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  2. Bis(diphenylphosphino)methane - Wikipedia

    en.wikipedia.org/wiki/Bis(diphenylphosphino)methane

    1,1-Bis(diphenylphosphino)methane (dppm), is an organophosphorus compound with the formula CH 2 (PPh 2) 2. Dppm, a white, crystalline powder, is used in inorganic and organometallic chemistry as a ligand. [1] It is more specifically a chelating ligand because it is a ligand that can bond to metals with two phosphorus donor atoms.

  3. Tetrakis (3,5-bis (trifluoromethyl)phenyl)borate - Wikipedia

    en.wikipedia.org/wiki/Tetrakis(3,5-bis(trifluoro...

    The [BAr F 4] − anion with four fluorinated aryl groups distributed tetrahedrally about a central boron atom. Tetrakis[3,5-bis(trifluoromethyl)phenyl]borate is an anion with chemical formula [{3,5-(CF 3) 2 C 6 H 3} 4 B] −, which is commonly abbreviated as [BAr F 4] −, indicating the presence of fluorinated aryl (Ar F) groups.

  4. Bis(benzene)chromium - Wikipedia

    en.wikipedia.org/wiki/Bis(benzene)chromium

    Bis(benzene)chromium is the organometallic compound with the formula Cr(η 6-C 6 H 6) 2. It is sometimes called dibenzenechromium. It is sometimes called dibenzenechromium. The compound played an important role in the development of sandwich compounds in organometallic chemistry and is the prototypical complex containing two arene ligands .

  5. Bis(trimethylsilyl)amine - Wikipedia

    en.wikipedia.org/wiki/Bis(trimethylsilyl)amine

    Bis(trimethylsilyl)amine (also known as hexamethyldisilazane and HMDS) is an organosilicon compound with the molecular formula [(CH 3) 3 Si] 2 NH. The molecule is a derivative of ammonia with trimethylsilyl groups in place of two hydrogen atoms.

  6. 1,8-Bis (dimethylamino)naphthalene - Wikipedia

    en.wikipedia.org/wiki/1,8-Bis(dimethylamino...

    With a pK a of 12.34 [4] for its conjugate acid in aqueous solution, 1,8-bis(dimethylamino)naphthalene is one of the strongest organic bases. However, it only absorbs protons slowly—hence the trade name. The high basicity is attributed to the relief of strain upon protonation and/or the strong interaction between the nitrogen lone pairs. [3]

  7. Organobismuth chemistry - Wikipedia

    en.wikipedia.org/wiki/Organobismuth_chemistry

    For example: Me 3 Bi + SO 2 Cl 2 → Me 3 BiCl 2 + SO 2 Me 3 BiCl 2 + 2 MeLi → Me 5 Bi + 2 LiCl. Unstable, purple Ph 5 Bi was the first to be synthesized so. [6] Bi(V) easily forms an onium ion for example by protonation with p-toluenesulfonic acid: [19] Ph 5 Bi + HO 3 SAr → Ph 4 Bi + [O 3 SAr −] Pentaphenylbismuth forms an ate complex ...

  8. Bisoxazoline ligand - Wikipedia

    en.wikipedia.org/wiki/Bisoxazoline_ligand

    Bis(oxazoline) ligands (often abbreviated BOX ligands) are a class of privileged chiral ligands containing two oxazoline rings. They are typically C 2 ‑symmetric and exist in a wide variety of forms; with structures based around CH 2 or pyridine linkers being particularly common (often generalised BOX and PyBOX respectively).

  9. Disiamylborane - Wikipedia

    en.wikipedia.org/wiki/Disiamylborane

    Disiamylborane (bis(1,2-dimethylpropyl)borane) is an organoborane with the formula [((CH 3) 2 CHCH(CH 3)) 2 BH] 2 (abbreviation: Sia 2 BH). It is a colorless waxy solid that is used in organic synthesis for hydroboration–oxidation reactions. Like most dialkyl boron hydrides, it has a dimeric structure with bridging hydrides.