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Hypervalent Bonding in the OF(a4Σ), SF(a4Σ), SF5/SF6, and OSF4 Species

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Department of Chemistry, Laboratory of Physical Chemistry, National and Kapodistrian University of Athens, Panepistimiopolis, Athens 15771, Greece
Cite this: J. Phys. Chem. A 2018, 122, 8, 2178–2183
Publication Date (Web):February 12, 2018
https://doi.org/10.1021/acs.jpca.7b10750
Copyright © 2018 American Chemical Society

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    Abstract

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    Hypervalency has struggled the conventional wisdom of too many chemists for so many years. Numerous theories and bonding models have been introduced but the so-called “hypervalency” mystery remains. We offer a simple and appealing explanation for the bonding mechanism of OF(a4Σ), SF(a4Σ), SF5/SF6, and OSF4 based solely on the fact that excited and/or ionic states of the constituent fragments may and actually do occur in the ground states of so many “every day” molecules. In particular, and through multireference methods, we have found that the bonding in all the studied species is ionic in nature, perhaps contrary to the present status of our chemical beliefs. Although the “atoms in molecules” hypothesis is certainly not the only way to explain the formation of the chemical bond, we strongly believe that it is the simplest and most economical conceptual principle that should guide our chemical thinking.

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    Cited By

    This article is cited by 8 publications.

    1. Benjamin A. Jackson, Jordan Harshman, Evangelos Miliordos. Addressing the Hypervalent Model: A Straightforward Explanation of Traditionally Hypervalent Molecules. Journal of Chemical Education 2020, 97 (10) , 3638-3646. https://doi.org/10.1021/acs.jchemed.0c00368
    2. Prabhat Gautam, Yue Wang, Guoxian Zhang, Handong Sun, Julian M. W. Chan. Using the Negative Hyperconjugation Effect of Pentafluorosulfanyl Acceptors to Enhance Two-Photon Absorption in Push–Pull Chromophores. Chemistry of Materials 2018, 30 (20) , 7055-7066. https://doi.org/10.1021/acs.chemmater.8b02723
    3. Jonas O. Wenzel, Fabian Jester, Antonio Togni, David Rombach. Hydroamination of Triisopropylsilyl Acetylene Sulfur Pentafluoride – a Bench‐top Route to Pentafluorosulfanylated Enamines. Chemistry – A European Journal 2024, 30 (14) https://doi.org/10.1002/chem.202304015
    4. Ravi Kumar, Toshifumi Dohi, Viktor V. Zhdankin. Organohypervalent heterocycles. Chemical Society Reviews 2024, 221 https://doi.org/10.1039/D2CS01055K
    5. Yohsuke Yamamoto, Yuan Shi, Takashi Masui, Daigo Saito, Tatsuya Inoue, Hitomi Sato, Chisato Dohi, Emiko Muneta, Rong Shang, Masaaki Nakamoto. Synthesis and Characterization of Hypervalent Pentacoordinate Carbon Compounds Bearing a 7‐6‐7‐Ring Skeleton. Chemistry – A European Journal 2023, 29 (9) https://doi.org/10.1002/chem.202203162
    6. Abdulrahman Aldossary, Martin Head-Gordon. Non-iterative method for constructing valence antibonding molecular orbitals and a molecule-adapted minimum basis. The Journal of Chemical Physics 2022, 157 (9) https://doi.org/10.1063/5.0095443
    7. Chenting Yan, Masato Takeshita, Jun-ya Nakatsuji, Akihiro Kurosaki, Kaoko Sato, Rong Shang, Masaaki Nakamoto, Yohsuke Yamamoto, Yohei Adachi, Ko Furukawa, Ryohei Kishi, Masayoshi Nakano. Synthesis and properties of hypervalent electron-rich pentacoordinate nitrogen compounds. Chemical Science 2020, 11 (19) , 5082-5088. https://doi.org/10.1039/D0SC00002G
    8. Apostolos Kalemos, Isuru R. Ariyarathna, Shahriar N. Khan, Evangelos Miliordos, Aristides Mavridis. “Hypervalency” and the chemical bond. Computational and Theoretical Chemistry 2019, 1153 , 65-74. https://doi.org/10.1016/j.comptc.2019.02.014

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