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cis–trans Isomerism among the Octahedral Diaquabis(optically active C-substituted ethylenediamine)nickel(II) Complexes and Their Thermal Reaction Products. An Explanation for a Variety in Colors and Stereochemistry of Lifschitz Complexes
http://hdl.handle.net/2297/37514
http://hdl.handle.net/2297/375141610242c-d4eb-401d-a53c-c7f4e6cc0c22
名前 / ファイル | ライセンス | アクション |
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LE-PR-IHARA-Y-3025-3029.pdf (399.2 kB)
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Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2017-10-02 | |||||
タイトル | ||||||
タイトル | cis–trans Isomerism among the Octahedral Diaquabis(optically active C-substituted ethylenediamine)nickel(II) Complexes and Their Thermal Reaction Products. An Explanation for a Variety in Colors and Stereochemistry of Lifschitz Complexes | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
著者 |
Ihara, Yoshinori
× Ihara, Yoshinori× Sakino, Tomomi× Ishikawa, Mieko× Koyata, Takanori |
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書誌情報 |
Bulletin of the Chemical Society of Japan 巻 70, 号 12, p. 3025-3029, 発行日 1997-01-01 |
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ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 0009-2673 | |||||
NCID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AA12026255 | |||||
DOI | ||||||
関連タイプ | isIdenticalTo | |||||
識別子タイプ | DOI | |||||
関連識別子 | 10.1246/bcsj.70.3025 | |||||
出版者 | ||||||
出版者 | 日本化学会=The Chemical Society of Japan | |||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | The solid-phase thermal reactions of trans-diaquabis(diamine)nickel(II) complexes (trans-[Ni(diamine)2(H2O)2]X2) were investigated by means of TG/DTA and DSC, and high-temperature electronic spectrometry, where the diamine is an optically active diamine such as (1S,2S)-1,2-diphenyl-1,2-ethanediamine or (S)-4-methyl-1,2-pentanediamine, and X is Cl−, Br−, or NO3−. Several complexes were peculiarly transformed into cis-[NiX2(diamine)2] upon thermal deaquation-anation, and then isomerized to trans-[NiX2(diamine)2] upon further heating. The results were in contrast to the reactions of the complexes with the corresponding racemic diamines which underwent a simple deaquation-anation, retaining an original trans configuration. The differences must come from a slight difference in the conformation of diamine ligands between trans-[Ni(R-diamine)(S-diamine)(H2O)2]X2 which is obtained for the rac-diamines and trans-[Ni(R- or S-diamine)2(H2O)2]X2 which is obtained for the optically active diamines. | |||||
権利 | ||||||
権利情報 | Copyright © 日本化学会 The Chemical Society of Japan|許可を得て登録 | |||||
著者版フラグ | ||||||
出版タイプ | VoR | |||||
出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 | |||||
関連URI | ||||||
識別子タイプ | URI | |||||
関連識別子 | http://www.chemistry.or.jp/ | |||||
関連URI | ||||||
識別子タイプ | URI | |||||
関連識別子 | https://www.jstage.jst.go.jp/article/bcsj/70/12/70_12_3025/_article |