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Deoxycholic acid hydrogen bonding

Adequate x-ray crystallographic studies have been made of some of the structures in Table VII. The end-view cross section of channels in urea- -paraffin complexes is shown in Figure 5 53). The urea (and thiourea) molecules are hydrogen bonded to create hollow cylindrical channels whose walls are helices of linked urea or thiourea. These helices can be right or left handed in a given crystal (but not both). In the orthorhombic structure of the deoxycholic acid complex with acetic acid having a =... [Pg.23]

The most common hosts for inclusion polymerization are urea, thiourea, perhydrotriphenylene (PHTP), deoxycholic acid (DCA), apocholic acid (ACA) and tris(o-phenylenedioxy)cyclotriphosphazene (TPP)(Fig. 2). They have the common feature of forming channel-like clathrates, but differ in many specific properties. For instance, urea and thiourea have a rigid structure in which the host molecules are connected by hydrogen bonds and possess a high selectivity towards the guests. In urea channels are rather narrow whereas in thiourea they are wider as a consequence, linear molecules include only in urea and branched or cyclic molecules in thiourea. On the contrary, chainnels existing in PHTP clathrates are very flexible and can accomodate linear, branched and cyclic molecules. [Pg.81]

The crystalline 1 1 complex of deoxycholic acid and acetic acid comprises chains of hydrogen-bonded acetic acid molecules occupying wide tunnels between... [Pg.280]

Porous host substructures with parallel channels are typical of many inclusion compounds formed by bile acids and their derivatives (see Deoxycholic, Cholic, and Apocholic Acids). In this class of compounds, host molecules are always optically active, and the resulting host networks are chiral. The best known among them are inclusion compounds of deoxycholic acid (DCA) (also known as choleic acidsj. With most guests. DCA molecules assemble via hydrogen bonds into a coiTugated... [Pg.224]

Amide- and Urea-Based Anion Receptors, p. 51 Amino Acids Applications, p. 42 Chiral Guest Recognition, p. 236 Deoxycholic, Cholic, and Apocholic Acids, p. 441 Fluorescence Sensing of Anions, p. 566 Guanidinium-Based Anion Receptors, p. 615 Hydrogen Bonding, p. 658 lonophores, p. 760... [Pg.1370]


See other pages where Deoxycholic acid hydrogen bonding is mentioned: [Pg.70]    [Pg.196]    [Pg.170]    [Pg.20]    [Pg.24]    [Pg.99]    [Pg.70]    [Pg.60]    [Pg.579]    [Pg.236]    [Pg.224]    [Pg.70]    [Pg.473]    [Pg.358]    [Pg.138]    [Pg.169]    [Pg.441]    [Pg.619]    [Pg.164]    [Pg.261]    [Pg.262]    [Pg.322]    [Pg.991]    [Pg.2360]    [Pg.193]    [Pg.195]   
See also in sourсe #XX -- [ Pg.91 ]




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