Nonactin 及其阳离子复合物的光学活性

IF 2.8 4区 化学 Q2 CHEMISTRY, ANALYTICAL
Chirality Pub Date : 2024-07-21 DOI:10.1002/chir.23703
Afton Gustafson, Bart Kahr
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引用次数: 0

摘要

Nonactin 是一种非反常(S4 对称)的光学活性天然产物,在所有频率和温度下的溶液中,其特定旋转均为零。所有具有光学活性的非反相天然产物都具有特定的零旋转,这是具有相等和相反特征值的双偶极(磁电或回旋)张量的空间平均的结果。空间平均中产生的零点与光学失活中产生的零点原则上是不同的,尽管在实践中并不一定。非活素在定向时具有可测量的光学活性。本文通过计算研究了壬内酯及其阳离子复合物(同样为 S4 对称)光学活性的各向异性,以强调光学活性与手性之间的不恰当联系。计算结果表明,壬乳蛋白大环的构象在络合时发生的变化是导致计算出的光学活性降低的主要原因;而金属则是偶然因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Optical Activity of Nonactin and Its Cation Complexes

Optical Activity of Nonactin and Its Cation Complexes

Nonactin is a non-enantiomorphous (S4 symmetric), optically active natural product with a specific rotation of zero in solutions at all frequencies and temperatures. All optically active, non-enantiomorphous natural products have specific rotations of zero as a consequence of the spatial average of bisignate chiroptical (magnetoelectric or gyration) tensors with equal and opposite eigenvalues. Zeros that arise in the spatial average are distinct in principle, though not necessarily in practice, from zeros that arise in optical inactivity—chiroptical tensors with zero values for all elements as in centric molecules. Nonactin would be measurably optically active when oriented. The anisotropy of the optical activity of nonactin and its cation complexes, likewise S4 symmetric, are studied here by computation to emphasize the infelicitous linkage between optical activity and chirality. Computations show that changes in the conformation of the nonactin macrocycle upon complexation principally are responsible for diminishing the computed optical activity; the metals are incidental.

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来源期刊
Chirality
Chirality 医学-分析化学
CiteScore
4.40
自引率
5.00%
发文量
124
审稿时长
1 months
期刊介绍: The main aim of the journal is to publish original contributions of scientific work on the role of chirality in chemistry and biochemistry in respect to biological, chemical, materials, pharmacological, spectroscopic and physical properties. Papers on the chemistry (physiochemical, preparative synthetic, and analytical), physics, pharmacology, clinical pharmacology, toxicology, and other biological aspects of chiral molecules will be published.
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