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  2. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    The F 2 molecule is commonly described as having exactly one bond (in other words, a bond order of 1) provided by one p electron per atom, as are other halogen X 2 molecules. However, the heavier halogens' p electron orbitals partly mix with those of d orbitals, which results in an increased effective bond order; for example, chlorine has a ...

  3. Single bond - Wikipedia

    en.wikipedia.org/wiki/Single_bond

    The increase in component bonds is the reason for this attraction increase as more electrons are shared between the bonded atoms (Moore, Stanitski, and Jurs 343). Single bonds are often seen in diatomic molecules. Examples of this use of single bonds include H 2, F 2, and HCl. Single bonds are also seen in molecules made up of more than two atoms.

  4. Covalent radius of fluorine - Wikipedia

    en.wikipedia.org/wiki/Covalent_radius_of_fluorine

    The covalent radius is defined as half the bond lengths between two neutral atoms of the same kind connected with a single bond. By this definition, the covalent radius of F is 71 pm. However, the F-F bond in F 2 is abnormally weak and long. Besides, almost all bonds to fluorine are highly polar because of its large electronegativity, so the ...

  5. Molecular binding - Wikipedia

    en.wikipedia.org/wiki/Molecular_binding

    Among the tightest known protein–protein complexes is that between the enzyme angiogenin and ribonuclease inhibitor; the dissociation constant for the human proteins is 5x10 −16 mol/L. [3] [4] Another biological example is the binding protein streptavidin, which has extraordinarily high affinity for biotin (vitamin B7/H, dissociation ...

  6. Diatomic molecule - Wikipedia

    en.wikipedia.org/wiki/Diatomic_molecule

    All diatomic molecules are linear and characterized by a single parameter which is the bond length or distance between the two atoms. Diatomic nitrogen has a triple bond, diatomic oxygen has a double bond, and diatomic hydrogen, fluorine, chlorine, iodine, and bromine all have single bonds. [6]

  7. Carbon–fluorine bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–fluorine_bond

    Carbon–fluorine bonds can have a bond dissociation energy (BDE) of up to 130 kcal/mol. [2] The BDE (strength of the bond) of C–F is higher than other carbon–halogen and carbon–hydrogen bonds. For example, the BDEs of the C–X bond within a CH 3 –X molecule is 115, 104.9, 83.7, 72.1, and 57.6 kcal/mol for X = fluorine, hydrogen ...

  8. Fluorine - Wikipedia

    en.wikipedia.org/wiki/Fluorine

    2 K 2 MnF 6 + 4 SbF 5 → 4 KSbF 6 + 2 MnF 3 + F 2 ↑ Christe later commented that the reactants "had been known for more than 100 years and even Moissan could have come up with this scheme." [ 178 ] As late as 2008, some references still asserted that fluorine was too reactive for any chemical isolation.

  9. Double bond rule - Wikipedia

    en.wikipedia.org/wiki/Double_bond_rule

    Moreover, the multiple bonds of the elements with n=2 are much stronger than usual, because lone pair repulsion weakens their sigma bonding but not their pi bonding. [2] An example is the rapid polymerization that occurs upon condensation of disulfur , the heavy analogue of O 2 .