Jove
Visualize
お問い合わせ
JoVE
x logofacebook logolinkedin logoyoutube logo
JoVEについて
概要リーダーシップブログJoVEヘルプセンター
著者向け
出版プロセス編集委員会範囲と方針査読よくある質問投稿
図書館員向け
推薦の声購読アクセスリソース図書館諮問委員会よくある質問
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experimentsアーカイブ
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教員リソースセンター教員サイト
利用規約
プライバシーポリシー
ポリシー

関連する概念動画

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

こちらも読む

関連記事

共著者、ジャーナル、引用グラフによってこの研究に関連する記事。

並び替え
Same author

Flash Communication: A Metal-First Approach to Ruthenium Complexes of a Boryl-Centered POBOP Pincer Ligand.

Organometallics·2026
Same author

A Thiosemicarbazone-Derived Fluorescent Probe for the Detection of Silver Ions and Bioimaging Application.

Journal of fluorescence·2026
Same author

Synthesis of sulfanyl derivatives of 1,2,4-triazoles <i>via</i> an acid catalyzed intramolecular cyclization of isothiosemicarbazones: structural characterization, <i>E</i>/<i>Z</i> isomerism, mechanistic insights and <i>in vitro</i> cytotoxicity.

RSC advances·2026
Same author

Fluoride ion chelation <i>via</i> pnictogen bonding using a distibora[1.1]ferrocenophane.

Chemical communications (Cambridge, England)·2026
Same author

Rational Design of Enzyme-Responsive Fluorescent Organoruthenium Prodrug for Real-Time Tracking of Cargo Release and Cytotoxicity.

Inorganic chemistry·2026
Same author

Structural and Electronic Complexities of a Sulfur-Bridged Di-Iron Complex Composed of Mono- and Di-Nitrosyl Units.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2025

関連する実験動画

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

3.1K

予期せぬB/Alトランセレメント Rhピンサー複合体内

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
まとめ

研究者はアルミニウムやボロン中心でロジウムピンチャー複合体を合成した. 予期せぬB/Al転移は,アルミニウム部位を改変しようとすると発生し,代わりにボロン複合体を生成した.

科学分野:

  • 有機金属化学
  • 協調化学
  • メイングループ 化学

背景:

  • ピンサー複合体は,その三角調節により,ユニークな反応性を提供します.
  • アルミニウムとボロンは,それぞれメイングループと有機金属化学の重要な元素です.
  • 低座標の主なグループ要素の安定化と反応性を理解することは極めて重要です.

研究 の 目的:

  • bis (N-ピロリル) アルミニル (PAlP) とボリル (PBP) ユニットを含む新しいロジウムピンカー複合体を合成し,特徴づけること.
  • PAlPロジウム複合体のアルミニル部位の反応性を調査する.
  • 3つの座標のアルミニウムセンターへのアクセス方法を探求する.

主な方法:

  • PAlPとPBPロジウムジカルボニル複合体の合成
  • (PAlpyP) Rh(CO) 2におけるアルミニル部位を安定させるためのピリジンの調整.
  • BF3·Et2OとB(C6F5) 3を用いたルイス酸媒介のピリジン抽出を含む反応.

主要な成果:

  • ピリジンによって安定した4座標のアルミニウム中心で (PAlpyP) Rh ((CO) 2の合成が成功しました.

さらに関連する動画

Author Spotlight: Evaluating Biophysical Assays for Characterizing PROTACS Ternary Complexes
07:22

Author Spotlight: Evaluating Biophysical Assays for Characterizing PROTACS Ternary Complexes

Published on: January 12, 2024

4.1K
Isolation of Cognate RNA-protein Complexes from Cells Using Oligonucleotide-directed Elution
10:53

Isolation of Cognate RNA-protein Complexes from Cells Using Oligonucleotide-directed Elution

Published on: January 16, 2017

9.3K

関連する実験動画

Last 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

3.1K
Author Spotlight: Evaluating Biophysical Assays for Characterizing PROTACS Ternary Complexes
07:22

Author Spotlight: Evaluating Biophysical Assays for Characterizing PROTACS Ternary Complexes

Published on: January 12, 2024

4.1K
Isolation of Cognate RNA-protein Complexes from Cells Using Oligonucleotide-directed Elution
10:53

Isolation of Cognate RNA-protein Complexes from Cells Using Oligonucleotide-directed Elution

Published on: January 16, 2017

9.3K
  • BF3·Et2Oで治療した際に予期せぬB/ Al転移が起こり, (PBP) RhCO2複合体を形成し,ピンサー構造を保ちました.
  • B ((C6F5) 3を用いたピリジン抽出の試みは,イソカルボニルブリッジングによるPAlP複合体の二元化につながった.
  • 結論:

    • ピリジンの調整は,ロジウムピンサー複合体の4座標アルミニルサイトを安定させるのに有効である.
    • ルイス酸媒介反応は予期せぬB/Al転移を引き起こし,ボリル複合体に対する代替経路を提供する.
    • アルミニルピンサー複合体の反応性は抽出剤に敏感であり,特定の条件下で二分化につながる.