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- W1504671809 abstract "Photodissociation of a series of complexes Mg+–C6H5X (X=H, F, Cl, Br) has been studied. The formation of Mg+ was found to be the predominant dissociation pathway. We monitored the photodissociation product as a function of the excitation wavelength in a broad spectral region. Experiments on the complexes with different halide substitutions showed similar action spectra. This is explained by a similar structure shared by these complexes with Mg+ being above the benzene ring. In the photodissociation of Mg+–(C6H5F), MgF+ is also formed besides Mg+. The action spectra corresponding to these two channels were found to be different, and the MgF+ channel is believed to be from a different isomer. The experimental results are consistent with our quantum ab initio calculations." @default.
- W1504671809 created "2016-06-24" @default.
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- W1504671809 date "2000-06-15" @default.
- W1504671809 modified "2023-10-12" @default.
- W1504671809 title "Photodissociation spectroscopy of Mg+–C6H5X (X=H, F, Cl, Br)" @default.
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- W1504671809 doi "https://doi.org/10.1063/1.481706" @default.
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