The increasing efficiency of the inorganic-organic hybrid halides has revolutionised photovoltaic research.

Thus the two halides had similar effects on open state preference.

Methyl halides are volatile one-carbon compounds responsible for substantial depletion of stratospheric ozone.

The mixed tertiary amines are produced by the action of alkyl halides on the primary amines.

The methyl halides come off as a gas that can be collected and converted into gasoline.

Key to the success of this strategy is the combination of C-F cleavage with alkyl halides activation.

These results demonstrate the potential for industrial production of methyl halides from nonfood sources to make gasoline.

The yeast eats the acetate and converts it into methyl halides, molecules traditionally used as agricultural fumigants.

Treatment of the latter derivatives with alkyl or cycloalkyl halides in alkaline medium gave the required title compounds.

Through effective reductive activation, covalent functionalization of the charged BP by reaction with organic alkyl halides is achieved.

Gas-phase mass spectrometric studies and calculations were performed for the reaction of naked phenylium ion with several benzene halides.

This simplified perspective based on extensive experimental and theoretical analysis provides a platform from which to understand structure-property relationships in functional perovskite halides.

The role of bridging halides in the structure and magnetic properties of the complexes are investigated, and a possible magneto-structural correlation has been established.

Perovskite halides are broadly classified as hybrid organic-inorganic and all-inorganic analogues depending on the chemical nature of the A cation in the ABX3-type structure.

Influence of spin density of bridging halides on the magnitude of coupling constants has been discussed with the help of density functional theory (DFT) calculations.

Herein, we report our latest experimental investigations of halide-π interactions in solution.