Multinuclear NMR Spectroscopy Research Articles

Synthesis and Fluorescence Studies of Diborene Coinage Metal Complexes.

Nine different coinage metal (Cu, Ag) π complexes of diborenes with various anionic diborene (aryl, heteroaryl) and metal substituents (Cl, Br, C6F5, C2SiMe3), stabilizing neutral donors (N-heterocyclic carbene = NHC, phosphine), configurations (cis/trans, acyclic/cyclic diborene), and charges (neutral, cationic) were synthesized and characterized by multinuclear NMR spectroscopy and X-ray crystallographic analyses. Their optical properties were investigated by UV-vis absorption and steady-state as well as time-resolved luminescence spectroscopy in solution and the solid state to gain insights into the excited-state behavior of this unusual class of photoactive compounds and to provide structure-property relationships. The structural and electronic modification of the (B═B)···M motif greatly influences not only the visible light absorption but also the photostability and quantum yields, which can reach high values of up to f = 0.42. The lifetimes are found in the nanosecond regime, providing estimated radiative rate constants over a wide range of kr = 1.3-14 × 107 s-1, indicative of fluorescence. Intersystem crossing (ISC) is sufficiently slow for prompt emission from the S1 state to be observed, while the spin-orbit coupling in the T1 state is too weak for phosphorescence to occur at room temperature. ISC can be accelerated, however, by modifying diborene ligand substitution and the coinage metal center, hinting at the potential for exploiting the properties of long-lived triplet excited states of metal diborene complexes in the future.

1-Nitramino-5-aminotetrazole – A simple accessible highly energetic building block

The highly energetic 1-nitrimino-5-aminotetrazole moiety can be obtained by direct nitration of 1,5-diaminotetrazole. The hydroxylammonium, 3,6,7-triamino-[1,2,4]triazolo[4,3-b][1,2,4]triazolium (HTATOT) and potassium derivatives were synthesized in this study through acid-base reaction because of the expected promising properties. Especially the potassium derivative shows interesting characteristics for a use as primary explosive. All new compounds were characterized through multinuclear NMR and IR spectroscopy. The purities were checked via CHNO elemental analysis and the compounds’ sensitivities (IS, FS, ESD) were measured using the BAM 1 of 6 method. Based on the crystallographic densities (low-temperature X-ray diffraction experiments) and the calculated heats of formation (atomization method based on CBS-4M level of theory), the performance data were calculated using the EXPLO5 code. The potassium derivative thereby shows interesting properties for possible use as metal-free primary explosive (positive PETN initiation, Td ​= ​180 ​°C). The hydroxylammonium derivative shows astonishing detonation properties (vD ​= ​9697 ​m·s−1, p ​= ​38.1 ​GPa).

Simple and energetic: Novel combination of furoxan and 1,2,4-triazole rings in the synthesis of energetic materials

Two novel representatives of energetic (1,2,4-triazolyl)furoxans were prepared from the readily available (furoxanyl)amidrazones. Synthesized compounds were thoroughly characterized with IR and multinuclear NMR spectroscopy, elemental analysis and X-ray diffraction data. Analysis of structural features supported by quantum-chemical calculations revealed the main reasons for experimentally observed difference in thermal stability and mechanical sensitivity of both compounds. It was found that 3-cyano-4-(1H-1,2,4-triazol-3-yl)furoxan is more thermally stable (Td: 229 ​°C) than 4-azido-3-(1H-1,2,4-triazol-3-yl)furoxan (Td: 154 ​°C) and the latter compound is also more sensitive to impact and friction. In addition, both heterocyclic assemblies have high detonation parameters (vD: 7.0–8.0 ​km·s−1; p: 22–29 ​GPa) exceeding those of benchmark explosives trinitrotoluene and hexanitrostilbene which enable their usability for various energetic applications.

Access to Monomeric Lead(II) Hydrides with Remarkable Thermostability and Their Use in Catalytic Hydroboration of Carbonyl Derivatives.

