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Linnett is Back: Chemical Bonding through the Lens of Born Maxima
María Menéndez-Herrero1, Evelio Francisco1, Ángel Martín Pendás1
1Departamento de Química Física y Analítica. Facultad de Química, Universidad de Oviedo, 33006 Oviedo, Spain.
Abstract:
The classical Lewis-Langmuir electron pair model remains central to chemical bonding theories despite its inherent contradictions with quantum mechanical principles such as antisymmetry. This paper revisits the long-forgotten Linnett's double quartet (LDQ) model, which integrates spin considerations into chemical bonding. We demonstrate that the distribution of electrons at the maxima of the square of the wave function (Born maxima) highlights the rigidity of the same-spin electron blocks and validates the LDQ framework in atoms and molecules. A generalized LDQ model accounts for all bond types, including covalent, polar covalent, ionic, dative, and electron-deficient, and directly incorporates electron correlation effects, providing a rigorous yet intuitive approach to bonding. This perspective also reveals fundamental flaws in conventional mean-field descriptions that ignore the correlated motion of electrons. By bridging traditional and quantum paradigms, the generalized LDQ model offers a robust tool for understanding chemical bonding, with implications for education, experimental design, and theoretical advancements.
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Atoms participate in a chemical bond formation to acquire a completed valence-shell electron configuration similar to that of the noble gas nearest to it in atomic number. Ionic, covalent, and metallic bonds are some of the important types of chemical bonds. Bond energy and bond length determine the strength of a chemical bond.
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An ionic bond is formed due to electrostatic attraction between cations and anions. Often, the ions are formed by the transfer of electrons...

