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Electron Configuration of Multielectron Atoms03:26

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The alkali metal sodium (atomic number 11) has one more electron than the neon atom. This electron must go into the lowest-energy subshell available, the 3s orbital, giving a 1s22s22p63s1 configuration. The electrons occupying the outermost shell orbital(s) (highest value of n) are called valence electrons, and those occupying the inner shell orbitals are called core electrons. Since the core electron shells correspond to noble gas electron configurations, we can abbreviate electron...
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Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
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Coordination compounds and complexes exhibit different colors, geometries, and magnetic behavior, depending on the metal atom/ion and ligands from which they are composed. In an attempt to explain the bonding and structure of coordination complexes, Linus Pauling proposed the valence bond theory, or VBT, using the concepts of hybridization and the overlapping of the atomic orbitals. According to VBT, the central metal atom or ion (Lewis acid) hybridizes to provide empty orbitals of suitable...
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Isomerism in Complexes
Isomers are different chemical species that have the same chemical formula.
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In complexation reactions, metal atoms or cations interact with ligands to form donor-acceptor adducts called metal complexes. Ligands that bind through one donor site are monodentate, ligands with two donor sites are bidentate, and those with more than two donor sites are polydentate ligands. For example, ethylene diamine is a bidentate ligand that binds through two nitrogen donor atoms, forming a five-membered ring. EDTA is a polydentate ligand that binds through four oxygen and two nitrogen...
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Combining Solid-state and Solution-based Techniques: Synthesis and Reactivity of ChalcogenidoplumbatesII or IV
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(IV) 复合物

Ning Wang1, Xiaoyu Li2, Hui Guo3

  • 1Spin-X Institute, School of Chemistry and Chemical Engineering, State Key Laboratory of Luminescent Materials and Devices, South China University of Technology, Guangzhou 510641, China.

Journal of the American Chemical Society
|December 9, 2025
PubMed
概括
此摘要是机器生成的。

研究人员合成了第一个四价酸复合物,其中包括 (IV) 和. 这些复合物表现出独特的结合和反应性,进步有机金属化学.

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科学领域:

  • 有机金属化学
  • 兰化物化学
  • 无机化学

背景情况:

  • 四价合物复合物的发展落后于三价合物.
  • 在稳定不寻常的氧化状态方面,酸对象至关重要.

研究的目的:

  • 合成和描述第一个四价酸复合物.
  • 研究这些新型复合物的电子结构和结合.
  • 探索这些化合物的初步反应性.

主要方法:

  • [ImtBuN) 3CeIVP (SiMe3) Ar]复合物的合成.
  • 单晶X射线衍射用于结构特征.
  • 计算研究 (DFT) 来分析结合.
  • 使用亚化物和二化合物的初步反应性研究.

主要成果:

  • 成功合成和结构特征两个四价复合物.
  • 观察到不同的几何形状 (金字塔形与三角形平面形) 和Ce-P键特性.
  • 计算分析显示了对Ce-P σ和π键的显著f-轨道贡献.
  • 复合物1显示添加反应,而不是氧化还原过程,与测试试剂.

结论:

  • 建立了第一个四价酸复合物.
  • 证明了联体环境对Ce-P结合和几何学的影响.
  • 突出了f轨道参与结合的重要性.
  • 表示与氧化还原行为不同的独特反应模式.