 13/15 element cationic chains remained unreported prior to this study.
Purpose of the Study:
- To synthesize and characterize novel mixed Group 13/15 element cationic chain compounds.
- To explore the reactivity of pnictogenboranes with monohalideboranes.
- To investigate the structural and electronic properties of these new cationic chains.
Main Methods:
- Synthesis of cationic chain compounds using pnictogenboranes (H2EBH2⋅NMe3, E=P, As) and monohalideboranes.
- Characterization via X-ray structure analysis, NMR spectroscopy, IR spectroscopy, and mass spectrometry.
- Density Functional Theory (DFT) calculations to elucidate reaction pathways, stability, and charge distribution.
Main Results:
- Successful synthesis of mixed Group 13/15 cationic chain compounds with the general formula [Me3N⋅BH2EH2BH2⋅NMe3][X] (E=P, As; X=AlCl4, I) and [Me3N⋅BH2PH2BH2PH2BH2⋅NMe3][X] (X=I, VCl4(thf)2).
- Comprehensive characterization confirmed the structures and properties of the synthesized compounds.
- DFT calculations supported the experimental findings, revealing high thermodynamic stability and detailed charge distribution.
Conclusions:
- This work reports the first examples of mixed Group 13/15 element cationic chains.
- The synthesized compounds are structurally characterized and their stability is confirmed.
- The study provides insights into the formation and properties of these novel inorganic cationic structures.
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Acidity of 1-Alkynes
The acidic strength of hydrocarbons follows the order: Alkynes > Alkenes > Alkanes. The strength of an acid is commonly expressed in units of pKa — the lower the pKa, the stronger the acid. Among the hydrocarbons, terminal alkynes have lower pKa values and are, therefore, more acidic. For example, the pKa values for ethane, ethene, and acetylene are 51, 44, and 25, respectively, as shown here.
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
Electrophilic Addition to Alkynes: Halogenation
Halogenation is another class of electrophilic addition reactions where a halogen molecule gets added across a π bond. In alkynes, the presence of two π bonds allows for the addition of two equivalents of halogens (bromine or chlorine). The addition of the first halogen molecule forms a trans-dihaloalkene as the major product and the cis isomer as the minor product. Subsequent addition of the second equivalent yields the tetrahalide.

