Isostructural Cocrystals of 1,3,5-Trinitrobenzene Assembled by Halogen Bonding

被引:58
作者
Bennion, Jonathan C. [1 ,2 ]
Vogt, Leslie [3 ]
Tuckerman, Mark E. [3 ,4 ,5 ]
Matzger, Adam J. [1 ,2 ]
机构
[1] Univ Michigan, Dept Chem, 930 North Univ Ave, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Macromol Sci & Engn Program, 930 North Univ Ave, Ann Arbor, MI 48109 USA
[3] NYU, Dept Chem, New York, NY 10003 USA
[4] NYU, Courant Inst Math Sci, New York, NY 10003 USA
[5] NYU Shanghai, NYU ECNU Ctr Computat Chem, 3663 Zhongshan Rd North, Shanghai 200062, Peoples R China
关键词
ENERGETIC COCRYSTALS; DENSITY; POLYMORPHISM; SENSITIVITY; STACKING; HNIW;
D O I
10.1021/acs.cgd.6b00753
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Two isostructural energetic cocrystals containing 1,3,5-trinitrobenzene (TNB) were obtained with the energetic materials 1,3,5-triiodo-2,4,6-trinitrobenzene (TITNB) and 1,3,5-tribromo-2,4,6-trinitrobenzene (TBTNB) in ratios of 2:1 TNB/TITNB (1) and 2:1 TNB/TBTNB (2). These materials contain the shortest nitro-iodo and second shortest nitro-bromo interactions seen in the Cambridge Structural Database for organohalides. Computational studies indicate that the cocrystals are more stable than their respective component crystals by 11.5 kJ/mol for 1 and 8.2 kJ/mol for 2. While the formation of an isostructural 2:1 cocrystal with 1,3,5-trichloro-2,4,6-trinitrobenzene (TCTNB) was calculated to be favorable by 8.5 kJ/mol, only a physical mixture of the two coformers was obtained experimentally. Both 1 and 2 possess high crystallographic densities (2.203 and 1.980 g/cm(3), respectively) and were found to be insensitive in small-scale impact drop tests, possessing sensitivity between that of TNB and TXTNB (X = I or Br). The halogen content of the two cocrystals suggests application as insensitive biocidal energetics. Halogen bonding, facilitated by the strong polarization induced by aromatic ring nitration, plays a critical role in the formation of these cocrystals and offers a promising route to the development of new energetic cocrystals.
引用
收藏
页码:4688 / 4693
页数:6
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