• 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

超铀有机金属化学。

Transuranium organometallic chemistry.

作者信息

Réant Benjamin L L, Deakin Cameron N, MacKenzie Ross E, Goodwin Conrad A P

机构信息

Centre for Radiochemistry Research, The University of Manchester, Manchester, UK.

出版信息

Nat Rev Chem. 2025 Aug 13. doi: 10.1038/s41570-025-00732-4.

DOI:10.1038/s41570-025-00732-4
PMID:40804532
Abstract

Coordination chemistry is a tool to reveal the hidden nature of elements through controlled manipulation of their environment, and the benefits that this understanding has brought society are numerous. For a chemist, the actinide series represents an intriguing frontier wherein conventional chemical intuition yields to relativistic effects and atypical technical challenges influence the pace of progress. Much of the chemical understanding of transuranium elements was developed during and shortly after the Manhattan Project and was borne out of practical needs. Although theoretical interest in their fundamental bonding and behaviour has always existed, synthesis-led exploration was often not possible. Synthetic, analytical and computational advancements in the twenty-first century have changed this, and contemporary synthetic transuranium coordination chemistry has begun to reveal that their properties are more nuanced than previously appreciated. In this Review, we discuss the discovery of transuranium elements, their history and the logistical demands inherent to chemical advancement in the area, and present key progress in transuranium organometallic and selected metal-organic chemistry, with a focus on how the field has begun to mature.

摘要

配位化学是一种通过对元素环境进行可控操纵来揭示其隐藏本质的工具,这种认识给社会带来的益处众多。对于化学家而言,锕系元素代表着一个引人入胜的前沿领域,在其中传统化学直觉让位于相对论效应,而非典型的技术挑战影响着进展的速度。对超铀元素的许多化学认识是在曼哈顿计划期间及之后不久发展起来的,并且源于实际需求。尽管对其基本键合和行为的理论兴趣一直存在,但以合成为主导的探索往往是不可能的。21世纪的合成、分析和计算进展改变了这一状况,当代合成超铀配位化学已开始揭示其性质比以前所认识的更为细微。在本综述中,我们讨论超铀元素的发现、它们的历史以及该领域化学进展所固有的后勤需求,并介绍超铀有机金属化学和选定的金属有机化学的关键进展,重点关注该领域是如何开始走向成熟的。

相似文献

1
Transuranium organometallic chemistry.超铀有机金属化学。
Nat Rev Chem. 2025 Aug 13. doi: 10.1038/s41570-025-00732-4.
2
Prescription of Controlled Substances: Benefits and Risks管制药品的处方:益处与风险
3
The Lived Experience of Autistic Adults in Employment: A Systematic Search and Synthesis.成年自闭症患者的就业生活经历:系统检索与综述
Autism Adulthood. 2024 Dec 2;6(4):495-509. doi: 10.1089/aut.2022.0114. eCollection 2024 Dec.
4
Short-Term Memory Impairment短期记忆障碍
5
Sexual Harassment and Prevention Training性骚扰与预防培训
6
Health professionals' experience of teamwork education in acute hospital settings: a systematic review of qualitative literature.医疗专业人员在急症医院环境中团队合作教育的经验:对定性文献的系统综述
JBI Database System Rev Implement Rep. 2016 Apr;14(4):96-137. doi: 10.11124/JBISRIR-2016-1843.
7
The use of Open Dialogue in Trauma Informed Care services for mental health consumers and their family networks: A scoping review.创伤知情护理服务中使用开放对话模式为心理健康消费者及其家庭网络提供服务:范围综述。
J Psychiatr Ment Health Nurs. 2024 Aug;31(4):681-698. doi: 10.1111/jpm.13023. Epub 2024 Jan 17.
8
Survivor, family and professional experiences of psychosocial interventions for sexual abuse and violence: a qualitative evidence synthesis.性虐待和暴力的心理社会干预的幸存者、家庭和专业人员的经验:定性证据综合。
Cochrane Database Syst Rev. 2022 Oct 4;10(10):CD013648. doi: 10.1002/14651858.CD013648.pub2.
9
Access Points: Understanding Special Interests Through Autistic Narratives.切入点:通过自闭症患者的叙述理解特殊利益群体。
Autism Adulthood. 2025 Feb 5;7(1):100-111. doi: 10.1089/aut.2023.0157. eCollection 2025 Feb.
10
A Spectrum of Understanding: A Qualitative Exploration of Autistic Adults' Understandings and Perceptions of Friendship(s).理解的光谱:对自闭症成年人对友谊的理解与认知的质性探索
Autism Adulthood. 2024 Dec 2;6(4):438-450. doi: 10.1089/aut.2023.0051. eCollection 2024 Dec.

