Comparing the performance of aliphatic azido nitramines, nitrate esters, and nitro compounds: theoretical design and investigation

2015 ◽  
Vol 93 (11) ◽  
pp. 1232-1238
Author(s):  
Junqing Yang ◽  
Guixiang Wang ◽  
Xuedong Gong ◽  
Xiaoan Wei
Keyword(s):  
Thermal Stability ◽  
Thermodynamic Properties ◽  
Density Functional ◽  
Density Functional Theory Method ◽  
Nitro Compounds ◽  
Oxygen Balance ◽  
Nitrate Esters ◽  
Energetic Properties ◽  
The Density Functional Theory ◽  
Theoretical Investigations

To improve the low density and oxygen balance of the pure azido compounds, experimental research has been devoted to developing the modified azido compounds, such as azido nitramines, azido nitrate esters, and azido nitro compounds. Using the experimental methods to obtain a compound with suitable performance needs more resources than using theoretical tests, which makes the theoretical investigations meaningful. In this work, three azido compounds (I, II, and III) and their 27 modified derivatives were designed and studied using the density functional theory method. Results show that –NNO2, –NO2, and –ONO2 all can improve the thermodynamic and energetic properties and the increment increases with the increasing number of substituent groups. The contribution to the thermodynamic properties is –ONO2 > –NO2 > –NNO2 and that to the energetic properties is –NNO2 > –ONO2 > –NO2. The azido nitramines possess the best energetic properties and azido nitrate esters have the best thermodynamic properties. These substituents slightly decrease the thermal stability and the azido nitrate esters possess the lowest thermal stability. Systematical inspection of the substituent effect can direct experimental researchers to synthesize modified azido compounds purposefully and selectively.

Synthesis, Structure, and Theoretical Investigations of an Alkaline Earth Vanadate Oxide Compound (Ca4V4O14): Electronic, Optical, and Chemical Bond Properties

2011 ◽  
Vol 64 (7) ◽  
pp. 973 ◽  
Author(s):  
Yi-Ping Tong ◽  
Guo-Tian Luo ◽  
Zhen Jin ◽  
Yan-Wen Lin
Keyword(s):  
Density Functional ◽  
Density Functional Theory Method ◽  
Dielectric Constants ◽  
Static Case ◽  
Oxide Compound ◽  
Structural Distortions ◽  
The Density Functional Theory ◽  
Theoretical Investigations ◽  
Jahn Teller ◽  
Jahn Teller Effect

One novel purely inorganic d0 polyoxovanadate compound Ca4V4O14 (1) was obtained and characterized structurally. The chain-like [V4O14]8– anion, built up from distorted VO5 trigonal bipyramids and VO4 tetrahedras is rarely observed. The reason for structural distortions is ascribed to the second-order Jahn-Teller effect. The band structure, the density of states, linear optical response functions, the dielectric constants of the static case ϵ(0), and refractive indexes were calculated by the density functional theory method. The nature of the V–O and Ca–O bonds, and of the electronic absorption peak are discussed in detail.

Design of new aliphatic azido nitro compounds as plasticizer: an initial exploration on AFCTEE (1-azido-formic acid 1,1,1-trinitro-ethyl ester)

2015 ◽  
Vol 93 (7) ◽  
pp. 690-695 ◽  
Author(s):  
Junqing Yang ◽  
Xuedong Gong ◽  
Guixiang Wang
Keyword(s):  
Thermal Stability ◽  
Formic Acid ◽  
Ethyl Ester ◽  
Chemical Stability ◽  
Density Functional ◽  
High Energy ◽  
Nitro Compounds ◽  
Functional Theory ◽  
Energetic Properties ◽  
Initial Exploration

To explore new high-energy azido nitro compounds as plasticizers for propellants, AFCTEE (1-azido-formic acid 1,1,1-trinitro-ethyl ester) was designed and studied using density functional theory. The predicted density of AFCTEE, 1.90 gcm−3, is comparable to that of HMX (1,3,5,7-tetranitro-1,3,5,7-tetraazacyclooctane) and much higher than that of general organic azido compounds. AFCTEE possesses higher energetic properties and chemical stability than the promising azido nitro plasticizer DAMNP (1,3-diazido-2-methyl-2-nitropropane) and the conventional plasticizer NG (nitroglycerine), and it has a moderate thermal stability. The pyrolysis of AFCTEE starts from the rupture of C–NO2 and then the breakage of N–N2 via Curtius rearrangement. This work is the initial exploration for AFCTEE, aiming at the energetics, spectra (IR, NMR, and UV), stability, and decomposition mechanism. Compared with DAMNP, the advantages of superior energetic properties and chemical stability suggest AFCTEE is a promising energetic azido nitro compound and is worth further investigation.

scholarly journals First-Principles Study of Mechanical and Thermodynamic Properties of Binary and Ternary CoX (X = W and Mo) Intermetallic Compounds

