The Phenoxyl Radical–Water Complex—A Matrix Isolation and Computational Study
Wolfram Sander, Saonli Roy, Iakov Polyak, Juan Manuel Ramírez‐Anguita, Elsa Sánchez‐García
Abstract
Wolfram Sander, Saonli Roy, Iakov Polyak, Juan Manuel Ramírez‐Anguita, Elsa Sánchez‐García
Abstract
The phenoxyl radical 1 was generated in high yields by flash vacuum pyrolysis of allyl phenyl ether 2 with subsequent trapping of the products in argon at 3 K. In water-doped argon matrices, an OH···O complex between 1 and water is formed that could be characterized by IR spectroscopy. Several isotopomers of the complex were generated, and the IR spectra compared to results of density functional theory calculations. Other dimers between 1 and water were not found under these conditions. QM/MM calculations in simulated argon matrices reveal that an OH···π complex is unstable even at a time scale of picoseconds. This finding has implications on the related interaction between the tyrosyl radical and the water in biological systems.
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The phenoxyl radical 1 was generated in high yields by flash vacuum pyrolysis of allyl phenyl ether 2 with subsequent trapping of the products in argon at 3 K. In water-doped argon matrices, an OH···O complex between 1 and water is formed that could be characterized by IR spectroscopy. Several isotopomers of the complex were generated, and the IR spectra compared to results of density functional theory calculations. Other dimers between 1 and water were not found under these conditions. QM/MM calculations in simulated argon matrices reveal that an OH···π complex is unstable even at a time scale of picoseconds. This finding has implications on the related interaction between the tyrosyl radical and the water in biological systems.
Key concepts: Chemistry, Matrix isolation, Isotopomers, Flash vacuum pyrolysis, Argon, Picosecond, Photochemistry, Density functional theory