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  1. Monatshefte für Chemie - Chemical Monthly
  2. Monatshefte für Chemie - Chemical Monthly : Volume 136
  3. Monatshefte für Chemie - Chemical Monthly : Volume 136, Issue 6, June 2005
  4. Today’s View of the Chemical Bond
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Monatshefte für Chemie - Chemical Monthly : Volume 148
Monatshefte für Chemie - Chemical Monthly : Volume 147
Monatshefte für Chemie - Chemical Monthly : Volume 146
Monatshefte für Chemie - Chemical Monthly : Volume 145
Monatshefte für Chemie - Chemical Monthly : Volume 144
Monatshefte für Chemie - Chemical Monthly : Volume 143
Monatshefte für Chemie - Chemical Monthly : Volume 142
Monatshefte für Chemie - Chemical Monthly : Volume 141
Monatshefte für Chemie - Chemical Monthly : Volume 140
Monatshefte für Chemie - Chemical Monthly : Volume 139
Monatshefte für Chemie - Chemical Monthly : Volume 138
Monatshefte für Chemie - Chemical Monthly : Volume 137
Monatshefte für Chemie - Chemical Monthly : Volume 136
Monatshefte für Chemie - Chemical Monthly : Volume 136, Issue 12, December 2005
Monatshefte für Chemie - Chemical Monthly : Volume 136, Issue 11, November 2005
Monatshefte für Chemie - Chemical Monthly : Volume 136, Issue 10, October 2005
Monatshefte für Chemie - Chemical Monthly : Volume 136, Issue 9, September 2005
Monatshefte für Chemie - Chemical Monthly : Volume 136, Issue 8, August 2005
Monatshefte für Chemie - Chemical Monthly : Volume 136, Issue 7, July 2005
Monatshefte für Chemie - Chemical Monthly : Volume 136, Issue 6, June 2005
Editorial: The Nature of the Chemical Bond Revisited
Historical Aspects of the Chemical Bond. Chemical Relationality versus Physical Objectivity
The Quantum Mechanical Basis of Conceptual Chemistry
The Topological Analysis of the Electron Localization Function. A Key for a Position Space Representation of Chemical Bonds
Today’s View of the Chemical Bond
Chemical Bonding in Molecules and Complexes Containing d-Elements Based on DFT
Recent Development of Relativistic Molecular Theory
Magnetic Orbitals and Mechanisms of Exchange I. Direct Exchange
Magnetic Orbitals and Mechanisms of Exchange II. Superexchange
Aromaticity Index Can Predict and Explain the Stability of Polycyclic Conjugated Hydrocarbons
Cyclic Conjugation Energy Effects in Polycyclic π-Electron Systems
New Keys for Old Keywords. Case Studies within the Updated Paradigms of the Hybridization and Aromaticity
Theoretical Study of Chemical Binding of Noble Gas Atom and Transition Metal Complexes: Ng–NiCO, Ng–NiN2, Ng–CoCO (Ng = He–Xe)
Chemical Bonds and Spin State Splittings in Spin Crossover Complexes. A DFT and QTAIM Analysis
Monatshefte für Chemie - Chemical Monthly : Volume 136, Issue 5, May 2005
Monatshefte für Chemie - Chemical Monthly : Volume 136, Issue 4, April 2005
Monatshefte für Chemie - Chemical Monthly : Volume 136, Issue 3, March 2005
Monatshefte für Chemie - Chemical Monthly : Volume 136, Issue 2, February 2005
Monatshefte für Chemie - Chemical Monthly : Volume 136, Issue 1, January 2005
Monatshefte für Chemie - Chemical Monthly : Volume 135
Monatshefte für Chemie - Chemical Monthly : Volume 134
Monatshefte für Chemie - Chemical Monthly : Volume 133
Monatshefte für Chemie - Chemical Monthly : Volume 132
Monatshefte für Chemie - Chemical Monthly : Volume 131
Monatshefte für Chemie - Chemical Monthly : Volume 130
Monatshefte für Chemie - Chemical Monthly : Volume 129
Monatshefte für Chemie - Chemical Monthly : Volume 128

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Today’s View of the Chemical Bond

Content Provider Springer Nature Link
Author Boča, Roman Linert, Wolfgang
Copyright Year 2005
Abstract The chemical bond is a stabilization of a system with a characteristic nuclear configuration, electronic structure, and a set of physico-chemical properties. The physical origin of the chemical bond lies in an acceleration of the electrons by a joint potential of several nuclei. The quantitative description of the chemical bond in the dihydrogen molecule can be treated within the MO or VB method. Both of them have some intrinsic drawbacks which can be overcome when the MO method is followed by the configuration interaction, and the limited VB method by its complete counterpart that includes the “ionic structures”. In the end, both results are equivalent as they include the correlation energy. The amplitudes of the two-electron wave functions show that the maximum probability is obtained when the electrons are correlated – kept apart at the individual centers. This condition is very natural for the limited VB; it includes a part of the correlation energy. Therefore the VB method is a better reference for the evaluation of the exchange coupling constant that separates the ground singlet state from the lowest triplet one.
Starting Page 881
Ending Page 923
Page Count 43
File Format PDF
ISSN 00269247
Journal Monatshefte für Chemie - Chemical Monthly
Volume Number 136
Issue Number 6
e-ISSN 14344475
Language English
Publisher Springer-Verlag
Publisher Date 2005-06-10
Publisher Place Vienna
Access Restriction One Nation One Subscription (ONOS)
Subject Keyword Chemistry/Food Science Analytical Chemistry Inorganic Chemistry Organic Chemistry Physical Chemistry Theoretical and Computational Chemistry
Content Type Text
Resource Type Article
Subject Chemistry
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