Title of article :
Contrasting modes of bonding for copper(I), silver(I), and gold(I) in dithioimidodiphosphinato metallacycles
Author/Authors :
Herndon، William C. نويسنده , , Haiduc، Ionel نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2001
Abstract :
Photochemical reaction between biphenyl and carbon tetrachloride is studied with nanosecond time-resolved infrared spectroscopy and picosecond time-resolved fluorescence spectroscopy. Fluorescence lifetime of biphenyl in carbon tetrachloride solutions is measured with a picosecond time-resolved fluorescence spectrometer. The recorded lifetime is 3.8 ps, shorter than fluorescence lifetime in cyclohexane by a factor of four thousand. After the photoexcitation of biphenyl in carbon tetrachloride, the trichloromethyl (CCl3) radical is formed as a reaction intermediate, which is confirmed by the detection of the radicalʹs 896 cm-1 infrared band with nanosecond time-resolved infrared spectroscopy. One of the Cl atoms in solvent carbon tetrachloride is transferred to biphenyl to form the CCl3 radical and a biphenyl–Cl adduct. Together with the already reported spectroscopic detection of the CCl3 radical as an intermediate in photochemical reactions of trans-stilbene or anthracene with carbon tetrachloride, it is likely that this series of reactions are common for aromatic molecules.
Keywords :
Cu, Ag, and Au complexes , Dithioimidodiphosphinato ligand , DFT calculations
Journal title :
Journal of Molecular Structure
Journal title :
Journal of Molecular Structure