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Molecular structures connectivity

A major disadvantage of a matrix representation for a molecular graph is that the number of entries increases with the square of the number of atoms in the molecule. What is needed is a representation of a molecular graph where the number of entries increases only as a linear function of the number of atoms in the molecule. Such a representation can be obtained by listing, in tabular form only the atoms and the bonds of a molecular structure. In this case, the indices of the row and column of a matrix entry can be used for identifying an entry. In essence, one has to distinguish each atom and each bond in a molecule. This is achieved by a list of the atoms and a list of the bonds giving the coimections between the atoms. Such a representation is called a connection table (CT). [Pg.40]

Deficiencies in Representing Molecular Structures by a Connection Table... [Pg.63]

The concept of connection tablc.s, a.s shown. so far, cannot represent adequately quite a number of molecular structures. Basically, a connection table represents only a single valence bond structure. Thus, any chemical species that cannot he described adequately by a single valence bond (VB) structure with single or multiple bonds between two atom.s is not handled accurately. [Pg.63]

RAMSES is usually generated from molecular structures in a VB representation. The details of the connection table (localized charges, lone pairs, and bond orders) are kept within the model and are accessible for further processes. Bond orders are stored with the n-systems, while the number of free electrons is stored with the atoms. Upon modification oF a molecule (e.g., in systems dealing with reactions), the VB representation has to be generated in an adapted Form from the RAMSES notation. [Pg.69]

Z-matriccs arc commonly used as input to quantum mechanical ab initio and serai-empirical) calculations as they properly describe the spatial arrangement of the atoms of a molecule. Note that there is no explicit information on the connectivity present in the Z-matrix, as there is, c.g., in a connection table, but quantum mechanics derives the bonding and non-bonding intramolecular interactions from the molecular electronic wavefunction, starting from atomic wavefiinctions and a crude 3D structure. In contrast to that, most of the molecular mechanics packages require the initial molecular geometry as 3D Cartesian coordinates plus the connection table, as they have to assign appropriate force constants and potentials to each atom and each bond in order to relax and optimi-/e the molecular structure. Furthermore, Cartesian coordinates are preferable to internal coordinates if the spatial situations of ensembles of different molecules have to be compared. Of course, both representations are interconvertible. [Pg.94]

An alternative way to represent molecules is to use a linear notation. A linear notation uses alphanumeric characters to code the molecular structure. These have the advantage of being much more compact than the connection table and so can be particularly useful for transmif-ting information about large numbers of molecules. The most famous of the early line notations is the Wiswesser line notation [Wiswesser 1954] the-SMILES notation is a more recent example that is increasingly popular [Weininger 1988]. To construct the Wiswesser... [Pg.659]

In biological systems molecular assemblies connected by non-covalent interactions are as common as biopolymers. Examples arc protein and DNA helices, enzyme-substrate and multienzyme complexes, bilayer lipid membranes (BLMs), and aggregates of biopolymers forming various aqueous gels, e.g, the eye lens. About 50% of the organic substances in humans are accounted for by the membrane structures of cells, which constitute the medium for the vast majority of biochemical reactions. Evidently organic synthesis should also develop tools to mimic the Structure and propertiesof biopolymer, biomembrane, and gel structures in aqueous media. [Pg.350]

Strkcttire inflkence. The specificity of interphase transfer in the micellar-extraction systems is the independent and cooperative influence of the substrate molecular structure - the first-order molecular connectivity indexes) and hydrophobicity (log P - the distribution coefficient value in the water-octanole system) on its distribution between the water and the surfactant-rich phases. The possibility of substrates distribution and their D-values prediction in the cloud point extraction systems using regressions, which consider the log P and values was shown. Here the specificity of the micellar extraction is determined by the appearance of the host-guest phenomenon at molecular level and the high level of stmctural organization of the micellar phase itself. [Pg.268]

On the basis of data obtained the possibility of substrates distribution and their D-values prediction using the regressions which consider the hydrophobicity and stmcture of amines was investigated. The hydrophobicity of amines was estimated by the distribution coefficient value in the water-octanole system (Ig P). The molecular structure of aromatic amines was characterized by the first-order molecular connectivity indexes ( x)- H was shown the independent and cooperative influence of the Ig P and parameters of amines on their distribution. Evidently, this fact demonstrates the host-guest phenomenon which is inherent to the organized media. The obtained in the research data were used for optimization of the conditions of micellar-extraction preconcentrating of metal ions with amines into the NS-rich phase with the following determination by atomic-absorption method. [Pg.276]

Knowing the substitution pattern of both benzene rings A and B, one can deduce the molecular structure from the CH connectivities of the CH COSY and CH COLOC plots. The interpretation of both experiments leads firstly to the correlation Table 41.1. [Pg.216]

