quantized interaction - definição. O que é quantized interaction. Significado, conceito
Diclib.com
Dicionário ChatGPT
Digite uma palavra ou frase em qualquer idioma 👆
Idioma:

Tradução e análise de palavras por inteligência artificial ChatGPT

Nesta página você pode obter uma análise detalhada de uma palavra ou frase, produzida usando a melhor tecnologia de inteligência artificial até o momento:

  • como a palavra é usada
  • frequência de uso
  • é usado com mais frequência na fala oral ou escrita
  • opções de tradução de palavras
  • exemplos de uso (várias frases com tradução)
  • etimologia

O que (quem) é quantized interaction - definição

QUANTIZED FLUX CIRCULATION OF SOME PHYSICAL QUANTITY
Quantized Vortices; Quantized vortices; Quantized vortex; Quantum vortices
  • arxiv=1807.06746}}</ref>

Cation–pi interaction         
  • Fig. 1: Examples of π-π. CH-π, and π-cation interactions
  • Fig. 2: The Stoddart synthesis of [2]catenane
  • 275px
  • Cationic [[Acetylcholine]] binding to a [[tryptophan]] residue of the nicotinamide acetylcholine receptor via a cation–π effect.
  • quadrupole]] charge distribution.
  • Binding energy (in kcal/mol) for Na<sup>+</sup> to benzene with prototypical substituents.<ref name="electrostaticmodel" />
  • 450px
  • Cyclophane host–guest complex
  • 450px
  • Cation–π interaction in indole-3-acetic acid choline ester compared to neutral analog
  • 450px
  • Quadrupole moments of benzene and hexafluorobenzene. The polarity is inverted due to differences in electronegativity for hydrogen and fluorine relative to carbon; the inverted quadrupole moment of hexafluorobenzene is necessary for anion-pi interactions.
  • 350px
  • Calculated interaction energies of methylamonium and benzene in a variety of solvents
  • Cyclization of squalene to form hopene
NONCOVALENT MOLECULAR INTERACTION BETWEEN THE FACE OF AN ELECTRON-RICH Π SYSTEM AND AN ADJACENT CATION; EXAMPLE OF NONCOVALENT BONDING BETWEEN A MONOPOLE (CATION) AND A QUADRUPOLE (Π SYSTEM)
Cation-pi interaction; Anion-pi interaction; Anion–pi interaction; Cation-π interaction; Cation–pi interaction
Cation–π interaction is a noncovalent molecular interaction between the face of an electron-rich π system (e.g.
Cation–π interaction         
  • Fig. 1: Examples of π-π. CH-π, and π-cation interactions
  • Fig. 2: The Stoddart synthesis of [2]catenane
  • 275px
  • Cationic [[Acetylcholine]] binding to a [[tryptophan]] residue of the nicotinamide acetylcholine receptor via a cation–π effect.
  • quadrupole]] charge distribution.
  • Binding energy (in kcal/mol) for Na<sup>+</sup> to benzene with prototypical substituents.<ref name="electrostaticmodel" />
  • 450px
  • Cyclophane host–guest complex
  • 450px
  • Cation–π interaction in indole-3-acetic acid choline ester compared to neutral analog
  • 450px
  • Quadrupole moments of benzene and hexafluorobenzene. The polarity is inverted due to differences in electronegativity for hydrogen and fluorine relative to carbon; the inverted quadrupole moment of hexafluorobenzene is necessary for anion-pi interactions.
  • 350px
  • Calculated interaction energies of methylamonium and benzene in a variety of solvents
  • Cyclization of squalene to form hopene
NONCOVALENT MOLECULAR INTERACTION BETWEEN THE FACE OF AN ELECTRON-RICH Π SYSTEM AND AN ADJACENT CATION; EXAMPLE OF NONCOVALENT BONDING BETWEEN A MONOPOLE (CATION) AND A QUADRUPOLE (Π SYSTEM)
Cation-pi interaction; Anion-pi interaction; Anion–pi interaction; Cation-π interaction; Cation–pi interaction
Cation–π interaction is a noncovalent molecular interaction between the face of an electron-rich π system (e.g.
Configuration interaction         
POST-HARTREE–FOCK LINEAR VARIATIONAL METHOD FOR SOLVING THE NONRELATIVISTIC SCHRÖDINGER EQUATION
Configuration interaction singles; Configuration Interaction Singles
Configuration interaction (CI) is a post-Hartree–Fock linear variational method for solving the nonrelativistic Schrödinger equation within the Born–Oppenheimer approximation for a quantum chemical multi-electron system. Mathematically, configuration simply describes the linear combination of Slater determinants used for the wave function.

Wikipédia

Quantum vortex

In physics, a quantum vortex represents a quantized flux circulation of some physical quantity. In most cases, quantum vortices are a type of topological defect exhibited in superfluids and superconductors. The existence of quantum vortices was first predicted by Lars Onsager in 1949 in connection with superfluid helium. Onsager reasoned that quantisation of vorticity is a direct consequence of the existence of a superfluid order parameter as a spatially continuous wavefunction. Onsager also pointed out that quantum vortices describe the circulation of superfluid and conjectured that their excitations are responsible for superfluid phase transitions. These ideas of Onsager were further developed by Richard Feynman in 1955 and in 1957 were applied to describe the magnetic phase diagram of type-II superconductors by Alexei Alexeyevich Abrikosov. In 1935 Fritz London published a very closely related work on magnetic flux quantization in superconductors. London's fluxoid can also be viewed as a quantum vortex.

Quantum vortices are observed experimentally in type-II superconductors (the Abrikosov vortex), liquid helium, and atomic gases (see Bose–Einstein condensate), as well as in photon fields (optical vortex) and exciton-polariton superfluids.

In a superfluid, a quantum vortex "carries" quantized orbital angular momentum, thus allowing the superfluid to rotate; in a superconductor, the vortex carries quantized magnetic flux.

The term "quantum vortex" is also used in the study of few body problems. Under the De Broglie–Bohm theory, it is possible to derive a "velocity field" from the wave function. In this context, quantum vortices are zeros on the wave function, around which this velocity field has a solenoidal shape, similar to that of irrotational vortex on potential flows of traditional fluid dynamics.