本文引用的文献

1
Berkelium-carbon bonding in a tetravalent berkelocene.四价锫茂中的锫-碳键合
Science. 2025 Feb 28;387(6737):974-978. doi: 10.1126/science.adr3346. Epub 2025 Feb 27.
2
Tetravalent Terbium Chelates: Stability Enhancement and Property Tuning.四价铽螯合物:稳定性增强与性能调控
Precis Chem. 2023 Oct 2;1(10):583-591. doi: 10.1021/prechem.3c00065. eCollection 2023 Dec 25.
3
Proton-Coupled Electron Transfer at the Pu Couple.钚电对处的质子耦合电子转移
J Am Chem Soc. 2024 Aug 7;146(31):21859-21867. doi: 10.1021/jacs.4c06319. Epub 2024 Jul 25.
4
Progress in Nonaqueous Molecular Uranium Chemistry: Where to Next?非水相分子铀化学的进展:下一步何去何从?
Inorg Chem. 2024 May 27;63(21):9366-9384. doi: 10.1021/acs.inorgchem.3c04533. Epub 2024 May 13.
5
A tetrahedral neptunium(V) complex.一种四面体钚(V)配合物。
Nat Chem. 2024 Sep;16(9):1490-1495. doi: 10.1038/s41557-024-01529-6. Epub 2024 May 6.
6
N-Heterocyclic Carbene to Actinide d-Based π-bonding Correlates with Observed Metal-Carbene Bond Length Shortening Versus Lanthanide Congeners.N-杂环卡宾与锕系元素基于d轨道的π键合与观察到的金属-卡宾键长相对于镧系同系物的缩短相关。
J Am Chem Soc. 2024 Apr 17;146(15):10367-10380. doi: 10.1021/jacs.3c12721. Epub 2024 Apr 3.
7
A tetravalent praseodymium complex with field-induced slow magnetic relaxation.一种具有场致慢磁弛豫的四价镨配合物。
Dalton Trans. 2024 Mar 26;53(13):5779-5783. doi: 10.1039/d4dt00052h.
8
Carbene Complexes of Plutonium: Structure, Bonding, and Divergent Reactivity to Lanthanide Analogs.钚的卡宾配合物:结构、键合及与镧系类似物的不同反应性
J Am Chem Soc. 2024 Feb 14;146(6):4098-4111. doi: 10.1021/jacs.3c12719. Epub 2024 Feb 1.
9
Substituent Positioning Effects on the Magnetic Properties of Sandwich-Type Erbium(III) Complexes with Bis(trimethylsilyl)-Substituted Cyclooctatetraenyl Ligands.取代基位置对含双(三甲基硅基)取代环辛四烯基配体的夹心型铒(III)配合物磁性的影响
Inorg Chem. 2024 May 27;63(21):9511-9519. doi: 10.1021/acs.inorgchem.3c03369. Epub 2023 Dec 22.
10
Synthesis and comparison of iso-structural f-block metal complexes (Ce, U, Np, Pu) featuring -arene interactions.具有芳基相互作用的等结构f区金属配合物(铈、铀、镎、钚)的合成与比较
Chem Sci. 2023 Jun 20;14(27):7438-7446. doi: 10.1039/d3sc02194g. eCollection 2023 Jul 12.