一种具有强烈铁磁相互作用的稳定基基替代基离子: 5,10-二-5,10-二氨酸替代 5,10-二烯-5,10-二氨酸基离子
Shinsuke Hiraoka1, Toshihiro Okamoto, Masatoshi Kozaki
1Departments of Chemistry and Materials Science, Graduate School of Science, Osaka City University, Sugimoto, Sumiyoshi-ku, Osaka 558-8585, Japan.
Journal of the American Chemical Society
|January 8, 2004
概括
研究人员开发了一种稳定的基质替代基离子,这是有机磁铁的关键组成部分. 这种新材料具有强烈的铁磁相互作用,为先进的磁性应用铺平了道路.
科学领域:
- 有机化学 有机化学
- 材料科学是一种材料科学.
- 磁力学 磁力学 是一种
背景情况:
- 有机磁铁对于它们的潜在应用是可取的.
- 开发具有强大的分子内相互作用的稳定旋转构建块至关重要.
研究的目的:
- 合成和描述一种具有铁磁性质的新型基质替代基离子.
- 为了评估其稳定性和磁相互作用强度,以便在有机磁铁中潜在使用.
主要方法:
- 制备2 - 尼特罗尼尔氧化物替代的5,10 - 双-5,10 - 双氨酸基离子 (1+).
- 在环境条件下评估化合物的稳定性.
- 分子内铁磁相互作用的量化 (J/kB).
主要成果:
- 成功合成了一种稳定的根基替代的基离子,标记为1+.
- 该化合物在室温的空气条件下表现出稳定性.
- 观察到一个显著的铁磁内分子相互作用 (J/kB) 超过+700K.
结论:
- 合成的基离子是有机磁体的一个有希望的构建块.
- 它的稳定性和强烈的铁磁合使其对开发新的磁性材料具有吸引力.
相关概念视频
Acid/Base Strengths and Dissociation Constants
The relative strength of an acid or base is the extent to which it ionizes when dissolved in water. If the ionization reaction is essentially complete, the acid or base is termed strong; if relatively little ionization occurs, the acid or base is weak. There are many more weak acids and bases than strong ones. The most common strong acids and bases are listed below:
Relative Strengths of Conjugate Acid-Base Pairs
Brønsted-Lowry acid-base chemistry is the transfer of protons; thus, logic suggests a relation between the relative strengths of conjugate acid-base pairs. The strength of an acid or base is quantified in its ionization constant, Ka or Kb, which represents the extent of the acid or base ionization reaction. For the conjugate acid-base pair HA / A−, the ionization equilibrium equations and ionization constant expressions are
Lewis Acids and Bases
In 1923, G. N. Lewis proposed a generalized definition of acid-base behavior in which acids and bases are identified by their ability to accept or to donate a pair of electrons and form a coordinate covalent bond.
A coordinate covalent bond (or dative bond) occurs when one of the atoms in the bond provides both bonding electrons. For example, a coordinate covalent bond occurs when a water molecule combines with a hydrogen ion to form a hydronium ion. A coordinate covalent bond also results when...
A coordinate covalent bond (or dative bond) occurs when one of the atoms in the bond provides both bonding electrons. For example, a coordinate covalent bond occurs when a water molecule combines with a hydrogen ion to form a hydronium ion. A coordinate covalent bond also results when...
Lewis Acids and Bases
This lesson delves into Lewis acids and bases in the context of the octet rule for electron-deficient compounds. Here, the concept is discussed, emphasizing the group 13 elements like boron or aluminium. Since group 13 elements possess three valence electrons, they form trivalent compounds with a sextet of electrons and a vacant orbital for the central atom. Consequently, these electron-deficient compounds accept electrons from other species to complete their octet in a chemical reaction. They...
Nucleophiles
The word “nucleophile” has a Greek root and translates to nucleus-loving. Nucleophiles are either negatively charged or neutral species with a pair of electrons in a high-energy occupied molecular orbital (HOMO). As these species tend to donate electron pairs, nucleophiles are considered Lewis bases as well. Negatively charged species, like OH−, Cl−, or HS−, with one or several pairs of electrons, are typically nucleophiles. Similarly, neutral species such as ammonia, amines, water, and alcohol...
Relative Reactivity of Carboxylic Acid Derivatives
Carboxylic acid derivatives such as acid halides, anhydrides, esters, and amides undergo nucleophilic acyl substitution reactions with varying degrees of reactivity.
A key factor in assessing the reactivity of the acid derivatives is the basicity of the substituent or the leaving group. The lower the basicity of the leaving group, the higher the reactivity of the derivative. The basicity of the leaving group follows this order:
Halide ions < Acyloxy ions < Alkoxy ions < Amine ions
A key factor in assessing the reactivity of the acid derivatives is the basicity of the substituent or the leaving group. The lower the basicity of the leaving group, the higher the reactivity of the derivative. The basicity of the leaving group follows this order:
Halide ions < Acyloxy ions < Alkoxy ions < Amine ions


