Sušanj Ruđer, Nemec Vinko, Bedeković Nikola, Cinčić Dominik
Department of Chemistry, Faculty of Science, University of Zagreb, Horvatovac 102a, 10000 Zagreb, Croatia.
Cryst Growth Des. 2022 Sep 7;22(9):5135-5142. doi: 10.1021/acs.cgd.2c00665. Epub 2022 Aug 1.
In this study, we investigate the halogen bond acceptor potential of oxygen and nitrogen atoms of morpholine and piperazine fragments when they are peripherally located on ,, or ,, acceptor molecules. We synthesized four acceptor molecules derived from either acetylacetone or benzoylacetone and cocrystallized them with 1,4-diiodotetrafluorobenzene and 1,3,5-triiodotrifluorobenzene. This resulted in eight cocrystals featuring different topicities and geometric dispositions of donor atoms. In all cocrystals, halogen bonds are formed with either the morpholinyl oxygen atom or the terminal piperazine nitrogen atom. The I···O halogen bonds feature lower relative shortening values than I···N, I···O, and I···N halogen bonds. The N and O halogen bond acceptor sites were evaluated through calculations of molecular electrostatic potential values.
在本研究中,我们研究了吗啉和哌嗪片段中的氧原子和氮原子在外围位于受体分子上时的卤键受体潜力。我们合成了四种源自乙酰丙酮或苯甲酰丙酮的受体分子,并将它们与1,4 - 二碘四氟苯和1,3,5 - 三碘三氟苯共结晶。这产生了八个具有不同给体原子拓扑和几何排列的共晶体。在所有共晶体中,卤键是与吗啉基氧原子或末端哌嗪氮原子形成的。I···O卤键的相对缩短值低于I···N、I···O和I···N卤键。通过计算分子静电势值评估了N和O卤键受体位点。