Materials ◽  
2021 ◽  
Vol 14 (6) ◽  
pp. 1404
Author(s):  
Yunfei Yang ◽  
Changhao Wang ◽  
Junhao Sun ◽  
Shilei Li ◽  
Wei Liu ◽  
...  
Keyword(s):  
Free Energy ◽  
Thermodynamic Properties ◽  
Gibbs Free Energy ◽  
Density Functional ◽  
Vibrational Entropy ◽  
Functional Theory ◽  
Lattice Constants ◽  
The Density Functional Theory ◽  
Ductile Behavior ◽  
Pseudo Potential

In this study, the structural, elastic, and thermodynamic properties of DO19 and L12 structured Co3X (X = W, Mo or both W and Mo) and μ structured Co7X6 were investigated using the density functional theory implemented in the pseudo-potential plane wave. The obtained lattice constants were observed to be in good agreement with the available experimental data. With respect to the calculated mechanical properties and Poisson’s ratio, the DO19-Co3X, L12-Co3X, and μ-Co7X6 compounds were noted to be mechanically stable and possessed an optimal ductile behavior; however, L12-Co3X exhibited higher strength and brittleness than DO19-Co3X. Moreover, the quasi-harmonic Debye–Grüneisen approach was confirmed to be valid in describing the temperature-dependent thermodynamic properties of the Co3X and Co7X6 compounds, including heat capacity, vibrational entropy, and Gibbs free energy. Based on the calculated Gibbs free energy of DO19-Co3X and L12-Co7X6, the phase transformation temperatures for DO19-Co3X to L12-Co7X6 were determined and obtained values were noted to match well with the experiment results.

Study of the Stability and Chemical Reactivity of a Series of Tetrazole Pyrimidine Hybrids by the Density Functional Theory Method (DFT)

2021 ◽  
Vol 37 (4) ◽  
pp. 805-812
Author(s):  
Ahissandonatien Ehouman ◽  
Adjoumanirodrigue Kouakou ◽  
Fatogoma Diarrassouba ◽  
Hakim Abdel Aziz Ouattara ◽  
Paulin Marius Niamien
Keyword(s):  
Density Functional ◽  
Theoretical Study ◽  
Molecular Descriptors ◽  
Chemical Reactivity ◽  
Density Functional Theory Method ◽  
Functional Theory ◽  
Reactivity Descriptors ◽  
The Density Functional Theory ◽  
The Stability ◽  
Global Reactivity Descriptors

Our theoretical study of stability and reactivity was carried out on six (06) molecules of a series of pyrimidine tetrazole hybrids (PTH) substituted with H, F, Cl, Br, OCH3 and CH3 atoms and groups of atoms using the density function theory (DFT). Analysis of the thermodynamic formation quantities confirmed the formation and existence of the series of molecules studied. Quantum chemical calculations at the B3LYP / 6-311G (d, p) level of theory determined molecular descriptors. Global reactivity descriptors were also determined and analyzed. Thus, the results showed that the compound PTH_1 is the most stable, and PTH_5 is the most reactive and nucleophilic. Similarly, the compound PTH_4 is the most electrophilic. The analysis of the local descriptors and the boundary molecular orbitals allowed us to identify the preferred atoms for electrophilic and nucleophilic attacks.

scholarly journals Practical and Theoretical Study on the Inhibitory Influences of New Azomethine Derivatives Containing an 8-Hydroxyquinoline Moiety for the Corrosion of Carbon Steel in 1 M HCl

2018 ◽  
Vol 34 (6) ◽  
pp. 3016-3029 ◽  
Author(s):  
A. El-Yaktini ◽  
A. Lachiri ◽  
M. El-Faydy ◽  
F. Benhiba ◽  
H. Zarrok ◽  
...  
Keyword(s):  
Carbon Steel ◽  
Density Functional ◽  
Electrochemical Impedance ◽  
Density Functional Theory Method ◽  
Steel Corrosion ◽  
Experimental Results ◽  
Chemical Parameters ◽  
Functional Theory ◽  
The Density Functional Theory ◽  
Inhibition Ability

The inhibition ability of a new Azomethine derivatives containing the 8-hydroxyquinoline (BDHQ and MDHQ) towards carbon steel corrosion in HCl solution was studied at various concentrations and temperatures using weight loss, polarization curves and electrochemical impedance spectroscopy (EIS) methods. The experimental results reveal that BDHQ and MDHQ are efficient mixed type corrosion inhibitors, and their inhibition efficiencies increase with increasing concentration. The adsorption of these inhibitors on mild steel surface obeys Langmuir isotherm. Quantum chemical parameters are calculated using the Density Functional Theory method (DFT) and Monte Carlo simulations. Correlation between theoretical and experimental results is discussed.

