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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.
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 ...
A chiral molecule or ion exists in two stereoisomers that are mirror images of each other, [5] called enantiomers; they are often distinguished as either "right-handed" or "left-handed" by their absolute configuration or some other criterion. The two enantiomers have the same chemical properties, except when reacting with other chiral compounds.
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.
The solution to this gives the atomic displacement due to the phonon, which is given by ,,, = (),, (,) [(,)] where the atomic position i is described by l, m, and κ, which represent the specific atomic layer, l, the particular unit cell it is in, m, and the position of the atom with respect to its own unit cell, κ. The term x(l,m) is the ...
Conduction heat flux q k for ideal gas is derived with the gas kinetic theory or the Boltzmann transport equations, and the thermal conductivity is =, -, where u f 2 1/2 is the RMS (root mean square) thermal velocity (3k B T/m from the MB distribution function, m: atomic mass) and τ f-f is the relaxation time (or intercollision time period ...
In chemistry, such a molecule is called an enantiomer or is said to exhibit chirality or enantiomerism. The term "chiral" comes from the Greek word for the human hand, which itself exhibits such non-superimposeability of the left hand precisely over the right.
In chemistry, absolute configuration refers to the spatial arrangement of atoms within a molecular entity (or group) that is chiral, and its resultant stereochemical description. [1] Absolute configuration is typically relevant in organic molecules where carbon is bonded to four different substituents.