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  2. Extended Hückel method - Wikipedia

    en.wikipedia.org/wiki/Extended_Hückel_method

    It is common in many theoretical studies to use the extended Hückel molecular orbitals as a preliminary step to determining the molecular orbitals by a more sophisticated method such as the CNDO/2 method and ab initio quantum chemistry methods. Since the extended Hückel basis set is fixed, the monoparticle calculated wavefunctions must be ...

  3. Hückel method - Wikipedia

    en.wikipedia.org/wiki/Hückel_method

    The Hückel method or Hückel molecular orbital theory, proposed by Erich Hückel in 1930, is a simple method for calculating molecular orbitals as linear combinations of atomic orbitals. The theory predicts the molecular orbitals for π-electrons in π-delocalized molecules , such as ethylene , benzene , butadiene , and pyridine .

  4. Semi-empirical quantum chemistry method - Wikipedia

    en.wikipedia.org/wiki/Semi-empirical_quantum...

    The NOTCH method [26] includes many new, physically-motivated terms compared to the NDDO family of methods, is much less empirical than the other semi-empirical methods (almost all of its parameters are determined non-empirically), provides robust accuracy for bonds between uncommon element combinations, and is applicable to ground and excited ...

  5. Möbius aromaticity - Wikipedia

    en.wikipedia.org/wiki/Möbius_aromaticity

    A Hückel-Möbius aromaticity switch (2007) has been described based on a 28 pi-electron porphyrin system: [11] [note 2] The phenylene rings in this molecule are free to rotate forming a set of conformers: one with a Möbius half-twist and another with a Hückel double-twist (a figure-eight configuration) of roughly equal energy.

  6. Hückel's rule - Wikipedia

    en.wikipedia.org/wiki/Hückel's_rule

    In organic chemistry, Hückel's rule predicts that a planar ring molecule will have aromatic properties if it has 4n + 2 π-electrons, where n is a non-negative integer. The quantum mechanical basis for its formulation was first worked out by physical chemist Erich Hückel in 1931.

  7. Möbius–Hückel concept - Wikipedia

    en.wikipedia.org/wiki/Möbius–Hückel_concept

    Möbius–Hückel correlation diagram; two modes of butadiene to cyclobutene conversion. It has been noted that for every degeneracy along a reaction coordinate there is a molecular orbital crossing. [4] Thus for the butadiene to cyclobutene conversion, the two Möbius (here conrotatory) and Hückel (here disrotatory) modes are shown in Figure 5.

  8. Three Hours To Change Your Life - images.huffingtonpost.com

    images.huffingtonpost.com/2013-01-04-ThreeHours...

    an excerpt of the book Your Best Year Yet! by Jinny S. Ditzler This document is a 35-page excerpt, including the Welcome chapter of the book and Part 1: The Principles of Best Year Yet – three hours to change your life First published by HarperCollins in 1994 and by Warner Books in 1998

  9. DLVO theory - Wikipedia

    en.wikipedia.org/wiki/DLVO_theory

    In 1923, Peter Debye and Erich Hückel reported the first successful theory for the distribution of charges in ionic solutions. [7] The framework of linearized Debye–Hückel theory subsequently was applied to colloidal dispersions by S. Levine and G. P. Dube [8] [9] who found that charged colloidal particles should experience a strong medium-range repulsion and a weaker long-range attraction.