首页> 外文期刊>The Journal of Chemical Physics >MAGNETIC FIELD INDUCED ALIGNMENT-ORIENTATION CONVERSION - NONLINEAR ENERGY SHIFT AND PREDISSOCIATION IN TE-2 B1(U) STATE
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MAGNETIC FIELD INDUCED ALIGNMENT-ORIENTATION CONVERSION - NONLINEAR ENERGY SHIFT AND PREDISSOCIATION IN TE-2 B1(U) STATE

机译:TE-2 B1(U)态中的磁场诱导的对准方向转换-非线性能量转换和预离解

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The paper analyzes magnetic field induced alignment-orientation conversion (AOC) phenomenon caused by simultaneous effect of quadratic terms in Zeeman energy shift and magnetic predissociation (PD), producing asymmetry either in energy splitting omega(MM+/-1)not equal omega-(M-/+1-M) or in relaxation of coherence Gamma(MM+/-1)(not equal Gamma)-(M-/+-M) between coherently excited M, M+/-1 magnetic sublevels. The AOC is registered via the appearance of circular polarization (C) of fluorescence under linearly polarized excitation. The unified perturbation treatment of a molecule in external magnetic held B is presented, accounting for magnetic and intramolecular perturbations via interaction with bonded or continuum states, considering Hund's (c)-case coupling and dividing the intramolecular perturbation operator into homogeneous (Delta Omega=0) and heterogeneous (Delta Omega=+/-1) parts. Explicit expressions up to B-2 terms are given for energy shift and PD rate, adapted to 1(u) state in conditions relevant to the B-3 Sigma(u)(-) complex of Te-2 molecule. Numeric simulation revealed that nonlinear magnetic energy shift and heterogeneous magnetic PD produce dispersion type fluorescence circularity signals C(B) of different sign. Fitting of experimental data on B1(u)(-), upsilon(J)=2(96) state of Te-130(2) molecule allowed to determine the electronic matrix element of paramagnetic Hamiltonian (Omega=0(H) over cap(pm)Omega=1)=G(+/-)=2.7, as well as the natural C-upsilon(het) = +/-6 s(-1/2) and the magnetic alpha(upsilon)(het) = -/+ 9 X 10(3) s-1/2 T-1 rate constants of heterogeneous PD, supposing that the B1(u)(-) state PD takes place through O-u(-) state continuum. As a result, magnetic AOC represents a sensitive method to investigate molecular structure and intramolecular interaction between both bonded and continuum states. Additionally, it has been shown that the magnetic PD effect leads to strong amplification of nonzero field level crossing signals caused by B-2 terms in Zeeman energy shift. (C) 1996 American Institute of Physics. [References: 30]
机译:本文分析了由二次项在Zeeman能量位移和磁预离解(PD)的同时作用引起的磁场感应的取向定向转换(AOC)现象,在能量分裂欧米伽(MM +/- 1)不等于欧米伽-( M-/ + 1-M)或在相干激发的M,M +/- 1磁性子能级之间的相干性Gamma(MM +/- 1)(不等于Gamma)-(M-/ +-M)中松弛。通过在线性偏振激发下出现荧光的圆偏振(C)来记录AOC。提出了对外部磁保持B中分子的统一扰动处理,考虑了与键或连续态相互作用引起的磁和分子内扰动,考虑了Hund's(c)-case耦合并将分子内扰动算子划分为均质(Delta Omega = 0 )和非均质(Delta Omega = + /-1)部分。给出了能量转移和PD速率的最高B-2项的明确表达,在与Te-2分子的B-3 Sigma(u)(-)络合物相关的条件下适应1(u)状态。数值模拟表明,非线性磁能转移和异质磁PD产生不同符号的色散型荧光圆度信号C(B)。将实验数据拟合到Te-130(2)分子的B1(u)(-),upsilon(J)= 2(96)状态可确定顺磁性哈密顿电子矩阵元素(Omega = 0 (H) cap(pm) Omega = 1)= G(+/-)= 2.7,以及自然C-upsilon(het)= +/- 6 s(-1/2)和磁性alpha(upsilon)( het)=-/ +异构PD的9 X 10(3)s-1 / 2 T-1速率常数,假设B1(u)(-)状态PD通过Ou(-)状态连续体发生。结果,磁性AOC代表了一种研究键合态和连续态之间分子结构和分子内相互作用的灵敏方法。另外,已经表明,磁性PD效应导致在塞曼能移中由B-2项引起的非零场电平交叉信号的强烈放大。 (C)1996年美国物理研究所。 [参考:30]

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