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类金属铝和镓簇合物:分子尺度上的元素修饰?

Metalloid aluminum and gallium clusters: element modifications on the molecular scale?

作者信息

Schnepf Andreas, Schnöckel Hansgeorg

机构信息

Institut für Anorganische Chemie Universität Karlsruhe TH Engesserstrasse, Geb.30.45, 76128 Karlsruhe, Germany.

出版信息

Angew Chem Int Ed Engl. 2002 Oct 4;41(19):3532-52, 3511. doi: 10.1002/1521-3773(20021004)41:19<3532::AID-ANIE3532>3.0.CO;2-4.

Abstract

As members of the same group in the periodic table, the industrially significant elements aluminum and gallium exhibit strong similarities in the majority of their compounds. In contrast there are significant differences in the structures of the two elemental forms: Aluminum forms a typical closest-packed metallic structure whereas gallium demonstrates a diversity of molecular bonding principles in its seven structural modifications. It can therefore be expected that differences between Al and Ga compounds will arise when, as for the elemental forms, many metal-metal bonds are formed. To synthesize such cluster compounds, we have developed the following synthesis procedure: Starting from gaseous monohalides at around 1000 degrees C, metastable solutions are generated from which the elements ultimately precipitate by means of a disproportionation reaction at room temperature. On the way to the elemental forms, molecular Al and Ga cluster compounds can be obtained by selection of suitable ligands (protecting groups), in which a core of Al or Ga atoms are protected from the formation of the solid element by a ligand shell. Since the arrangement of atoms in such clusters corresponds to that in the elements, we have designated these clusters as metalloid or elementoid. In accordance with the Greek word [see text] (ideal, prototype), the atomic arrangement in metalloid clusters represents the prototypic or ideal atomic arrangement in the elements at the molecular level. The largest clusters of this type contain 77 Al or 84 Ga atoms and have diameters of up to two nanometers. They hold the world record with respect to the naked metal-atom core for structurally characterized metalloid clusters.

摘要

作为元素周期表中同一族的成员,具有工业重要性的元素铝和镓在其大多数化合物中表现出很强的相似性。相比之下,这两种单质形式的结构存在显著差异:铝形成典型的密堆积金属结构,而镓在其七种结构变体中展现出多种分子键合原理。因此可以预期,如同单质形式那样,当形成许多金属 - 金属键时,铝和镓的化合物之间会出现差异。为了合成这类簇合物,我们开发了以下合成方法:从约1000摄氏度的气态单卤化物开始,生成亚稳溶液,元素最终通过室温下的歧化反应从该溶液中沉淀出来。在形成单质形式的过程中,通过选择合适的配体(保护基团)可以获得分子铝和镓簇合物,其中铝或镓原子的核心被配体壳层保护,避免形成固态元素。由于这类簇合物中的原子排列与元素中的原子排列相对应,我们将这些簇合物称为类金属或类元素。根据希腊词[见原文](理想的、原型),类金属簇合物中的原子排列代表了元素在分子水平上的原型或理想原子排列。这类最大的簇合物包含77个铝原子或84个镓原子,直径可达两纳米。就结构表征的类金属簇合物的裸金属原子核心而言,它们保持着世界纪录。

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