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本文引用的文献

1
Enantioselective Inclusion Complexation of N-Nitrosopiperidines by Steroidal Bile Acids.
Angew Chem Int Ed Engl. 1999 Feb 1;38(3):392-395. doi: 10.1002/(SICI)1521-3773(19990201)38:3<392::AID-ANIE392>3.0.CO;2-H.
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Interpretation of experiments on metabolic processes, using isotopic tracer elements.利用同位素示踪元素对代谢过程实验的解读。
Nature. 1948 Dec 18;162(4129):963. doi: 10.1038/162963b0.
3
Dependence of the enantioselectivity on reversion of layer directions in cholamide inclusion compounds.对映选择性对胆酰胺包合物中层方向反转的依赖性。
Chem Commun (Camb). 2007 Nov 7(41):4257-9. doi: 10.1039/b705822e.
4
Supramolecular tilt chirality in crystals of steroids and alkaloids.类固醇和生物碱晶体中的超分子倾斜手性
Chirality. 2008 Mar;20(3-4):330-6. doi: 10.1002/chir.20443.
5
Crystalline host-guest assemblies of steroidal and related molecules: diversity, hierarchy, and supramolecular chirality.甾体及相关分子的晶体主客体组装体:多样性、层级结构和超分子手性
Acc Chem Res. 2007 Aug;40(8):694-702. doi: 10.1021/ar700017a. Epub 2007 Jun 9.
6
Topological study of pseudo-cubic hydrogen-bond networks in a binary system composed of primary ammonium carboxylates: an analogue of an ice cube.由伯铵羧酸盐组成的二元体系中伪立方氢键网络的拓扑学研究:冰块的类似物。
Chemistry. 2007;13(15):4163-8. doi: 10.1002/chem.200700099.
7
Supramolecular tilt chirality derived from symmetrical benzene molecules: handedness of the 2(1) helical assembly.
Chem Asian J. 2007 Feb 5;2(2):230-8. doi: 10.1002/asia.200600332.
8
Well-designed supramolecular clusters comprising triphenylmethylamine and various sulfonic acids.由三苯甲基胺和各种磺酸组成的精心设计的超分子簇。
Angew Chem Int Ed Engl. 2007;46(13):2220-3. doi: 10.1002/anie.200603841.
9
Supramolecular chirality in layered crystals of achiral ammonium salts and fatty acids: A hierarchical interpretation.非手性铵盐与脂肪酸层状晶体中的超分子手性:一种层级解释。
Angew Chem Int Ed Engl. 2006 Jun 19;45(25):4142-5. doi: 10.1002/anie.200504424.
10
Bile acid derivatives as enantiodifferentiating host molecules in inclusion processes.胆汁酸衍生物作为包合过程中的对映体识别主体分子。
Chirality. 2005 Mar;17(3):121-30. doi: 10.1002/chir.20126.

胆汁酸及其衍生物晶体聚集体中的超分子手性;三轴、倾斜、螺旋和束状手性。

Supramolecular chirality in crystalline assemblies of bile acids and their derivatives; three-axial, tilt, helical, and bundle chirality.

作者信息

Miyata Mikiji, Tohnai Norimitsu, Hisaki Ichiro

机构信息

Department of Material and Life Science, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan.

出版信息

Molecules. 2007 Aug 22;12(8):1973-2000. doi: 10.3390/12081973.

DOI:10.3390/12081973
PMID:17960100
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6149093/
Abstract

Steroidal bile acids and their derivatives exhibit characteristic inclusion behaviors in the crystalline state. Their crystals present varied assemblies due to asymmetric molecular structures, which relate to supramolecular properties through cooperative weak interactions. An overview indicates that the steroidal assemblies lie in an intermediate position among various molecules and have hierarchical structures such as primary, secondary, tertiary, and host-guest assemblies like proteins. Such an interpretation brought about the idea that the assemblies with dimensionality present supramolecular chirality such as three-axial, tilt, helical, bundle, and complementary chirality. This concept of the supramolecular chirality enables us to understand formation of chiral crystals starting from the molecular chirality of the steroidal molecules.

摘要

甾体胆汁酸及其衍生物在晶体状态下表现出独特的包合行为。由于其不对称的分子结构,它们的晶体呈现出多样的组装形式,这些组装形式通过协同弱相互作用与超分子性质相关。概述表明,甾体组装体处于各种分子的中间位置,并具有诸如一级、二级、三级等层次结构,以及类似蛋白质的主客体组装结构。这样的解释引出了一个观点,即具有维度性的组装体呈现出超分子手性,如三轴、倾斜、螺旋、束状和互补手性。超分子手性的这一概念使我们能够从甾体分子的分子手性出发理解手性晶体的形成。