Supramolecular Architectures of 2-(3-(4-acetoxyphenyl)propanoyl)benzene-1,3,5-triyl triacetate (1) and 4-(3-(4-acetoxyphenyl)propanoyl)-5-hydroxy-1,3-phenylene diacetate (2)  

Supramolecular Architectures of 2-(3-(4-acetoxyphenyl)propanoyl)benzene-1,3,5-triyl triacetate (1) and 4-(3-(4-acetoxyphenyl)propanoyl)-5-hydroxy-1,3-phenylene diacetate (2)

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作  者:Li Wang Rui Xu Li Wang;Rui Xu(The First Affiliated Hospital of Xi’an Medical University, Xi’an, China)

机构地区:[1]The First Affiliated Hospital of Xi’an Medical University, Xi’an, China

出  处:《International Journal of Organic Chemistry》2022年第4期200-207,共8页有机化学国际期刊(英文)

摘  要:2-(3-(4-acetoxyphenyl)propanoyl)benzene-1,3,5-triyl triacetate (1), C<sub>25</sub>H<sub>22</sub>O<sub>9</sub> and 4-(3-(4-acetoxyphenyl)propanoyl)-5-hydroxy-1,3-phenylene diacetate (2), C<sub>21</sub>H<sub>20</sub>O<sub>8</sub> were formed via esterification of phloretin and acetic anhydride, respectively. Their structures all reveal three-dimensional framework structures. In (1), the molecule, which contains two intramolecular O&ctdot;O interactions, is existed as dimer that forms classic cyclic R<sup>2</sup><sub>2</sub> (9) C-H&ctdot;O hydrogen bonding interactions. The molecules are linked by a combination of C-H&ctdot;O and C-H&ctdot;π(arene) hydrogen bonds. It is interesting that two molecules of the dimer occur different intermolecular interactions. In (2), several weak C-H&ctdot;O interactions of the types Caryl-H&ctdot;O, C<sub>sp</sub><sup>3</sup>-H&ctdot;O and intramolecular hydrogen bond O-H&ctdot;O are present. Both molecules give cyclic R<sup>2</sup><sub>2</sub> (4) motif. These hydrogen bonds and interactions appear to play an important role in controlling the molecular conformation.2-(3-(4-acetoxyphenyl)propanoyl)benzene-1,3,5-triyl triacetate (1), C<sub>25</sub>H<sub>22</sub>O<sub>9</sub> and 4-(3-(4-acetoxyphenyl)propanoyl)-5-hydroxy-1,3-phenylene diacetate (2), C<sub>21</sub>H<sub>20</sub>O<sub>8</sub> were formed via esterification of phloretin and acetic anhydride, respectively. Their structures all reveal three-dimensional framework structures. In (1), the molecule, which contains two intramolecular O&ctdot;O interactions, is existed as dimer that forms classic cyclic R<sup>2</sup><sub>2</sub> (9) C-H&ctdot;O hydrogen bonding interactions. The molecules are linked by a combination of C-H&ctdot;O and C-H&ctdot;π(arene) hydrogen bonds. It is interesting that two molecules of the dimer occur different intermolecular interactions. In (2), several weak C-H&ctdot;O interactions of the types Caryl-H&ctdot;O, C<sub>sp</sub><sup>3</sup>-H&ctdot;O and intramolecular hydrogen bond O-H&ctdot;O are present. Both molecules give cyclic R<sup>2</sup><sub>2</sub> (4) motif. These hydrogen bonds and interactions appear to play an important role in controlling the molecular conformation.

关 键 词:Phloretin Derivatives Crystal Structure Hydrogen Bonds 

分 类 号:O626[理学—有机化学]

 

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