We report on the remarkable stability of unprecedented, monomeric lead(II) hydrides M+[LPb(II)H]- (M[1-H]), where L = 2,6-bis(3,5-diphenylpyrrolyl)pyridine and M = (18-crown-6)potassium or ([2.2.2]-cryptand)potassium. The half-life of [K18c6][1-H] of ∼2 days in tetrahydrofuran at 25 °C is significantly longer than those reported for dimeric lead(II) hydrides supported by bulky terphenyl ligands (few hours at low temperatures), which are the only examples known for lead(II) hydride compounds. The presence of a Pb-H bond in [1-H]- was unambiguously identified by multinuclear NMR spectroscopy. Remarkably, a 1H resonance of the hydride ligand was found at δ = 41.43 ppm (1JPbH = 1312 Hz). For reactivity study, [1-H]- serves as an excellent hydroboration catalyst with high turnover numbers and turnover frequencies for several carbonyl compounds.

Solution-Grown Ternary Semiconductors: Nanostructuring and Stereoelectronic Lone Pair Distortions in I–V–VI2 Materials

Alkali pnictogen dichalcogenides─I–V–VI2 or APnCh2─have been identified as promising semiconducting materials for energy conversion devices. However, the controlled nanoscale synthesis and our understanding of the effects of cation ordering and stereochemically active lone pairs on the structures of these ternary compounds remain underdeveloped. Here, we use solution-phase chemistry to synthesize a family of APnCh2 materials, including LiSbSe2, NaSbS2, NaSbSe2, NaBiS2, and NaBiSe2. Our approach utilizes alkali metal hydrides (AH) or carboxylates, A(O2CR), PnPh3, and elemental chalcogens as synthetic precursors and oleylamine or 1-octadecene as solvents. Synthetic manipulation via fine-tuning of reaction temperature enables control over the degree of ordering caused by the Sb 5s2 lone pair-induced distortions in NaSbS2. Pair distribution function analysis demonstrates that the structure of the Sb-containing phases deviates much more from a disordered rock salt structure than that of the Bi-containing phases. This local distortion, induced by the Sb lone pair, leads to a previously unreported noncentrosymmetric NaSbS2 crystal structure, which is additionally supported by second-harmonic generation measurements. Infrared and multinuclear solid-state NMR spectroscopies show that oleylamine or chelating carboxylates and, in some cases, unreacted precursors (LiH and PnPh3) remain bound to the nanocrystalline surfaces. A deeper understanding of the local atomic environment, long-range ordering, surface chemistry, and optoelectronic properties of these materials may speed up their fundamental study and application.

Dynamics of Formation of Binuclear Metal Complexes: A New Cu(I) Compound with N‐(2‐thiophenecarbonyl)‐N’‐(3‐Cl, 4‐F‐phenyl)thiourea as Ligand

AbstractHerein we report the synthesis and characterization of a new copper(I) complex with triphenylphosphine (PPh3) and N‐(2‐thiophenecarbonyl)‐N’‐(3‐Cl, 4‐F‐phenyl)thiourea (HL), as ligands. The complex was characterized by vibrational (FTIR and FT‐Raman) and multinuclear (1H, 13C {1H}, 31P{1H}) NMR spectroscopies. The crystalline structure of the complex was determined by single‐crystal X‐ray diffraction, confirming that a neutral binuclear compound, identified as [Cu(PPh3)(L‐κ2‐N,μ‐S)]2, was obtained. The anionic thiourea ligand coordinates to the metal through the sulfur and nitrogen atoms in an unusual bidentate κ2‐N,μ‐S coordination mode. The complex is a dimer sited on a crystallographic center of symmetry. Each Cu2(μ‐S)2 cation bridges trough the sulfur atoms of two symmetry related thiourea moieties and is also coordinated to the nitrogen atom of the thiourea ligand and the phosphorus atom from PPh3 co‐ligand, forming a slightly distorted tetrahedral geometry. An intramolecular N−H⋅⋅⋅O=C hydrogen bond is observed in the anionic ligand, forming a six‐membered ring that stabilizes the N−H thioamide group. Hirshfeld surface analysis shows that the molecules are connected by weak intermolecular contacts C⋅⋅⋅C, H⋅⋅⋅C and H⋅⋅⋅H which add to the stability of the crystalline packing. The in vitro cytotoxicity study of the complex indicates that it is more active against human lung carcinoma cells (A549), when compared to the free ligand.

