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Molecular structures diagrams

Figure 6.4. Molecular structure diagram of [ PPh3 2Cu(SEt)2ln(SEt)2], indicating tunable sites. Figure 6.4. Molecular structure diagram of [ PPh3 2Cu(SEt)2ln(SEt)2], indicating tunable sites.
CAS CHEMICAL REGISTRY 8,000,000 compounds CHEMICAL ABSTRACTS SERVICE The world s largest file of substance information, including coordination compounds, polymers, incompletely defined substances, alloys, mixtures, and minerals. In each record, the registry number is linked to molecular structure diagram, molecular formula, CA index name, synonyms, and the ten most recent references in Chemical Abstracts. Easy crossover to the bibliographic file... [Pg.26]

CAS Registry Numbers are assigned in sequential order as substances are entered into the CAS Chemical Registry System database for the first time the numbers have no chemical significance. CAS Registry Numbers link the molecular structure diagram, systematic CA index name, synonyms, molecular formula,... [Pg.253]

FIGURE 9.41 One-Dimensional Chain, (a) Cu(ll) Linker, (b) Portion of the chain within the solid state. (Molecular structure diagrams created with CIF data, with hydrogen atoms omitted for clarity). [Pg.350]

Figure 10 The dipyridyl tetrapropoxycalix[4]arene-PdCl2 complex 44 has two axles, but its crystal structure (rotated 90° with respect to the molecular structure diagram) reveals clear wheel-and-axle topology. " ... Figure 10 The dipyridyl tetrapropoxycalix[4]arene-PdCl2 complex 44 has two axles, but its crystal structure (rotated 90° with respect to the molecular structure diagram) reveals clear wheel-and-axle topology. " ...
Charles Coulson contributed to physics, chemistry and mathematics, emphasising that, in order to demonstrate their undoubted explanatory power, the mathematical models of quantum chemistry would need to be tailored to provide qualitative, contrastive chemical explanations grounded in molecular structure diagrams. Yet he was also doubtful of the long-term explanatory role of the chemical bond. Although it is central to chemical explanation, Coulson felt that chemistry would need to outgrow the notion. [Pg.159]

Drawing-, text-, and structure-input tools are provided that enable easy generation of flow charts, textual annotations or labels, structures, or reaction schemes. It is also possible to select different representation styles for bond types, ring sizes, molecular orbitals, and reaction arrows. The structure diagrams can be verified according to free valences or atom labels. Properties such as molecular... [Pg.140]

Factual databases may provide the electronic version of printed catalogs on chemical compoimds. The catalogs of different suppliers of chemicals serve to identify chemical compounds with their appropriate synonyms, molecular formulas, molecular weight, structure diagrams, and - of course - the price. Sometimes the data are linked to other databases that contain additional information. Structure and substructure search possibihties have now been included in most of the databases of chemical suppliers. [Pg.240]

Seddon, G. M., Tariq, R. H., Dos Santos Viega, A. (1982). The visualisation of spatial transformations in diagrams of molecular structures. European Journal of Science Education, 4, 409 20. [Pg.30]

Seddon, G. M., Shubbar, K. E. (1984). The elfects of presentation mode and colour in teaching visualization of rotation in diagrams of molecular structures. Research in Science and Technological Education, 2(2), 167-176. [Pg.30]

Figure 3.3 Molecular structure of G-protein-coupled receptors. In (a) the electron density map of bovine rhodopsin is shown as obtained by cryoelectron microscopy of two-dimensional arrays of receptors embedded in lipid membrane. The electron densities show seven peaks reflecting the seven a-helices which are predicted to cross the cell membrane. In (b) is shown a helical-wheel diagram of the receptor orientated according to the electron density map shown in (a). The diagram is seen as the receptor would be viewed from outside the cell membrane. The agonist binding pocket is illustrated by the hatched region between TM3, TM5 and TM6. (From Schertler et al. 1993 and Baldwin 1993, reproduced from Schwartz 1996). Reprinted with permission from Textbook of Receptor Pharmacology. Eds Foreman, JC and Johansen, T. Copyright CRC Press, Boca Raton, Florida... Figure 3.3 Molecular structure of G-protein-coupled receptors. In (a) the electron density map of bovine rhodopsin is shown as obtained by cryoelectron microscopy of two-dimensional arrays of receptors embedded in lipid membrane. The electron densities show seven peaks reflecting the seven a-helices which are predicted to cross the cell membrane. In (b) is shown a helical-wheel diagram of the receptor orientated according to the electron density map shown in (a). The diagram is seen as the receptor would be viewed from outside the cell membrane. The agonist binding pocket is illustrated by the hatched region between TM3, TM5 and TM6. (From Schertler et al. 1993 and Baldwin 1993, reproduced from Schwartz 1996). Reprinted with permission from Textbook of Receptor Pharmacology. Eds Foreman, JC and Johansen, T. Copyright CRC Press, Boca Raton, Florida...
Fig. 5. A schematic band structure and molecular orbital diagram for a conjugated polymer containing no mid-gap states. Fig. 5. A schematic band structure and molecular orbital diagram for a conjugated polymer containing no mid-gap states.
Fig. 9 (a) Molecular structures of novel ESIPT dyes, 2,5,-bis[5-(4-t-butylphenyl)-[l,3,4]oxadia-zol-2-yl]-phenol (SOX), and 2,5-bis[5-(4-t-butylphenyl)-[l,3,4]oxadiazol-2-yl]-benzene-l,4,-diol (DOX). (b) Emission colors in the Commission Internationale de L Eclariage (CEE) chromaticity diagram. The inner oval and the filled circle at coordinate (x,y) of (0.33, 0.33) indicate the white region and the ideal color, respectively. Note that PS and PVK denote polystyrene and poly (N-vinylcarbazole) film (reprint from ref. [91], Copyright 2005 Wiley-VCH)... [Pg.240]

Figure 4. Views of DMBA, BP, 5,6-dimethylchrysene, 5,12-dimethyl-chrysene and 5-methyl chrysene. These illustrate the distortions that occur as a result of steric effects. These and many subsequent representations of molecular structure are stereoviews and may be viewed with stereoglasses alternatively the reader can focus his eyes on the two images until an image between them begins to form and then allow his eyes to relax until the central image becomes three-dimensional. This process calls for patience and may take a minute or so. The reader who does not wish to do this may simply inspect one of the two diagrams for each structure. Figure 4. Views of DMBA, BP, 5,6-dimethylchrysene, 5,12-dimethyl-chrysene and 5-methyl chrysene. These illustrate the distortions that occur as a result of steric effects. These and many subsequent representations of molecular structure are stereoviews and may be viewed with stereoglasses alternatively the reader can focus his eyes on the two images until an image between them begins to form and then allow his eyes to relax until the central image becomes three-dimensional. This process calls for patience and may take a minute or so. The reader who does not wish to do this may simply inspect one of the two diagrams for each structure.

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Molecular diagram

Structural diagrams

Structure diagram

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