Determination of dipole moments in ground and excited states of molecules in solution and in the gas phase

溶液和气相中分子基态和激发态偶极矩的测定

• 批准号: 456557001
• 负责人: Professor Dr. Michael Schmitt
• 金额: --
• 依托单位: Arbeitsgruppe Hochauflösende UV-Laserspektroskopie
• 依托单位国家: 德国
• 项目类别: Research Grants
• 资助国家: 德国
• 项目状态: 未结题
• 来源: https://gepris.dfg.de/gepris/projekt/456557001?language=en
• 关键词: Determination; dipole; moments; ground; excited

Molecular dipole moments in electronically excited states are determined by the change of the electron distribution due to the excitation and therefore provide important information about the nature of the excited states. High-resolution spectroscopic methods exist for small and medium-sized molecules, which allow both the magnitude and the direction of the dipole moment in the excited state to be determined with great accuracy. This primarily includes rovibronic strong spectroscopy of molecules in a supersonic jet. Unfortunately, this method cannot be extended to large molecules. On the one hand, many large molecules (more than 20 heavy atoms) cannot be transferred into the gas phase without decomposition, which is essential for molecular beam technologies. In addition, the moments of inertia of large molecules are also large, so that the rotational transitions can no longer be completely resolved. However, this is essential for the interpretation of the rotationally resolved spectra in the electric field. For this reason, many methods have been developed in the past decades that are able to determine information about the dipole moment in excited states of molecules in solution. Despite the limited information from these experiments that can be traced back to the original works by Onsager, Lippert and Mataga, they have found widespread use in the form of solvatochromic shifts. The reason for this is the intuitive comprehensibility of the concept and the easy viability using commercial fluorescence and absorption spectrometers. On the other hand, the method of solvatochromic shifts has fundamental problems. The variation of the solvent leads to differing interactions with the dissolved molecule, which results in spectral shifts that deviate strongly from a linear relationship that is predicted according to Lippert and Mataga. In addition, the size of the solvent cavity via the Onsager radius is included in the third power in the evaluation, so that slight deviations in the cavity size lead to widely varying results for the dipole moments. Both problems can be avoided by changing the solvent polarity function not by varying the solvent but by varying the temperature in a single solvent. The spectral shifts that can be achieved are smaller than in solvatochromism, but on the other hand the type of interaction between solvent and solvate is always the same. We circumvent the problem of the difficult to determine (theoretical) Onsager radius by directly determining the volume of the solvent cavities experimentally from the densities of the solutions. With these two variations, the relationship between the solvent polarity function and the spectral shifts is actually linear, as is assumed in theory.

电子激发态的分子偶极矩由激发引起的电子分布变化决定，因此提供了有关激发态性质的重要信息。高分辨率的光谱方法存在于小分子和中等大小的分子中，这使得激发态的偶极矩的大小和方向都可以非常准确地确定。这主要包括超音速射流中分子的旋转振动强光谱。不幸的是，这种方法不能扩展到大分子。一方面，许多大分子（超过20个重原子）无法在不分解的情况下转移到气相中，这对于分子束技术至关重要。此外，大分子的惯性矩也很大，因此转动跃迁不再能完全分辨。然而，这是必不可少的旋转分辨光谱在电场中的解释。由于这个原因，在过去的几十年中已经开发了许多方法，这些方法能够确定溶液中分子激发态的偶极矩信息。尽管从这些实验中得到的信息有限，但可以追溯到Onsager，Lippert和Mataga的原始作品，他们发现溶剂化变色位移的形式得到了广泛的应用。其原因是概念的直观可理解性和使用商业荧光和吸收光谱仪的简单可行性。另一方面，溶致变色位移方法存在根本问题。溶剂的变化导致与溶解分子的不同相互作用，这导致光谱偏移强烈偏离根据Lippert和Mataga预测的线性关系。此外，通过Onsager半径的溶剂腔的大小被包括在评估的三次方中，使得腔大小的微小偏差导致偶极矩的广泛变化的结果。这两个问题都可以通过改变溶剂极性函数来避免，不是通过改变溶剂，而是通过改变单一溶剂中的温度。可以实现的光谱位移小于溶剂化变色，但另一方面，溶剂和溶剂化物之间的相互作用类型总是相同的。我们规避的问题，难以确定（理论）Onsager半径直接确定的溶剂腔的体积实验从溶液的密度。在这两种情况下，溶剂极性函数和光谱位移之间的关系实际上是线性的，正如理论上所假设的那样。