Reversible Multielectron Release from Redox-Active Three-Dimensional Molecular Barrels with Ruthenium-Alkenyl Moieties.

Three-dimensional molecular barrels Ru6-4 and Ru6-5 were synthesized in high yields from dinuclear ruthenium-vinyl clamps and tritopic triphenylamine-derived carboxylate linkers and characterized by multinuclear NMR spectroscopy including 1H-1H COSY and 1H DOSY measurements, high-resolution electrospray ionization mass spectrometry, and X-ray crystallography. The metal frameworks of the cages adopt the shape of twisted trigonal prisms, and they crystallize as racemic mixtures of interdigitating Δ- and Λ-enantiomers with a tight columnar packing in Ru6-4. Electrochemical studies and redox titrations revealed that the cages are able to release up to 11 electrons on the voltammetric timescale and that their cage structures persist up to the hexacation level. IR and UV-vis-near-infrared spectroelectrochemical studies confirm substituent-dependent intramolecular electronic communication within the π-conjugated 1,3-divinylphenylene backbone in the tricationic states, where all three divinylphenylene-bridged diruthenium clamps are present in mixed-valent radical cation states. The formation of 1:3 charge-transfer salts with 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane as the electron acceptor is also demonstrated.

New Phosphonite Ligands with High Steric Demand and Low Basicity: Synthesis, Structural Properties and Cyclometalated Complexes of Pt(II)

Two phosphonite ligands bearing the highly sterically demanding 2,6-bis (2,6-dimethylphenyl)phenyl group (ArXyl2), PArXyl2(OPhNO2)2 and PArXyl2(OPhNO2,Me)2, were prepared from the parent dihalophosphines PArXyl2X2 (X = Cl, Br) and the corresponding phenols, 4-nitrophenol and 4-nitro-2,6-dimethylphenol, respectively. DFT methods were used to examine their structural features and to determine three steric descriptors, namely the Tolman cone angle, the percentage of buried volume, and the percentage of the coordination sphere protected by the ligand. A comparison with the related terphenyl phosphines is also provided. Reactions of PArXyl2(OPhNO2)2 and PArXyl2(OPhNO2,Me)2 with several Pt(II) precursors were investigated, revealing a high tendency of both phosphonites to undergo C-H activation processes and generate five- or six-membered cyclometalated structures. The coordination chemistry of the new ligands was explored with isolation, among others, of three carbonyl complexes, 1-3∙CO, and the triphenylphosphine adduct 3∙PPh3. X-ray diffraction methods permitted the determination of the solid-state structures of the mononuclear methyl carbonyl complex 1∙CO, the dinuclear chloride-bridged complex 2 and the doubly cyclometalated complex 3∙SMe2, including the conformations adopted by the ligands upon coordination. All of the new compounds were characterized by multinuclear NMR spectroscopy in solution.

Synthesis, Coordination Chemistry, and Mechanistic Studies of P,N-Type Phosphaalkene-Based Rh(I) Complexes.

