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  2. Phonon - Wikipedia

    en.wikipedia.org/wiki/Phonon

    A phonon is a collective excitation in a periodic, elastic arrangement of atoms or molecules in condensed matter, specifically in solids and some liquids.A type of quasiparticle in physics, [1] a phonon is an excited state in the quantum mechanical quantization of the modes of vibrations for elastic structures of interacting particles.

  3. Chirality (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Chirality_(chemistry)

    A chiral substance is enantiopure when only one of two possible enantiomers is present so that all molecules within a sample have the same chirality sense. Use of homochiral as a synonym is strongly discouraged. [22] A chiral substance is enantioenriched or heterochiral when its enantiomeric ratio is greater than 50:50 but less than 100:0. [23]

  4. Chirality - Wikipedia

    en.wikipedia.org/wiki/Chirality

    The term "chiral" in general is used to describe the object that is non-superposable on its mirror image. [18] In chemistry, chirality usually refers to molecules. Two mirror images of a chiral molecule are called enantiomers or optical isomers. Pairs of enantiomers are often designated as "right-", "left-handed" or, if they have no bias ...

  5. Chirality (physics) - Wikipedia

    en.wikipedia.org/wiki/Chirality_(physics)

    A theory that is asymmetric with respect to chiralities is called a chiral theory, while a non-chiral (i.e., parity-symmetric) theory is sometimes called a vector theory. Many pieces of the Standard Model of physics are non-chiral, which is traceable to anomaly cancellation in chiral theories.

  6. Asymmetric hydrogenation - Wikipedia

    en.wikipedia.org/wiki/Asymmetric_hydrogenation

    Chiral phosphine ligands, especially C 2-symmetric ligands, are the source of chirality in most asymmetric hydrogenation catalysts. Of these the BINAP ligand is well-known, as a result of its Nobel Prize-winning application in the Noyori asymmetric hydrogenation. [3] Chiral phosphine ligands can be generally classified as mono- or bidentate ...

  7. Chiral inversion - Wikipedia

    en.wikipedia.org/wiki/Chiral_inversion

    Chiral inversion is the process of conversion of one enantiomer of a chiral molecule to its mirror-image version with no other change in the molecule. [1] [2] [3] [4]Chiral inversion happens depending on various factors (viz. biological-, solvent-, light-, temperature- induced, etc.) and the energy barrier energy barrier associated with the stereogenic element present in the chiral molecule. 2 ...

  8. Chiral media - Wikipedia

    en.wikipedia.org/wiki/Chiral_media

    The term chiral / ˈ k aɪ r əl / describes an object, especially a molecule, which has or produces a non-superposable mirror image of itself. In chemistry, such a molecule is called an enantiomer or is said to exhibit chirality or enantiomerism.

  9. Umklapp scattering - Wikipedia

    en.wikipedia.org/wiki/Umklapp_scattering

    These processes are called Umklapp scattering and change the total phonon momentum. Umklapp scattering is the dominant process for electrical resistivity at low temperatures for low defect crystals [1] (as opposed to phonon-electron scattering, which dominates at high temperatures, and high-defect lattices which lead to scattering at any ...

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