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    Kanazawa University research  132  0 Kommentare Solvent effects of siloxanes on donor-acceptor interactions

    KANAZAWA, Japan, May 11, 2021 /PRNewswire/ -- Researchers at Kanazawa University report in Chemical Communications how solvents influence the strength of donor–acceptor interactions.  They found that silicone solvents, providing low compatibility, intensify donor–acceptor interactions between aromatic molecules compared to hydrocarbon solvents.

    Aromatic donor–acceptor (D–A) interactions are a type of non-covalent bond between a donor (electron-rich) and an acceptor (electron-deficient) aromatic molecules. Aromatic molecules feature one or more rings with 'delocalized' electrons. The aromatic D–A interactions are widely used for building supramolecular structures, which are assembly of molecules formed by non-covalent bonds like building blocks. The supramolecular structures have smart properties such as external stimuli-responsiveness and self-repairing. The stability and smart properties of supramolecular architectures formed by D-A interactions depend on characteristics of the D–A interactions in various circumstances. Shogo Amemori and colleagues from Kanazawa University have now investigated the solvent effects on a strength of D–A interactions. Their findings provide important insights into the origin of aromatic D–A interactions and new molecular design of supramolecular architectures.

    The researchers worked with organic compounds known as pyromellitic diimide (PMDI) and pyrene (Py) derivatives as acceptors and donors, respectively. The strength of the D–A interaction between the PMDI and Py derivatives was evaluated by the association constant of the D–A interaction, in which a higher association constant means stronger D–A interactions.

    Amemori and colleagues used solvents with a variety of polarity for the evaluation of solvent effect on the D-A interaction. Polarity is related to the separation of charge (into positive and negative components) within a molecule; in low-polarity molecules, the charge separation is small.  As most previous studies focused on low-polarity solvents belonging to the class of aliphatic molecules, the scientists explored another class of compounds, the so-called poly(dimethylsiloxanes) (PDMS) or oligo(dimethylsiloxane) (ODMS).  These molecules consist of backbone of silicon-oxygen bonds fully covered organic groups, and, as solvents, generally lead to low-polarity.

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    Kanazawa University research Solvent effects of siloxanes on donor-acceptor interactions KANAZAWA, Japan, May 11, 2021 /PRNewswire/ - Researchers at Kanazawa University report in Chemical Communications how solvents influence the strength of donor–acceptor interactions.  They found that silicone solvents, providing low compatibility, …