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Conformal groups

Conformation Groups that favor a flattening of the pyranose, a consequence of oxonium ion formation, increase the rate of reactivity. Ley uses 3,4-spiroketals to enforce chairlike structure on the pyranose ring, thus deactivating them toward reaction. [Pg.217]

Fig. 37. plot for the cis-proline (type VI) turns from Chou and Fasman (1977), plus the two examples in the Bence-Jones protein REI. Arrows point from position 2 to position 3 (the proline) for each example. The two conformational groups are labeled as Via and VIb. [Pg.212]

In the crystal state most stereoregular polymers have helical conformations. Group s(M/N) 1 comprises all the isotactic vinyl polymers [polypropylene, polybutene, polystyrene, etc., M/N = 3/1 poly-o-methylstyrene, etc., 4/1 ... [Pg.47]

The conformal group 0(1,3), if the Yang-Mills equations are defined in Minkowski space... [Pg.272]

In this section we describe the general approach to constructing conformally invariant ansatzes applicable to any (linear or nonlinear) system of partial differential equations, on whose solution set a linear covariant representation of the conformal group 0(1,3) is realized. Since the majority of the equations of the relativistic physics, including the Klein-Gordon-Fock, Maxwell, massless Dirac, and Yang-Mills equations, respect this requirement, they can be handled within the framework of this approach. [Pg.275]

Analysis of the symmetry groups of the equations of relativistic physics shows that for the majority of them the generators of the Poincare, extended Poincare, and conformal groups can be represented in the following form [19,21,33,48] ... [Pg.279]

Classification of inequivalent subalgebras of the algebras p(l,3), p(1.3), c(l,3) within actions of different automorphism groups [including the groups P(l, 3), P(l, 3) and 0(1,3)] is already available [30]. Since we will concentrate on conformally invariant systems, it is natural to restrict our disscussion to the classification of subalgebras of c(l, 3) that are inequivalent within the action of the conformal group 0(1, 3). [Pg.283]

Note that the conformal group C(l,3) generated by the infinitesimal operators (27) acts in the space of independent variables R1 3 only. That is why the basis operators of the algebra c l, 3) act in the space of dependent variables R4 as zero operators. [Pg.283]

The maximal symmetry group admitted by Eqs. (46) is the group C(l, 3)<8> SU(2) [17], where 0(1, 3) is the 15-parameter conformal group generated by the following vector fields... [Pg.301]

As we have mentioned in the introduction, the maximal symmetry group admitted by Eqs. (99) is the 16-parameter group C( 1,3) <8> H. This group is the direct product of the conformal group C( 1,3) generated by the Lie vector fields... [Pg.333]

In what follows we exploit invariance of the Maxwell equations under the conformal group C(l, 3) in order to construct their invariant solutions. [Pg.335]

J. P. Vigier, D. Bohm, M. Flato, and D. Sternheimer, Conformal group symmetry on elementary particles, Nuovo Cimento 38, 1941 (1965). [Pg.193]

Structure Configuration Conformation Group antiparallel to N Expected Product... [Pg.45]

Moreover, in 1970, Polyakov discovered that the correlation functions of a critical magnetic system have invariance properties for transformations belonging to the special conformal group. Then, in 1984, Belavin, Polyakov, and Zamolodchikov showed that these conformal transformations are really important in two dimensions. Since that time, research in this domain led to very interesting results. Thus exact values of the main exponents associated with two-dimensional polymer solutions, were found in 1986 by Saleur and Duplantier. [Pg.470]

Actually, at the critical point the system is also invariant fot transformations belonging to the conformal group dilatation is only one element of this group. However, this more powerful invariance has been taken into account only very recently and only in two dimensions (see Section 4.2). [Pg.470]

As early as 1970, Polyakov51 showed that at the critical point, a critical system is invariant for transformations belonging to the conformal group. Thus, as this group is rather rich in two dimensions, these invariance properties could later52 be used to make precise studies of critical phenomena and, in particular, to find exact values of critical exponents. [Pg.521]

This invariance is trivial, but as was shown by Polyakov in 1970,51 a critical system is also invariant for transformations belonging to the conformal group. [Pg.526]

The conformal group consists of a set of point transformations preserving angles. In other words, if a conformal transformation transforms a point M into M, the neighbourhood of M can be deduced from the neighbourhood of M by local rotation and dilatation. [Pg.526]

The special conformal group is a subgroup of the conformal group and it is generated by the following transformations (r - r )... [Pg.526]

The conformal invariance properties of critical systems are certainly important for any space dimension, but even more so in two dimensions because the two-dimensional conformal group is very rich. This essential fact was clearly recognized and exploited by Belavin, Polyakov, and Zamolodchikov in 1984.52 Their theory is not simple, but very interesting it is presently developing (1990) and consequendy certain points remain obscure. Here, we shall give only an idea of this method, in spite of the fact that it has already led to fundamental results. In particular, as we shall see, it provided the means for the calculation the exact values of the exponents aM defined in Section 3.3 of the present chapter [see (12.3.68)]. [Pg.527]

Fig. 28.14. A general process for the rational design of peptide mimetics (A) identification of crucial pharmacophoric groups, (B) determination of the spatial arrangement of these groups, and (C) use of a template to mount the key functional groups in their proper conformation. Groups highlighted with an asterisk comprise the pharmacophore of the heptapeptide. (From Harrold MW. Preparing students for future therapies the development of novel agents to control the renin-angiotensin system. Am J Pharm Educ 1997 61 173-178 with permission.)... Fig. 28.14. A general process for the rational design of peptide mimetics (A) identification of crucial pharmacophoric groups, (B) determination of the spatial arrangement of these groups, and (C) use of a template to mount the key functional groups in their proper conformation. Groups highlighted with an asterisk comprise the pharmacophore of the heptapeptide. (From Harrold MW. Preparing students for future therapies the development of novel agents to control the renin-angiotensin system. Am J Pharm Educ 1997 61 173-178 with permission.)...

See other pages where Conformal groups is mentioned: [Pg.67]    [Pg.78]    [Pg.79]    [Pg.81]    [Pg.273]    [Pg.273]    [Pg.274]    [Pg.278]    [Pg.278]    [Pg.279]    [Pg.349]    [Pg.711]    [Pg.4]    [Pg.110]    [Pg.527]    [Pg.877]    [Pg.94]    [Pg.643]    [Pg.59]   


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Acyl groups, conformation

Amide group conformation

Amino group conformation

Amylose hydroxymethyl group conformation

Benassi, R., Folli. U„ Schenetti, L., Taddei F., The Conformations of Acyl Groups

Carboxyl groups anti conformation

Carboxylate groups anti conformation

Chair conformations placing groups

Conformal groups Yang-Mills equations

Conformal groups symmetry properties

Conformation of acyl groups

Conformation side group

Conformational Preference of the Sulfinyl Group in Six-Membered Heterocycles

Conformational Selection Using a 3,5-O-Di-tert-Butylsilylidene Protecting Group

Conformational restriction methyl groups

Conformational studies peptide group interactions

Conformations of acyl groups in heterocyclic

Conformations of acyl groups in heterocyclic compounds

Conformations, anomeric effect groups

Conformer pendant group

Conformity to the group

Group folded conformation

Hydroxymethyl group conformation

Mesogenic groups macromolecule conformation

Methoxy groups, conformational

Methoxy groups, conformational stabilization

Methyl group conformation

Methyl group conformational effects

Parallel Conformation of 2-Cyanoethyl Group

Perpendicular Conformation of 2-Cyanoethyl Group

Phosphodiester group, conformation

Prosthetic groups conformations

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