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Synthesis and Properties of Pentacoordinated Phosphorus Compounds with Anti-apicophilic Arrangement
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- Kobayashi Junji
- Graduate School of Science, The University of Tokyo
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- Kawashima Takayuki
- Graduate School of Science, The University of Tokyo
Bibliographic Information
- Other Title
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- アピコフィリシティー則に反した5配位リン化合物の合成と性質
- アピコフィリシティーソク ニ ハンシタ 5ハイイ リン カゴウブツ ノ ゴウセイ ト セイシツ
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Description
Since the synthesis of the first pentacoordinated organophosphorus compound, Ph5P, by Wittig, the chemistry of pentacoordinated phosphorus compounds has been extensively expanded. Pentacoordinated phosphorus compounds usually take a trigonal bipyramidal structure with two distinctive sites; apical and equatorial positions. In the trigonal bipyramidal structure, electronegative and small substituents prefer the apical positions. Such properties are widely recognized as the apicophilicity rule. However, several examples breaking the apicophilicity rule have been reported in the past few decades and novel properties and reactivities of these new classes of compounds have been found. In this review, the synthesis of novel pentacoordinated phosphoranes with anti-apicophilic arrangement will be introduced, as well as their structures, spectroscopic properties, and reactivities.
Journal
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- Journal of Synthetic Organic Chemistry, Japan
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Journal of Synthetic Organic Chemistry, Japan 67 (8), 787-797, 2009
The Society of Synthetic Organic Chemistry, Japan
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Keywords
Details 詳細情報について
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- CRID
- 1390282680289562368
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- NII Article ID
- 10025399710
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- NII Book ID
- AN0024521X
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- COI
- 1:CAS:528:DC%2BD1MXhtVagsrnM
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- ISSN
- 18836526
- 00379980
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- NDL BIB ID
- 10338582
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- Text Lang
- ja
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- Data Source
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- JaLC
- NDL Search
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed