Common hydrogen bonds
The concept of supramolecular chemistry can be applied to the design of new pharmaceutical materials affording new compositions of matter with desirable composition, structure and properties.
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The design of a two-molecule, or binary, compound using complementary molecules represents an example of an application of crystal engineering. Crystal engineering is the understanding of intermolecular interactions, in the context of crystal packing, in the design of new solid materials.
By identifying reliable connectors through molecular recognition or self-assembly, one can build predictable architectures. The study of supramolecular synthesis was accomplished using known pharmaceutical molecules such as Nifedipine calcium channel blocker used for cardiovascular diseases and Phenytoin used as an anticonvulsant drug and model compounds containing synthons common in pharmaceutical common hydrogen bonds Crown ethers and Trimesic acid with ether linkages and carboxylic acid dimers, respectively with complementary molecular additives.
The co-crystals formed were characterized by various techniques IR, m. These crystalline assemblies could afford improved solubility, dissolution rate, stability and bioavailability.
Graduate Theses and Dissertations.]
Common hydrogen bonds - message simply
Structure[ edit ] The structure of hydrogen disulfide is similar to that of hydrogen peroxide , with C2 point group symmetry. Both molecules are distinctly nonplanar. The dihedral angle is Fractional distillation of this oil gives hydrogen disulfide separate from any other polysulfides mostly trisulfide. Trost and Hornberger [6] have calculated that while an isolated DSSD molecule would spontaneously oscillate between left and right chiral forms with a period of 5. common hydrogen bonds.Common hydrogen bonds Video
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