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Ball-and-stick drawing

Fig. 18.3 Ball and stick drawing of the centro-symmetric [H2NEt2]2Zr2Clio. Atom labels, bond distances and hydrogen bonds are labeled on the left side of the figure and Zr-CI-H-N hydrogen-bond angles are labeled on the right side of the figure. Fig. 18.3 Ball and stick drawing of the centro-symmetric [H2NEt2]2Zr2Clio. Atom labels, bond distances and hydrogen bonds are labeled on the left side of the figure and Zr-CI-H-N hydrogen-bond angles are labeled on the right side of the figure.
Fig. 1 Ball and stick drawings of the structures of (a) [Fe(F2o-TPP)(CPh2)] 0.5C6H6 0.5CH2Cl2 and (b) [Fe(F2o-TPP)(CPh2)(MeIni)]. The solvent molecules and/or hydrogen atoms are not shown [22]... Fig. 1 Ball and stick drawings of the structures of (a) [Fe(F2o-TPP)(CPh2)] 0.5C6H6 0.5CH2Cl2 and (b) [Fe(F2o-TPP)(CPh2)(MeIni)]. The solvent molecules and/or hydrogen atoms are not shown [22]...
Representations of tetrahedral methane (a) space-filling model (b) ball-and-stick model (c) ball-and-stick model, highlighting the tetrahedral faces (d) ball-and-stick drawing using wedge representations for the out-of-plane bonds. [Pg.603]

One of the most popular zeolites for photochemical studies faujasite (FAU) is depicted in Fig. 1. Fig. la is a ball and stick drawing which not only shows the... [Pg.226]

Figure 16. Ball and stick drawing of 2-0-(4-0-sulfo-a-L-fucopyranosyl)-4-0-sulfo-a-L-fucopyranose ("fucobiose") in the < , y = 0 reference conformation as in Fig. 1. Structural characteristics of rigid sulfated fucose residue deduced from energy minimization with MM2 to be reported elsewhere. Figure 16. Ball and stick drawing of 2-0-(4-0-sulfo-a-L-fucopyranosyl)-4-0-sulfo-a-L-fucopyranose ("fucobiose") in the < , y = 0 reference conformation as in Fig. 1. Structural characteristics of rigid sulfated fucose residue deduced from energy minimization with MM2 to be reported elsewhere.
Figure 6. Ball and stick drawing of the dominant (1) and minor (2) conformers from the lowest energy two-state structural solution D A. (Reproduced from ref. 40. Copyright 1986 American Chemical Society.)... Figure 6. Ball and stick drawing of the dominant (1) and minor (2) conformers from the lowest energy two-state structural solution D A. (Reproduced from ref. 40. Copyright 1986 American Chemical Society.)...
I wish to thank Andrew B. Carrell, who assisted with many of the calculations and figure preparations necessary for the production of this chapter. I also thank H. L. Carrell, G. D. Markham, A. S. Mildvan, and E. K. Patterson for many helpful discussions. Ball-and-stick drawings were drawn with the computer program VIEW (Carrell, 1976). Use of the Cambridge Structural Database (Allen etal., 1979) and the Protein Data Bank (Bernstein el al., 1977) is acknowledged. This work was supported by National Institutes of Health grants GM 44360, CA 10925, and CA 06927 and by an appropriation from the Commonwealth of Pennsylvania. [Pg.66]

Figure 5 A ball and stick drawing depicting the molecular structure of the Mn2(NSi2Me6)4 molecule... Figure 5 A ball and stick drawing depicting the molecular structure of the Mn2(NSi2Me6)4 molecule...
A ball-and-stick drawing is a simple skeletal model, in which the representation of the bond is generalized to a cylinder, and a disc is added at the position of each atom. Additional information may thereby be displayed in that different atom types may be distinguished by size and shading, and bonds of different appearance may be drawn. To create the line segments corresponding to a pure skeletal model, one needs only copy the coordinates of each pair of bonded atoms as the line segment end-points. To create ball-and-stick pictures, one must ... [Pg.54]

Line drawings Each atom is represented as a disc. The picture is a limit of the ball-and-stick drawings as the radius of each atomic ball is made in proportional to the van der Waals radius. [Pg.54]

