Use of Ab Initio Theory in Studying Various Chemical Systems

Abstract

Using ab initio calculations to supplement existing experimental data, a variety of chemical phenomena have been investigated. These include: the effects of substituents on altering carbon-hydrogen and silicon-hydrogen bond strengths, the mode by which the empty orbital on boron alters the properties of an adjacent phosphorous atom, and the effect of substituents on the singlet- triplet energy gap in a non-Kekule molecule. It has been found that substituents can alter the strength of carbon-hydrogen and silicon-hydrogen bonds through both pi delocalization and omega electron donation/withdrawal. The prediction has been made that two BH2 groups cooperate and hence increase the calculated pi bond strength in diboryl phosphine. Last, that the strength of the carbonyl bond has been shown to be largely responsible for reducing the singlet-triplet energy gap in oxyallyl to near degeneracy and in causing dimethyloxyallyl to have a predicted singlet electronic ground state. Thesis.

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Document Details

Document Type
Technical Report
Publication Date
Jan 01, 1990
Accession Number
ADA220913

Entities

People

  • Michael B. Coolidge

Organizations

  • Air Force Institute of Technology

Tags

Communities of Interest

  • Advanced Electronics
  • Energy and Power Technologies

DTIC Thesaurus Topics

  • Chemical Compounds
  • Chemical Reactions
  • Chemical Synthesis
  • Chemistry
  • Computational Chemistry
  • Computational Chemistry Methods
  • Crystal Structure
  • Electron Density
  • Electronic Structure Theory
  • Energy
  • Exclusion Principle
  • Kinetic Energy
  • Molecular Orbital Theory
  • Organic Chemistry
  • Potential Energy
  • Quantum Chemistry
  • Quantum Properties

Fields of Study

  • Chemistry
  • Physics

Readers

  • Organic Chemistry
  • Quantum Chemistry
  • Quantum spin resonance or Electron Paramagnetic Resonance spectroscopy.

Technology Areas

  • Microelectronics
  • Space