Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Project functional

In order to proceed further, it is now necessary to study the linear dependence of the projected functions 0V 02, 03>. . . which is done by investigating their overlap matrix... [Pg.289]

The layout of Tables 12.3 and 12.4 is similar to that of Tables 11.5 and 11.6 described in Section 11.3.1. There is, nevertheless, one point concerning the Num. row that merits further coimnent. In Chapter 6 we discussed how the symmetric group projections interact with spatial syimnetiy projections. Functions 1, 2, and 4 are members of one constellation, and the corresponding coefficients may not be entirely independent. There are three linearly independent E+ symmetry functions from the five standard tableaux of this configuration. The 1, 2, and 4 coefficients are thus possibly partly independent and partly coimected by group theory. In none... [Pg.164]

Figure B.l. A commutative diagram for the proof of Proposition B.2. The functions tti and 712 are the natural projection functions. The function i is the inclusion function any element of SU(V) is automatically an element of C(V). Figure B.l. A commutative diagram for the proof of Proposition B.2. The functions tti and 712 are the natural projection functions. The function i is the inclusion function any element of SU(V) is automatically an element of C(V).
CDD also has Projects functionality that enhances the capability to share research data securely using CDD (Fig. 3). This enables users of CDD to organize their data within a vault into projects and invite individual vault members to be able to access specific projects, allowing for more flexible data sharing and... [Pg.142]

Of course, the choice of the projecting function P(x) of Eq. (17-36) is not unique. The choice depends on the purpose. For example, when the angle of the hydrogen... [Pg.474]

To understand this, take the matrix group G — GL2, with H the upper triangular group. Here G acts on k1 = kei ke2, and H is the stabilizer of ev In fact G acts transitively on the set of one-dimensional subspaces and since H is the stabilizer of one of them, the coset space is the collection of those subspaces. But they form the projective line over k, which is basically different from the kind of subsets of fc" that we have considered. In the complex case, for instance, it is the Riemann sphere, and all analytic functions on it are constant whereas on subsets of n-space we always have the coordinate projection functions. [Pg.130]

The operator Idc>projects functions onto the core states. Thus in Eq. (D-1) the operator I — removed from (p> those terms that could be expanded in c>. In... [Pg.544]

It is not possible, however, to simply project the product functions a > b > with Ag and thoi to use these functions in Rayleigh-Schrdding perturbation theory, for two reasons. First, the projected functions Ag a > lb > are not eigenfunctions of the unperturbed hamiltonian Hq = -h H since H, which corresponds to a certain assignment of electrons to each subsystan A or B, does not... [Pg.12]

This rdation shows how the action of the antisymmetiizer can mix different orders in perturbation theory. Secondly, the projected functions Ag 0 > 0 > do not form an orthogonal set in the antisymmetric subspace of the Hilbert space L2(r3nj. jf excited states (a > and b > in order to obtain a complete... [Pg.13]

This relation shows how the action of the antisymmetrizer can mix different orders in perturbation theory. Secondly, the projected functions AglO ) 0 > do not form an orthogonal set in the antisymmetric subspace of the Hilbert space L2(r3N) if we take all excited states a > and b > in order to obtain a complete set a > b >, the projections As a > b > form a linearly dependent set. Expanding a given (antisymmetric) function in this overcomplete set is always possible, but the expansion coefficients are not uniquely defined. How the different symmetry adapted perturbation theories that have been formulated since the original treatment by Eisenschitz and London in 1930 , actually deal with these two problems can be read in the following reviews Usually, the first order interaction... [Pg.13]

A. Streitweiser, Jr., J. B. Collins, J. M. McKelvey, D. Grier, J. Sender, and A. G. Toczko, Proc. Natl. Acad. Sci. USA, 76, 2499 (1979). Integrated Spatial Electron Populations in Molecules The Electron Projection Function. [Pg.267]

From the Pauli principle follows that the projected function J4ab o. rather than should be considered as the correct zeroth-order wave function in the perturbation theory of intermolecular interactions. Here J4ab is the usual intermolecular antisymmetrization operator and is (the lowest) eigenfunction of, the sum of... [Pg.1052]

In 1980, Farmer, with great foresight, proposed the use of cyclohexane as a scaffold to project functionality as a mimetic of protein secondary structures... [Pg.251]

Guengerich, F.P. (1998). The environmental genome project Functional analysis of polymorphisms. Environ. Health Perspect. 106, 365-368. [Pg.469]

There are several problems encountered in combination of SIMS and EPMA images. Due to the change of the sample holder, the images sometimes have different orientations. SIMS and EPMA have different projection functions, i.e. the projection of different concentrations to the resulting image intensity values is non-monotonic and non-linear. EPMA and SIMS micrographs also exhibit various artefacts, e.g. lateral distortion of the SIMS distributions [26]. Most of these distortions are both local and non-linear. All the above... [Pg.528]

We assume that a molecule, such as NH3, belongs to the point group Csv, and that it has three equivalent bonds represented b3rfunctions 1, 4 2, and Si s, as well as a lone-pair orbital 4 which is not equivalent to the bond orbitals. The z axis is the principal axis. If we act on the i j with the projection operator for the Xth rep, the result will be a linear combination of the functions in 4, that transform like the Xth rep. In this manner we can project new functions d> each of which is a linear combination of the "iTj. The inverse of the transformation that takes the 4 y into the is the transformation that gives us the in terms of the To keep the computation down to a minimum we will treat the projected functions 4> not as linear combinations of s, p, p , and p but as the combinations of the base functions of the axial rotation group so, pi, po, and p i. Thus, there are only three functions involved, namely, 00, 01, and 0 i. These functions transform according to the A(0o) and E [Pg.317]

This means that two functions that transform according to different irreducible representations are orthogonal, and that a projection of an already projected function changes nothing. Here is the proof. After noting that RS = Q,... [Pg.1094]

Use the Image Stacks Z Project function to project the movie to a series of 2D images. [Pg.303]


See other pages where Project functional is mentioned: [Pg.50]    [Pg.191]    [Pg.53]    [Pg.29]    [Pg.282]    [Pg.192]    [Pg.569]    [Pg.216]    [Pg.146]    [Pg.19]    [Pg.479]    [Pg.387]    [Pg.391]    [Pg.113]    [Pg.1027]    [Pg.324]    [Pg.385]    [Pg.12]    [Pg.191]    [Pg.224]    [Pg.452]    [Pg.1031]    [Pg.311]    [Pg.311]    [Pg.312]    [Pg.1259]    [Pg.718]    [Pg.508]    [Pg.495]   
See also in sourсe #XX -- [ Pg.83 ]




SEARCH



Correlation function projection

Functional genomics projects

Matrix element between projected functions

Model function and projection operators

Project and Functional Teams

Project engineering functional safety assessment

Project, generally manager, specific functions

Projected electron density function

Projected functions

Projected functions

Projection wave function

© 2024 chempedia.info