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  2. Coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Coupling_reaction

    In one important reaction type, a main group organometallic compound of the type R-M (where R = organic group, M = main group centre metal atom) reacts with an organic halide of the type R'-X with formation of a new carbon-carbon bond in the product R-R'. The most common type of coupling reaction is the cross coupling reaction. [1] [2] [3]

  3. Transition metal hydride - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_hydride

    Ternary metal hydrides have the formula A x MH n, where A + is an alkali or alkaline earth metal cation, e.g. K + and Mg 2+.A celebrated example is K 2 ReH 9, a salt containing two K + ions and the ReH 9 2− anion.

  4. Cross-coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Cross-coupling_reaction

    Often, however, cross-coupling refers to a metal-catalyzed reaction of a nucleophilic partner with an electrophilic partner. Mechanism proposed for Kumada coupling (L = Ligand , Ar = Aryl ). In such cases, the mechanism generally involves reductive elimination of R-R' from L n MR(R') (L = spectator ligand ).

  5. Non-covalent interaction - Wikipedia

    en.wikipedia.org/wiki/Non-covalent_interaction

    Figure 1. Anionic Lewis base forming a halogen bond with electron-withdrawn bromine (Lewis acid) Halogen bonding is a type of non-covalent interaction which does not involve the formation nor breaking of actual bonds, but rather is similar to the dipole–dipole interaction known as hydrogen bonding.

  6. Hydrogen-bond catalysis - Wikipedia

    en.wikipedia.org/wiki/Hydrogen-bond_catalysis

    Hydrogen-bond catalysis is a type of organocatalysis that relies on use of hydrogen bonding interactions to accelerate and control organic reactions. In biological systems, hydrogen bonding plays a key role in many enzymatic reactions, both in orienting the substrate molecules and lowering barriers to reaction. [ 1 ]

  7. Methylene imine - Wikipedia

    en.wikipedia.org/wiki/Methylene_imine

    Methylene imine is an organic compound with the chemical formula H 2 C=NH. The simplest imine , it is a stable, colorless gas that has been detected throughout the universe. [ 1 ] Structural parameters determined by microwave spectroscopy include a C=N bond length of 1.27 Å , an N–H bond length of 1.02 Å and an H−N=C bond angle of 110.5 ...

  8. Lone pair - Wikipedia

    en.wikipedia.org/wiki/Lone_pair

    The s character rich O σ(out) lone pair orbital (also notated n O (σ)) is an ~sp 0.7 hybrid (~40% p character, 60% s character), while the p lone pair orbital (also notated n O (π)) consists of 100% p character. Both models are of value and represent the same total electron density, with the orbitals related by a unitary transformation.

  9. List of alternative nonmetal classes - Wikipedia

    en.wikipedia.org/wiki/List_of_alternative...

    Cressey 2010, "Chemists re-define hydrogen bond", Nature newsblog, accessed 23 August 2017; Cronyn MW 2003, "The prope; Dingle A 2017, The elements: An encyclopedic tour of the periodic table, Quad Books, Brighton, ISBN 978-0-85762-505-2; Dinwiddle R, Lamb H, Franceschetti DR & Viney M (eds) 2018, How science works, Dorling Kindersley, London

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