Feynman diagramIn theoretical physics, a Feynman diagram is a pictorial representation of the mathematical expressions describing the behavior and interaction of subatomic particles. The scheme is named after American physicist Richard Feynman, who introduced the diagrams in 1948. The interaction of subatomic particles can be complex and difficult to understand; Feynman diagrams give a simple visualization of what would otherwise be an arcane and abstract formula.
Scalar field theoryIn theoretical physics, scalar field theory can refer to a relativistically invariant classical or quantum theory of scalar fields. A scalar field is invariant under any Lorentz transformation. The only fundamental scalar quantum field that has been observed in nature is the Higgs field. However, scalar quantum fields feature in the effective field theory descriptions of many physical phenomena. An example is the pion, which is actually a pseudoscalar.
Coupling constantIn physics, a coupling constant or gauge coupling parameter (or, more simply, a coupling), is a number that determines the strength of the force exerted in an interaction. Originally, the coupling constant related the force acting between two static bodies to the "charges" of the bodies (i.e. the electric charge for electrostatic and the mass for Newtonian gravity) divided by the distance squared, , between the bodies; thus: in for Newtonian gravity and in for electrostatic.
Quartic interactionIn quantum field theory, a quartic interaction is a type of self-interaction in a scalar field. Other types of quartic interactions may be found under the topic of four-fermion interactions. A classical free scalar field satisfies the Klein–Gordon equation. If a scalar field is denoted , a quartic interaction is represented by adding a potential energy term to the Lagrangian density. The coupling constant is dimensionless in 4-dimensional spacetime. This article uses the metric signature for Minkowski space.
Lerch zeta functionIn mathematics, the Lerch zeta function, sometimes called the Hurwitz–Lerch zeta function, is a special function that generalizes the Hurwitz zeta function and the polylogarithm. It is named after Czech mathematician Mathias Lerch, who published a paper about the function in 1887. The Lerch zeta function is given by A related function, the Lerch transcendent, is given by The transcendent only converges for any real number , where: or and .
Multivalued functionIn mathematics, a multivalued function, also called multifunction and many-valued function, is a set-valued function with continuity properties that allow considering it locally as an ordinary function. Multivalued functions arise commonly in applications of the implicit function theorem, since this theorem can be viewed as asserting the existence of a multivalued function. In particular, the inverse function of a differentiable function is a multivalued function, and is single-valued only when the original function is monotonic.
Beta function (physics)In theoretical physics, specifically quantum field theory, a beta function, β(g), encodes the dependence of a coupling parameter, g, on the energy scale, μ, of a given physical process described by quantum field theory. It is defined as and, because of the underlying renormalization group, it has no explicit dependence on μ, so it only depends on μ implicitly through g. This dependence on the energy scale thus specified is known as the running of the coupling parameter, a fundamental feature of scale-dependence in quantum field theory, and its explicit computation is achievable through a variety of mathematical techniques.
Hurwitz zeta functionIn mathematics, the Hurwitz zeta function is one of the many zeta functions. It is formally defined for complex variables s with Re(s) > 1 and a ≠ 0, −1, −2, ... by This series is absolutely convergent for the given values of s and a and can be extended to a meromorphic function defined for all s ≠ 1. The Riemann zeta function is ζ(s,1). The Hurwitz zeta function is named after Adolf Hurwitz, who introduced it in 1882. The Hurwitz zeta function has an integral representation for and (This integral can be viewed as a Mellin transform.
Boiling pointThe boiling point of a substance is the temperature at which the vapor pressure of a liquid equals the pressure surrounding the liquid and the liquid changes into a vapor. The boiling point of a liquid varies depending upon the surrounding environmental pressure. A liquid in a partial vacuum, i.e., under a lower pressure, has a lower boiling point than when that liquid is at atmospheric pressure. Because of this, water boils at under standard pressure at sea level, but at at altitude.
Melting pointThe melting point (or, rarely, liquefaction point) of a substance is the temperature at which it changes state from solid to liquid. At the melting point the solid and liquid phase exist in equilibrium. The melting point of a substance depends on pressure and is usually specified at a standard pressure such as 1 atmosphere or 100 kPa. When considered as the temperature of the reverse change from liquid to solid, it is referred to as the freezing point or crystallization point.
