一种[Mn8] 缺陷超四面体 T3 及其二聚体[Mn16] 类似物

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Antonis Anastassiades, Dimitris I. Alexandropoulos, Ashlyn Hale, George Christou, Spyros P. Perlepes and Anastasios J. Tasiopoulos*, 
{"title":"一种[Mn8] 缺陷超四面体 T3 及其二聚体[Mn16] 类似物","authors":"Antonis Anastassiades,&nbsp;Dimitris I. Alexandropoulos,&nbsp;Ashlyn Hale,&nbsp;George Christou,&nbsp;Spyros P. Perlepes and Anastasios J. Tasiopoulos*,&nbsp;","doi":"10.1021/acs.cgd.4c0110010.1021/acs.cgd.4c01100","DOIUrl":null,"url":null,"abstract":"<p >The initial use of 2-(pyridin-2-yl)propane-1,3-diol (pypdH<sub>2</sub>) in Mn cluster chemistry has afforded two new mixed-valence polynuclear Mn clusters, namely, [Mn<sub>8</sub>Ο<sub>5</sub>(pypd)(hmp)<sub>3</sub>(O<sub>2</sub>CCMe<sub>3</sub>)<sub>8</sub>] (<b>1</b>) and [Mn<sub>16</sub>Ο<sub>10</sub>(N<sub>3</sub>)<sub>2</sub>(pypd)<sub>2</sub>{(py)<sub>2</sub>CO<sub>2</sub>}<sub>4</sub>(O<sub>2</sub>CEt)<sub>12</sub>] (<b>2</b>) (hmp<sup>–</sup> = deprotonated 2-hydroxymethylpyridine; (py)<sub>2</sub>CO<sub>2</sub><sup>2–</sup> = deprotonated gem-diol form of di-2-pyridyl ketone). Compound <b>1</b> features a novel [Mn<sup>III</sup><sub>7</sub>Mn<sup>II</sup>(μ<sub>4</sub>-O)<sub>2</sub>(μ<sub>3</sub>-O)<sub>3</sub>(μ-OR)<sub>5</sub>]<sup>8+</sup> structural core resembling a supertetrahedron T3, lacking two apexes, while complex <b>2</b> has a [Mn<sup>III</sup><sub>14</sub>Mn<sup>II</sup><sub>2</sub>(μ<sub>4</sub>-O)<sub>4</sub>(μ<sub>3</sub>-O)<sub>6</sub>(μ-N<sub>3</sub>)<sub>2</sub>(μ<sub>3</sub>-OR)<sub>2</sub>(μ-OR)<sub>8</sub>]<sup>14+</sup> core consisting of two [Mn<sub>8</sub>] subunits related to <b>1</b> and thus is a dimeric analogue of <b>1</b>. Direct current (dc) magnetic susceptibility studies revealed the presence of dominant antiferromagentic exchange interactions between the Mn ions in complexes <b>1</b> and <b>2</b> and small ground state spin values for both compounds. Overall, this work highlights the capability of polyol-like chelates like pypdH<sub>2</sub> to stabilize high nuclearity 3d metal clusters based on polynuclear building blocks.</p><p >The initial use of 2-(pyridin-2-yl)propane-1,3-diol ligand in Mn cluster chemistry has afforded two new polynuclear [Mn<sub>8</sub>] and [Mn<sub>16</sub>] clusters. They feature novel, structurally related [Mn<sup>III</sup><sub>7</sub>Mn<sup>II</sup>(μ<sub>4</sub>-O)<sub>2</sub>(μ<sub>3</sub>-O)<sub>3</sub>(μ-OR)<sub>5</sub>]<sup>8+</sup> (<b>1</b>) and [Mn<sup>III</sup><sub>14</sub>Mn<sup>II</sup><sub>2</sub>(μ<sub>4</sub>-O)<sub>4</sub>(μ<sub>3</sub>-O)<sub>6</sub>(μ-N<sub>3</sub>)<sub>2</sub>(μ<sub>3</sub>-OR)<sub>2</sub>(μ-OR)<sub>8</sub>]<sup>14+</sup> (<b>2</b>) cores consisting of one and two (connected) defective supertetrahedra T3, lacking two apexes, respectively. Magnetism studies revealed dominant antiferromagentic exchange interactions and small spin ground state values for both compounds.