The synthesis of P,N-phosphaalkene ligands, py-CH═PMes* (1, py = 2-pyridyl, Mes* = 2,4,6-tBu-C6H2) and the novel quin-CH═PMes* (2, quin = 2-quinolinyl) is described. The reaction with [Rh(μ-Cl)cod]2 produces Rh(I) bis(phosphaalkene) chlorido complexes 3 and 4 with distorted trigonal bipyramidal coordination environments. Complexes 3 and 4 show a pronounced metal-to-ligand charge transfer (MLCT) from Rh into the ligand P═C π* orbitals. Upon heating, quinoline-based complex 4 undergoes twofold C-H bond activation at the o-tBu groups of the Mes* substituents to yield the cationic bis(phosphaindane) Rh(I) complex 5, which could not be observed for the pyridine-based analogue 3. Using sub- or superstoichiometric amounts of AgOTf the C-H bond activation at an o-tBu group of one or at both Mes* was detected, respectively. Density functional theory (DFT) studies suggest an oxidative proton shift pathway as an alternative to a previously reported high-barrier oxidative addition at Rh(I). The Rh(I) mono- and bis(phosphaindane) triflate complexes 6 and 7, respectively, undergo deprotonation at the benzylic CH2 group of the phosphaindane unit in the presence of KOtBu to furnish neutral, distorted square-planar Rh(I) complexes 8 and 9, respectively, with one of the P,N ligands being dearomatized. All complexes were fully characterized, including multinuclear NMR, vibrational, and ultraviolet-visible (UV-vis) spectroscopy, as well as single-crystal X-ray and elemental analysis.

Noncovalent Synergy: Aurophilicity and Aryl Stacking in Bis(gold(I)aryl)-dmpm Complexes.

Bis(dimethylphosphino)methane (dmpm) was used as a ligand to synthesize four semi-supported dinuclear gold(I) complexes, dmpm(AuR)2 (R = Cl, C6H5, C6Cl5, and C6F5), which were studied concerning the synergistic effects of two weak noncovalent interactions: aurophilic and aryl-aryl stacking interactions. The chloro-substituted complex was synthesized by the ligand substitution of (tht)AuCl with dmpm and further functionalized by the reaction with PhMgBr or in situ-generated C6Cl5Li to afford the phenyl- and pentachlorophenyl-substituted compounds, respectively. The pentafluorophenyl-substituted gold complex was generated by the ligand substitution of (tht)Au(C6F5) with dmpm. All complexes were characterized by multinuclear NMR spectroscopy, CHN analyses, and X-ray diffraction experiments. Additionally, the basic photoluminescence properties of dmpm(AuCl)2, dmpm(AuC6Cl5)2, and dmpm(AuC6F5)2 were examined. The aggregation behavior of dmpm(AuC6F5)2 was further investigated by variable-temperature diffusion-ordered NMR spectroscopy experiments.

Dinuclear gold(I) Complexes with Bidentate NHC Ligands as Precursors for Alkynyl Complexes via Mechanochemistry.

The use of alkynyl gold(I) complexes covers different research fields, such as bioinorganic chemistry, catalysis, and material science, considering the luminescent properties of the complexes. Regarding this last application, we report here the synthesis of three novel dinuclear gold(I) complexes of the general formula [(diNHC)(Au-C≡CPh)2]: two Au-C≡CPh units are connected by a bridging di(N-heterocyclic carbene) ligand, which should favor the establishment of semi-supported aurophilic interactions. The complexes can be easily synthesized through mechanochemistry upon reacting the pristine dibromido complexes [(diNHC)(AuBr)2] with phenylacetylene and KOH. Interestingly, we were also able to isolate the monosubstituted complex [(diNHC)(Au-C≡CPh)(AuBr)]. The gold(I) species were fully characterized by multinuclear NMR spectroscopy and mass spectrometry. The emission properties were also evaluated, and the salient data are comparable to those of analogous compounds reported in the literature.

Single-Site Iridium Picolinamide Catalyst Immobilized onto Silica for the Hydrogenation of CO2 and the Dehydrogenation of Formic Acid.

