三金属化物内体金属烯的对称衍生物,Sc3N@C80
Erick B Iezzi1, James C Duchamp, Kim Harich
1Department of Chemistry, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061, USA.
Journal of the American Chemical Society
|January 24, 2002
概括
研究人员创建了第一个功能化的三金属化模板 (TNT) 内体金属烯衍生物. 这种新型的Sc3N@C80化合物是使用先进的光谱技术合成和表征的.
科学领域:
- * 富勒烯化学 富勒烯化学
- * 超分子化学 超分子化学
- * 材料科学 材料科学
背景情况:
- * 内膜金属烯 (EMF) 是封装金属离子或的烯.
- *三金属化物模板 (TNT) 电磁场,像Sc3N@C80一样,具有独特的电子和结构性质.
- * 电磁场的功能化对于将其属性定制为特定应用至关重要.
研究的目的:
- * 合成TNT内体金属烯的第一个功能化衍生物.
- * 描述新型功能化的电磁场的结构和特性.
主要方法:
- * Sc3N@C80与6,7-dimethoxyisochroman-3-one (13C标记) 的反应.
- *使用高性能液态染色学 (HPLC) 净化反应混合物.
- *使用1HNMR,13CNMR和MALDI-TOF质谱法对纯化单吸管进行表征.
主要成果:
- *成功合成了Sc3N@C80.0的13C标记单添加物.
- * 反应主要产生单个单添加物产物.
- * 结构分析表明,衍生发生在Sc3N@C80的[5,6]环结处.
结论:
- * 该研究报告了第一个成功的功能化三金属化物模板内体金属烯.
- * 一种新型对称单通道被合成和特征化.
- *这些发现为进一步探索和应用功能化的TNT电磁场开辟了道路.
相关概念视频
Metallic Solids
Metallic solids such as crystals of copper, aluminum, and iron are formed by metal atoms. The structure of metallic crystals is often described as a uniform distribution of atomic nuclei within a “sea” of delocalized electrons. The atoms within such a metallic solid are held together by a unique force known as metallic bonding that gives rise to many useful and varied bulk properties.
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and malleability. Many...
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and malleability. Many...
Coordination Compounds and Nomenclature
In most main group element compounds, the valence electrons of the isolated atoms combine to form chemical bonds that satisfy the octet rule. For instance, the four valence electrons of carbon overlap with electrons from four hydrogen atoms to form CH4. The one valence electron leaves sodium and adds to the seven valence electrons of chlorine to form the ionic formula unit NaCl (Figure 1a). Transition metals do not normally bond in this fashion. They primarily form coordinate covalent bonds, a...
Structural Isomerism
Isomerism in Complexes
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can be...
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can be...
Valence Bond Theory
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...
Chirality at Nitrogen, Phosphorus, and Sulfur
Chirality is most prevalent in carbon-based tetrahedral compounds, but this important facet of molecular symmetry extends to sp3-hybridized nitrogen, phosphorus and sulfur centers, including trivalent molecules with lone pairs. Here, the lone pair behaves as a functional group in addition to the other three substituents to form an analogous tetrahedral center that can be chiral.
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
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Properties of Organometallic Compounds
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