Manke Kara J, Vervoort Tyson R, Kuwata Keith T, Varberg Thomas D
Department of Chemistry, Macalester College, St Paul, MN 55105, USA.
J Chem Phys. 2008 Mar 14;128(10):104302. doi: 10.1063/1.2837470.
The B (2)Phi(5/2)-X(1) (2)Delta(3/2)(0,0) band at 778 nm and the C (2)Delta(3/2)-X(1) (2)Delta(3/2)(0,0) band at 737 nm of tantalum oxide (TaO) were recorded by laser excitation spectroscopy using a hollow cathode sputtering source to generate the molecules. The hyperfine structure arising from the (181)Ta (I=72) nucleus was measured at sub-Doppler resolution using the technique of intermodulated fluorescence spectroscopy. The hyperfine structure was assigned and fitted in order to derive accurate values for the magnetic dipole and electric quadrupole interactions. The magnetic hyperfine constant for the ground electronic state was also calculated using the density functional theory as h(3/2)=625 MHz, in good agreement with the experimental value of 647+/-10 MHz. This result suggests that the X (2)Delta ground state of TaO is well described by a pure deltasigma(2) electronic configuration, where the unpaired electron is located in a Ta 5ddelta orbital.
利用空心阴极溅射源产生氧化钽(TaO)分子,通过激光激发光谱记录了氧化钽在778nm处的B (2)Phi(5/2)-X(1) (2)Delta(3/2)(0,0)带和在737nm处的C (2)Delta(3/2)-X(1) (2)Delta(3/2)(0,0)带。采用互调荧光光谱技术在亚多普勒分辨率下测量了由(181)Ta(I = 72)核产生的超精细结构。对超精细结构进行了归属和拟合,以得出磁偶极和电四极相互作用的准确值。还使用密度泛函理论计算了基态电子态的磁超精细常数,结果为h(3/2)=625 MHz,与647±10 MHz的实验值吻合良好。该结果表明,TaO的X (2)Delta基态可以用纯deltasigma(2)电子构型很好地描述,其中未配对电子位于Ta 5ddelta轨道。