The development of an efficient heterogeneous catalyst for storing H2 into CO2 and releasing it from the produced formic acid, when needed, is a crucial target for overcoming some intrinsic criticalities of green hydrogen exploitation, such as high flammability, low density, and handling. Herein, we report an efficient heterogeneous catalyst for both reactions prepared by immobilizing a molecular iridium organometallic catalyst onto a high-surface mesoporous silica, through a sol–gel methodology. The presence of tailored single-metal catalytic sites, derived by a suitable choice of ligands with desired steric and electronic characteristics, in combination with optimized support features, makes the immobilized catalyst highly active. Furthermore, the information derived from multinuclear DNP-enhanced NMR spectroscopy, elemental analysis, and Ir L3-edge XAS indicates the formation of cationic iridium sites. It is quite remarkable to note that the immobilized catalyst shows essentially the same catalytic activity as its molecular analogue in the hydrogenation of CO2. In the reverse reaction of HCOOH dehydrogenation, it is approximately twice less active but has no induction period.

Synthesis, characterization and gas phase conformational properties of chlorodifluoroacetylsulfenyl chloride, CF2ClC(O)SCl

The simple chlorodifluoroacetylsulfenyl chloride species, CF2ClC(O)SCl, has been synthetized for the first time by the reaction between chlorodifluorothioacetic acid, CF2ClC(O)SH, and elemental chlorine. This sulfenyl carbonyl derivative has been exhaustively characterized by multinuclear (19F and 13C) NMR, FTIR, and FT-Raman spectroscopies. Conformational properties were investigated using gas-phase infrared and liquid Raman spectroscopy techniques, in combination with quantum chemical calculations at the B3LYP/6-311+G(3df) level of approximation. The coexistence of two forms, characterized by two orientations (gauche and syn) of the C-Cl single bond of the –CF2Cl group with respect to the C=O double bond, is confirmed in the gas phase. The synperiplanar (syn) conformation in the sulfenylcarbonyl chloride moiety is characterized by the C=O double bond and the S-Cl single bond adopting a mutual synperiplanar orientation. The lowest energy conformation is the gauche-syn, with the second anti-syn form higher in energy by around 1.0 kcal/mol.

Structurally characterized aluminum alkoxide derivatives for aerosol spray materials production

The synthesis of a family of aluminum alkoxides was undertaken via the reaction of trimethyl aluminum (Al(CH3)3) using a series of sterically varied ortho-substituted phenols (H-OAr), including: 2-methyl phenol (H-oMP), 2-isopropyl phenol (H-oPP), 2-phenyl phenol (H-oPhP), 2,6-di-methyl phenol (H-DMP), 2,6-di-isopropyl phenol (H-DIP), and 2,6-di-phenyl phenol (H-DPhP). The products isolated using the least sterically encumbered phenoxides proved to generate the homoleptic compounds: [(oMP)Al((μ-oMP)2Al(oMP)2)2] (1), and [Al(μ-oPP)(oPP)2]2 (2), [Al(μ-oPP)(oPP)2(THF)]2 (2-THF), and [Al(μ-oPhP)(oPhP)2]2 (3). As the steric bulk was increased only partial substitution was achieved forming the alkyl, alkoxide compounds: [Al(μ-OAr)(CH3)(OAr)]2 (OAr = trans-DMP (4a), cis-DIP (5a), trans-DPhP (6a)). Sub-stoichiometric metathesis reactions for the smaller OAr ligands were undertaken to produce a series of [Al(CH3)3-x(OAr)x]2 where × = 2: OAr = trans-oMP (1a); x = 1, OAr = oMP (1b), and DMP (4b). Alternatively, the use of neo-pentanol (H-ONep) led to the homoleptic species [(ONep)Al((μ-ONep)2Al(ONep)2)2] (7) and heteroleptic [Al(μ-ONep)(CH3)2]2 (7b). Efforts to generate 7 from [Al(OPri)3]4 resulted in the production of the mixed ligated species [Al4(μ-OPri)6(ONep)6] (8). The compounds were fully characterized using a variety of analytical tools as well as multinuclear NMR (1H, 13C, 27Al) spectroscopy. Select species were used for aerosol spray pyrolysis for the anticipated production of alumina (Al2O3) materials. The final products from 1, 1b, 7, and 7b proved to generate amorphous mesoparticles of size 2.1(0.1), 2.6(0.2), 2.7(0.2), and 2.5(0.2) μm, respectively as determined by SEM and pXRD analyses. Data collected using Single Particle Aerosol Mass Spectrometry (SPAMS) revealed that Al0 particles had been produced instead of the expected Al2O3 ceramic materials.

