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A highly-flexible cyclic-decavanadate ligand for interconversion of dinuclear- and trinuclear-cobalt(II) and manganese(II) cores
https://doi.org/10.24517/00049601
https://doi.org/10.24517/0004960135e253df-2f42-4f06-be8d-3d298f9e0a2f
| 名前 / ファイル | ライセンス | アクション |
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SC-PR-HAYASHI-Y-37666.pdf (1.1 MB)
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| Item type | 学術雑誌論文 / Journal Article(1) | |||||||
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| 公開日 | 2017-12-25 | |||||||
| タイトル | ||||||||
| タイトル | A highly-flexible cyclic-decavanadate ligand for interconversion of dinuclear- and trinuclear-cobalt(II) and manganese(II) cores | |||||||
| 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 | |||||||
| ID登録 | ||||||||
| ID登録 | 10.24517/00049601 | |||||||
| ID登録タイプ | JaLC | |||||||
| 著者 |
Maruyama, Tatsuya
× Maruyama, Tatsuya× Kikukawa, Yuji× Sakiyama, Hiroshi× Katayama, Misaki× Inada, Yasuhiro× Hayashi, Yoshihito |
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| 著者別表示 |
林, 宜仁
× 林, 宜仁
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| 提供者所属 | ||||||||
| 内容記述タイプ | Other | |||||||
| 内容記述 | 金沢大学理工研究域物質化学系 | |||||||
| 書誌情報 |
RSC Advances 巻 7, 号 60, p. 37666-37674, 発行日 2017 |
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| ISSN | ||||||||
| 収録物識別子タイプ | ISSN | |||||||
| 収録物識別子 | 2046-2069 | |||||||
| DOI | ||||||||
| 関連タイプ | isIdenticalTo | |||||||
| 識別子タイプ | DOI | |||||||
| 関連識別子 | 10.1039/c7ra05941h | |||||||
| 出版者 | ||||||||
| 出版者 | Royal Society of Chemistry | |||||||
| 抄録 | ||||||||
| 内容記述タイプ | Abstract | |||||||
| 内容記述 | The structure transformation of multinuclear-metal-cores can change catalytic, optical, and magnetic properties. Cyclic decavanadate ligands exhibit versatility in the number and the direction of the coordination sites by changing the conformation to stabilize various multinuclear-metal-cores, while organic multinucleating ligands require specific design for each of the multimetal complexes due to their structure directing ability. The flexibility of cyclic decavanadate ligands is demonstrated here to achieve accommodation of dinuclear or trinuclear units by using the same ligand. The reaction of a dinuclear-cobalt-core-containing decavanadate [Co2(H2O)2V10O30]6- (Co2) with 1 equiv. of Co(OAc)2 (OAc = acetate) gave a trinuclear-cobalt-core-containing decavanadate [Co3(H2O)(OAc)V10O30]5- (Co3) in high yield. The central cobalt core exhibited an incomplete-cubane-type structure. The decavanadate ring contracts to accommodate a smaller dinuclear unit by taking a wavy conformation and expands to accommodate the larger trinuclear unit. The reverse reaction quantitatively proceeded by the addition of 5 equiv. of [VO3]- with respect to Co3. Although a trinuclear-manganese-core-containing decavanadate [Mn3(H2O)(OAc)V10O30]5- (Mn3) possesses the same structure as that of Co3, the addition of 5 equiv. of [VO3]- yielded a different structure of a dinuclear-manganese-core-containing decavanadate [Mn2V10O30]6- (Mn2) with two cyclic pentavanadate ligands sandwiching the manganese core. Thus, the conformations of the cyclic decavanadates are rearranged to respond to the central metal core structures. EXAFS study suggests both manganese complexes maintain the molecular structure in solution. The simultaneous analyses of the magnetic susceptibility data and the magnetization data revealed the switch of magnetic interaction modes from ferromagnetic in dinuclear complexes to mixed ferromagnetic and antiferromagnetic interactions in trinuclear complexes: the ferromagnetic interaction in dinuclear units of Co2 (J = 8.05 cm-1) and Mn2 (J = 0.76 cm-1) (Hex = -JS1S2), and the ferromagnetic and antiferromagnetic interactions in Co3 (J = -1.59 cm-1 and J′ = 13.6 cm-1) and Mn3 (J = -2.20 cm-1 and J′ = 0.07 cm-1) (Hex = -JSA1SA2 - J′[SA1SB + SA2SB]) were studied. © 2017 The Royal Society of Chemistry. | |||||||
| 権利 | ||||||||
| 権利情報 | Copyright © 2017 The Royal Society of Chemistry. | |||||||
| 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 | |||||||