</p>","PeriodicalId":3,"journal":{"name":"ACS Applied Electronic Materials","volume":null,"pages":null},"PeriodicalIF":4.3000,"publicationDate":"2024-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/epdf/10.1021/acs.cgd.4c01100","citationCount":"0","resultStr":"{\"title\":\"A [Mn8] Defective Supertetrahedron T3 and Its Dimeric [Mn16] Analogue\",\"authors\":\"Antonis Anastassiades,&nbsp;Dimitris I. Alexandropoulos,&nbsp;Ashlyn Hale,&nbsp;George Christou,&nbsp;Spyros P. Perlepes and Anastasios J. Tasiopoulos*,&nbsp;\",\"doi\":\"10.1021/acs.cgd.4c0110010.1021/acs.cgd.4c01100\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The initial use of 2-(pyridin-2-yl)propane-1,3-diol (pypdH<sub>2</sub>) in Mn cluster chemistry has afforded two new mixed-valence polynuclear Mn clusters, namely, [Mn<sub>8</sub>Ο<sub>5</sub>(pypd)(hmp)<sub>3</sub>(O<sub>2</sub>CCMe<sub>3</sub>)<sub>8</sub>] (<b>1</b>) and [Mn<sub>16</sub>Ο<sub>10</sub>(N<sub>3</sub>)<sub>2</sub>(pypd)<sub>2</sub>{(py)<sub>2</sub>CO<sub>2</sub>}<sub>4</sub>(O<sub>2</sub>CEt)<sub>12</sub>] (<b>2</b>) (hmp<sup>–</sup> = deprotonated 2-hydroxymethylpyridine; (py)<sub>2</sub>CO<sub>2</sub><sup>2–</sup> = deprotonated gem-diol form of di-2-pyridyl ketone). Compound <b>1</b> features a novel [Mn<sup>III</sup><sub>7</sub>Mn<sup>II</sup>(μ<sub>4</sub>-O)<sub>2</sub>(μ<sub>3</sub>-O)<sub>3</sub>(μ-OR)<sub>5</sub>]<sup>8+</sup> structural core resembling a supertetrahedron T3, lacking two apexes, while complex <b>2</b> has a [Mn<sup>III</sup><sub>14</sub>Mn<sup>II</sup><sub>2</sub>(μ<sub>4</sub>-O)<sub>4</sub>(μ<sub>3</sub>-O)<sub>6</sub>(μ-N<sub>3</sub>)<sub>2</sub>(μ<sub>3</sub>-OR)<sub>2</sub>(μ-OR)<sub>8</sub>]<sup>14+</sup> core consisting of two [Mn<sub>8</sub>] subunits related to <b>1</b> and thus is a dimeric analogue of <b>1</b>. Direct current (dc) magnetic susceptibility studies revealed the presence of dominant antiferromagentic exchange interactions between the Mn ions in complexes <b>1</b> and <b>2</b> and small ground state spin values for both compounds. Overall, this work highlights the capability of polyol-like chelates like pypdH<sub>2</sub> to stabilize high nuclearity 3d metal clusters based on polynuclear building blocks.</p><p >The initial use of 2-(pyridin-2-yl)propane-1,3-diol ligand in Mn cluster chemistry has afforded two new polynuclear [Mn<sub>8</sub>] and [Mn<sub>16</sub>] clusters. They feature novel, structurally related [Mn<sup>III</sup><sub>7</sub>Mn<sup>II</sup>(μ<sub>4</sub>-O)<sub>2</sub>(μ<sub>3</sub>-O)<sub>3</sub>(μ-OR)<sub>5</sub>]<sup>8+</sup> (<b>1</b>) and [Mn<sup>III</sup><sub>14</sub>Mn<sup>II</sup><sub>2</sub>(μ<sub>4</sub>-O)<sub>4</sub>(μ<sub>3</sub>-O)<sub>6</sub>(μ-N<sub>3</sub>)<sub>2</sub>(μ<sub>3</sub>-OR)<sub>2</sub>(μ-OR)<sub>8</sub>]<sup>14+</sup> (<b>2</b>) cores consisting of one and two (connected) defective supertetrahedra T3, lacking two apexes, respectively. Magnetism studies revealed dominant antiferromagentic exchange interactions and small spin ground state values for both compounds.</p>\",\"PeriodicalId\":3,\"journal\":{\"name\":\"ACS Applied Electronic Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2024-10-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.acs.org/doi/epdf/10.1021/acs.cgd.4c01100\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Electronic Materials\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.cgd.4c01100\",\"RegionNum\":3,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENGINEERING, ELECTRICAL & ELECTRONIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Electronic Materials","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.cgd.4c01100","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, ELECTRICAL & ELECTRONIC","Score":null,"Total":0}
引用次数: 0

