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Axial loading is defined as applying a force on a structure directly along a given axis of said structure. [1] In the medical field, the term refers to the application of weight or force along the course of the long axis of the body. [2] The application of an axial load on the human spine can result in vertebral compression fractures. [3]
Mesons named with the letter "f" are scalar mesons (as opposed to a pseudo-scalar meson), and mesons named with the letter "a" are axial-vector mesons (as opposed to an ordinary vector meson) a.k.a. an isoscalar vector meson, while the letters "b" and "h" refer to axial-vector mesons with positive parity, negative C-parity, and quantum numbers I G of 1 + and 0 − respectively.
An atom bonded to 5 other atoms (and no lone pairs) forms a trigonal bipyramid with two axial and three equatorial positions, but in the seesaw geometry one of the atoms is replaced by a lone pair of electrons, which is always in an equatorial position. This is true because the lone pair occupies more space near the central atom (A) than does a ...
The T-shaped geometry is related to the trigonal bipyramidal molecular geometry for AX 5 molecules with three equatorial and two axial ligands. In an AX 3 E 2 molecule, the two lone pairs occupy two equatorial positions, and the three ligand atoms occupy the two axial positions as well as one equatorial position. The three atoms bond at 90 ...
[18]: 1165 Examples of this include the octacyanomolybdate (Mo(CN) 4− 8) and octafluorozirconate (ZrF 4− 8) anions. [18]: 1165 The nonahydridorhenate ion (ReH 2− 9) in potassium nonahydridorhenate is a rare example of a compound with a steric number of 9, which has a tricapped trigonal prismatic geometry. [13]: 254 [18]
The α- and β-anomers of D-glucopyranose.. In organic chemistry, the anomeric effect or Edward-Lemieux effect (after J. T. Edward and Raymond Lemieux) is a stereoelectronic effect that describes the tendency of heteroatomic substituents adjacent to a heteroatom within a cyclohexane ring to prefer the axial orientation instead of the less-hindered equatorial orientation that would be expected ...
In chemistry, a trigonal pyramid is a molecular geometry with one atom at the apex and three atoms at the corners of a trigonal base, resembling a tetrahedron (not to be confused with the tetrahedral geometry). When all three atoms at the corners are identical, the molecule belongs to point group C 3v.
Atropisomers exhibit axial chirality (planar chirality). When the barrier to racemization is high, as illustrated by the BINAP ligands, the phenomenon becomes of practical value in asymmetric synthesis. Methaqualone, the anxiolytic and hypnotic-sedative, is a classical example of a drug molecule that exhibits the phenomenon of atropisomerism. [9]