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Group properties table

The study of the molar volumes of hydrocarbons by Kopp in 1855 provided the earliest example of the addivitity of group properties. Table 5 and 6 list the molecular volume and the contribution of each atom and functional group to this volume as determined by both the 0.002 and 0.001 au envelope of the charge density for a number of hydrocarbons obtained from 6-31G /6-31G calculations. Table 5 also lists the fraction of the total electronic charge of the atom contained within the stated envelope" ". ... [Pg.52]

Chemical reactivity and group trends Table 10.2 Some physical properties of Group 14 elements... [Pg.373]

From the comparison of the results, it can be inferred that copper ions exchanged in the ZSM-5 zeolites assumes a bidentate (sites 12 and II) or tridentate coordination (sites M5, Z6, and M7). These two groups differ also in the molecular properties (Table 2.2). The I-centers are characterized by lower values of the valence index and greater partial charges, QCu, in comparison to the M and Z centers, which is associated with the deeper laying HOMO and LUMO levels. In the M5, Z6, and M7 sites Cu1 ions exhibit more covalent character, and the frontier orbitals have less negative energies. As a result, the chemical hardness of the I-centers, located at the channel intersections, is smaller than those located on the walls of the ZSM-5 zeolite. [Pg.32]

Physical and chemical properties. Only the physical and chemical properties which have an effect on the crystal growth of these materials are mentioned. The physical properties are grouped in table II. [Pg.97]

Because of the group property of closure all operations of any group can be presented in the form of a multiplication table that contains all elements of the group, e.g. [Pg.57]

Vibrations may be decomposed into three orthogonal components Ta (a = x, y, z) in three directions. These displacements have the same symmetry properties as cartesian coordinates. Likewise, any rotation may be decomposed into components Ra. The i.r. spanned by translations and rotations must clearly follow the appropriate symmetry type of the point-group character table. In quantum formalism, a transition will be allowed only if the symmetry product of the initial and final-state wave functions contains the symmetry species of the operator appropriate to the transition process. Definition of the symmetry product will be explained in terms of a simple example. [Pg.298]

Figure 3. Possible preparation of polymeric model membranes (X = polymerizable group). (a)-(c) Polymerization preserving head group properties, (d) Polymerization preserving chain mobility (30). Corresponding monomers see Table 1. Figure 3. Possible preparation of polymeric model membranes (X = polymerizable group). (a)-(c) Polymerization preserving head group properties, (d) Polymerization preserving chain mobility (30). Corresponding monomers see Table 1.
The second approach to modify the physical properties is through end-group modifications. Table 22.5 shows three different end groups with rather different properties. By using an epoxy compound or a di-primary glycol, the physical properties can be much improved. [Pg.727]

INVERSE are the inverse operator list, and the Gensym symbol for it, respectively. The CLASS property value is another Gensym atom which has as its value a list of all of the operators in that class. (In this simple case, the value of // CLS-1 is the list (// GRP-1), etc.) The remaining pairs in each property list represent the group multiplication table. For any particular group multiplication, an element of the group list at the top of Table I pertains to the right operator, the property indicator pertains to the left operator, and the property value pertains to the product. For example, for the product of the permutation operator (123) with itself,... [Pg.180]

Enzyme Properties. The two isolated veratryl alcohol oxidases had very similar properties (Table I). The difference in isoelectric points might be accounted for by aspartate content all other amino acid contents except glycine were the same within experimental error (5%). The specific activities (veratryl alcohol as substrate) were significantly different, but both enzymes contained a flavin prosthetic group (25) and converted one molecule of oxygen to one molecule of hydrogen peroxide during alcohol oxidation. [Pg.474]

All the vinylogous systems 22-32 exhibit the same pattern of redox properties. The position of the potentials Ei and E2, or better E = (Ei + E2>/2 of a certain vinyl-ogue is mainly determined by the heterocyclic end groups (cf. Table 8). [Pg.17]

The members of symmetry groups are symmetry operations the combination rule is successive operation. The identity element is the operation of doing nothing at all. The group properties can be demonstrated by forming a multiplication table. Let us label the rows of the table by the first operation and the columns by the second operation. Note that this order is important because most groups are not commutative. The C3V group multiplication table is as follows ... [Pg.670]

Table 4.1. A systematic comparison of the group properties of a collection of synthetic chemicais and a coiiection of naturaiiy occurring chemicals, both collections heid by a pharmaceuticai company. Table 4.1. A systematic comparison of the group properties of a collection of synthetic chemicais and a coiiection of naturaiiy occurring chemicals, both collections heid by a pharmaceuticai company.
STRUCTURE AND PROPERTIES Table 1-3 Some Common Functional Groups... [Pg.8]

An additional modification of lignins with hydroxyl or amine group-containing compounds was found to further improve the product properties (Table III). [Pg.253]

Losartan was the first ATI antagonist to be used clinically. It has a complicated effect, since its major metabolite (E-3174) is about ten times more potent as an inhibitor of angiotensin II than losartan itself. Candesartan cilexetil is the only compound in this group which is a real prodrug. It is hydrolysed by the liver to the active form, candesartan. Differences between drugs in this class are largely accounted for by their pharmacokinetic properties (Table 8.2). [Pg.143]

Fig. 4a-d. Possible ways to synthesize polymeric model membranes7) (X = polymerizable group), a —c Polymerization with preservation of head group properties d polymerization with preservation of chain mobility. For examples of corresponding monomers, see Table 1... [Pg.5]

Hydrogen is often placed by itself in the Periodic Table. This is because the properties of hydrogen are unique. However, profitable comparisons can be made with the other elements. It is often shown at the top of either Group I or Group VII, but it cannot fit easily into the trends shown by either group see Table 9.7. [Pg.157]

A subset H of G, H c G, that is itself a group with the same law of binary composition, is a subgroup of G. Any subset of G that satisfies closure will be a subgroup of G, since the other group properties are then automatically fulfilled. The region of the multiplication table of S(3) in Table 1.3 in a box shows that the subset P0 Pi P2 is closed, so that this set is a... [Pg.6]

The complete set of point symmetry operators that is generated from the operators Ri R2... that are associated with the symmetry elements (as shown, for example, in Table 2.2) by forming all possible products like R, Ry and including E, satisfies the necessary group properties the set is complete (satisfies closure), it contains E, associativity is satisfied, and each element (symmetry operator) has an inverse. That this is so may be verified in any particular case we shall see an example presently. Such groups of point symmetry operators are called point groups. For example, if a system has an S4 axis and no... [Pg.30]


See other pages where Group properties table is mentioned: [Pg.175]    [Pg.569]    [Pg.425]    [Pg.583]    [Pg.21]    [Pg.490]    [Pg.112]    [Pg.777]    [Pg.1489]    [Pg.70]    [Pg.677]    [Pg.51]    [Pg.298]    [Pg.425]    [Pg.39]    [Pg.127]    [Pg.512]    [Pg.115]    [Pg.92]    [Pg.45]    [Pg.286]    [Pg.294]    [Pg.103]    [Pg.77]    [Pg.111]    [Pg.202]    [Pg.149]    [Pg.2]    [Pg.5]   
See also in sourсe #XX -- [ Pg.658 , Pg.702 ]




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