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相关概念视频

Valence Bond Theory02:42

Valence Bond Theory

10.3K
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...
10.3K
Complexation Equilibria: The Chelate Effect01:19

Complexation Equilibria: The Chelate Effect

902
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...
902
Reduction of Alkynes to trans-Alkenes: Sodium in Liquid Ammonia02:10

Reduction of Alkynes to trans-Alkenes: Sodium in Liquid Ammonia

10.1K
Alkynes can be reduced to trans-alkenes using sodium or lithium in liquid ammonia. The reaction, known as dissolving metal reduction, proceeds with an anti addition of hydrogen across the carbon–carbon triple bond to form the trans product. Since ammonia exists as a gas (bp = −33°C) at room temperature, the reaction is carried out at low temperatures using a mixture of dry ice (sublimes at −78°C) and acetone. 
When dissolved in liquid ammonia, an alkali metal, such as sodium,...
10.1K
Metal-Ligand Bonds02:51

Metal-Ligand Bonds

23.0K
The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
23.0K
Post-translational Translocation of Proteins to the RER01:27

Post-translational Translocation of Proteins to the RER

7.0K
A sizable fraction of proteins destined for ER are first synthesized in the cell cytosol and then transported across the ER membrane–a process called post-translational translocation. Similar to cotranslationally translocated proteins, these proteins also use the Sec translocon complex to enter the ER lumen.
Targeting proteins to the ER
Hsp40 and Hsp70 chaperone molecules bind the translated proteins in the cytosol to prevent their folding. The chaperone binding helps to keep the signal...
7.0K
Alkenes via Reductive Coupling of Aldehydes or Ketones: McMurry Reaction01:22

Alkenes via Reductive Coupling of Aldehydes or Ketones: McMurry Reaction

2.2K
The radical dimerization of ketones or aldehydes gives vicinal diols through a pinacol coupling reaction. However, the behavior of titanium metals used for the reaction as a source of electrons is unusual. When the reaction is carried out in the presence of titanium, diols can be isolated at low temperatures. Else titanium further reacts with diols, forming alkenes through the McMurry reaction.
2.2K

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相关实验视频

Updated: Nov 27, 2025

Line Shape Analysis of Dynamic NMR Spectra for Characterizing Coordination Sphere Rearrangements at a Chiral Rhenium Polyhydride Complex
10:52

Line Shape Analysis of Dynamic NMR Spectra for Characterizing Coordination Sphere Rearrangements at a Chiral Rhenium Polyhydride Complex

Published on: July 27, 2022

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在Rh复合体内发生意想不到的B/Al转移

Qingheng Lai1, Nattamai Bhuvanesh1, Oleg V Ozerov1

  • 1Department of Chemistry, Texas A&M University, 3255 TAMU, College Station, Texas 77842, United States.

Journal of the American Chemical Society
|December 2, 2020
PubMed
概括

研究人员用或中心合成了钉复合物. 在试图修改位时发生了意想不到的B/Al转化,产生复合物.

科学领域:

  • 有机金属化学
  • 协调化学
  • 主要组化学

背景情况:

  • 由于它们的三角协调, 复合体具有独特的反应性.
  • 和分别是主要组和有机金属化学中的关键元素.
  • 了解低坐标主组元素的稳定性和反应性至关重要.

研究的目的:

  • 合成和描述具有 bis (N-pyrrolyl) aluminyl (PAlP) 和 boryl (PBP) 单元的新型复合物.
  • 研究PAlP复合体中的基位点的反应性.
  • 探索在框架内访问三坐标中心的方法.

主要方法:

  • 合成PAlP和PBP二复合物
  • 在 (PAlpyP) Rh(CO) 2中稳定的协调.
  • 使用BF3·Et2O和B(C6F5) 3进行易斯酸介导的化反应.

主要成果:

  • 通过胺稳定四坐标中心成功合成 (PAlpyP) Rh ((CO) 2.
  • 在用BF3·Et2O治疗时发生了意想不到的B/ Al转移,形成了 (PBP) Rh (CO) 2复合体,同时保留了子结构.

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  • 试图用B(C6F5) 3抽取皮里丁,通过同碳酸桥接导致PAlP复合物的二元化.
  • 结论:

    • 皮里丁的协调有效地稳定了复合体中的四坐标位.
    • 易斯酸介导反应可以诱导意想不到的B/Al转化,为烯复合物提供替代途径.
    • 基复合物的反应性对抽象剂敏感,在某些条件下导致二元化.