Energetic but insensitive spiro‐tetrahydrotetrazines based on oxetane‐3‐one

AbstractEnergetic oxetanes were first described in the 1970s, such as 3,3‐bis(azidomethyl)oxetanes (BAMO) and 3‐(nitratomethyl)‐3‐(methyl)oxetanes (NIMMO). Over the past few years, oxetanes were hardly available only as special‐purpose chemicals for the pharmaceutical industry. Oxetan‐3‐one is condensed with energetic compounds with a hydrazino function such as amino‐nitroguanidine and picryl hydrazine to form energetic Schiff bases. Hydrazinolysis of the guanidine derivatives lead to energetic spiro‐tetrahydrotetrazines which are quite rare in literature. All products were characterized by their crystal structure using single‐crystal X‐ray diffraction. Furthermore, the new compounds were analyzed using IR, EA, DTA, and multinuclear NMR spectroscopy (1H and 13C). The sensitivities towards external stimuli such as friction and impact were determined according to BAM standards and the energetic performances were calculated using the EXPLO5 code.

Structural Diversity of Lithium Oligo-α-Pyridylamides

Lithium oligo-α-pyridylamides are useful intermediates in coordination chemistry. Upon trans-metalation they have afforded a variety of extended metal atom chains (EMACs), which are currently investigated as molecular wires and single-molecule magnets. However, structural information on this class of compounds is scarce. Two trilithium salts of a new, sterically encumbered oligo-α-pyridylamido ligand were isolated in crystalline form and structurally characterized in the solid state and in solution. Lithiation of N2-(trimethylsilyl)-N6-{6-[(trimethylsilyl)amino]pyridin-2-yl}pyridine-2,6-diamine (H3L) with n-BuLi in thf yielded dimeric adduct [Li6L2(thf)6] (1), which was crystallized from n-hexane/thf as 1·C6H14. Crystals of a tetra-thf solvate with formula [Li6L2(thf)4] (2) were also obtained. The compounds feature two twisted L3− ligands exhibiting a cis-cis conformation and whose five nitrogen donors are all engaged in metal coordination. The six Li+ ions per molecule display coordination numbers ranging from 3 to 5. Compound 1·C6H14 was investigated by multinuclear 1D and 2D NMR spectroscopy, including 1H DOSY experiments, which indicated retention of the dimeric structure in benzene-d6 solution. To the best of our knowledge, 1 and 2 are the longest-chain lithium oligo-α-pyridylamides structurally authenticated so far, thereby qualifying as appealing intermediates to access high-nuclearity EMACs by trans-metalation.

Unexpected White Phosphorus (P4 ) Activation Modes with Silylene-Substituted o-Carboranes and Access to an Isolable 1,3-Diphospha-2,4-disilabutadiene.

New types of metal‐free white phosphorus (P4) activation are reported. While the phosphine‐silylene‐substituted dicarborane 1, CB‐SiP (CB=ortho‐C,C′‐C2B10H10, Si=PhC(tBuN)2Si, P=P[N(tBu)CH2]2), activates white phosphorus in a 2 : 1 molar ratio to yield the P5‐chain containing species 2, the analogous bis(silylene)‐substituted compound 3, CB‐Si2 , reacts with P4 in the molar ratio of 2 : 1 to furnish the first isolable 1,3‐diphospha‐2,4‐disilabutadiene (Si=P−Si=P‐containing) compound 4. For the latter reaction, two intermediates having a CB‐Si2P4 and CB‐Si2P2 core could be observed by multinuclear NMR spectroscopy. The compounds 2 and 4 were characterized including single‐crystal X‐ray diffraction analyses. Their electronic structures and mechanisms were investigated by density functional theory calculations.

