Item type |
デフォルトアイテムタイプ_(フル)(1) |
公開日 |
2025-01-20 |
タイトル |
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タイトル |
Reactivity of Organoiridium Tungsten Oxide Clusters with Transition Metal Aquo Cations |
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言語 |
en |
作成者 |
Sugiarto
Mitsuhashi, Ryoji
Sadakane, Masahiro
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アクセス権 |
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アクセス権 |
open access |
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アクセス権URI |
http://purl.org/coar/access_right/c_abf2 |
権利情報 |
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言語 |
en |
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権利情報 |
This document is the Accepted Manuscript version of a Published Work that appeared in final form in Inorganic Chemistry, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.inorgchem.4c00076 |
権利情報 |
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言語 |
en |
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権利情報 |
This is not the published version. Please cite only the published version. |
権利情報 |
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言語 |
ja |
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権利情報 |
この論文は出版社版ではありません。引用の際には出版社版をご確認、ご利用ください。 |
内容記述 |
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内容記述 |
Organometallic–polyoxometalate (POM) complexes form a unique class of molecular organometallic oxides characterized by the dynamic behavior of the organometallic cations. Herein, we investigated the reactivity of Cp*Ir-octatungstate clusters (where Cp* represents pentamethylcyclopentadienyl, C5Me5–) with Werner-type transition-metal aquo cations. The addition of Ag+, Co2+, Ni2+, and M3+ (M = Cr, Fe, or In) cations to the aqueous solution of Cp*Ir-octatungstate clusters resulted in the formation of [{Ag(OH2)2}2{Cp*Ir(OH2)}2{Cp*IrW3O12(OH)}2(WO2)2] (1), Co1.5K0.8Na0.2[{trans-Co(OH2)2}{Cp*IrW3O12(OH)}2(WO2)1.3{cis-Co(OH2)2}0.7] (2-Co), Ni0.2K1.4Na0.2[{Ni(OH2)4}2{Cp*IrW3O12(OH)}2(WO2)1.1{cis-Ni(OH2)2}0.9] (2-Ni), and [{M(OH2)4}2{Cp*IrW3O12(OH)}2{cis-M(OH2)2}2](NO3)2 (M = Cr, 3-Cr; Fe, 3-Fe; or In, 3-In), respectively. All clusters share the same cubane-type {Cp*IrW3O12(OH)}5– building block, representing the first examples of organoiridium-POMs functionalized by transition-metal aquo cations. These compounds are insoluble in water, facilitating the evaluation of their heterogeneous water-oxidation properties. Notably, 2-Co generates the highest catalytic water oxidation current. This work provides a new synthetic method to introduce metal–aquo complexes on an organometallic oxide cluster, producing multimetallic molecules that model the catalytic sites of complex oxides. |
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言語 |
en |
内容記述 |
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内容記述タイプ |
Other |
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内容記述 |
This study was commissioned by the New Energy and Industrial Technology and Development Organization (NEDO) of Japan (project JPNP20005). We acknowledge support from the JSPS KAKENHI Grant-in-Aid for Transformative Research Area (A) “Supra-ceramics" (JP22H05144), the JSPS Core-to-Core program, and the International Network on Polyoxometalate Science at Hiroshima University. The magnetic measurements were conducted at the Institute of Molecular Science, supported by ARIM of the MEXT (project JPMXP1223MS1015). |
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言語 |
en |
出版者 |
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出版者 |
American Chemical Society |
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言語 |
en |
言語 |
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言語 |
eng |
資源タイプ |
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資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
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資源タイプ |
journal article |
出版タイプ |
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出版タイプ |
AM |
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出版タイプResource |
http://purl.org/coar/version/c_ab4af688f83e57aa |
関連情報 |
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関連タイプ |
isVersionOf |
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識別子タイプ |
DOI |
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関連識別子 |
https://doi.org/10.1021/acs.inorgchem.4c00076 |
助成情報 |
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助成機関名 |
日本学術振興会 |
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言語 |
ja |
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研究課題番号URI |
https://kaken.nii.ac.jp/ja/grant/KAKENHI-PLANNED-22H05144/ |
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研究課題番号 |
22H05144 |
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研究課題名 |
超セラミックスの次元・形態制御 |
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言語 |
ja |
助成情報 |
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助成機関名 |
Japan Society for the Promotion of Science |
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言語 |
en |
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研究課題名 |
Controls of Structural dimensionality and Crystal morphology of Supra-ceramics |
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言語 |
en |
開始ページ |
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開始ページ |
5672 |
書誌情報 |
en : Inorganic Chemistry
巻 63,
号 12,
p. 5672-5680,
発行日 2024-03-12
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旧ID |
56135 |