Fig. 3 Structural changes of tubulin subunits upon MT disassembly, a Structure of a 3 subunit of the T2R complex (pdb id 1SA0 [15]). The monomer is sub-divided in an N-terminal domain (blue) with bound GDP (ball-and-stick drawing, grey), the central helix H7 yellow), an intermediate domain green), and the C-terminal helices red), b Comparison of the 3 subunit conformation in the T2R complex (same color code as in a) and in a straight protofilament (nucleotide binding domain and C-terminal helix hairpin in cyan, H7 helix in salmon, intermediate domain in pink, pdb id 1JFF [70]) after superposition of the secondary structural elements of their N-terminal domain, c Schematic representation recapitulating the movements between straight and curved tubulin monomers (domains are color-coded as in a the nucleotide is depicted as a red sphere)... Fig. 3 Structural changes of tubulin subunits upon MT disassembly, a Structure of a 3 subunit of the T2R complex (pdb id 1SA0 [15]). The monomer is sub-divided in an N-terminal domain (blue) with bound GDP (ball-and-stick drawing, grey), the central helix H7 yellow), an intermediate domain green), and the C-terminal helices red), b Comparison of the 3 subunit conformation in the T2R complex (same color code as in a) and in a straight protofilament (nucleotide binding domain and C-terminal helix hairpin in cyan, H7 helix in salmon, intermediate domain in pink, pdb id 1JFF [70]) after superposition of the secondary structural elements of their N-terminal domain, c Schematic representation recapitulating the movements between straight and curved tubulin monomers (domains are color-coded as in a the nucleotide is depicted as a red sphere)...
Fig. 5. Ball and stick drawing of the W2(/i-CSiMe3 2(CH2SiMe3)4 f 2-C2(Ph)Me molecule. The carbon atoms of the alkyne C-4 and C-5 and the /i-CSiMe3 ligands, C-22 and C-27, and the two tungsten atoms lie in a plane. Fig. 5. Ball and stick drawing of the W2(/i-CSiMe3 2(CH2SiMe3)4 f 2-C2(Ph)Me molecule. The carbon atoms of the alkyne C-4 and C-5 and the /i-CSiMe3 ligands, C-22 and C-27, and the two tungsten atoms lie in a plane.
Fig. 6. Ball and stick drawing of the (Me3SiCH2)4W2(M-CSiMe3) /i-C(SiMe3)C-(CH2)CHMe molecule. Selected bond distances associated with the central W2(//-CSiMe3)- >i-C(SiMe3)C(CH2)CHMe moiety are shown. Fig. 6. Ball and stick drawing of the (Me3SiCH2)4W2(M-CSiMe3) /i-C(SiMe3)C-(CH2)CHMe molecule. Selected bond distances associated with the central W2(//-CSiMe3)- >i-C(SiMe3)C(CH2)CHMe moiety are shown.
I THF crystallizes from hexane as a dimer. The central four membered ring is formed by the two lithium atoms and two metallated carbon atoms. The carbon atoms show two lithium contacts. Similarly, the lithium atoms have two carbon contacts. An intramolecular coordination of the piperidino nitrogen and the oxygen of the THF molecule complete the coordination sphere of lithium. A ball and stick drawing of the molecular structure of I THF and selected bond distances and angles are given in Fig. 1. [Pg.208]

Figure 36. The crystal structure (ball-and-stick drawing) of [NaTi(0-/-Pr)5] . [Adapted from (184).]... Figure 36. The crystal structure (ball-and-stick drawing) of [NaTi(0-/-Pr)5] . [Adapted from (184).]...
FIQURE 9.9—COnt d (b) Top views. Both parts include computer-generated spacefilling models (bottom). The top half of each part shows corresponding ball-and-stick drawings. [Pg.244]

Fig. 4a ODCase active-site (pyrimidine-binding region) with BMP bound from E. colL a Ball-and-stick drawing of polar and hydrophobic residues based on the crystallographi-cally determined coordinates. Bonds in BMP are darker than those in the active-site residues. b line drawing of polar active-site residues (bold) and their interactions with bound BMP... Fig. 4a ODCase active-site (pyrimidine-binding region) with BMP bound from E. colL a Ball-and-stick drawing of polar and hydrophobic residues based on the crystallographi-cally determined coordinates. Bonds in BMP are darker than those in the active-site residues. b line drawing of polar active-site residues (bold) and their interactions with bound BMP...
Figure 2.10 Ball-and-stick drawing of a pterin chelating molybdenum complex [Mo205(xanthopterinate)2p". Red, oxygen green, molybdenum blue, nitrogen grey, carbon. Figure 2.10 Ball-and-stick drawing of a pterin chelating molybdenum complex [Mo205(xanthopterinate)2p". Red, oxygen green, molybdenum blue, nitrogen grey, carbon.
Figure 2.11 A ball-and-stick drawing of 16 (left) and depiction of its bent alloxazine ligand TMAZH. Figure 2.11 A ball-and-stick drawing of 16 (left) and depiction of its bent alloxazine ligand TMAZH.
Figure 5. Ball-and-stick drawing of the (H20)2 CBEC geometry, obtained by the state-averaged FORS-MCSCF method. Figure 5. Ball-and-stick drawing of the (H20)2 CBEC geometry, obtained by the state-averaged FORS-MCSCF method.
The figure that follows shows ball-and-stick drawings... [Pg.357]


See other pages where Ball-and-stick drawing is mentioned: [Pg.49]    [Pg.258]    [Pg.260]    [Pg.114]    [Pg.106]    [Pg.111]    [Pg.789]    [Pg.322]    [Pg.187]    [Pg.2]    [Pg.111]    [Pg.538]    [Pg.375]    [Pg.375]    [Pg.18]    [Pg.407]    [Pg.357]   
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