The hydrogen bond is the most important of all directional intermolecular interactions. It is
operative in determining molecular conformation, molecular aggregation, and the function of …

A hydrogen bond, X− H⊙⊙⊙ A, is an interaction wherein a hydrogen atom is attracted to
two atoms, X and A, rather than just one and so acts like a bridge between them. This …

Phosphorescence has rarely been observed in pure organic chromophore systems at room
temperature. We herein report efficient phosphorescence from the crystals of benzophenone …

The Cambridge Structural Database (CSD) and its associated software systems have
formed the basis for more than 800 research applications in structural chemistry …

Electronic differences between inorganic (M− X) and organic (C− X) halogens in conjunction
with the anisotropic charge distribution associated with terminal halogens have been …

A single crystal of 1-butyl-3-methylimidazolium chloride [bmim] Cl, a prototype ionic liquid,
has successfully been prepared and an X-ray crystallographic analysis has been performed …

Through the years the GRID force field has been tuned to fit experimental observations in
crystal structures. This paper describes the determination of the hydrogen bonding pattern …

This review provides a comparative assessment of hydrogen bonding (HB) interactions with
halogen (X) acceptors. Based on the data available in the literature we selected various inter …

Contacts of the type C− H⊙⊙⊙ X where X= F, Cl, Br, I, O, S, or N were analyzed statistically
using structures available in the Cambridge Structural Database. For this analysis, the cone …

The Cambridge Structural Database is a storehouse of over 250 000 small-molecule organic
and organometallic crystal structures. Statistical analysis of structural data provides a better …