• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

较重的磷族元素亚胺配合物[(ArE)M(CO)](E = As、Sb和Bi;M = Cr、Mo、W和Fe)的结构与键合的比较研究

A comparative study of the structure and bonding in heavier pnictinidene complexes [(ArE)M(CO)] (E = As, Sb and Bi; M = Cr, Mo, W and Fe).

作者信息

Vránová Iva, Kremláček Vít, Erben Milan, Turek Jan, Jambor Roman, Růžička Aleš, Alonso Mercedes, Dostál Libor

机构信息

Department of General and Inorganic Chemistry, Faculty of Chemical Technology, University of Pardubice, Studentská 573, CZ - 532 10, Pardubice, Czech Republic.

Eenheid Algemene Chemie (ALGC), Member of the QCMM VUB-UGent Alliance Research Group, Vrije Universiteit Brussel, Pleinlaan 2, 1050 Brussels, Belgium.

出版信息

Dalton Trans. 2017 Mar 14;46(11):3556-3568. doi: 10.1039/c7dt00095b.

DOI:10.1039/c7dt00095b
PMID:28240753
Abstract

N,C,N-Chelated pnictinidenes ArE [where E = As (1), Sb (2) or Bi (3); Ar = CH-2,6-(CH[double bond, length as m-dash]Nt-Bu)] were used as ligands for the coordination of transition metal carbonyls. Thus, the reaction of 1-3 with [M(CO)THF] (where M = Cr, W) or [Mo(CO)(MeN)] gave complexes [(ArE)M(CO)] [where E = As and M = Cr (1a), Mo (1b), W (1c); E = Sb and M = Cr (2a), Mo (2b), W (2c); E = Bi and M = Cr (3a), Mo (3b), W (3c)]. Analogously, the treatment of 1-3 with [Fe(CO)] resulted in the formation of the complexes [(ArE)Fe(CO)] [where E = As (1d), Sb (2d) or Bi (3d)]. All compounds were characterized by H and C NMR spectroscopy, Raman, IR and UV-Vis spectroscopy. The molecular structures of the majority of the compounds (except 1b and 1c) were also determined by the single-crystal X-ray diffraction analysis. Furthermore, the structure and bonding of the title compounds have also been thoroughly investigated using a computational approach.

摘要

N、C、N-螯合的磷族元素化合物ArE(其中E = As(1)、Sb(2)或Bi(3);Ar = CH-2,6-(CH[双键,长度如间位短线]-Nt-Bu))被用作过渡金属羰基配合物的配体。因此,1-3与[M(CO)THF](其中M = Cr、W)或[Mo(CO)(MeN)]反应得到配合物[(ArE)M(CO)](其中E = As且M = Cr(1a)、Mo(1b)、W(1c);E = Sb且M = Cr(2a)、Mo(2b)、W(2c);E = Bi且M = Cr(3a)、Mo(3b)、W(3c))。类似地,1-3与[Fe(CO)]反应生成配合物[(ArE)Fe(CO)](其中E = As(1d)、Sb(2d)或Bi(3d))。所有化合物均通过氢谱和碳谱核磁共振、拉曼光谱、红外光谱和紫外-可见光谱进行表征。大多数化合物(1b和1c除外)的分子结构也通过单晶X射线衍射分析确定。此外,还使用计算方法对标题化合物的结构和键合进行了深入研究。

相似文献

1
A comparative study of the structure and bonding in heavier pnictinidene complexes [(ArE)M(CO)] (E = As, Sb and Bi; M = Cr, Mo, W and Fe).较重的磷族元素亚胺配合物[(ArE)M(CO)](E = As、Sb和Bi;M = Cr、Mo、W和Fe)的结构与键合的比较研究
Dalton Trans. 2017 Mar 14;46(11):3556-3568. doi: 10.1039/c7dt00095b.
2
Heavier pnictinidene gold(i) complexes.更重的磷属元素金(i)配合物。
Dalton Trans. 2018 Oct 23;47(41):14503-14514. doi: 10.1039/c8dt03022g.
3
Singlet diradical complexes of chromium, molybdenum, and tungsten with azo anion radical ligands from M(CO)6 precursors.由M(CO)₆前体形成的铬、钼和钨与偶氮阴离子自由基配体的单线态双自由基配合物。
Inorg Chem. 2007 Oct 15;46(21):8584-93. doi: 10.1021/ic700584x. Epub 2007 Sep 22.
4
Hydrophosphination reactions with transition metal ferrocenylphosphine complexes.与过渡金属二茂铁基膦配合物的氢膦化反应。
Dalton Trans. 2016 Feb 7;45(5):2208-17. doi: 10.1039/c5dt03374h. Epub 2015 Nov 18.
5
Synthesis and structural characterization of heteroboroxines with MB2O3 core (M = Sb, Bi, Sn).具有 MB2O3 核(M = Sb、Bi、Sn)的杂硼氧烷的合成与结构表征。
Inorg Chem. 2013 Feb 4;52(3):1424-31. doi: 10.1021/ic302153s. Epub 2013 Jan 17.
6
New Metallacarborane Chemistry: Molybdenum and Tungsten Carbonyl Multidecker Sandwiches. Cluster Dimers Linked via Metal-Metal Bonds(1).新型金属碳硼烷化学:钼和钨羰基多层夹心化合物。通过金属-金属键连接的簇二聚体(1)。
Inorg Chem. 1998 Jan 12;37(1):102-111. doi: 10.1021/ic971297d.
7
New bonding modes for boraamidinate ligands in heavy group 15 complexes: fluxional behavior of the 1:2 complexes, LiM[PhB(NtBu)2]2 (M = As, Sb, Bi).重15族配合物中硼脒基配体的新键合模式:1:2配合物LiM[PhB(NtBu)₂]₂(M = As、Sb、Bi)的动态行为
Inorg Chem. 2007 Apr 2;46(7):2627-36. doi: 10.1021/ic0622757. Epub 2007 Feb 28.
8
Facile activation of alkynes with a boraguanidinato-stabilized germylene: a combined experimental and theoretical study.硼胍基稳定的亚锗烯对炔烃的简便活化:实验与理论相结合的研究
Dalton Trans. 2017 Sep 28;46(36):12339-12353. doi: 10.1039/c7dt01950e. Epub 2017 Sep 11.
9
Li/X phosphinidenoid pentacarbonylmetal complexes: a combined experimental and theoretical study on structures and spectroscopic properties.锂/膦亚磷烯五羰基金属配合物:结构和光谱性质的实验与理论综合研究。
Inorg Chem. 2013 Mar 18;52(6):3313-25. doi: 10.1021/ic302786v. Epub 2013 Mar 7.
10
M2(hpp)4Cl2 and M2(hpp)4, where M = Mo and W: preparations, structure and bonding, and comparisons with C2, C2H2, and C2Cl2 and the hypothetical molecules M2(hpp)4(H)2.M2(hpp)4Cl2 和 M2(hpp)4,其中 M = 钼(Mo)和钨(W):制备、结构与键合,以及与 C2、C2H2 和 C2Cl2 及假设分子 M2(hpp)4(H)2 的比较
J Am Chem Soc. 2003 Dec 24;125(51):16040-9. doi: 10.1021/ja0301065.

