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Map -plane

MATLAB code for the calculation of electron density maps (plane group p2) ... [Pg.112]

See also Calculus Computer-Aided Design and Manufacturing Computer Science Geometry Maps and Mapping Plane Surveying Trigonometry. [Pg.901]

Thus, x(, ri) and y(, ri) are likewise harmonic, but in the variables % and r. Equations 8-54 and 8-55 are simpler than Equations 8-21 and 8-22, with P = Q = 0. The use of our reciprocity relationships shows that there exists a duality between physical and mapped planes, and vice versa, for conformal transformations that is, Equations 8-50 and 8-51 are mirror images of Equations 8-54 and 8-55. One might have anticipated this type of reversibility, but it is not direetly evident from Equations 8-21 and 8-22. Equations 8-54 and 8-55 are consistent with Thompson s original Equations 8-21 and 8-22. Use of the Cauehy-Riemann eonditions in the transformed plane, that is. Equations 8-52 and 8-53, in Equations 8-14 to 8-16, leads to a = y and 3 = 0. [Pg.166]

FIGURE 4 Mapping of ellipsoid onto a mapping plane. [Pg.111]

Structural maps display the top (and sometimes the base) of the reservoir surface below the datum level. The depth values are always true vertical sub sea. One could say that the contours of structure maps provide a picture of the subsurface topography. They display the shape and extent of a hydrocarbon accumulation and indicate the dip and strike of the structure. The dip is defined as the angle of a plane with the horizontal, and Is perpendicular to the strike, which runs along the plane. [Pg.140]

The projection model (equations 1, 2) describes the mapping of 3D points = m,yw,2wY to 2D image points Pi = (ii,j/i) in a virtual, undistorted image plane. The... [Pg.485]

T- and mapped to the image plane considering scaling (Si,Sy) of the coordinate axes and a shift Ci,Cy) of the center of the coordinate system. The distance between X-ray source and image intensifier tube is called /. [Pg.486]

Pulsed-force mode AFM (PFM-AFM) is a method introduced for fast mapping of local stiffness and adliesion with lower required data storage than recording force-distance curves at each point on the x-y plane [115]. A sinusoidal or triangular modulation is applied between the tip and sample (either via lever or sample piezo) at a lower frequency than that of either the piezo or cantilever resonance frequency. Tip and sample then come... [Pg.1700]

Figure C3.6.4 Single-handed chaotic attractor and next-amplitude map reconstmcted from experimental data for tire BZ reaction, (a) The reconstmcted attractor projected onto tire + x)) plane (see tire text for a... Figure C3.6.4 Single-handed chaotic attractor and next-amplitude map reconstmcted from experimental data for tire BZ reaction, (a) The reconstmcted attractor projected onto tire + x)) plane (see tire text for a...
We now examine how a next-amplitude-map was obtained from tire attractor shown in figure C3.6.4(a) [171. Consider tire plane in tliis space whose projection is tire dashed curve i.e. a plane ortliogonal to tire (X (tj + t)) plane. Then, for tire /ctli intersection of tire (continuous) trajectory witli tliis plane, tliere will be a data point X (ti + r), X (ti + 2r))on tire attractor tliat lies closest to tire intersection of tire continuous trajectory. A second discretization produces tire set Xt- = k = 1,2,., I This set is used in tire constmction... [Pg.3061]

View the contour map m several planes to see the general Torm of the distiibiiiioii. As long as you don t alter the molecular coordinates, you don t need to repeat th e wave function calculation. Use the left mouse button and the IlyperChem Rotation or Translation tools (or Tool icons ) to change the view of amolecnle without changing its atomic coordinates. [Pg.136]

The structure of ethylene and the orbital hybridization model for its double bond were presented m Section 2 20 and are briefly reviewed m Figure 5 1 Ethylene is planar each carbon is sp hybridized and the double bond is considered to have a a component and a TT component The ct component arises from overlap of sp hybrid orbitals along a line connecting the two carbons the tt component via a side by side overlap of two p orbitals Regions of high electron density attributed to the tt electrons appear above and below the plane of the molecule and are clearly evident m the electrostatic potential map Most of the reactions of ethylene and other alkenes involve these electrons... [Pg.190]

FIGURE 5 1 (a) The planar framework of u bonds in ethylene showing bond distances and angles (b) and (c) The p orbitals of two sp hybridized carbons overlap to produce a tt bond (d) The electrostatic potential map shows a region of high negative potential due to the tt elec trons above and below the plane of the atoms... [Pg.191]

FIGURE 9 3 Electro static potential maps of eth yiene and acetylene The region of highest negative charge (red) is associated with the TT bonds and lies between the two carbons in both This electron rich re gion IS above and below the plane of the molecule in ethylene Because acetylene has two TT bonds a band of high electron density encir cles the molecule... [Pg.366]

FIGURE 113 (a) The framework of bonds shown in the tube model of benzene are cr bonds (b) Each carbon is sp hybridized and has a 2p orbital perpendicular to the cr framework Overlap of the 2p orbitals generates a tt system encompass mg the entire ring (c) Electrostatic potential map of benzene The red area in the center corresponds to the region above and below the plane of the ring where the tt electrons are concentrated... [Pg.430]

The electrostatic potential map of benzene (Figure 11 3c) shows regions of high electron density above and below the plane of the ring which is where we expect the most loosely held electrons (the rr electrons) to be In Chapter 12 we will see how this region of high electron density is responsible for the characteristic chemical reactivity of benzene and its relatives... [Pg.430]

In the x-ray portion of the spectmm, scientific CCDs have been utilized as imaging spectrometers for astronomical mapping of the sun (45), galactic diffuse x-ray background (46), and other x-ray sources. Additionally, scientific CCDs designed for x-ray detection are also used in the fields of x-ray diffraction, materials analysis, medicine, and dentistry. CCD focal planes designed for infrared photon detection have also been demonstrated in InSb (47) and HgCdTe (48) but are not available commercially. [Pg.430]


See other pages where Map -plane is mentioned: [Pg.42]    [Pg.120]    [Pg.161]    [Pg.265]    [Pg.109]    [Pg.85]    [Pg.82]    [Pg.198]    [Pg.1204]    [Pg.111]    [Pg.42]    [Pg.120]    [Pg.161]    [Pg.265]    [Pg.109]    [Pg.85]    [Pg.82]    [Pg.198]    [Pg.1204]    [Pg.111]    [Pg.16]    [Pg.136]    [Pg.142]    [Pg.204]    [Pg.209]    [Pg.488]    [Pg.678]    [Pg.1376]    [Pg.1806]    [Pg.2270]    [Pg.2488]    [Pg.2552]    [Pg.2856]    [Pg.3061]    [Pg.3062]    [Pg.350]    [Pg.98]    [Pg.664]    [Pg.116]    [Pg.393]    [Pg.607]    [Pg.622]    [Pg.219]   
See also in sourсe #XX -- [ Pg.99 ]




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Patterson maps Harker planes

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