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Optical Stark spectroscopy of the $\tilde B{}^1A^{\prime \prime} $B̃1A′′(000)←$\tilde X{}^1A^\prime $X̃1A′(000) system of copper hydroxide
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The $\tilde B{}^1A^{\prime \prime} $B̃1A′′(000)←$\tilde X{}^1A^\prime $X̃1A′(000) band system of a cold beam of CuOH has been studied field-free and in the presence of a static electric field. The Stark tuning of the low-J levels of the $\tilde X{}^1A^\prime $X̃1A′(000) state were analyzed to give a value of 3.968(32) D for the a-component of the permanent electric dipole moment, μa. An upper limit of 0.3 D for μa($\tilde B{}^1A^{\prime \prime} $B̃1A′′) is established from the lack of observable Stark tuning for the low-J levels of the $\tilde B{}^1A^{\prime \prime} $B̃1A′′(000) state. The experimental value for μa($\tilde X{}^1A^\prime $X̃1A′) is compared to theoretical predictions and other Cu-containing molecules. A molecular orbital correlation diagram is used to rationalize the large change in μa upon excitation. The electronegativity of OH was determined to be 2.81 from a comparison of the determined μa with the experimental μ values for CuF, CuO, and CuS.
Title: Optical Stark spectroscopy of the $\tilde B{}^1A^{\prime \prime} $B̃1A′′(000)←$\tilde X{}^1A^\prime $X̃1A′(000) system of copper hydroxide
Description:
The $\tilde B{}^1A^{\prime \prime} $B̃1A′′(000)←$\tilde X{}^1A^\prime $X̃1A′(000) band system of a cold beam of CuOH has been studied field-free and in the presence of a static electric field.
The Stark tuning of the low-J levels of the $\tilde X{}^1A^\prime $X̃1A′(000) state were analyzed to give a value of 3.
968(32) D for the a-component of the permanent electric dipole moment, μa.
An upper limit of 0.
3 D for μa($\tilde B{}^1A^{\prime \prime} $B̃1A′′) is established from the lack of observable Stark tuning for the low-J levels of the $\tilde B{}^1A^{\prime \prime} $B̃1A′′(000) state.
The experimental value for μa($\tilde X{}^1A^\prime $X̃1A′) is compared to theoretical predictions and other Cu-containing molecules.
A molecular orbital correlation diagram is used to rationalize the large change in μa upon excitation.
The electronegativity of OH was determined to be 2.
81 from a comparison of the determined μa with the experimental μ values for CuF, CuO, and CuS.
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