• 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

含氮配体二硝酰胺根(N(NO2)2(-))、4,5-二氰基-1,2,3-三唑(C4N5(-))和二氰胺根(N(CN)2(-))的第一类锕系元素配合物。

First actinide complexes of the nitrogen-containing ligands dinitramide (N(NO2)2(-)), 4,5-Dicyano-1,2,3-triazolate (C4N5(-)), and dicyanamide (N(CN)2(-)).

机构信息

Department of Chemistry Ludwig-Maximilians University, Butenandtstrasse 5-13 (Haus D), D-81377, Munich, Germany.

出版信息

Inorg Chem. 2010 Mar 15;49(6):2674-83. doi: 10.1021/ic901820b.

DOI:10.1021/ic901820b
PMID:20141179
Abstract

The syntheses and characterization of uranyl complexes of nitrogen-containing ligands are reported. For the first time, an actinide complex containing dinitramide ligands coordinated to the actinide center in UO(2)(N(NO(2))(2))(2)(OP(NMe(2))(3))(2) (1) has been isolated and structurally characterized. Using an excess of OP(NMe(2))(3), the dinitramide ligands were replaced by OP(NMe(2))(3) ligands resulting in the formation of the salt [UO(2)(OP(NMe(2))(3))(4)]N(NO(2))(2) (2). Both complexes 1 and 2 were characterized using IR, Raman, as well as (1)H, (13)C, (14)N and (31)P{(1)H} NMR spectroscopy, in addition to C/H/N analysis. The structures of 1 and 2 were determined by single crystal X-ray diffraction. 1: monoclinic, P2(1)/n, a = 12.5389(3), b = 7.9496(2), c = 15.8172(4) A, beta = 110.842(3) degrees , V = 1473.48(6) A(3), Z = 2. 2: orthorhombic, Pbca, a = 14.5640(6), b = 15.3697(6), c = 45.7789(18) A, V = 10247.3(7) A(3), Z = 8. The related complex [UO(2)(N(CN)(2))(2)(OP(NMe(2))(3))(2)] (3) containing the dicyanamide ligand (N(CN)(2)(-)) coordinated to the U(VI) center was synthesized and characterized using IR, Raman, (1)H, (13)C and (31)P{(1)H} NMR spectroscopy. The structure of 3 was determined using single crystal X-ray diffraction and revealed a dinuclear complex containing both terminal and bridging N(CN)(2)(-) ligands. 3: monoclinic, P2(1)/c, a = 15.5873(9), b = 14.2132(6), c = 13.2006(5) A, beta = 100.029(3) degrees, V = 2879.8(2) A(3), Z = 2. Finally, in this investigation of the coordination of relatively nitrogen-rich ligands to uranium centers, the synthesis, characterization, and isolation of the first U(VI) complex showing coordination of the triazolate ligand via a ring nitrogen atom is reported in UO(2)((NC)(2)C(2)N(3))(2)(OPPh(3))(3) (4). Complex 4 was characterized using IR, Raman, (1)H, (13)C and (31)P{(1)H} NMR spectroscopy. The solid state structure of 4 was determined using single crystal X-ray diffraction. 4: monoclinic, P2(1)/n, a = 18.9970(2), b = 31.9500(3), c = 20.1133(2) A, beta = 111.4449(4) degrees, V = 11362.69(19) A(3), Z = 8. To the best of our knowledge, compounds 1 and 2 are the first structurally characterized complexes where a dinitramide ligand is coordinated to an f-block center. Complex 3 is the first structurally characterized actinide dicyanamide complex and a rare example of a dinuclear uranyl complex showing a 12 membered U-N-C ring formed by bridging dicyanamide ligands between two uranyl centers. Finally, complex 4 is the first isolated and structurally characterized uranium complex containing a triazolate ligand coordinated to the U(VI) center. Complexes 3 and 4 are examples of uranyl complexes containing ligands coordinated via nitrogen atoms to the U(VI) center. Whereas the dinitramide ligand can coordinate via N or O atoms, in complex 1, the N(NO(2))(2) ligand acts as a bidentate chelate ligand, and only coordination via the oxygen atoms to the U(VI) center was observed in the crystalline state.