Unexpected White Phosphorus (P4) Activation Modes with Silylene‐Substitutedo‐Carboranes and Access to an Isolable 1,3‐Diphospha‐2,4‐disilabutadiene

AbstractNew types of metal‐free white phosphorus (P4) activation are reported. While the phosphine‐silylene‐substituted dicarborane1, CB‐SiP(CB=ortho‐C,C′‐C2B10H10,Si=PhC(tBuN)2Si,P=P[N(tBu)CH2]2), activates white phosphorus in a 2 : 1 molar ratio to yield the P5‐chain containing species2, the analogous bis(silylene)‐substituted compound3, CB‐Si2,reacts with P4in the molar ratio of 2 : 1 to furnish the first isolable 1,3‐diphospha‐2,4‐disilabutadiene (Si=P−Si=P‐containing) compound4. For the latter reaction, two intermediates having a CB‐Si2P4and CB‐Si2P2core could be observed by multinuclear NMR spectroscopy. The compounds2and4were characterized including single‐crystal X‐ray diffraction analyses. Their electronic structures and mechanisms were investigated by density functional theory calculations.

3D honeycomb construction of N-fluorodinitromethyl substituted polynitroazoles based on hydrogen-bonded staggered conformation: Toward high-density melt-cast explosive instead of TNT

N-fluorodinitromethyl-functionalized polynitro-triazole/pyrazole were synthesized and characterized by IR spectrum, elemental analysis, multinuclear NMR spectroscopy as well as differential scanning calorimetry. The crystal packing characteristic of honeycomb construction for 5a and inter/intramolecular interactions were thoroughly explored. Compound 5a melts at 74°C and decomposes at 167°C, while compound 5b melts at 47°C and decomposes at 209°C. Further structural analysis was not performed for 5b as its melt point indicates that it is not appropriate for melt-cast explosive. Both new compounds show zero oxygen balance, high density (1.88 g cm−3), negative heats of formation (-101.3 kJ mol−1 for 5a, -123.3 kJ mol−1 for 5b), acceptable sensitivities (IS > 10 J, FS > 168 N) and high detonation performances (vD > 8591 m s−1, P > 32.7 GPa). The resluts of physicochemical properties and detonation performance suggest that 5a could be used as an applicable melt-cast explosive and a replacer for TNT.

Tuning the Properties of 5-Azido and 5-Nitramino-tetrazoles by Diverse Functionalization - General Concepts for Future Energetic Materials.

5‐Azido and 5‐nitraminotetrazole backbones are established heterocyclic motifs in the research field of energetic materials synthesis. Despite the high energy content of the compounds, the problem with many derivatives is that their sensitivities are far too high. Functionalization of one of the ring nitrogen atoms is the aim of this study to adjust the sensitivity by inserting nitratoethyl, azidoethyl and methyl groups. In this context, derivatives of 2‐(2‐azidoethyl)‐5‐nitraminotetrazoles (2, 2 a–2 d), as well as 1‐nitrato and 1‐azidoethyl substituted 5‐azidotetrazole (7 and 10) and the methylation products of 5‐azidotetrazole (5‐azido‐1‐methyl‐tetrazole, 11 and 5‐azido‐2‐methyl‐tetrazole, 12) were prepared. The obtained nitrogen‐rich compounds were extensively characterized through multinuclear NMR spectroscopy and IR spectroscopy. The structural confinement was checked by X‐ray diffraction experiments. The pure samples (verified by elemental analysis) were investigated regarding their behavior toward friction, impact (BAM methods) and electrostatic discharge as well as heating (DTA and DSC). For all metal‐free compounds the detonation properties were computed with the EXPLO5 code using their density and heat of formation, calculated based on CBS‐4 M level of theory.