高値ニッケル (IV) オキシド複合体の一時的形成と反応性
Sandeep K Padamati1, Davide Angelone1,2, Apparao Draksharapu1
1Molecular Inorganic Chemistry, Stratingh Institute for Chemistry, Faculty of Science and Engineering, University of Groningen , Nijenborgh 4, 9747AG, Groningen, The Netherlands.
Journal of the American Chemical Society
|June 6, 2017
まとめ
研究者は,室温で形成された新しい二核ニッケル (IV) オキシドブリッジ複合体について報告しています. この高価ニッケル-酸素種は,選択的酸化反応における塩化ナトリウム反応性を制御するための新しい可能性を提供します.
科学分野:
- 無機化学
- 有機金属化学
- カタリシス
背景:
- 高価金属オクソ種は酸化触媒における重要な中間物質である.
- 二核の高価ニッケル複合体の安定化と特徴付けは大きな課題を提示しています.
- Ni ((IV) O種の電子的および構造的性質を理解することは,それらの触媒的可能性を解き放つための鍵です.
研究 の 目的:
- 新型反応性高い二核ニッケル (IV) オキシドブリッジ複合体を合成し,特徴づけること.
- Ni ((IV) O種の構造的および電子的性質を調査する.
- 選択的酸化のための有機基質とのこの複合体の反応性を調査する.
主な方法:
- 二核ニッケル (IV) オキシドブリッジ複合体と塩化ナトリウムとの反応による合成
- 紫外線吸収,共振ラーマン,1H NMR,EPR,X線吸収スペクトロスコーピーを用いた構造と電子的特徴付け.
- 密度関数理論 (DFT) の方法とESI質量スペクトロメトリを用いた計算分析.
主要な成果:
- 安定した二核ニッケル (IV) オキシドブリッジ複合体,L2Ni (IV) 2 (μ-O) 3+が室温で形成される.
- 詳細な構造とスペクトル学的な証拠は,Ni (IV) -O結合と二核核を確認します.
- 有機基質との反応性の実証,選択的酸化の可能性を示す.
結論:
- 高値二核ニッケル (IV) オキシドブリッジ複合体の成功合成と特徴付け
- このNi ((IV) O種は,基本的な反応性を研究し,新しい触媒酸化方法を開発するためのプラットフォームを提供します.
- 選択的有機変異における制御された塩化ナトリウム反応性への道を開く.
関連する概念動画
Formation of Complex Ions
26.5K
A type of Lewis acid-base chemistry involves the formation of a complex ion (or a coordination complex) comprising a central atom, typically a transition metal cation, surrounded by ions or molecules called ligands. These ligands can be neutral molecules like H2O or NH3, or ions such as CN− or OH−. Often, the ligands act as Lewis bases, donating a pair of electrons to the central atom. These types of Lewis acid-base reactions are examples of a broad subdiscipline called coordination...
26.5K
Properties of Transition Metals
30.3K
Transition metals are defined as those elements that have partially filled d orbitals. As shown in Figure 1, the d-block elements in groups 3–12 are transition elements. The f-block elements, also called inner transition metals (the lanthanides and actinides), also meet this criterion because the d orbital is partially occupied before the f orbitals.
30.3K
Valence Bond Theory
11.4K
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...
11.4K
Complexation Equilibria: Factors Influencing Stability of Complexes
890
In complexation reactions, metal cations are the electron pair acceptors, and the ligands are the electron pair donors. The stability of the metal complexes depends primarily on the complexing ability of the central metal ion and the nature of the ligands. Generally, the complexing ability of the metal ion depends on the size and charge of the ion. As the metal ion size increases, the stability of the metal complexes decreases, provided that the valency of the metal ion and the ligands remain...
890
Ionic Bonding and Electron Transfer
51.6K
Ions are atoms or molecules bearing an electrical charge. A cation (a positive ion) forms when a neutral atom loses one or more electrons from its valence shell, and an anion (a negative ion) forms when a neutral atom gains one or more electrons in its valence shell. Compounds composed of ions are called ionic compounds (or salts), and their constituent ions are held together by ionic bonds: electrostatic forces of attraction between oppositely charged cations and anions.
51.6K
Coordination Number and Geometry
19.3K
For transition metal complexes, the coordination number determines the geometry around the central metal ion. Table 1 compares coordination numbers to molecular geometry. The most common structures of the complexes in coordination compounds are octahedral, tetrahedral, and square planar.
19.3K


