Related Experiment Video
Updated: Apr 3, 2026

13:58
Probing C84-embedded Si Substrate Using Scanning Probe Microscopy and Molecular Dynamics
Published on: September 28, 2016
12.3K
Preparation, Structural Determination, and Characterization of Electronic Properties of Bis-Silylated and
Masahiro Kako1, Kyosuke Miyabe2, Kumiko Sato3
1Department of Engineering Science, The University of Electro-Communications, Chofu 182-8585 (Japan). kako@e-one.uec.ac.jp.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|September 22, 2015
Abstract
No abstract available in PubMed .
More Related Videos
Related Concept Videos
Preparation and Reactions of Sulfides
6.0K
Sulfides are the sulfur analog of ethers, just as thiols are the sulfur analog of alcohol. Like ethers, sulfides also consist of two hydrocarbon groups bonded to the central sulfur atom. Depending upon the type of groups present, sulfides can be symmetrical or asymmetrical. Symmetrical sulfides can be prepared via an SN2 reaction between 2 equivalents of an alkyl halide and one equivalent of sodium sulfide.
6.0K
Predicting Molecular Geometry
47.1K
VSEPR Theory for Determination of Electron Pair Geometries
47.1K
Chirality at Nitrogen, Phosphorus, and Sulfur
7.5K
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...
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
7.5K

