Literature DB >> 30901207

Orthophosphate and Sulfate Utilization for C-E (E = P, S) Bond Formation via Trichlorosilyl Phosphide and Sulfide Anions.

Michael B Geeson1, Pablo Ríos1, Wesley J Transue1, Christopher C Cummins1.   

Abstract

Reduction of phosphoric acid (H3PO4) or tetra- n-butylammonium bisulfate ([TBA][HSO4]) with trichlorosilane leads to the formation of the bis(trichlorosilyl)phosphide ([P(SiCl3)2]-, 1) and trichlorosilylsulfide ([Cl3SiS]-, 2) anions, respectively. Balanced equations for the formation of the TBA salts of anions 1 and 2 were formulated based on the identification of hexachlorodisiloxane and hydrogen gas as byproducts arising from these reductive processes: i) [H2PO4]- + 10HSiCl3 → 1 + 4O(SiCl3)2 + 6H2 for P and ii) [HSO4]- + 9HSiCl3 → 2 + 4O(SiCl3)2 + 5H2 for S. Hydrogen gas was identified by its subsequent use to hydrogenate an alkene ((-)-terpinen-4-ol) using Crabtree's catalyst ([(COD)Ir(py)(PCy3)][PF6], COD = 1,5-cyclooctadiene, py = pyridine, Cy = cyclohexyl). Phosphide 1 was generated in situ by the reaction of phosphoric acid and trichlorosilane and used to convert an alkyl chloride (1-chlorooctane) to the corresponding primary phosphine, which was isolated in 41% yield. Anion 1 was also prepared from [TBA][H2PO4] and isolated in 62% yield on a gram scale. Treatment of [TBA]1 with an excess of benzyl chloride leads to the formation of tetrabenzylphosphonium chloride, which was isolated in 61% yield. Sulfide 2 was used as a thionation reagent, converting benzophenone to thiobenzophenone in 62% yield. It also converted benzyl bromide to benzyl mercaptan in 55% yield. The TBA salt of trimetaphosphate ([TBA]3[P3O9]·2H2O), also a precursor to anion 1, was found to react with either trichlorosilane or silicon(IV) chloride to provide bis(trimetaphosphate)silicate, [TBA]2[Si(P3O9)2], characterized by NMR spectroscopy, X-ray crystallography, and elemental analysis. Trichlorosilane reduction of [TBA]2[Si(P3O9)2] also provided anion 1. The electronic structures of 1 and 2 were investigated using a suite of theoretical methods; the computational studies suggest that the trichlorosilyl ligand is a good π-acceptor and forms σ-bonds with a high degree of s character.

Entities:  

Year:  2019        PMID: 30901207     DOI: 10.1021/jacs.9b01475

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  6 in total

1.  Synthesis of monophosphines directly from white phosphorus.

Authors:  Daniel J Scott; Jose Cammarata; Maximilian Schimpf; Robert Wolf
Journal:  Nat Chem       Date:  2021-04-05       Impact factor: 24.427

Review 2.  Let's Make White Phosphorus Obsolete.

Authors:  Michael B Geeson; Christopher C Cummins
Journal:  ACS Cent Sci       Date:  2020-05-18       Impact factor: 14.553

Review 3.  Transition-Metal-Mediated Functionalization of White Phosphorus.

Authors:  Christian M Hoidn; Daniel J Scott; Robert Wolf
Journal:  Chemistry       Date:  2020-11-18       Impact factor: 5.236

4.  Sustainable Production of Reduced Phosphorus Compounds: Mechanochemical Hydride Phosphorylation Using Condensed Phosphates as a Route to Phosphite.

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Review 5.  Recent Breakthroughs in P4 Chemistry: Towards Practical, Direct Transformations into P1 Compounds.

Authors:  Daniel J Scott
Journal:  Angew Chem Int Ed Engl       Date:  2022-05-25       Impact factor: 16.823

6.  Binding, Release and Functionalization of Intact Pnictogen Tetrahedra Coordinated to Dicopper Complexes.

Authors:  Martin Piesch; Amélie Nicolay; Maria Haimerl; Michael Seidl; Gábor Balázs; T Don Tilley; Manfred Scheer
Journal:  Chemistry       Date:  2022-06-23       Impact factor: 5.020

  6 in total

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