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The Quantum-Mechanical Model of an Atom02:45

The Quantum-Mechanical Model of an Atom

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Shortly after de Broglie published his ideas that the electron in a hydrogen atom could be better thought of as being a circular standing wave instead of a particle moving in quantized circular orbits, Erwin Schrödinger extended de Broglie’s work by deriving what is now known as the Schrödinger equation. When Schrödinger applied his equation to hydrogen-like atoms, he was able to reproduce Bohr’s expression for the energy and, thus, the Rydberg formula governing hydrogen spectra.
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Thomson's e/m Experiment01:19

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In a beam of charged particles created by a heated cathode, the particles move at different speeds. However, many applications need a beam with uniform particle speeds. An arrangement known as a velocity selector uses electric and magnetic fields to pick particles with a particular speed from the beam.
A particle with charge q, speed v, and mass m enters an area from the top, where the magnetic and electric fields are perpendicular both to the particle's motion and to one another. The magnetic...
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Electron Behavior00:54

Electron Behavior

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Overview
Electrons are negatively charged subatomic particles that are attracted to an orbit around the positively-charged nucleus of an atom. They reside in locations that are associated with energy levels called shells and are further organized into sub-shells and orbitals within each shell.
Electrons Orbit the Nucleus
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Electron Behavior01:09

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Electrons are negatively charged subatomic particles attracted to and orbit around the positively-charged nucleus of an atom. They reside in spaces associated with energy levels called shells and are further organized into subshells and orbitals within each shell.
Electrons Orbit the Nucleus
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The Uncertainty Principle04:08

The Uncertainty Principle

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Werner Heisenberg considered the limits of how accurately one can measure properties of an electron or other microscopic particles. He determined that there is a fundamental limit to how accurately one can measure both a particle’s position and its momentum simultaneously. The more accurate the measurement of the momentum of a particle is known, the less accurate the position at that time is known and vice versa. This is what is now called the Heisenberg uncertainty principle. He...
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π Electron Effects on Chemical Shift: Overview01:27

π Electron Effects on Chemical Shift: Overview

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An applied magnetic field causes loosely bound π-electrons in organic molecules to circulate, producing a local or induced diamagnetic field over a large spatial volume. As the molecules tumble in solution, the field generated by π-electrons in spherical substituents results in a zero net field. However, the net field generated by π-electrons in non-spherical substituents is not zero. The effect of this induced field depends on the orientation of the molecule with respect to B0,...
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Related Experiment Video

Updated: Mar 23, 2026

Dependence of Laser-induced Breakdown Spectroscopy Results on Pulse Energies and Timing Parameters Using Soil Simulants
08:53

Dependence of Laser-induced Breakdown Spectroscopy Results on Pulse Energies and Timing Parameters Using Soil Simulants

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Expanding the usage of the Source Function to experimental electron densities.

Jacob Overgaard1

  • 1Department of Chemistry and Centre for Materials Crystallography, Aarhus University, Langelandsgade, 140 DK-8000 Aarhus C, Denmark.

Acta Crystallographica Section B, Structural Science, Crystal Engineering and Materials
|April 7, 2016
PubMed
Summary

The Source Function reveals chemical bonding insights in solids using X-ray data. Electronic delocalization in aromatic systems is accurately measured and transferable between similar chemical structures.

Keywords:
Source Functionchemical transferabilityelectron density

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Area of Science:

  • Solid-state chemistry
  • Quantum chemistry
  • Crystallography

Background:

  • The Source Function offers a theoretical and experimental approach to understanding chemical bonds in solid materials.
  • Investigating electronic delocalization in aromatic systems is crucial for predicting material properties.

Discussion:

  • X-ray derived electron densities provide a quantitative measure of electronic delocalization.
  • The transferability of these electronic contributions between analogous chemical systems is demonstrated.

Key Insights:

  • The Source Function accurately quantifies electronic delocalization in aromatic compounds.
  • Electron density data from X-ray diffraction is a reliable tool for studying chemical bonding.
  • Observed electronic delocalization patterns are transferable, simplifying analysis across similar molecules.

Outlook:

  • Further application of the Source Function to diverse solid-state systems.
  • Exploring the predictive power of transferable electronic delocalization for novel material design.
  • Integrating theoretical calculations with experimental X-ray data for enhanced chemical bonding analysis.