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自旋-轨道耦合、杜施insky旋转和位移矢量对二苯甲酮及其稠合类似物芴酮系间窜越速率的影响:一种基于含时相关函数的方法。

The influence of spin-orbit coupling, Duschinsky rotation and displacement vector on the rate of intersystem crossing of benzophenone and its fused analog fluorenone: a time dependent correlation function based approach.

作者信息

Karak Pijush, Chakrabarti Swapan

机构信息

Department of Chemistry, University of Calcutta, 92 A.P.C Road, Kolkata - 700009, West Bengal, India.

出版信息

Phys Chem Chem Phys. 2020 Nov 4;22(42):24399-24409. doi: 10.1039/d0cp04713a.

Abstract

To understand the effect of structural rigidity or flexibility on the intersystem crossing rate, herein we have adopted a time dependent correlation function based approach, an appropriate method for a harmonic oscillator under Condon approximation. Following this technique, we have developed generalized codes for calculating the rate of intersystem crossing (ISC) both at 0 K and at finite temperature. Since the rate of ISC is a measurable quantity, we have separated the real and imaginary parts of the complex correlation function carefully and eliminated the imaginary part by exploiting the odd nature of this function. Using this simplified method, we have calculated the ISC rate constant (kISC) of two molecules, namely, benzophenone and its fused analog, fluorenone. The calculations clearly elucidate that kISC of benzophenone is 103 times larger compared to that of fluorenone. Interestingly, our analyses reveal that the combined effect of spin-orbit coupling and the number of normal modes could increase the rate of ISC of benzophenone by three orders in comparison to that of fluorenone. Furthermore, the Duschinsky rotation matrix (J) and displacement vectors (D) could influence the rate of ISC by one order each, indicating that the overall rate of ISC of benzophenone could have been 105 times higher than that of fluorenone if the latter two factors, namely, J and D have practically no impact on the rate of ISC of fluorenone. However, it has been found that albeit J can't alter the rate of ISC of fluorenone, D indeed can change the rate by two orders, thereby keeping the overall ratio of the rate of ISC of benzophenone and fluorenone as 103. The present study elucidates that none of the above mentioned factors alone can explain the relative rate of ISC of the studied systems; rather a complex interplay between all these factors makes the rate of ISC of benzophenone 103 times higher than that of fluorenone.

摘要

为了理解结构刚性或柔韧性对系间窜越速率的影响,在此我们采用了一种基于含时相关函数的方法,这是一种在康登近似下适用于简谐振子的合适方法。遵循该技术,我们开发了用于计算零开尔文和有限温度下系间窜越(ISC)速率的通用代码。由于ISC速率是一个可测量的量,我们仔细分离了复相关函数的实部和虚部,并利用该函数的奇性消除了虚部。使用这种简化方法,我们计算了两种分子,即二苯甲酮及其稠合类似物芴酮的ISC速率常数(kISC)。计算结果清楚地表明,二苯甲酮的kISC比芴酮的大103倍。有趣的是,我们的分析表明,与芴酮相比,自旋 - 轨道耦合和简正模式数量的综合作用可使二苯甲酮的ISC速率提高三个数量级。此外,杜施insky旋转矩阵(J)和位移矢量(D)各自可使ISC速率改变一个数量级,这表明如果后两个因素,即J和D对芴酮的ISC速率实际上没有影响,那么二苯甲酮的总体ISC速率可能比芴酮高105倍。然而,已发现尽管J不能改变芴酮的ISC速率,但D确实可以使速率改变两个数量级,从而使二苯甲酮和芴酮的ISC速率的总体比值保持为103。本研究表明,上述任何一个因素都不能单独解释所研究体系的ISC相对速率;相反,所有这些因素之间的复杂相互作用使得二苯甲酮的ISC速率比芴酮高103倍。

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