热力光谱学与晶体结构立体化学配位的验证

Q2 Chemistry
George E. Tranter, Delphine D. Le Pevelen
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引用次数: 9

摘要

手性分子的绝对立体化学是通过x射线晶体学分析理想地建立到原子分辨率的。然而,光谱学,即电子圆二色性(ECD)、旋光色散(ORD)、振动圆二色性(VCD)和拉曼光学活性(ROA),在建立相对和绝对立体化学以及确定光学纯度方面发挥着重要的补充作用。摘要简要介绍了热学光谱,并指出了它们的优缺点。应用ECD来验证选择用于晶体学分析的单晶确实是块体材料的代表。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Chiroptical spectroscopy and the validation of crystal structure stereochemical assignments

Chiroptical spectroscopy and the validation of crystal structure stereochemical assignments

The absolute stereochemistry of chiral molecules is ideally established to atomic resolution by X-ray crystallographic analysis. However, chiroptical spectroscopies, namely electronic circular dichroism (ECD), optical rotatory dispersion (ORD), vibrational circular dichroism (VCD) and Raman optical activity (ROA), play important complementary roles in establishing relative and absolute sterochemistries as well as allowing determinations of optical purity. A brief summary of chiroptical spectroscopies is presented, along with guidance to their advantages and disadvantages. The application of ECD to verifying that single crystals selected for crystallographic analysis are indeed representative of bulk material is described.

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来源期刊
Tetrahedron, asymmetry
Tetrahedron, asymmetry 化学-无机化学与核化学
CiteScore
4.70
自引率
0.00%
发文量
0
审稿时长
1 months
期刊介绍: Cessation. Tetrahedron: Asymmetry presents experimental or theoretical research results of outstanding significance and timeliness on asymmetry in organic, inorganic, organometallic and physical chemistry, as well as its application to related disciplines, especially bio-organic chemistry. The journal publishes critical reviews, original research articles and preliminary communications dealing with all aspects of the chemical, physical and theoretical properties of non-racemic organic and inorganic materials and processes. Topics relevant to the journal include: the physico-chemical and biological properties of enantiomers; strategies and methodologies of asymmetric synthesis; resolution; chirality recognition and enhancement; analytical techniques for assessing enantiomeric purity and the unambiguous determination of absolute configuration; and molecular graphics and modelling methods for interpreting and predicting asymmetric phenomena. Papers describing the synthesis or properties of non-racemic molecules will be required to include a separate statement in the form of a Stereochemistry Abstract, for publication in the same issue, of the criteria used for the assignment of configuration and enantiomeric purity.
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