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  2. Halogen bond - Wikipedia

    en.wikipedia.org/wiki/Halogen_bond

    The strength and directionality of halogen bonds are a key tool in the discipline of crystal engineering, which attempts to shape crystal structures through close control of intermolecular interactions. [32] Halogen bonds can stabilize copolymers [33] [34] or induce mesomorphism in otherwise isotropic liquids. [35]

  3. Bond-dissociation energy - Wikipedia

    en.wikipedia.org/wiki/Bond-dissociation_energy

    The term bond-dissociation energy is similar to the related notion of bond-dissociation enthalpy (or bond enthalpy), which is sometimes used interchangeably.However, some authors make the distinction that the bond-dissociation energy (D 0) refers to the enthalpy change at 0 K, while the term bond-dissociation enthalpy is used for the enthalpy change at 298 K (unambiguously denoted DH° 298).

  4. 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 ...

  5. Polyhalogen ions - Wikipedia

    en.wikipedia.org/wiki/Polyhalogen_ions

    Even though they have a reduced bond order, all three halogen atoms are tightly bound. The fluorine–fluorine bond of trifluoride, with bond order 0.5, has a bond-strength is 30 kcal/mol, only 8 kcal/mol less than the fluorine–fluorine bond in difluorine whose bond order is 1. [7]

  6. Dehalogenation - Wikipedia

    en.wikipedia.org/wiki/Dehalogenation

    The rate of dehalogenation depends on the strength of the bond between the carbon and halogen atom. The bond dissociation energies of carbon-halogen bonds are described as: H 3 C−I (234 kJ/mol), H 3 C−Br (293 kJ/mol), H 3 C−Cl (351 kJ/mol), and H 3 C−F (452 kJ/mol). Thus, for the same structures the bond dissociation rate for ...

  7. Inductive effect - Wikipedia

    en.wikipedia.org/wiki/Inductive_effect

    The strength of inductive effect is also dependent on the distance between the substituent group and the main group that react; the longer the distance, the weaker the effect. Inductive effects can be expressed quantitatively through the Hammett equation , which describes the relationship between reaction rates and equilibrium constants with ...

  8. Interhalogen - Wikipedia

    en.wikipedia.org/wiki/Interhalogen

    Most interhalogens are halogen fluorides, and all but three (IBr, AtBr, and AtI) of the remainder are halogen chlorides. Chlorine and bromine can each bond to five fluorine atoms, and iodine can bond to seven. AX and AX 3 interhalogens can form between two halogens whose electronegativities are relatively close to one another. When ...

  9. Halogen - Wikipedia

    en.wikipedia.org/wiki/Halogen

    The halogens (/ ˈ h æ l ə dʒ ə n, ˈ h eɪ-,-l oʊ-,-ˌ dʒ ɛ n / [1] [2] [3]) are a group in the periodic table consisting of six chemically related elements: fluorine (F), chlorine (Cl), bromine (Br), iodine (I), and the radioactive elements astatine (At) and tennessine (Ts), though some authors [4] would exclude tennessine as its chemistry is unknown and is theoretically expected to ...