引用本文的文献

1
Nature of the heavy formal double bonds As[double bond, length as m-dash]Ch, Sb[double bond, length as m-dash]Ch and Bi[double bond, length as m-dash]Ch (Ch = S, Se, Te) in NCN-pincer supported arsinidene, stibinidene and bismuthinidene chalcogenides.NCN钳形配体支持的胂烯、亚锑烯和亚铋烯硫族化物中重形式双键As[双键,长度用m破折号表示]Ch、Sb[双键,长度用m破折号表示]Ch和Bi[双键,长度用m破折号表示]Ch(Ch = S、Se、Te)的性质
Chem Sci. 2025 Jul 18. doi: 10.1039/d5sc03320a.
2
Bis(amidophenolate)-supported pnictoranides: Lewis acid-induced electromerism in a bismuth complex.双(酰胺基酚盐)支撑的磷族元素化物:铋配合物中路易斯酸诱导的电子异构现象
Chem Sci. 2025 Jul 8;16(31):14178-14185. doi: 10.1039/d5sc03374h. eCollection 2025 Aug 6.
3
Synthesis, Structure, and Electronic Properties of [Cr@SnSb(en)]: A Cr Octahedron Encapsulated in a Zintl-Ion Ligand.
[Cr@SnSb(en)]的合成、结构及电子性质:包裹于津特耳离子配体中的铬八面体
J Am Chem Soc. 2025 Jul 16;147(28):24309-24316. doi: 10.1021/jacs.5c00515. Epub 2025 Jul 7.
4
Multi-Talented Bismuthinidenes: Double C(sp)─I Bond Activation Using Single or Two Bi Centers.多才多艺的双铋烯:利用单个或两个铋中心实现双C(sp)─I键活化
Chemistry. 2025 Jun 12;31(33):e202500620. doi: 10.1002/chem.202500620. Epub 2025 May 15.
5
Combining geometric constraint and redox non-innocence within an ambiphilic PBiP pincer ligand.在双亲和性PBiP钳形配体中结合几何约束和氧化还原非无害性。
Chem Sci. 2024 Mar 18;15(16):6036-6043. doi: 10.1039/d4sc00197d. eCollection 2024 Apr 24.
6
Triplet bismuthinidenes featuring unprecedented giant and positive zero field splittings.具有前所未有的巨大正零场分裂的三重态双铋烯
Natl Sci Rev. 2023 Jun 12;10(10):nwad169. doi: 10.1093/nsr/nwad169. eCollection 2023 Oct.
7
Isolation and characterization of bis(silylene)-stabilized antimony(I) and bismuth(I) cations.双(硅亚基)稳定的一价锑和一价铋阳离子的分离与特性研究。
Nat Commun. 2023 May 23;14(1):2968. doi: 10.1038/s41467-023-38606-2.
8
Isolation of an Arsenic Diradicaloid with a Cyclic C As -Core.一种具有环状C-As核心的砷双自由基的分离。
Angew Chem Int Ed Engl. 2022 Aug 22;61(34):e202207415. doi: 10.1002/anie.202207415. Epub 2022 Jul 13.
9
Unveiling the Electronic Structure of the Bi(+1)/Bi(+3) Redox Couple on NCN and NNN Pincer Complexes.揭示NCN和NNN钳形配合物上Bi(+1)/Bi(+3)氧化还原对的电子结构。
Inorg Chem. 2021 Dec 6;60(23):17657-17668. doi: 10.1021/acs.inorgchem.1c02252. Epub 2021 Nov 12.
10
Phosphine-Stabilized Pnictinidenes.磷化氢稳定的磷族元素单原子化合物
Chemistry. 2021 Oct 7;27(56):14073-14080. doi: 10.1002/chem.202102320. Epub 2021 Aug 20.