Advancement and stabilization of copper(ii) azide by the use of triazole- and tetrazole ligands – enhanced primary explosives??
Materials Advances Pub Date: 2021-11-11 DOI: 10.1039/D1MA00588J
Abstract
Copper(II) (cupric) and copper(I) (cuprous) azide are both very powerful primary explosives with good thermal stabilities. However, both suffer from extreme sensitivities, which makes them unsuitable for any application. One brilliant concept for the synthesis of new ecofriendly, non-water soluble, and very powerful primary explosives is the assembly of ligands in the coordination sphere of copper(II) azide. Blocking of possible coordination sites through endothermic azoles allows the desensitization of copper(II) azide and leads to compounds with manageable sensitivities. 13 different nitrogen-rich tri- and tetrazole derivatives were used for the synthesis of energetic copper(II) azide complexes. The water insoluble compounds are highly promising candidates for the replacement of lead and perchlorate containing primary explosives. For the characterization, the complexes were analyzed by single crystal X-ray diffraction, elemental analysis (EA), infrared (IR) spectroscopy, and differential thermal analysis (DTA) measurements with heating rates of 5 °C min?1. The bulk material purity of selected complexes was confirmed by X-ray powder diffraction. The sensitivities toward impact (IS), friction (FS), and electrostatic discharge (ESD) of all synthesized compounds were tested and determined according to BAM (Bundesanstalt für Materialforschung und -prüfung) standards. The most promising compounds were investigated in copper shell initiation experiments with PETN as main charge.
Recommended Literature
- [1] An integrated process of CO2 capture and in situ hydrogenation to formate using a tunable ethoxyl-functionalized amidine and Rh/bisphosphine system? Yu-Nong Li,Liang-Nian He,Xian-Dong Lang,Xiao-Fang Liu,Shuai ZhangRSC Adv., 2014,4, 49995-50002 10.1039/C4RA08740B
- [2] Acetyl group orientation modulates the electronic ground-state asymmetry of the special pair in purple bacterial reaction centers P. K. Wawrzyniak,M. T. P. Beerepoot,H. J. M. de Groot,F. BudaPhys. Chem. Chem. Phys., 2011,13, 10270-10279 10.1039/C1CP20213H
- [3] An astrophysically-relevant mechanism for amino acid enantiomer enrichment Stephen P. Fletcher,Richard B. C. Jagt,Ben L. FeringaChem. Commun., 2007, 2578-2580 10.1039/B702882B
- [4] An approach to biodegradable star polymeric architectures using disulfide coupling? Jingquan Liu,Huiyun Liu,Zhongfan Jia,Volga Bulmus,Thomas P. DavisChem. Commun., 2008, 6582-6584 10.1039/B817037A
- [5] An inter-tangled network of redox-active and conducting polymers as a cathode for ultrafast rechargeable batteries Jieun Kim,Han-Saem Park,Tae-Hee Kim,Sung Yeol Kim,Hyun-Kon SongPhys. Chem. Chem. Phys., 2014,16, 5295-5300 10.1039/C3CP54624A
- [6] An Appraisal of pH triggered Bacitracin drug release, through composite hydrogel systems RabailGul,MariamMir,MurtazaNAli 10.1177/08853282231160212
- [7] An artificial CO-releasing metalloprotein built by histidine-selective metallation? Inês S. Albuquerque,Hélia F. Jeremias,Miguel Chaves-Ferreira,Dijana Matak-Vinkovic,Omar Boutureira,Carlos C. Rom?oChem. Commun., 2015,51, 3993-3996 10.1039/C4CC10204E
- [8] An artificial photosynthesis system comprising a covalent triazine framework as an electron relay facilitator for photochemical carbon dioxide reduction? Siquan Zhang,Shengyao Wang,Liping Guo,Hao Chen,Bien Tan,Shangbin JinJ. Mater. Chem. C, 2020,8, 192-200 10.1039/C9TC05297F
- [9] An aptasensor for detection of potassium ions based on RecJf exonuclease mediated signal amplification Bidou Wang,Xifeng ChenAnalyst, 2014,139, 5695-5699 10.1039/C4AN01350F
- [10] Acenaphthenic hopanoids, a novel series of aromatised Teresita Carrillo-Hernández,Philippe Schaeffer,Pierre AlbrechtChem. Commun., 2001, 1976-1977 10.1039/B105198A
Journal Name:Materials Advances
research_products
-
CAS no.: 89640-58-4