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Anions, representation

I could be improved, including the need to incorporate water molecules and use a appropriate representation of the chloride anion. [Pg.418]

This redueible representation (the oeeupaney of two e orbitals in the anion gives rise to more than one state, so the direet produet e x e eontains more than one symmetry eomponent) ean be deeomposed into pure symmetry eomponents (labels F are used to denote the irredueible symmetries) by using the deeomposition formula given in Appendix... [Pg.269]

Fig. 7. Representive stmctures for compounds of molybdenum(0) (a) Mo(CO)g (b) tris(acetonitrile)tris(carbonyl)molybdenum(0) (c) bis(l,2-diphenylphosphinoethane) bis (dinitrogen) molybdenum(0), [R2PCH2CH2PR2]2Mo(N2)2, where R = CgH, also known as Mo(dppe)2(N2)2, where dppe = 1,2 — diphenylphosphinoethane (d) cyclopentadienyl tricarbonyl molybdenum(0) anion, CpMo(CO)3, where Cp = cyclopentadienyl (e)... Fig. 7. Representive stmctures for compounds of molybdenum(0) (a) Mo(CO)g (b) tris(acetonitrile)tris(carbonyl)molybdenum(0) (c) bis(l,2-diphenylphosphinoethane) bis (dinitrogen) molybdenum(0), [R2PCH2CH2PR2]2Mo(N2)2, where R = CgH, also known as Mo(dppe)2(N2)2, where dppe = 1,2 — diphenylphosphinoethane (d) cyclopentadienyl tricarbonyl molybdenum(0) anion, CpMo(CO)3, where Cp = cyclopentadienyl (e)...
Condensation occurs most readily at a pH value equal to the piC of the participating silanol group. This representation becomes less vaUd at pH values above 10, where the rate constant of the depolymerization reaction k 2 ) becomes significant and at very low pH values where acids exert a catalytic influence on polymerization. The piC of monosilicic acid is 9.91 0.04 (51). The piC value of Si—OH decreases to 6.5 in higher order sihcate polymers (52), which is consistent with piC values of 6.8 0.2 reported for the surface silanol groups of sihca gel (53). Thus, the acidity of silanol functionahties increases as the degree of polymerization of the anion increases. However, the exact relationship between the connectivity of the silanol sihcon and SiOH acidity is not known. [Pg.6]

Pig. 3. Representation of the electrical double layer at a metal electrode—solution interface for the case where anions occupy the inner Helmholtz plane... [Pg.510]

Eig. 2. Schematic representation of (a) cation-exchange resin, and (b), anion-exchange resin. [Pg.172]

Figure 9,5 Schematic representations of the structures of cyclic melasilicate anions with rf = 3. 4, 6, and 8. Figure 9,5 Schematic representations of the structures of cyclic melasilicate anions with rf = 3. 4, 6, and 8.
Figure 12.11 Schematic representation of the structures of polycyclic polyphosphide anions (open circles P, shaded circles P") (a) Pj ", (b) fPj Xr, (c) P8 i. (d) Pii -... Figure 12.11 Schematic representation of the structures of polycyclic polyphosphide anions (open circles P, shaded circles P") (a) Pj ", (b) fPj Xr, (c) P8 i. (d) Pii -...
Figure 12.29 Schematic representation of the boatshaped anion [(NH)4P406(0H)2] -showing important dimensions and the positions of H bonds. Figure 12.29 Schematic representation of the boatshaped anion [(NH)4P406(0H)2] -showing important dimensions and the positions of H bonds.
Figure 13.12 Schematic representation of the structure of the complex anion LSbjCIiiO] " showing the two different coordination geometries about Sb and the unique quadruply bridging Cl atom. Figure 13.12 Schematic representation of the structure of the complex anion LSbjCIiiO] " showing the two different coordination geometries about Sb and the unique quadruply bridging Cl atom.
Figure 13.13 Schematic representation of the anion structure in M2IAS2F10OJ.H2O. Figure 13.13 Schematic representation of the anion structure in M2IAS2F10OJ.H2O.
Figure 13.14 Schematic representation of the structure of (a) the trimeric anion [Sb.iFi203l, and (b) the dimeric anion fAs2F Figure 13.14 Schematic representation of the structure of (a) the trimeric anion [Sb.iFi203l, and (b) the dimeric anion fAs2F<vOrl. ...
Schematic representation of defect clusters in Fei- jO. The normal NaCl-type structure (a) has Fe (small open circles) and O (large dark circles) at alternate comers of the cube. In the 4 1 cluster (h), four octahedral Fe" sites are left vacant and an Fe" ion (grey) occupies the cube centre, thus being tetrahedrally coordinated by the 40. In (c) a more extended 13 4 cluster is shown in which, again, all anion sites are occupied but the 13 octahedral Fe sites are vacant and four Fe occupy a tetrahedral array of cube centres. Schematic representation of defect clusters in Fei- jO. The normal NaCl-type structure (a) has Fe (small open circles) and O (large dark circles) at alternate comers of the cube. In the 4 1 cluster (h), four octahedral Fe" sites are left vacant and an Fe" ion (grey) occupies the cube centre, thus being tetrahedrally coordinated by the 40. In (c) a more extended 13 4 cluster is shown in which, again, all anion sites are occupied but the 13 octahedral Fe sites are vacant and four Fe occupy a tetrahedral array of cube centres.
The four oxygen anions in the tetrahedron are balanced by the -i-4 oxidation state of the silicon cation, while the four oxygen anions connecting the aluminum cation are not balanced. This results in -1 net charge, which should be balanced. Metal cations such as Na", Mg ", or protons (H" ) balance the charge of the alumina tetrahedra. A two-dimensional representation of an H-zeolite tetrahedra is shown ... [Pg.70]

