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  2. Tris(trimethylsilyl)phosphine - Wikipedia

    en.wikipedia.org/wiki/Tris(trimethylsilyl)phosphine

    Tris(trimethylsilyl)phosphine is prepared by treating trimethylsilyl chloride, white phosphorus, and sodium-potassium alloy: [2] 1/4 P 4 + 3 Me 3 SiCl + 3 K → P(SiMe 3) 3 + 3 KCl. Several other methods exist. [1] Copper phosphide cluster Cu 96 P 30 {P(SiMe 3) 2} 6 (PEt 3) 18 with C and H atoms omitted for clarity (red=Cu, purple=P, tan=Si ...

  3. Trimethylsilyl group - Wikipedia

    en.wikipedia.org/wiki/Trimethylsilyl_group

    A trimethylsilyl group (abbreviated TMS) is a functional group in organic chemistry.This group consists of three methyl groups bonded to a silicon atom [−Si(CH 3) 3], which is in turn bonded to the rest of a molecule.

  4. Diethylphosphite - Wikipedia

    en.wikipedia.org/wiki/Diethylphosphite

    Many analogues of diethyl phosphite can be prepared. [4] [5] Despite being named as a phosphite the compound exists overwhelmingly in its phosphonate form, (C 2 H 5 O) 2 P(O)H, a property it shares with its parent acid phosphorous acid. Nonetheless many of its reactions appear to proceed via the minor phosphorus(III) tautomer. [6]

  5. Dimethyl methylphosphonate - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_methylphosphonate

    Dimethyl methylphosphonate can be prepared from trimethyl phosphite and a halomethane (e.g. iodomethane) via the Michaelis–Arbuzov reaction. [2]Dimethyl methylphosphonate is a schedule 2 chemical as it may be used in the production of chemical weapons.

  6. Trimethyl phosphite - Wikipedia

    en.wikipedia.org/wiki/Trimethyl_phosphite

    P(OCH 3) 3 → CH 3 P(O)(OCH 3) 2. As a ligand, trimethyl phosphite has a smaller cone angle and better acceptor properties relative to trimethylphosphine. A representative derivative is the colorless tetrahedral complex Ni(P(OMe) 3) 4 (m.p. 108 °C). [4] The tridentate ligand called the Kläui ligand is derived from trimethyl phosphite. The ...

  7. Triethyl phosphonoacetate - Wikipedia

    en.wikipedia.org/wiki/Triethyl_phosphonoacetate

    Triethyl phosphonoacetate is a reagent for organic synthesis used in the Horner-Wadsworth-Emmons reaction (HWE) or the Horner-Emmons modification.. Triethyl phosphonoacetate can be added dropwise to sodium methoxide solution to prepare a phosphonate anion.

  8. Michaelis–Arbuzov reaction - Wikipedia

    en.wikipedia.org/wiki/Michaelis–Arbuzov_reaction

    [2] [3] This reaction is widely used for the synthesis of various phosphonates, phosphinates, and phosphine oxides. Several reviews have been published. [4] [5] The reaction also occurs for coordinated phosphite ligands, as illustrated by the demethylation of {(C 5 H 5)Co[(CH 3 O) 3 P] 3} 2+ to give {(C 5 H 5)Co[(CH 3 O) 2 PO] 3} −, which is ...

  9. Dimethylphosphite - Wikipedia

    en.wikipedia.org/wiki/Dimethylphosphite

    Dimethylphosphite is an organophosphorus compound with the formula (CH 3 O) 2 P(O)H, known as dimethyl hydrogen phosphite (DMHP). Dimethylphosphite, is a minor tautomer of the phosphorus(V) derivative. It is a reagent for generating other organophosphorus compounds, exploiting the high reactivity of the P-H bond. The molecule is tetrahedral. It ...