Dirichlet beta functionIn mathematics, the Dirichlet beta function (also known as the Catalan beta function) is a special function, closely related to the Riemann zeta function. It is a particular Dirichlet L-function, the L-function for the alternating character of period four. The Dirichlet beta function is defined as or, equivalently, In each case, it is assumed that Re(s) > 0. Alternatively, the following definition, in terms of the Hurwitz zeta function, is valid in the whole complex s-plane: Another equivalent definition, in terms of the Lerch transcendent, is: which is once again valid for all complex values of s.
Riemann zeta functionThe Riemann zeta function or Euler–Riemann zeta function, denoted by the Greek letter ζ (zeta), is a mathematical function of a complex variable defined as for , and its analytic continuation elsewhere. The Riemann zeta function plays a pivotal role in analytic number theory, and has applications in physics, probability theory, and applied statistics. Leonhard Euler first introduced and studied the function over the reals in the first half of the eighteenth century.
Cross-coupling reactionIn organic chemistry, a cross-coupling reaction is a reaction where two different fragments are joined. Cross-couplings are a subset of the more general coupling reactions. Often cross-coupling reactions require metal catalysts. One important reaction type is this: (R, R' = organic fragments, usually aryle; M = main group center such as Li or MgX; X = halide) These reactions are used to form carbon–carbon bonds but also carbon-heteroatom bonds. Cross-coupling reaction are a subset of coupling reactions.
PropagatorIn quantum mechanics and quantum field theory, the propagator is a function that specifies the probability amplitude for a particle to travel from one place to another in a given period of time, or to travel with a certain energy and momentum. In Feynman diagrams, which serve to calculate the rate of collisions in quantum field theory, virtual particles contribute their propagator to the rate of the scattering event described by the respective diagram.
Polygamma functionIn mathematics, the polygamma function of order m is a meromorphic function on the complex numbers defined as the (m + 1)th derivative of the logarithm of the gamma function: Thus holds where ψ(z) is the digamma function and Γ(z) is the gamma function. They are holomorphic on . At all the nonpositive integers these polygamma functions have a pole of order m + 1. The function ψ(1)(z) is sometimes called the trigamma function. Digamma function#Integral representations When m > 0 and Re z > 0, the polygamma function equals where is the Hurwitz zeta function.
RenormalizationRenormalization is a collection of techniques in quantum field theory, statistical field theory, and the theory of self-similar geometric structures, that are used to treat infinities arising in calculated quantities by altering values of these quantities to compensate for effects of their self-interactions. But even if no infinities arose in loop diagrams in quantum field theory, it could be shown that it would be necessary to renormalize the mass and fields appearing in the original Lagrangian.
Coupling reactionIn organic chemistry, a coupling reaction is a type of reaction in which two reactant molecules are bonded together. Such reactions often require the aid of a metal catalyst. 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. Richard F.
Hiyama couplingThe Hiyama coupling is a palladium-catalyzed cross-coupling reaction of organosilanes with organic halides used in organic chemistry to form carbon–carbon bonds (C-C bonds). This reaction was discovered in 1988 by Tamejiro Hiyama and Yasuo Hatanaka as a method to form carbon-carbon bonds synthetically with chemo- and regioselectivity. The Hiyama coupling has been applied to the synthesis of various natural products.
Branch pointIn the mathematical field of complex analysis, a branch point of a multi-valued function (usually referred to as a "multifunction" in the context of complex analysis) is a point such that if the function is n-valued (has n values) at that point, all of its neighborhoods contain a point that has more than n values. Multi-valued functions are rigorously studied using Riemann surfaces, and the formal definition of branch points employs this concept.
Kumada couplingIn organic chemistry, the Kumada coupling is a type of cross coupling reaction, useful for generating carbon–carbon bonds by the reaction of a Grignard reagent and an organic halide. The procedure uses transition metal catalysts, typically nickel or palladium, to couple a combination of two alkyl, aryl or vinyl groups. The groups of Robert Corriu and Makoto Kumada reported the reaction independently in 1972. The reaction is notable for being among the first reported catalytic cross-coupling methods.
