enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Carbon–hydrogen bond activation - Wikipedia

    en.wikipedia.org/wiki/Carbon–hydrogen_bond...

    This species then binds to an alkane molecule, forming a σ-complex (coordination of a C-H bond). In a third step, the metal atom inserts into the C-H bond, cleaving it and yielding the alkyl (or aryl) metal hydride. The intermediates and their kinetics can be observed using time-resolved spectroscopic techniques (e.g. TR-IR, TR-XAS, TR-RIXS ...

  3. Carbon–hydrogen bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–hydrogen_bond

    The length of the carbonhydrogen bond varies slightly with the hybridisation of the carbon atom. A bond between a hydrogen atom and an sp 2 hybridised carbon atom is about 0.6% shorter than between hydrogen and sp 3 hybridised carbon. A bond between hydrogen and sp hybridised carbon is shorter still, about 3% shorter than sp 3 C-H.

  4. Agostic interaction - Wikipedia

    en.wikipedia.org/wiki/Agostic_interaction

    The term agostic is reserved to describe two-electron, three-center bonding interactions between carbon, hydrogen, and a metal. Two-electron three-center bonding is clearly implicated in the complexation of H 2, e.g., in W(CO) 3 (PCy 3) 2 H 2, which is closely related to the agostic complex shown in the figure. [8]

  5. Hydrogen bond - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_bond

    Consequently, hydrogen bonds between or within solute molecules dissolved in water are almost always unfavorable relative to hydrogen bonds between water and the donors and acceptors for hydrogen bonds on those solutes. [44] Hydrogen bonds between water molecules have an average lifetime of 10 −11 seconds, or 10 picoseconds. [45]

  6. Non-covalent interaction - Wikipedia

    en.wikipedia.org/wiki/Non-covalent_interaction

    A hydrogen bond (H-bond), is a specific type of interaction that involves dipole–dipole attraction between a partially positive hydrogen atom and a highly electronegative, partially negative oxygen, nitrogen, sulfur, or fluorine atom (not covalently bound to said hydrogen atom). It is not a covalent bond, but instead is classified as a strong ...

  7. C–H···O interaction - Wikipedia

    en.wikipedia.org/wiki/C–H···O_interaction

    Bond strength is less than 1 kcal/mol. In the case of aromatic C–H donors, C–H···O interactions are not linear due to influence of aromatic ring substituents near the interacting C-H group. [ 6 ] [ 7 ] If aromatic molecules involved in С–Н···О interaction belong to the group of polycyclic aromatic hydrocarbons , the strength of C ...

  8. Hydrogen compounds - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_compounds

    By some definitions, "organic" compounds are only required to contain carbon. However, most of them also contain hydrogen, and because it is the carbon-hydrogen bond that gives this class of compounds most of its particular chemical characteristics, carbon-hydrogen bonds are required in some definitions of the word "organic" in chemistry. [12]

  9. Host–guest chemistry - Wikipedia

    en.wikipedia.org/wiki/Host–guest_chemistry

    Host–guest chemistry encompasses the idea of molecular recognition and interactions through non-covalent bonding. Non-covalent bonding is critical in maintaining the 3D structure of large molecules, such as proteins and is involved in many biological processes in which large molecules bind specifically but transiently to one another.