Big Chemical Encyclopedia

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

Articles Figures Tables About

Resonance pivotal

Successive pivoting resonances of a covalent bond allows for electrical conduction to occur, as shown in Figure 1-1. A test of this theory was provided by gray and white tin. Gray tin is not metallic because all its valence orbitals are used for bonding and there is no metallic orbital available. White tin, on the other hand, has the metallic orbital available and therefore has metallic properties. [Pg.330]

Figure 1-1. Motion of an electron from the cathode to the anode by successive pivoting resonances of a covalent bond. Figure 1-1. Motion of an electron from the cathode to the anode by successive pivoting resonances of a covalent bond.
The compound Lajln has Tc = 10.4 K. Because La is hypoelectronic and In is hyperelectronic, I expect electron transfer to take place to the extent allowed by the approximate electroneutrality principle.13 The unit cube would then consist of 2 La, La, and In+, with In+ having no need for a metallic orbital and thus having valence 6 with the bonds showing mainly pivoting resonance among the twelve positions. The increase in valence of In and also of La (to 3 f ) and the assumption of the densely packed A15 structure account for the decrease in volume by 14.3%. Because the holes are fixed on the In + atoms, only the electrons move with the phonon, explaining the increase in Tc. [Pg.832]

Of course the above treatment is not definitive, but it does suggest that the antibonding a 2s MO mechanism can compare favourably with the pivotal resonance mechanism as the primary VB formulation for electron conduction in metallic lithium. [Pg.373]

Fe 2.22, Co 3.22, Ni 4.22. In this way the observed magnetic moments could be explained when he further assumed that these non-bonding d electrons have 2.44 3d orbitals at their disposal. For nickel thus 0.66 spins remain unpaired (2 X 2.44 — 4.22 — 0.66). The resulting unused orbital is 9 — 5.78 — 2.44 = 0.78, which Pauling then called the unstable orbital, but which he later recognized to be essential for the pivotal resonance and the conduction (metallic orbital). [Pg.316]

Another resonant frequency instmment is the TA Instmments dynamic mechanical analy2er (DMA). A bar-like specimen is clamped between two pivoted arms and sinusoidally oscillated at its resonant frequency with an ampHtude selected by the operator. An amount of energy equal to that dissipated by the specimen is added on each cycle to maintain a constant ampHtude. The flexural modulus, E is calculated from the resonant frequency, and the makeup energy represents a damping function, which can be related to the loss modulus, E". A newer version of this instmment, the TA Instmments 983 DMA, can also make measurements at fixed frequencies as weU as creep and stress—relaxation measurements. [Pg.199]

It is of interest to note that in order for a given atom to increase its ligancy beyond its covalency it is not necessary that this atom have an extra orbital, it is instead sufficient for the atoms that surround it to have extra orbitals. The valence bonds of the central atom may then resonate among their alternative positions by pivoting about the central atom. [Pg.381]

If we assume that particles detected using REVS are spherical and attached at a point to the surface of the resonator, we can determine the ratio between force applied tangentially to the surface of the particle and acceleration of the surface of the particle. We also assume that sphere is rolling, or pivoting about this attachment point, which we acknowledge is an approximation of the geometry of the virus-antibody interaction. The moment of inertia of the sphere about a central axis, /s is defined as ... [Pg.474]

In other words, for a sphere pivoting about an attachment point to a surface, the centre of mass of the sphere moves only 2/7th of the distance moved by the surface at full amplitude about the pivot point. The acceleration of a point on the surface of the resonator thus is given as ... [Pg.474]

Since the first crystallographic diffraction experiment was reported in 1912 [1], crystallography has been a major tool in the development of a variefy of chemical sciences. Over fhe pasf several decades if has been the second most important analytical method after nuclear magnetic resonance spectroscopy In chemistry, crystallography has been basic to the development of fields as diverse as organomefal-lic chemisfry and medicinal chemistry. It has had a pivotal role in the advancement of solid sfafe chemisfry. Diffraction studies are also now entrenched as a major research tool in structural biology. [Pg.85]


See other pages where Resonance pivotal is mentioned: [Pg.381]    [Pg.387]    [Pg.394]    [Pg.394]    [Pg.401]    [Pg.273]    [Pg.140]    [Pg.381]    [Pg.387]    [Pg.394]    [Pg.394]    [Pg.401]    [Pg.273]    [Pg.140]    [Pg.380]    [Pg.574]    [Pg.3]    [Pg.246]    [Pg.269]    [Pg.164]    [Pg.200]    [Pg.5]    [Pg.422]    [Pg.196]    [Pg.89]    [Pg.652]    [Pg.19]    [Pg.355]    [Pg.314]    [Pg.708]    [Pg.708]    [Pg.724]    [Pg.213]    [Pg.58]    [Pg.5]    [Pg.77]    [Pg.142]    [Pg.306]    [Pg.249]    [Pg.321]    [Pg.679]    [Pg.337]    [Pg.97]    [Pg.271]   
See also in sourсe #XX -- [ Pg.314 ]




SEARCH



Pivot

Pivoting

© 2024 chempedia.info