2023
DOI: 10.1021/acs.orglett.3c00149
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Challenging the Limitations of Tetranitro Biimidazole through Introducing a gem-Dinitromethyl Scaffold

Abstract: A gem-dinitromethyl group was successfully introduced into the TNBI•2H 2 O structure (TNBI: 4,4′,5,5′-tetranitro-2,2′-bi-1Himidazole) to obtain 1-(dinitromethyl)-4,4′,5,5′-tetranitro-1H,1′H-2,2′-biimidazole (DNM-TNBI). Benefiting from the transformation of an N-H proton into a gem-dinitromethyl group, the current limitations of TNBI were well solved. More importantly, DNM-TNBI has high density (1.92 g•cm −3 , 298 K), good oxygen balance (15.3%), and excellent detonation properties (D v = 9102 m•s −1 , P = 37.6… Show more

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Cited by 18 publications
(14 citation statements)
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“…A large number of energetic bonds −C–N–, −N–N–, –NN–, etc., in their structures, enhance the high heat of formation, density, and oxygen balance, thus improving the overall performance of the nitrogen-rich parent skeleton. Although there is a lack of a clear rule on the rational synthesis of such ideal energetic compounds, reasonable arrangement of oxidizing or energetic groups (–N 3 , –ONO 2 , –NO 2 , –NHNO 2 , etc.) to the heterocyclic backbone (through covalent or ionic bond) and a large number of inter- and intramolecular hydrogen bonding to avoid adverse ring strain might be helpful. …”
Section: Introductionmentioning
confidence: 99%
“…A large number of energetic bonds −C–N–, −N–N–, –NN–, etc., in their structures, enhance the high heat of formation, density, and oxygen balance, thus improving the overall performance of the nitrogen-rich parent skeleton. Although there is a lack of a clear rule on the rational synthesis of such ideal energetic compounds, reasonable arrangement of oxidizing or energetic groups (–N 3 , –ONO 2 , –NO 2 , –NHNO 2 , etc.) to the heterocyclic backbone (through covalent or ionic bond) and a large number of inter- and intramolecular hydrogen bonding to avoid adverse ring strain might be helpful. …”
Section: Introductionmentioning
confidence: 99%
“…Electrostatic potentials (ESPs) of compound 3 and 4 are calculated and analyzed by using Multiwfn v3.5 software. 42 The positive and negative potentials are indicated by red and blue sections, respectively. The essence of the hydrogen bond is electrostatic forces, and larger static potential differences are more favorable for hydrogen bond formation.…”
Section: Molecular Stabilitymentioning
confidence: 99%
“…18,19 Unfortunately, it has received little attention in the community of HEDMs. We have focused on exploring efficient methods to synthesize different types of energetic compounds, [20][21][22] and the classic Dimroth rearrangement is expected to access diversified energetic materials.…”
Section: Introductionmentioning
confidence: 99%