摘要

报告了含氮配体的铀酰配合物的合成和表征。首次分离并结构表征了含有 dinitramide 配体配位到 actinide 中心的铀酰配合物 UO(2)(N(NO(2))(2))(2)(OP(NMe(2))(3))(2) (1)。通过使用过量的 OP(NMe(2))(3),将 dinitramide 配体替换为 OP(NMe(2))(3)配体,得到盐 [UO(2)(OP(NMe(2))(3))(4)]N(NO(2))(2) (2)。使用红外、拉曼以及 1H、13C、14N 和 31P{(1)H} NMR 光谱,除了 C/H/N 分析之外,还对配合物 1 和 2 进行了表征。通过单晶 X 射线衍射确定了 1 和 2 的结构。1:单斜,P2(1)/n,a = 12.5389(3),b = 7.9496(2),c = 15.8172(4) A,β = 110.842(3)°,V = 1473.48(6) A(3),Z = 2。2:正交,Pbca,a = 14.5640(6),b = 15.3697(6),c = 45.7789(18) A,V = 10247.3(7) A(3),Z = 8。合成了含有 dicyanamide 配体 (N(CN)(2)(-)) 配位到 U(VI) 中心的相关配合物 [UO(2)(N(CN)(2))(2)(OP(NMe(2))(3))(2)] (3),并通过红外、拉曼、1H、13C 和 31P{(1)H} NMR 光谱对其进行了表征。通过单晶 X 射线衍射确定了 3 的结构,结果表明它是一种含有末端和桥接 N(CN)(2)(-) 配体的双核配合物。3:单斜,P2(1)/c,a = 15.5873(9),b = 14.2132(6),c = 13.2006(5) A,β = 100.029(3)°,V = 2879.8(2) A(3),Z = 2。最后,在这项对相对富氮配体与铀中心配位的研究中,首次报道了 U(VI) 配合物 UO(2)((NC)(2)C(2)N(3))(2)(OPPh(3))(3) (4),其显示通过环氮原子配位三唑配体。通过使用红外、拉曼、1H、13C 和 31P{(1)H} NMR 光谱对 4 进行了表征。通过单晶 X 射线衍射确定了 4 的固态结构。4:单斜,P2(1)/n,a = 18.9970(2),b = 31.9500(3),c = 20.1133(2) A,β = 111.4449(4)°,V = 11362.69(19) A(3),Z = 8。据我们所知,化合物 1 和 2 是首次结构表征的含有 dinitramide 配体配位到 f 区中心的配合物。3 是第一个结构表征的 actinide dicyanamide 配合物,也是一个罕见的双核铀酰配合物的例子,其通过桥连的二氰胺配体在两个铀酰中心之间形成 12 元 U-N-C 环。最后,配合物 4 是第一个分离并结构表征的含有三唑配体配位到 U(VI) 中心的铀酰配合物。配合物 3 和 4 是含有通过氮原子配位到 U(VI) 中心的配体的铀酰配合物的例子。尽管 dinitramide 配体可以通过 N 或 O 原子配位,但在配合物 1 中,N(NO(2))(2) 配体充当双齿螯合配体,并且在晶体状态下仅观察到与 U(VI) 中心的氧原子配位。

相似文献

1
First actinide complexes of the nitrogen-containing ligands dinitramide (N(NO2)2(-)), 4,5-Dicyano-1,2,3-triazolate (C4N5(-)), and dicyanamide (N(CN)2(-)).含氮配体二硝酰胺根(N(NO2)2(-))、4,5-二氰基-1,2,3-三唑(C4N5(-))和二氰胺根(N(CN)2(-))的第一类锕系元素配合物。
Inorg Chem. 2010 Mar 15;49(6):2674-83. doi: 10.1021/ic901820b.
2
First structurally characterized actinide isocyanates.首个得到结构表征的锕系异氰酸酯。
Inorg Chem. 2004 Nov 1;43(22):6860-2. doi: 10.1021/ic049078x.
3
Synthesis and characterization of heavier dioxouranium(VI) dihalides.重二卤化双氧铀(VI)的合成与表征
Inorg Chem. 2004 Nov 1;43(22):7120-6. doi: 10.1021/ic0354926.
4
Synthesis and characterization of 4,5-dicyano-2H-1,2,3-triazole and its sodium, ammonium, and guanidinium salts.4,5-二氰基-2H-1,2,3-三唑及其钠盐、铵盐和胍盐的合成与表征。
Inorg Chem. 2009 Feb 16;48(4):1731-43. doi: 10.1021/ic801793p.
5
Synthesis, structural characterization, and biological studies of new antimony(III) complexes with thiones. The influence of the solvent on the geometry of the complexes.新型含硫酮的锑(III)配合物的合成、结构表征及生物学研究。溶剂对配合物几何结构的影响。
Inorg Chem. 2007 Oct 15;46(21):8652-61. doi: 10.1021/ic700756e. Epub 2007 Sep 13.
6
Probing the chemistry, electronic structure and redox energetics in organometallic pentavalent uranium complexes.探究有机金属五价铀配合物的化学性质、电子结构和氧化还原能量学。
Inorg Chem. 2008 Dec 15;47(24):11879-91. doi: 10.1021/ic8017375.
7
Synthesis and characterization of novel rhenium(V) tetradentate N2O2 Schiff base monomer and dimer complexes.新型铼(V)四齿N2O2席夫碱单体和二聚体配合物的合成与表征
Inorg Chem. 2003 Oct 6;42(20):6519-27. doi: 10.1021/ic030240q.
8
Di- and tetranuclear metal complexes with phenoxo bridges: synthesis, structures, and photoluminescent and electroluminescent properties.含苯氧基桥联的双核和四核金属配合物:合成、结构以及光致发光和电致发光性质
Inorg Chem. 2006 Feb 20;45(4):1745-53. doi: 10.1021/ic051531x.
9
Self-assembly of cuII and niII [2 x 2] grid complexes and a binuclear CuII complex with a new semiflexible substituted pyrazine ligand: multiple anion encapsulation and magnetic properties.铜(II)和镍(II)[2×2]网格配合物以及一种含新型半柔性取代吡嗪配体的双核铜(II)配合物的自组装:多重阴离子包封及磁性质
Inorg Chem. 2004 Feb 9;43(3):1021-30. doi: 10.1021/ic030174s.
10
Novel metal-organic frameworks with specific topology from new tripodal ligands: 1,3,5-tris(1-imidazolyl)benzene and 1,3-bis(1-imidazolyl)-5-(imidazol-1-ylmethyl)benzene.新型三脚架配体衍生的具有特定拓扑结构的金属有机框架:1,3,5-三(1-咪唑基)苯和1,3-双(1-咪唑基)-5-(咪唑-1-基甲基)苯。
Inorg Chem. 2003 May 19;42(10):3168-75. doi: 10.1021/ic0206847.

引用本文的文献

1
Detection and identification of solids, surfaces, and solutions of uranium using vibrational spectroscopy.利用振动光谱法检测和识别铀的固体、表面及溶液。
Coord Chem Rev. 2018 Nov 1;374:314-344. doi: 10.1016/j.ccr.2018.07.010. Epub 2018 Jul 31.