Fig. 12. Schematic representation of the a-helix-inducing effect of specific bound anions like CIO4 or SCN" in the case of N-co-trialkylaled BPAA the extended helical conformation contracts by the insertion of the anions. The water molecules of the hydration shells are omitted 1091... Fig. 12. Schematic representation of the a-helix-inducing effect of specific bound anions like CIO4 or SCN" in the case of N-co-trialkylaled BPAA the extended helical conformation contracts by the insertion of the anions. The water molecules of the hydration shells are omitted 1091...
Assuming that the circles represent cations and squares represent anions, match the incomplete net ionic equations to their pictorial representations... [Pg.99]

Shown below is a representation of the ionic solid MX, where M cations are represented by squares and X anions are represented by circles. Fill in the box after the arrow to represent what happens to the solid after it has been completely dissolved in water. For simplicity, do not represent the water molecules. [Pg.448]

Scheme 8.12 Schematic representation of the oxiranyl anion strategy for the synthesis of trans-fused THPs. Scheme 8.12 Schematic representation of the oxiranyl anion strategy for the synthesis of trans-fused THPs.
Figure 3. Schematic representation of the lithium-ion conductor LiAICl4. The A1C14 may be considered as tetrahedral anions, as indicated by green. The lithium ions are located between them. Figure 3. Schematic representation of the lithium-ion conductor LiAICl4. The A1C14 may be considered as tetrahedral anions, as indicated by green. The lithium ions are located between them.
FIGURE 6-15 Schematic representation of the ion permeability modulation for cation-responsive voltammetric sensors based on negatively charged lipid membranes. Complexation of the guest cation to the phospholipid receptors causes an increase of the permeability for the anionic marker ion. (Reproduced with permission from reference 49.)... [Pg.187]

Figure 35. Schematic representation of the reversible variation of volume associated with the electrochemical switching of polypyrrole. Changes in free volume are mainly due to two effects electrostatic repulsions between fixed positive charges and exchange of cations, anions, and solvent molecules between the polymer and the solution. (Reprinted from T. F. Otero, H.-J. Grande, and J. Rodriguez, J. Phys. Chem. 101, 3688, 1997, Figs. 1, 3,6, 7, 13. Copyright 1997. Reprinted with the permission of the American Chemical Society.)... Figure 35. Schematic representation of the reversible variation of volume associated with the electrochemical switching of polypyrrole. Changes in free volume are mainly due to two effects electrostatic repulsions between fixed positive charges and exchange of cations, anions, and solvent molecules between the polymer and the solution. (Reprinted from T. F. Otero, H.-J. Grande, and J. Rodriguez, J. Phys. Chem. 101, 3688, 1997, Figs. 1, 3,6, 7, 13. Copyright 1997. Reprinted with the permission of the American Chemical Society.)...
In the anion radical of XXIII, the starting distorted structures belonging to the Og, bjg and b2u irreducible representations of point group D2k all converge into the unique set of bond lengths corresponding to... [Pg.31]

