enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Phosphite ester - Wikipedia

    en.wikipedia.org/wiki/Phosphite_ester

    Phosphite esters may be used as reducing agents in more specialised cases. For example, triethylphosphite is known to reduce certain hydroperoxides to alcohols formed by autoxidation [7] (scheme). In this process the phosphite is converted to a phosphate ester. This reaction type is also utilized in the Wender Taxol total synthesis.

  3. Ligand cone angle - Wikipedia

    en.wikipedia.org/wiki/Ligand_cone_angle

    In contrast, the solid-angle concept derives both bond length and the perimeter from empirical solid state crystal structures. [ 5 ] [ 6 ] There are advantages to each system. If the geometry of a ligand is known, either through crystallography or computations, an exact cone angle ( θ ) can be calculated.

  4. Organophosphorus chemistry - Wikipedia

    en.wikipedia.org/wiki/Organophosphorus_chemistry

    The P=O bond is very polar with a dipole moment of 4.51 D for triphenylphosphine oxide. [citation needed] Compounds related to phosphine oxides include phosphine imides (R 3 PNR') and related chalcogenides (R 3 PE, where E = S, Se, Te). These compounds are some of the most thermally stable organophosphorus compounds.

  5. Phosphonium - Wikipedia

    en.wikipedia.org/wiki/Phosphonium

    The Michaelis–Arbuzov reaction is the chemical reaction of a trivalent phosphorus ester with an alkyl halide to form a pentavalent phosphorus species and another alkyl halide. Commonly, the phosphorus substrate is a phosphite ester (P(OR) 3) and the alkylating agent is an alkyl iodide. [11] The mechanism of the Michaelis–Arbuzov reaction

  6. Trimethyl phosphite - Wikipedia

    en.wikipedia.org/wiki/Trimethyl_phosphite

    Trimethyl phosphite is an organophosphorus compound with the formula P(OCH 3) 3, often abbreviated P(OMe) 3.It is a colorless liquid with a highly pungent odor. It is the simplest phosphite ester and finds used as a ligand in organometallic chemistry and as a reagent in organic synthesis.

  7. Dimethylphenylphosphine - Wikipedia

    en.wikipedia.org/wiki/Dimethylphenylphosphine

    The ligand cone angle (θ) is the apex angle of a cylindrical cone, which is centered 2.28 Å from the center of the P atom. However, the cone angle of an unsymmetrical ligand cannot be determined in the same. In order to determine an effective cone angle for an unsymmetrical ligand PX 1 X 2 X 3, the following equation is used:

  8. Trimethylolpropane phosphite - Wikipedia

    en.wikipedia.org/wiki/Trimethylolpropane_phosphite

    Trimethylolpropane phosphite, C 2 H 5 C(CH 2 O) 3 P, is a phosphite ester used as a ligand in organometallic chemistry. Trimethylolpropane phosphite is sometimes abbreviated to EtCage. It is a white solid that is soluble in organic solvents. It is also highly toxic. [1]

  9. Bent's rule - Wikipedia

    en.wikipedia.org/wiki/Bent's_rule

    Yet, clearly the bond angles between all these molecules deviate from their ideal geometries in different ways. Bent's rule can help elucidate these apparent discrepancies. [5] [20] [21] Electronegative substituents will have more p character. [5] [20] Bond angle has a proportional relationship with s character and an inverse relationship with ...