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Related Concept Videos

[3,3] Sigmatropic Rearrangement of 1,5-Dienes: Cope Rearrangement01:21

[3,3] Sigmatropic Rearrangement of 1,5-Dienes: Cope Rearrangement

The Cope rearrangement is classified as a [3,3] sigmatropic shift in 1,5-dienes, leading to a more stable, isomeric 1,5-diene. The reaction involves a concerted movement of six electrons, four from two π bonds and two from a σ bond, via an energetically favorable chair-like transition state.
The Aufbau Principle and Hund's Rule03:02

The Aufbau Principle and Hund's Rule

To determine the electron configuration for any particular atom, we can build the structures in the order of atomic numbers. Beginning with hydrogen, and continuing across the periods of the periodic table, we add one proton at a time to the nucleus and one electron to the proper subshell until we have described the electron configurations of all the elements. This procedure is called the aufbau principle, from the German word aufbau (“to build up”). Each added electron occupies the subshell of...
The Seven Crystal Systems: Overview01:24

The Seven Crystal Systems: Overview

Crystals with various point group symmetries belong to different crystal classes, which are synonymous terms. Despite being in the same class, crystals may have distinct shapes, like cubes and octahedra. There are 32 three-dimensional point groups, all of which are systematically divided into seven crystal systems.The basic cubic crystal system, exemplified by NaCl, features orthogonal vectors (α = β = �� = 90°) of equal lengths (a = b = c). When specific requirements are not imposed on the...
Hückel's Rule Diagram of π MOs: Frost Circle01:08

Hückel's Rule Diagram of π MOs: Frost Circle

The Frost circle or the inscribed polygon method is a graphical method for determining the relative energies of π molecular orbitals (MOs) for planar, fully conjugated, and monocyclic compounds. This method was first described by A. A. Frost and Boris Musulin in 1953.
A Frost circle is constructed by drawing a polygon whose number of edges is equal to the number of carbons of the given cyclic system, with one of the vertices pointing down. Then, a circle is drawn enclosing the polygon so that...
Structural Isomerism02:34

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...
[3,3] Sigmatropic Rearrangement of Allyl Vinyl Ethers: Claisen Rearrangement01:24

[3,3] Sigmatropic Rearrangement of Allyl Vinyl Ethers: Claisen Rearrangement

The Claisen rearrangement is a [3,3] sigmatropic rearrangement of allyl vinyl ethers to unsaturated carbonyl compounds. The rearrangement is a concerted pericyclic reaction proceeding via a chair-like transition state.

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Related Experiment Video

Updated: Jun 1, 2026

Ultrahigh Density Array of Vertically Aligned Small-molecular Organic Nanowires on Arbitrary Substrates
08:07

Ultrahigh Density Array of Vertically Aligned Small-molecular Organic Nanowires on Arbitrary Substrates

Published on: June 18, 2013

Templating an organic array with Si(111)-7×7.

Alfred J Weymouth1, Roberto H Miwa, Graham J A Edge

  • 1Department of Physics, Engineering Physics & Astronomy, Queen's University, Kingston, Ontario, Canada K7L 3N6.

Chemical Communications (Cambridge, England)
|June 14, 2011
PubMed
Summary
This summary is machine-generated.

Steric hindrance prevents molecules from adsorbing near each other on silicon surfaces. This allows for the creation of ordered organic layers directly on the silicon surface reconstruction.

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Last Updated: Jun 1, 2026

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Probing C84-embedded Si Substrate Using Scanning Probe Microscopy and Molecular Dynamics
13:58

Probing C84-embedded Si Substrate Using Scanning Probe Microscopy and Molecular Dynamics

Published on: September 28, 2016

Area of Science:

  • Surface Science
  • Materials Chemistry
  • Nanotechnology

Background:

  • The silicon (111)-7×7 surface reconstruction presents unique adsorption sites.
  • Understanding molecular adsorption is crucial for surface functionalization and nanomaterial design.

Purpose of the Study:

  • To investigate the steric effects on molecular adsorption on the Si(111)-7×7 surface.
  • To explore the possibility of templating ordered organic layers on this surface.

Main Methods:

  • Simulations and experimental techniques were used to study molecular adsorption.
  • Analysis focused on the energetic equivalence of different adsorption geometries.

Main Results:

  • Nearest neighbor molecular adsorption is sterically hindered on the Si(111)-7×7 surface.
  • This steric effect breaks the energetic equivalence of corner and edge di-σ attachment sites.

Conclusions:

  • Steric hindrance can be utilized to control molecular assembly on surfaces.
  • Translationally ordered organic layers can be templated directly on the 7×7 surface reconstruction, opening new avenues for surface engineering.