Related Experiment Video
Updated: Aug 16, 2026

Facile Preparation of Ultrafine Aluminum Hydroxide Particles with or without Mesoporous MCM-41 in Ambient Environments
Published on: May 11, 2017
Chemistry of aluminium(I)
Herbert W Roesky1, S Shravan Kumar
1Institut für Anorganische Chemie der Georg-August-Universität Göttingen, Tammannstrasse 4, D-37077, Göttingen, Germany. hroesky@gwdg.de
Abstract:
In this article, we discuss the synthesis of tetrameric and monomeric aluminium(I) compounds. These compounds are prepared by reduction of the respective Al-X (X = halide) bond containing precursor. The tetrameric aluminium(I) compounds are synthesized by using sterically bulky ligands whereas a stable monomeric aluminium(I) compound is obtained using a monovalent chelating ligand. Theoretical studies are carried out on the monomer to understand the Lewis basicity. The presence of a lone pair of electrons plays an important role in the preparation of aluminium containing heterocyclic compounds, main group-main group and transition metal-main group compounds having donor-acceptor bonds by carrying out reactions with unsaturated compounds and Lewis acids.
Related Concept Videos
Acid Halides to Alcohols: LiAlH4 Reduction
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...
Alkali Metals
Table 1: Properties of the alkali metals
Ionic Bonding and Electron Transfer
Metallic Solids
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and malleability. Many...
Electron Configuration of Multielectron Atoms
Electrophilic Addition to Alkynes: Halogenation
Halogenation is another class of electrophilic addition reactions where a halogen molecule gets added across a π bond. In alkynes, the presence of two π bonds allows for the addition of two equivalents of halogens (bromine or chlorine). The addition of the first halogen molecule forms a trans-dihaloalkene as the major product and the cis isomer as the minor product. Subsequent addition of the second equivalent yields the tetrahalide.
