计算MCD光谱的高效协议在一个广泛的频率范围,结合共振和减弱的CC2二次响应理论
Josefine H Andersen1, Sonia Coriani1, Christof Hättig2
1Department of Chemistry, Technical University of Denmark, Kemitorvet Building 207, DK-2800 Kongens Lyngby, Denmark.
本研究引入了缓和和共振响应理论,用于准确的磁圆二元化 (MCD) 计算,克服复杂分子在高能区域的融合问题.
科学领域:
- 计算化学的计算化学
- 量子化学 是一个量子化学.
- 频谱学是一种光谱学.
背景情况:
- 结合集群响应理论使得高精度的光谱属性计算成为可能.
- 差异和缓慢的趋同阻碍了电子转换在密度较高的高能区域的计算.
研究的目的:
- 为了解决磁圆二元化 (MCD) 计算中的趋同问题.
- 为MCD实施减弱二次响应理论和共振响应理论.
- 为宽频MCD频谱提供一个有效的战略.
主要方法:
- 缓解二次响应理论的实施,以解决身份合集群单个和近似双重 (RI-CC2).
- 从共振响应理论中实现MCD术语.
- 对于四松胺 (2-8 eV) 的应用和与实验数据的比较.
主要成果:
- 和共振响应理论的结合有效地在广泛的频率范围内产生MCD光谱.
- 该协议对具有退化激发状态的高度对称分子有效.
- 计算时间由MCD圆性的构建块主导,而不是共振/减压方法本身.
结论:
- 和共振响应理论为计算MCD光谱提供了一个有效的策略.
- 该方法成功计算了密集电子状态的系统的MCD.
- 提供了使用开发程序的建议.
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