Sentence examples for intermolecular complexes from inspiring English sources

We report that PCPP can spontaneously self-assemble into intermolecular complexes with common formulation excipients − polyethers in aqueous solutions at neutral pH through the establishment of hydrogen bonds.

These apparent changes in fluorescence behaviour indicate the differences in the nature and number of intermolecular complexes and radiationless deactivation processes in various phases.

We propose a novel approach to modulate biomolecular interactions by de novo structure-based design of noncompetitive small molecules that bind to the intermolecular complexes and make molecular contacts with both interacting partners.

Our results show that these domains are composed of intermolecular complexes and their aggregates stabilized by the neutralization effect of GB, and linked together by formation of GB triple helices.

Titration in the presence of other ligands, rapidly provides information on the mechanism of action of the test compound, identifying the intermolecular complexes that are relevant for structure-based design.

Intermolecular interaction energies for representative configurations of intermolecular complexes were analyzed using the supermolecular approach at the MP2/6-311+G∗ level, which resulted in substantial interaction strengths for all the three forms of intermolecular interactions.

It has been found that dispersive interaction predominantly stabilizes the intermolecular complex formation of H2 on a variety of organic linkers.

The glass transition temperature of miscible blends showed a positive synergism due to the physical network resulting from intermolecular complex formation.

Intermolecular complex formation between mesogenic terphenyldiimide moieties of a thermotropic liquid-crystalline (LC) polyimide (P-11TPE) was studied by steady-state fluorescence and fluorescence lifetime measurements together with differential scanning calorimetry (d.s.c).s.c

The fluorescence peak wavelength of this intermolecular complex shifts slightly to shorter wavelength below the glass transition temperature and shifts abruptly to longer wavelength around crystallization, then shifts gradually to shorter wavelength again from various crystalline phases until the isotropic phase.

Due to near face-to-face and edge-to-face geometry accompanied by sterical hindrance, the intermolecular complex of the aromatic elements effectively prevents Aβ assembly.