The simplest way to treat the solvent molecules of an electrolyte explicitly is to represent them as hard spheres, whereas the electrostatic contribution of the solvent is expressed implicitly by a uniform dielectric medium in which charged hard-sphere ions interact. A schematic representation is shown in Figure 2(a) for the case of an idealized situation in which the cations, anions, and solvent have the same diameters. This is the solvent primitive model (SPM), first named by Davis and coworkers [15,16] but appearing earlier in other studies [17]. As shown in Figure 2(b), the interaction potential of a pair of particles (ions or solvent molecule), i and j, in the SPM are ... [Pg.627]

Figure 51-2. Diagrammatic representation (not to scale) of the binding of factors Va, Xa, Ca +, and prothrombin to the plasma membrane of the activated platelet. The sites of cleavage of prothrombin by factor Xa are indicated by two arrows. The part of prothrombin destined to form thrombin is labeled prethrombin.The Ca " is bound to anionic phospholipids of the plasma membrane of the activated platelet. Figure 51-2. Diagrammatic representation (not to scale) of the binding of factors Va, Xa, Ca +, and prothrombin to the plasma membrane of the activated platelet. The sites of cleavage of prothrombin by factor Xa are indicated by two arrows. The part of prothrombin destined to form thrombin is labeled prethrombin.The Ca " is bound to anionic phospholipids of the plasma membrane of the activated platelet.
Nitric acid is one of the six common strong acids. This means that when nitric acid dissolves in water, each acid molecule transfers a proton to a water molecule, generating a hydronium ion and the appropriate anion. Both the reaction and its molecular representation must show this proton transfer. [Pg.238]

Which of these options is the best Lewis structure Actually, no single Lewis structure by itself is an accurate representation of NO3. Any single structure of the anion shows nitrate with one NDO double bond and two N— O single bonds. In Section 9 1, we show that single and double bonds between the same types of atoms have different lengths and different energies. In contrast, experiments show that the three nitrate N—O bonds are identical. To show that the nitrate N—O bonds are all alike, we use a composite of the three equivalent Lewis structures. These are traditionally called resonance structures. Resonance stmctures are connected by double-headed arrows to emphasize that a complete depiction requires all of them. [Pg.599]

It is essential to realize that electrons In the nitrate anion do not flip back and forth among the three bonds, as implied by separate structures. The true character of the anion is a blend of the three, In which all three nitrogen-oxygen bonds are equivalent. The need to show several equivalent structures for such species reflects the fact that Lewis structures are approximate representations. They reveal much about how electrons are distributed in a molecule or ion, but they are imperfect instruments that cannot describe the entire story of chemical bonding, hi Chapter 10, we show how to interpret these structures from a more detailed bonding perspective. [Pg.600]

Figure 4. Schematic representation of separating motion of cation C from the reference ion A. A is another anion of the same kind, and C, plays a role of tranquilizer if the interaction of A -Ct is much stronger than that of A -C. Figure 4. Schematic representation of separating motion of cation C from the reference ion A. A is another anion of the same kind, and C, plays a role of tranquilizer if the interaction of A -Ct is much stronger than that of A -C.
Phase-transfer (PT) catalysts accelerate reactions of two immiscible reactants. Without a PT catalyst reactions between substances located in different phases are often slow or do not occur at all. The PT catalyst usually has the function of transferring anions, in the form of an ion pair, from the aqueous phase to the organic phase, in which the reaction with the water-insoluble reactant takes place (see schematic representation in Fig. 3.56). [Pg.117]


See other pages where Anions, representation is mentioned: [Pg.47]    [Pg.47]    [Pg.191]    [Pg.91]    [Pg.6]    [Pg.236]    [Pg.531]    [Pg.170]    [Pg.8]    [Pg.631]    [Pg.706]    [Pg.985]    [Pg.280]    [Pg.2]    [Pg.1074]    [Pg.222]    [Pg.19]    [Pg.142]    [Pg.143]    [Pg.89]    [Pg.1074]    [Pg.177]   
See also in sourсe #XX -- [ Pg.13 ]




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