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Cross-section of thallus of Ramalina lacera from HaZorea, November 1994, resuspended in the same site, retrieved in August 1995. Algal cells .

Cross-section of the 3D model of formic add , The van der Waals radius of each atom of the molecule is taken and by fusing the spheres the van der Waals surface is

Cross-section of the 600 MHz 3D NOESY-NOESY spectrum of met-myoglobin cyanide. The slice is taken at the 12-CH3 height. The inset shows the simulated cross-section involving the 12-CHj, 13-Ha and 13-Ha signals ,

Cross-section of the adiabatic reactor assembly.

Cross-section of the AF4 channel, scheme of size separation

Cross-section of the alveolar space in the lungs.

Cross-section of the APES along the Qb coordinate for the terms arising from the electronic configuration of Sis - Its main features are . The spin-triplet state is shown by dashed line

Cross-section of the APES of Cgo along the ective mode that takes the system from the undistorted high-spin minimum to the distorted low-spin minimum due to the multimode show that the lowest vibronic state associated with the electronic spin-doublet state is lower than that for the spin-quadruplet

Cross-section of the APES of Na4 along the e-mode distortion transforming the system from tetrahedral 0e PIT coupling

Cross-section of the APES of Na4 along the e-mode distortion transforming the system from tetrahedral Qts 0 to square-planar geometry due to the 8 e PJT coupling

Cross-section of the APES of Si4 along the hi-mode that distorts the system from square-planar to rhombic geometry due to the e PIT coupling between two excited states

Cross-section of the APES of Si4 along the hj-mode that distorts the system from square-planar to rhombic geometry due to the e PIT coupling between two excited states

Cross-section of the APES of the ozone molecule along the Qe component of the double degenerate e mode obtained by numerical ab initio calculations including the highly excited E state, explicitly demonstrating that the ground-state distorted configurations are due to the JTE in the excited state . The global minimum is at 2 0.69 A and the E-A avoided crossing takes place at Qe 0.35 A

Cross-section of the APES of the ozone molecule along the Qe component of the doubledegenerate e mode obtained by numerical ab initio calculations including the highly excited E state, exphcitly demonstrating that the ground state distorted configurations are due to the JTE in the excited state . The global minimum is at Qe 0.69A and the F-A avoided crossing takes place at Qe 0.35A

Cross-section of the block system, showing the process of cleaving the peptides off the solid phase.

Cross-section of the bridge deck in Saint-Pierre-la-Cour made with SFRC, y, 3 . Reproduced with permission from Behloul M., HPFRCC field applications

Cross-section of the bridges of open types with respective schematic diagrams of energy bands.

Cross-section of the C80 thermopile

Cross-section of the calorimeter of an enzyme thermistor with an aluminum constant temperature jacket. The two identical column ports

Cross-section of the cathode side. To reach the catalyst layer, oxygen in the channel must diffuse through the GDL

Cross-section of the column of the Topcon SM-700 700 Dual-Stage SEM, showing the high-resolution objective in the top stage and the versatile conical objective lens in the second stage.

Cross-section of the combined UPS-XPS-LEED system described by Bradshaw and Menzel

Cross-section of the composite containing the fabric , protective bonding layers and the PV cell.

Cross-section of the composite waveguide comprises two fibers of core radii p, and P2 with refractive-index profile n . The point P is defined by cylindrical polar coordinates r, and T2, 4 2 relative to the fiber axes, which are distance d apart.

Cross-section of the connector of the SPPl bacteriophage. The connector is a complex of the portal protein and two-head completion proteins, The section shows the X-ray structure of the portal protein fitted into a cryo-EM map. The X-ray structure has been modified from 13-mer into 12-mer, because the connector within the bacteriophage capsid has 12-fold symmetry whereas the portal protein before incorporation into the procapsid has 13-fold symmetry. The excellent fit of density confirms the 10 A resolution of the EM map



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