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・ Stereo Typical
・ Stereo World
・ Stereo Worxxx
・ Stereo-4
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・ Stereoautograph
・ Stereobelt
・ Stereoblindness
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・ Stereocaryum
・ Stereocaulaceae
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・ Stereocephalus
・ Stereocerus
Stereochemistry
・ Stereochemistry of ketonization of enols and enolates
・ Stereochilus (orchid)
・ Stereochlaena
・ Stereocilia
・ Stereocilia (inner ear)
・ Stereocilia Vol. 1
・ Stereocrea
・ Stereocyclops
・ Stereocyclops histrio
・ Stereocyclops incrassatus
・ Stereocyclops parkeri
・ Stereodmeta
・ Stereoelectroencephalography
・ Stereoelectronic effect


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Stereochemistry : ウィキペディア英語版
Stereochemistry

Stereochemistry, a subdiscipline of chemistry, involves the study of the relative spatial arrangement of atoms that form the structure of molecules and their manipulation. An important branch of stereochemistry is the study of chiral molecules.
Stereochemistry is also known as 3D chemistry because the prefix "stereo-" means "three-dimensionality".〔http://dictionary.reference.com/browse/stereo-〕
The study of stereochemistry focuses on stereoisomers and spans the entire spectrum of organic, inorganic, biological, physical and especially supramolecular chemistry. Stereochemistry includes methods for determining and describing these relationships; the effect on the physical or biological properties these relationships impart upon the molecules in question, and the manner in which these relationships influence the reactivity of the molecules in question (dynamic stereochemistry).
==History==
Louis Pasteur could rightly be described as the first stereochemist, having observed in 1849 that salts of tartaric acid collected from wine production vessels could rotate plane polarized light, but that salts from other sources did not. This property, the only physical property in which the two types of tartrate salts differed, is due to optical isomerism. In 1874, Jacobus Henricus van 't Hoff and Joseph Le Bel explained optical activity in terms of the tetrahedral arrangement of the atoms bound to carbon.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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