For most combinations of atoms, a number of molecular structures that differ fk m each other in the sequence of bonding of the atoms are possible. Each individual molecular assembly is called an isomer, and the constitution of a compound is the particular combination of bonds between atoms (molecular connectivity) which is characteristic of that structure. Propanal, allyl alcohol, acetone, 2-methyloxinine, and cyclopropanol each correspond to the molecular formula CjH O, but differ in constitution and are isomers of one another. [Pg.75]

The acids in Table 1.7 span a range of more than 70 units (10 ° in Kj. In this section we ll introduce some generalizations that will permit us to connect molecular structure with acidity, at least insofar- as trends in related compounds ar e concerned. The main ways in which structure affects acidity depend on ... [Pg.38]

We contend therefore that introduction of molecular modeling very early into the currieulum need not complicate or eonfuse the learning of organie chemistry, but rather assist the student in visualizing the structures of organic molecules and in learning the intimate connections between molecular structure and molecular properties. [Pg.314]

Even at the time-independent level, molecular structure and bonding often involve changes in the point group symmetry, so that inescapable connection seems to intertwine two issues better left apart. Dynamics simply makes such conceptual and procedural issues harder. [Pg.225]

Of the fundamental nonalternant hydrocarbons, only two prototypes were known about fifteen years ago azulene (XI, Fig. 5), the molecular structure of which was determined by Pfau and Plattner and fulvene (XIX) synthesized by Thiec and Wiemann. Early in the 1960 s many other interesting prototypes have come to be synthesized. Doering succeeded in synthesizing heptafulvene (XX) fulvalene (XXI) and heptafulvalene (XXIII). Prinzbach and Rosswog reported the synthesis of sesquifulvalene (XXII). Preparation of a condensed bicyclic nonalternant hydrocarbon, heptalene (VII), was reported by Dauben and Bertelli . On the other hand, its 5-membered analogue, pentalene (I), has remained, up to the present, unvanquished to many attempts made by synthetic chemists. Very recently, de Mayo and his associates have succeeded in synthesizing its closest derivative, 1-methylpentalene. It is added in this connection that dimethyl derivatives of condensed tricyclic nonaltemant hydrocarbons composed of 5- and 7-membered rings (XIV and XV), known as Hafner s hydrocarbons, were synthesized by Hafner and Schneider already in 1958. [Pg.4]

In terms of their molecular structures, the nucleotide and protein realms are usually considered to be rather independent of each other. However, these two families of molecules are covalently linked in the translational aminoacyl- RNAs and ribonucleoproteins as well as in the nucleoproteins involved in cellular and viral replication. In these hybrid biomolecules, a (deoxy)ribose phosphate moiety serves as the structural connection between the nucleoside and peptide moieties. [Pg.200]

Contemporary s Tithetic chemists know detailed information about molecular structures and use sophisticated computer programs to simulate a s Tithesis before trying it in the laboratory. Nevertheless, designing a chemical synthesis requires creativity and a thorough understanding of molecular structure and reactivity. No matter how complex, every chemical synthesis is built on the principles and concepts of general chemistry. One such principle is that quantitative relationships connect the amounts of materials consumed and the amounts of products formed in a chemical reaction. We can use these relationships to calculate the amounts of materials needed to make a desired amount of product and to analyze the efficiency of a chemical synthesis. The quantitative description of chemical reactions is the focus of Chapter 4. [Pg.201]

Although the work mentioned in this paper deals with only a small part of the subject the evidence which has been secured indicates that the idea of molecular compound formation should be thoroughly tested. Since the organic chemist specializes in problems connected with molecular structure and the residual aflSnity of atoms or groups he may iSnd this theory useful in the choice of negative catalysts for many purposes. [Pg.3]


See other pages where Molecular structures connectivity is mentioned: [Pg.359]    [Pg.658]    [Pg.211]    [Pg.3]    [Pg.7]    [Pg.228]    [Pg.123]    [Pg.3]    [Pg.28]    [Pg.253]    [Pg.284]    [Pg.267]    [Pg.51]    [Pg.238]    [Pg.13]    [Pg.331]    [Pg.337]    [Pg.355]    [Pg.372]    [Pg.189]    [Pg.450]    [Pg.67]    [Pg.222]    [Pg.119]    [Pg.208]    [Pg.417]    [Pg.253]    [Pg.108]    [Pg.93]    [Pg.114]    [Pg.456]    [Pg.96]   
See also in sourсe #XX -- [ Pg.37 ]




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Deficiencies in Representing Molecular Structures by a Connection Table

Molecular connectivity

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