Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Interactions edge-to-face

A number of papers deal with aspects of [Ru(phen)3] ". In the solid state, [Ru(phen)3] PF6]2 consists of racemic layers of cations, between which the anions reside. This contrasts with the structure of [Ru(bpy)3][PFg]2 which possesses homochiral layers. Racemic layers of [Ru(phen)3] " " cations are observed in the perchlorate salt. The structure of A-[Ru(phen)3][PF6]2 has been determined. Data for 335 M(phen), 159 M(phen)2, and 33M(phen)3 complexes from the Cambridge Structural Database have been analyzed and show that offset face-to-face inter-phen interactions are more common that edge-to-face interactions. ... [Pg.621]

The structure determination allows for an examination of the intermolecu-lar interactions of the three-component cocrystal (Fig. 17). Hydrogen bonding is observed between the carbonyls of BQ 21 and the hydroxyls of BN 20. A four-component u-stacking motif is apparent among two molecules each of BQ 21 and BN 20. Finally, edge-to-face interactions are observed with two molecules each of BQ 21 and AN 16. [Pg.68]

Fig. 14.1 Structures and crystalline order for benzene (1) and naphthalene (2) showing predominant edge-to-face interactions. Fig. 14.1 Structures and crystalline order for benzene (1) and naphthalene (2) showing predominant edge-to-face interactions.
Fig. 14.2 Anthracene and its native solid-state order, showing edge-to-face interactions. Fig. 14.2 Anthracene and its native solid-state order, showing edge-to-face interactions.
The addition of substituents to both the 9- and 10-positions of anthracene serves to disrupt the edge-to-face interactions of the molecule, preventing the adoption of a herringbone arrangement in the crystal. As long as the substituent groups are relatively small, the molecules will be able to adopt a n-stacked arrangement. 9,10-Dimethylanthracene (14) [28] and 9,10-bis(chloromethyl) anthracene (15) [29] are both excellent examples of the typical crystalline order of such species (Fig. 14.10). [Pg.517]

Fig. 21. Stereodrawing of L-arabinose bound to L-arabinose-binding protein from Escherichia coli. The edge-to-face interaction between tryptophan-16 and phenylalanine-17 gives rise to a hydrophobic surface that interacts with the hydrophobic portion of the sugar. Reproduced with permission from Quiocho and Vyas (1984). Fig. 21. Stereodrawing of L-arabinose bound to L-arabinose-binding protein from Escherichia coli. The edge-to-face interaction between tryptophan-16 and phenylalanine-17 gives rise to a hydrophobic surface that interacts with the hydrophobic portion of the sugar. Reproduced with permission from Quiocho and Vyas (1984).

See other pages where Interactions edge-to-face is mentioned: [Pg.238]    [Pg.100]    [Pg.141]    [Pg.93]    [Pg.239]    [Pg.269]    [Pg.161]    [Pg.252]    [Pg.68]    [Pg.68]    [Pg.480]    [Pg.63]    [Pg.64]    [Pg.78]    [Pg.58]    [Pg.63]    [Pg.64]    [Pg.208]    [Pg.40]    [Pg.154]    [Pg.512]    [Pg.512]    [Pg.514]    [Pg.515]    [Pg.517]    [Pg.519]    [Pg.519]    [Pg.520]    [Pg.522]    [Pg.522]    [Pg.524]    [Pg.524]    [Pg.528]    [Pg.528]    [Pg.529]    [Pg.534]    [Pg.542]    [Pg.162]    [Pg.166]    [Pg.169]   
See also in sourсe #XX -- [ Pg.66 ]

See also in sourсe #XX -- [ Pg.95 ]




SEARCH



Faces interactions

© 2024 chempedia.info