硫酸性金属有機構造物の超酸性-808
Juncong Jiang1, Felipe Gándara, Yue-Biao Zhang
1Department of Chemistry, University of California, Berkeley and Kavli Energy NanoSciences Institute at Berkeley , Berkeley, California 94720, United States.
Journal of the American Chemical Society
|August 27, 2014
まとめ
研究者らは,硫化金属有機フレームワーク (MOF) を使用した新しい固体超酸を開発しました. この新しいMOF素材は,例外的な酸性を示し,高度な触媒応用への道を切り開いています.
科学分野:
- 材料科学 材料科学とは
- 化学 化学は化学です.
- カタリシス カタリシス カタリシス
背景:
- 超酸性物質は,ハメット酸性関数 (H0) ≤ -12.12 を持つ高度に酸性物質である.
- 固体超酸は,液体酸よりも利点がありますが,新しい設計可能なシステムが必要です.
- メタル・オーガニック・フレームワーク (MOF) は,調節可能な構造を持つ多用途の多孔性材料です.
研究 の 目的:
- メタル・オーガニック・フレームワーク (MOF) に基づく新しい固体スーパーアシドを合成し,特徴づけること.
- 硫化MOFの超酸性材料としての可能性を調査する.
- MOF構造における超酸性の最初の証拠を提供すること.
主な方法:
- MOF-808-Pを硫酸で処理することによって硫化金属有機基板 (MOF-808-2.5SO4) の合成.
- ハメット酸性関数 (H0) を用いて材料の酸性の特徴づけ.
- シングルクリスタルX線 difraktion分析を用いた構造解明.
主要な成果:
- 硫化MOF,MOF-808-2.5SO4は,ハメット酸性関数 (H0) ≤-14.5.5のハメット酸性関数を示した.
- この酸度レベルは,材料が超酸性であることを確認します.
- 単結晶X線 difraktionは,超酸性の源としてジルコニウム結合硫酸塩基を特定しました.
結論:
- この研究は,金属有機フレームワーク (MOF) の超酸性の最初の事例を報告しています.
- 硫酸性MOFは,指定可能な固体超酸性物質の新しいクラスを表しています.
- これらの発見は,先進的な固体酸触媒の開発への道を開く.
さらに関連する動画
関連する概念動画
Acid Strength and Molecular Structure
25.9K
Binary Acids and Bases
In the absence of any leveling effect, the acid strength of binary compounds of hydrogen with nonmetals (A) increases as the H-A bond strength decreases down a group in the periodic table. For group 17, the order of increasing acidity is HF < HCl < HBr < HI. Likewise, for group 16, the order of increasing acid strength is H2O < H2S < H2Se < H2Te. Across a row in the periodic table, the acid strength of binary hydrogen compounds increases with...
In the absence of any leveling effect, the acid strength of binary compounds of hydrogen with nonmetals (A) increases as the H-A bond strength decreases down a group in the periodic table. For group 17, the order of increasing acidity is HF < HCl < HBr < HI. Likewise, for group 16, the order of increasing acid strength is H2O < H2S < H2Se < H2Te. Across a row in the periodic table, the acid strength of binary hydrogen compounds increases with...
25.9K
Crystal Field Theory - Octahedral Complexes
28.4K
Crystal Field Theory
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
28.4K
Ionic Crystal Structures
17.9K
Ionic crystals consist of two or more different kinds of ions that usually have different sizes. The packing of these ions into a crystal structure is more complex than the packing of metal atoms that are the same size.
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
17.9K
Metal-Ligand Bonds
19.2K
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...
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...
19.2K
Formation of Complex Ions
18.8K
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...
18.8K
Molecular Structure and Acidity
14.9K
An acid can be deprotonated to form a conjugate base or an anion. If the produced anion is more stable, then the acid is stronger. On the contrary, if the anion is unstable, then the acid is weaker. Hence, to determine the acidity of the compound, the stability of its conjugate base is studied using various factors.
The size effect explains the change in atomic size on acidity. When comparing the acids formed from elements that belong to the same column in the periodic table, their atomic sizes...
The size effect explains the change in atomic size on acidity. When comparing the acids formed from elements that belong to the same column in the periodic table, their atomic sizes...
14.9K


