不对称氟化镁β-二酮酸配合物的合成、结构和性质

IF 1.2 4区 化学 Q4 CHEMISTRY, INORGANIC & NUCLEAR
S. S. Krutskikh, D. V. Kochelakov, A. A. Nazarova, I. V. Korolkov, L. N. Zelenina, E. S. Vikulova
{"title":"不对称氟化镁β-二酮酸配合物的合成、结构和性质","authors":"S. S. Krutskikh,&nbsp;D. V. Kochelakov,&nbsp;A. A. Nazarova,&nbsp;I. V. Korolkov,&nbsp;L. N. Zelenina,&nbsp;E. S. Vikulova","doi":"10.1134/S0022476624110131","DOIUrl":null,"url":null,"abstract":"<p>New complexes of magnesium with asymmetric fluorinated β-diketones are synthesized: pentafluoropropionyl (Hpfpac, 6,6,6,5,5-pentafluorohexane-2,4-dione) and heptafluorobutyrylacetone (Hhfbac, 7,7,7,6,6,5,5-heptafluoroheptane-2,4-dione). The [Mg(H<sub>2</sub>O)(EtOH)(pfpac)<sub>2</sub>] <b>1</b> and [Mg(H<sub>2</sub>O)<sub>2</sub>(hfbac)<sub>2</sub>]·H<sub>2</sub>O <b>2 </b>phases are characterized by a number of methods. The structures of crystals of <b>1</b>, <b>2</b>, and [Mg(EtOH)<sub>2</sub>(hfbac)<sub>2</sub>] <b>3 </b>are determined by the single crystal X-ray diffraction analysis. Magnesium atoms have a distorted octahedral environment, and neutral ligands are in the <i>trans</i>-position. Molecules are involved in systems of OH⋯O<sub>dik</sub> hydrogen bonds, forming layers (<b>2</b>) or chains (<b>1</b>, <b>3</b>). A relative evaluation shows that <b>2</b> is more volatile than <b>1</b>. Structures of molecules and packing characters are compared with those of a series of related β-diketonate complexes. The effect of an increase in the ligand perfluoroalkyl chain (L = tfac, trifluoroacetylacetonate ion), including isoformular [Mg(H<sub>2</sub>O)<sub>2</sub>(L)<sub>2</sub>]·H<sub>2</sub>O, is shown.</p>","PeriodicalId":668,"journal":{"name":"Journal of Structural Chemistry","volume":"65 11","pages":"2260 - 2271"},"PeriodicalIF":1.2000,"publicationDate":"2024-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis, Structure, and Properties of Asymmetric Fluorinated Magnesium β-Diketonate Complexes\",\"authors\":\"S. S. Krutskikh,&nbsp;D. V. Kochelakov,&nbsp;A. A. Nazarova,&nbsp;I. V. Korolkov,&nbsp;L. N. Zelenina,&nbsp;E. S. Vikulova\",\"doi\":\"10.1134/S0022476624110131\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>New complexes of magnesium with asymmetric fluorinated β-diketones are synthesized: pentafluoropropionyl (Hpfpac, 6,6,6,5,5-pentafluorohexane-2,4-dione) and heptafluorobutyrylacetone (Hhfbac, 7,7,7,6,6,5,5-heptafluoroheptane-2,4-dione). The [Mg(H<sub>2</sub>O)(EtOH)(pfpac)<sub>2</sub>] <b>1</b> and [Mg(H<sub>2</sub>O)<sub>2</sub>(hfbac)<sub>2</sub>]·H<sub>2</sub>O <b>2 </b>phases are characterized by a number of methods. The structures of crystals of <b>1</b>, <b>2</b>, and [Mg(EtOH)<sub>2</sub>(hfbac)<sub>2</sub>] <b>3 </b>are determined by the single crystal X-ray diffraction analysis. Magnesium atoms have a distorted octahedral environment, and neutral ligands are in the <i>trans</i>-position. Molecules are involved in systems of OH⋯O<sub>dik</sub> hydrogen bonds, forming layers (<b>2</b>) or chains (<b>1</b>, <b>3</b>). A relative evaluation shows that <b>2</b> is more volatile than <b>1</b>. Structures of molecules and packing characters are compared with those of a series of related β-diketonate complexes. The effect of an increase in the ligand perfluoroalkyl chain (L = tfac, trifluoroacetylacetonate ion), including isoformular [Mg(H<sub>2</sub>O)<sub>2</sub>(L)<sub>2</sub>]·H<sub>2</sub>O, is shown.</p>\",\"PeriodicalId\":668,\"journal\":{\"name\":\"Journal of Structural Chemistry\",\"volume\":\"65 11\",\"pages\":\"2260 - 2271\"},\"PeriodicalIF\":1.2000,\"publicationDate\":\"2024-12-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Structural Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1134/S0022476624110131\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Structural Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1134/S0022476624110131","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0

摘要

合成了镁与不对称氟化β-二酮的新配合物:五氟丙炔(Hpfpac, 6,6,5,5-五氟己烷-2,4-二酮)和七氟丁基丙酮(Hhfbac, 7,7,7,6,6,5,5-七氟庚烷-2,4-二酮)。用多种方法对[Mg(H2O)(EtOH)(pfpac)2] 1和[Mg(H2O)2(hfbac)2]·H2O 2相进行表征。用单晶x射线衍射分析确定了1、2和[Mg(EtOH)2(hfbac)2] 3的晶体结构。镁原子具有扭曲的八面体环境,中性配体处于反位。分子参与OH⋯Odik氢键体系,形成层(2)或链(1,3)。相对评价表明2比1更具挥发性。并与一系列相关的β-二酮酸配合物的分子结构和包装特性进行了比较。显示了配体全氟烷基链(L = tfac,三氟乙酰丙酮离子)的增加,包括异构体[Mg(H2O)2(L)2]·H2O的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis, Structure, and Properties of Asymmetric Fluorinated Magnesium β-Diketonate Complexes

New complexes of magnesium with asymmetric fluorinated β-diketones are synthesized: pentafluoropropionyl (Hpfpac, 6,6,6,5,5-pentafluorohexane-2,4-dione) and heptafluorobutyrylacetone (Hhfbac, 7,7,7,6,6,5,5-heptafluoroheptane-2,4-dione). The [Mg(H2O)(EtOH)(pfpac)2] 1 and [Mg(H2O)2(hfbac)2]·H2O 2 phases are characterized by a number of methods. The structures of crystals of 1, 2, and [Mg(EtOH)2(hfbac)2] 3 are determined by the single crystal X-ray diffraction analysis. Magnesium atoms have a distorted octahedral environment, and neutral ligands are in the trans-position. Molecules are involved in systems of OH⋯Odik hydrogen bonds, forming layers (2) or chains (1, 3). A relative evaluation shows that 2 is more volatile than 1. Structures of molecules and packing characters are compared with those of a series of related β-diketonate complexes. The effect of an increase in the ligand perfluoroalkyl chain (L = tfac, trifluoroacetylacetonate ion), including isoformular [Mg(H2O)2(L)2]·H2O, is shown.

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
Journal of Structural Chemistry
Journal of Structural Chemistry 化学-无机化学与核化学
CiteScore
1.60
自引率
12.50%
发文量
142
审稿时长
8.3 months
期刊介绍: Journal is an interdisciplinary publication covering all aspects of structural chemistry, including the theory of molecular structure and chemical bond; the use of physical methods to study the electronic and spatial structure of chemical species; structural features of liquids, solutions, surfaces, supramolecular systems, nano- and solid materials; and the crystal structure of solids.
×
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