摘要

将 2-(吡啶-2-基)丙烷-1,3-二醇(pypdH2)首次用于锰簇化学反应中,产生了两种新的混合价多核锰簇、即 [Mn8Ο5(pypd)(hmp)3(O2CCMe3)8] (1) 和 [Mn16Ο10(N3)2(pypd)2{(py)2CO2}4(O2CEt)12] (2) (hmp- = 去质子化的 2-羟甲基吡啶;(py)2CO22- = 二-2-吡啶基酮的去质子化 gem-diol 形式)。化合物 1 具有新颖的[MnIII7MnII(μ4-O)2(μ3-O)3(μ-OR)5]8+结构核心,类似于缺乏两个顶点的超四面体 T3、而复合物 2 具有一个[MnIII14MnII2(μ4-O)4(μ3-O)6(μ-N3)2(μ3-OR)2(μ-OR)8]14+ 核心,由与 1 有关的两个[Mn8]亚基组成,因此是 1 的二聚类似物。直流磁感应强度研究表明,复合物 1 和 2 中的锰离子之间存在主要的反铁磁交换相互作用,而且这两种化合物的基态自旋值都很小。总之,这项工作突出了多元醇类螯合物(如 pypdH2)稳定基于多核结构单元的高核度 3d 金属簇的能力。它们具有结构相关的新型[MnIII7MnII(μ4-O)2(μ3-O)3(μ-OR)5]8+ (1)和[MnIII14MnII2(μ4-O)4(μ3-O)6(μ-N3)2(μ3-OR)2(μ-OR)8]14+ (2)核心,分别由一个和两个(相连)缺顶的缺陷超四面体 T3 组成。磁性研究表明,这两种化合物的反铁磁交换相互作用占主导地位,自旋基态值较小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A [Mn8] Defective Supertetrahedron T3 and Its Dimeric [Mn16] Analogue

The initial use of 2-(pyridin-2-yl)propane-1,3-diol (pypdH2) in Mn cluster chemistry has afforded two new mixed-valence polynuclear Mn clusters, namely, [Mn8Ο5(pypd)(hmp)3(O2CCMe3)8] (1) and [Mn16Ο10(N3)2(pypd)2{(py)2CO2}4(O2CEt)12] (2) (hmp = deprotonated 2-hydroxymethylpyridine; (py)2CO22– = deprotonated gem-diol form of di-2-pyridyl ketone). Compound 1 features a novel [MnIII7MnII4-O)23-O)3(μ-OR)5]8+ structural core resembling a supertetrahedron T3, lacking two apexes, while complex 2 has a [MnIII14MnII24-O)43-O)6(μ-N3)23-OR)2(μ-OR)8]14+ core consisting of two [Mn8] subunits related to 1 and thus is a dimeric analogue of 1. Direct current (dc) magnetic susceptibility studies revealed the presence of dominant antiferromagentic exchange interactions between the Mn ions in complexes 1 and 2 and small ground state spin values for both compounds. Overall, this work highlights the capability of polyol-like chelates like pypdH2 to stabilize high nuclearity 3d metal clusters based on polynuclear building blocks.

The initial use of 2-(pyridin-2-yl)propane-1,3-diol ligand in Mn cluster chemistry has afforded two new polynuclear [Mn8] and [Mn16] clusters. They feature novel, structurally related [MnIII7MnII4-O)23-O)3(μ-OR)5]8+ (1) and [MnIII14MnII24-O)43-O)6(μ-N3)23-OR)2(μ-OR)8]14+ (2) cores consisting of one and two (connected) defective supertetrahedra T3, lacking two apexes, respectively. Magnetism studies revealed dominant antiferromagentic exchange interactions and small spin ground state values for both compounds.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信