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Coupling of translational and rotational motion in chiral liquids in electromagnetic and circularly polarised electric fields

机译:电磁和圆极化电场中手性液体中平移和旋转运动的耦合

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Non-equilibrium molecular dynamics simulations of R and S enantiomers of 1,1-chlorofluoroethane, both for pure liquids and racemic mixtures, have been performed at 298 K in the absence and presence of both electromagnetic (em) and circularly polarised electric (CP) fields of varying frequency (100-2200 GHz) and intensity (0.025-0.2 V ? ~(-1) _(rms)). Significant non-thermal field effects were noted in the coupling of rotational and translational motion; for instance, in microwave and far-infrared (MWIR) em fields, marked increases in rotational and translational diffusion vis - vis the zero-field case took place at 0.025-0.1 V ? ~(-1) _(rms), with a reduction in translational diffusion vis - vis the zero-field case above 0.1 V ? ~(-1) _(rms) above 100 GHz. This was due to enhanced direct coupling of rotational motion with the more intense em field at the ideal intrinsic rotational coupling frequency (approximately 700 GHz) leading to such rapidly oscillating rotational motion that extent of translational motion was effectively reduced. In the case of CP fields, rotational and translational diffusion was also enhanced for all intensities, particularly at approximately 700 GHz. For both MWIR and CP fields, non-linear field effects were evident above around 0.1 V ? ~(-1) _(rms) intensity, in terms of enhancements in translational and rotational motion. Simulation of 90-10 mol. % liquid mixtures of a Lennard-Jones solvent with R and S enantiomer-solutes in MWIR and CP fields led to more limited promotion of rotational and translational diffusion, due primarily to increased frictional effects. For both em and CP fields, examination of the laboratory- and inertial-frame auto- and cross-correlation functions of velocity and angular velocity demonstrated the development of explicit coupling with the external fields at the applied frequencies, especially so in the more intense fields where nonlinear effects come into play. For racemic mixtures, elements of the laboratory- and inertial-frame velocity and angular velocity were found to couple with each other to a lesser extent.
机译:在不存在和存在电磁(em)和圆极化电(CP)的情况下,已在298 K下对纯液体和外消旋混合物进行的1,1-氯氟乙烷R和S对映异构体的非平衡分子动力学模拟频率(100-2200 GHz)和强度(0.025-0.2 V?〜(-1)_(rms))的磁场。在旋转和平移运动的耦合中注意到了显着的非热场效应。例如,在微波和远红外(MWIR)电磁场中,相对于零电场情况,旋转和平移扩散相对于0.025-0.1 V明显增加。 〜(-1)_(rms),相对于高于0.1 V的零场情况,其平移扩散减小了? 100 GHz以上的〜(-1)_(rms)。这是由于在理想的固有旋转耦合频率(大约700 GHz)下,旋转运动与更强的电磁场的直接耦合增强,从而导致旋转运动迅速振荡,从而有效降低了平移运动的程度。在CP场的情况下,对于所有强度,尤其是在大约700 GHz时,旋转和平移扩散也得到了增强。对于MWIR和CP场,非线性场效应在高于0.1 V?就平移和旋转运动的增强而言,〜(-1)_(rms)强度。模拟90-10 mol。 Lennard-Jones溶剂与R和S对映异构体-溶质在MWIR和CP领域中所占百分比的液体混合物,导致旋转和平移扩散的促进有限,这主要是由于摩擦效应的增加。对于em和CP场,对速度和角速度的实验室帧和惯性帧自相关函数和互相关函数的检查表明,在所施加的频率下,特别是在更强的场中,与外部场显式耦合的发展。在其中非线性效应起作用。对于外消旋混合物,发现实验室和惯性框架速度和角速度的元素在较小程度上相互耦合。

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