[go: up one dir, main page]

Klapötke et al., 2008 - Google Patents

Synthesis, Characterization and Explosive Properties of 1, 3‐Dimethyl‐5‐amino‐1H‐tetrazolium 5‐Nitrotetrazolate

Klapötke et al., 2008

Document ID
6605241266138083636
Author
Klapötke T
Miró Sabaté C
Rusan M
Publication year
Publication venue
Zeitschrift für anorganische und allgemeine Chemie

External Links

Snippet

Dimethyl‐5‐amino‐1H‐tetrazolium 5‐nitrotetrazolate (5b) was synthesized in high yield from 1, 4‐dimethyl‐5‐amino‐1H‐tetrazolium iodide (5a) and silver 5‐nitrotetrazolate. Both new compounds (5a and 5b) were characterized using vibrational (IR and Raman) and …
Continue reading at onlinelibrary.wiley.com (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B31/00Compositions containing an inorganic nitrogen-oxygen salt
    • C06B31/28Compositions containing an inorganic nitrogen-oxygen salt the salt being ammonium nitrate
    • C06B31/30Compositions containing an inorganic nitrogen-oxygen salt the salt being ammonium nitrate with vegetable matter; with resin; with rubber
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B25/00Compositions containing a nitrated organic compound
    • C06B25/34Compositions containing a nitrated organic compound the compound being a nitrated acyclic, alicyclic or heterocyclic amine
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B43/00EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES compositions characterised by explosive or thermic constituents not provided for in groups C06B25/00 - C06B41/00
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B25/00Compositions containing a nitrated organic compound
    • C06B25/18Compositions containing a nitrated organic compound the compound being nitrocellulose present as 10% or more by weight of the total composition
    • C06B25/24Compositions containing a nitrated organic compound the compound being nitrocellulose present as 10% or more by weight of the total composition with nitroglycerine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D257/00Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
    • C07D257/02Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B29/00Compositions containing an inorganic oxygen-halogen salt, e.g. chlorate, perchlorate
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B45/00Compositions or products which are defined by structure or arrangement of component of product
    • C06B45/04Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B41/00Compositions containing a nitrated metallo-organic compound
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06DMEANS FOR GENERATING SMOKE OR MIST; GAS-ATTACK COMPOSITIONS; GENERATION OF GAS FOR BLASTING OR PROPULSION (CHEMICAL PART)
    • C06D5/00Generation of pressure gas, e.g. for blasting cartridges, starting cartridges, rockets
    • C06D5/06Generation of pressure gas, e.g. for blasting cartridges, starting cartridges, rockets by reaction of two or more solids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00
    • C07D487/12Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
    • C07D487/14Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00Compounds containing elements of Groups 3 or 13 of the Periodic System
    • C07F5/02Boron compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C201/00Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic System
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C-Si linkages

Similar Documents

Publication Publication Date Title
Gidaspov et al. Novel trinitroethanol derivatives: high energetic 2-(2, 2, 2-trinitroethoxy)-1, 3, 5-triazines
Klapötke et al. Thermal stabilization of energetic materials by the aromatic nitrogen-rich 4, 4′, 5, 5′-tetraamino-3, 3′-bi-1, 2, 4-triazolium cation
Yadav et al. Facile fabrication of functionalized pyrimidine derivatives: constructing a new family of high performance and less sensitive energetic compounds
Klapoetke et al. Nitration Products of 5‐Amino‐1H‐tetrazole and Methyl‐5‐amino‐1H‐tetrazoles–Structures and Properties of Promising Energetic Materials
Klapötke et al. Neutral 5-nitrotetrazoles: Easy initiation with low pollution
Kettner et al. 5, 5′-Bis-(trinitromethyl)-3, 3′-bi-(1, 2, 4-oxadiazole): a stable ternary CNO-compound with high density
Lei et al. A facile strategy for synthesizing promising pyrazole-fused energetic compounds
Gidaspov et al. High-density insensitive energetic materials: 2, 4, 6-tris (2-fluoro-2, 2-dinitroethoxy)-1, 3, 5-triazine
Xu et al. 1-Nitro-2-trinitromethyl substituted imidazoles: a new family of high performance energetic materials
Haiges et al. 5-(Fluorodinitromethyl)-2 H-tetrazole and its tetrazolates–Preparation and Characterization of New High Energy Compounds
Aizikovich et al. The nitration pattern of energetic 3, 6-diamino-1, 2, 4, 5-tetrazine derivatives containing azole functional groups
Luk et al. Energetic N-azidomethyl derivatives of polynitro hexaazaisowurtzitanes series: CL-20 analogues having the highest enthalpy
Ma et al. Synthesis and thermal behavior of a fused, tricyclic pyridine-based energetic material: 4-amino-5-nitro-[1, 2, 5] oxadiazolo [3, 4-e] tetra-zolo [1, 5-a] pyridine-3-oxide
Klapötke et al. Hydrogen‐bonding Stabilization in Energetic Perchlorate Salts: 5‐Amino‐1H‐tetrazolium Perchlorate and its Adduct with 5‐Amino‐1H‐tetrazole
Kumar et al. Resolving synthetic challenges faced in the syntheses of asymmetric N, N′-ethylene-bridged energetic compounds
Mathpati et al. Potential energetic salts of 5, 5′-methylenedi (4H-1, 2, 4-triazole-3, 4-diamine) cation: Synthesis, characterization and detonation performance
Klapötke et al. N-Functionalisation of 5, 5′-bistetrazole providing 2, 2′-di (azidomethyl) bistetrazole: a melt-castable metal-free green primary explosive
Klapötke et al. Synthesis, Characterization and Explosive Properties of 1, 3‐Dimethyl‐5‐amino‐1H‐tetrazolium 5‐Nitrotetrazolate
Benz et al. Melt castable derivatives of pentaerythritol tetranitrate
Gospodinov et al. Energetic derivatives of 3, 3′, 5, 5′-tetranitro-4, 4′-bipyrazole (TNBPz): Synthesis, characterization and properties
Srinivas et al. Synthesis of nitrate ester and nitramine derivatives of polyfluoro alkyl compounds for high energy materials
Thaltiri et al. Efficient synthesis of N-methyltetranitropyrrole: A stable, insensitive and high energy melt-castable material
Gettings et al. Methyl sydnone imine and its energetic salts
Joo et al. Polynitramino compounds outperform PETN
Klapötke et al. 1, 5‐Diamino‐4‐methyltetrazolium 5‐Nitrotetrazolate–Synthesis, Testing and Scale‐up