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揭示手性有机-无机杂化金属卤化物中手性中心与金属卤化物之间的手性转移。

Unveiling Chirality Transfer between Chiral Centers and Metal Halides in Chiral Organic-Inorganic Hybrid Metal Halides.

作者信息

Han Xiang-Bin, Wang Wei, Jin Ming-Liang, Jing Chang-Qing, Zhang Jing-Meng, Fan Chang-Chun

机构信息

Jiangsu Key Laboratory for Science and Applications of Molecular Ferroelectrics and School of Chemistry and Chemical Engineering, Southeast University, Nanjing 211189, China.

出版信息

Inorg Chem. 2024 Oct 7;63(40):19030-19038. doi: 10.1021/acs.inorgchem.4c03606. Epub 2024 Sep 23.

Abstract

Chirality transfer refers to the process in which chiral cations compel the crystallization of the inorganic component into the Sohncke group. Enhancing the chirality of the inorganic component in chiral organic-inorganic hybrid metal halides (OIHMHs) through chirality transfer, aimed at improving chiroptical and spintronic properties, remains challenging due to the complexity of the underlying mechanism. To investigate this, we propose a novel concept─chirality transfer coefficient─as a means of quantifying the strength of chirality transfer in OIHMHs. A comparative study of OIHMHs with varying dimensionality, metal ions, and chiral centers was conducted to elucidate this mechanism. By analyzing factors such as hydrogen bonding, the number of chiral centers, dimensionality, helical geometry, and structural distortions, we found that chirality transfer is influenced by a combination of structural dimensions and the number of chiral centers. Importantly, our findings reveal that 0D, and 1D OIHMHs, particularly 1D with a zigzag chain configuration, exhibit stronger chirality transfer than their 2D counterparts. Moreover, in 2D OIHMHs, a reduction in the number of chiral centers enhances chirality transfer. However, no direct correlation was observed between chirality transfer and spin splitting. These insights contribute to a more comprehensive understanding of chirality transfer mechanisms and provide a strategic approach for enhancing the chirality transfer and associated physical properties in OIHMHs.

摘要

手性转移是指手性阳离子促使无机组分结晶成 Sohncke 群的过程。通过手性转移增强手性有机-无机杂化金属卤化物(OIHMHs)中无机组分的手性,以改善手性光学和自旋电子学性质,由于其潜在机制的复杂性,仍然具有挑战性。为了研究这一问题,我们提出了一个新颖的概念——手性转移系数,作为量化 OIHMHs 中手性转移强度的一种手段。对具有不同维度、金属离子和手性中心的 OIHMHs 进行了对比研究,以阐明这一机制。通过分析氢键、手性中心数量、维度、螺旋几何结构和结构畸变等因素,我们发现手性转移受结构维度和手性中心数量的综合影响。重要的是,我们的研究结果表明,0D 和 1D 的 OIHMHs,特别是具有锯齿链构型的 1D OIHMHs,比其 2D 对应物表现出更强的手性转移。此外,在 2D OIHMHs 中,手性中心数量的减少会增强手性转移。然而,未观察到手性转移与自旋分裂之间存在直接相关性。这些见解有助于更全面地理解手性转移机制,并为增强 OIHMHs 中的手性转移及相关物理性质提供了一种策略性方法。

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