Pressure effect on the structural, phonon, elastic and thermodynamic properties of L12phase RH3TA: First-principles calculations

2018 ◽  
Vol 32 (14) ◽  
pp. 1850169
Author(s):  
Leini Wang ◽  
Zhang Jian ◽  
Wei Ning
Keyword(s):  
Thermodynamic Properties ◽  
Density Functional ◽  
Harmonic Approximation ◽  
Debye Model ◽  
Approximation Model ◽  
Functional Theory ◽  
The Density Functional Theory ◽  
Relationship Of ◽  
G Ratio ◽  
Wide Pressure

The phonon, elastic and thermodynamic properties of L12phase Rh3Ta have been investigated by the density functional theory (DFT) approach combined with the quasi-harmonic approximation model. The results of the phonon band structure show that L12phase Rh3Ta possesses dynamical stability in the pressure range from 0–80 GPa due to the absence of imaginary frequencies. The pressure dependences with the elastic constants C[Formula: see text], shear modulus G, bulk modulus B, Young’s modulus Y, Poisson’s ratio and B/G ratio have been analyzed. The results of the elastic properties studies show that L12phase Rh3Ta compound is mechanically stable and possesses a higher hardness, improved ductility and plasticity under higher pressures. The pressure and temperature relationship of the thermodynamic properties, such as the Debye temperature [Formula: see text], heat capacity C[Formula: see text], thermal expansion coefficient [Formula: see text] and the Grüneisen parameter [Formula: see text] are predicted by the quasi-harmonic Debye model in a wide pressure (0–80 GPa) and temperature (0–750 K) ranges.

Ab Initio Calculations of New α-L5-7a and β-L5-7a Graphyne Polymorphic Varieties

2022 ◽  
Vol 1049 ◽  
pp. 180-185
Author(s):  
Viktor Mavrinskii ◽  
Evgeniy A. Belenkov
Keyword(s):  
Density Functional ◽  
Electronic States ◽  
Density Functional Theory Method ◽  
Geometric Optimization ◽  
Initial Structure ◽  
Functional Theory ◽  
Graphene Layers ◽  
Density Of Electronic States ◽  
Sublimation Energy ◽  
The Density Functional Theory

Calculations of the structural and energy parameters, band structure and density of electronic states of new structural varieties of graphyne have been performed by the density functional theory method. The initial structure of the nine polymorphs was theoretically constructed on the basis of the 5-7a graphene layer. As a result of the calculations, the structure of only five graphyne layers was found to be stable: α-L5-7a, β1-L5-7a, β2-L5-7a, β3-L5-7a and β4-L5-7a. The structure of layers γ1-L5-7a, γ2-L5-7a, and γ3-L5-7a is transformed into the structure of graphene layers by geometric optimization, and the graphyne layer γ4-L5-7a is transformed sp+sp2 layer L3-6-13. The sublimation energy of the stable graphyne polymorphs varies from 6.66 to 6.78 eV/atom. The density of electronic states at the Fermi energy level for all α-L5-7a and β-L5-7a layers of graphyne is different from zero, so the new graphyne polymorphs should have metallic properties.

Hydrogen-Bonded Interactions in the Systems L-Cysteine - H2SeO3 and L-Cysteine -H2SeO4

2013 ◽  
pp. 169-179
Author(s):  
Alexei N. Pankratov ◽  
Nikolay A. Bychkov ◽  
Olga M. Tsivileva
Keyword(s):  
Density Functional ◽  
Density Functional Theory Method ◽  
Thiol Group ◽  
Mutual Orientation ◽  
Theory Method ◽  
Functional Theory ◽  
Compound A ◽  
The Density Functional Theory ◽  
The Enthalpy Of Formation ◽  
Hydrogen Bonded

Using the density functional theory method at the B3LYP/6-31G(d,p) level of theory, the formation of hydrogen-bonded complexes of L-cysteine with selenious and selenic acids has been studied. In both cases of selenium-containing acids, the complexes occur preferably by cysteine carboxylic group, therewith the enthalpy of formation values consist from –19 to –21 kcal/mol, and free energy from –6 to –9 kcal/mol. Probably, the initial act of interaction in the system hydroxyl-containing selenium compound - a-amino acid, proceeding with mutual orientation of the reactants molecules and intermolecular hydrogen bonds formation, serves as a prerequisite for the thiol group capability of participating in the subsequent stages (including more completed transformations) of biologically important reactions.

scholarly journals Proposed Mechanism for the High-Yield Polymerization of Oxyethyl Propiolates with Rh Complex Catalyst Using the Density Functional Theory Method

Polymers ◽  
2019 ◽  
Vol 11 (1) ◽  
pp. 93 ◽  
Author(s):  
Yoshiaki Yoshida ◽  
Yasuteru Mawatari ◽  
Masayoshi Tabata
Keyword(s):  
Density Functional ◽  
Density Functional Theory Method ◽  
High Reactivity ◽  
High Yield ◽  
Complex Catalyst ◽  
Dft Methods ◽  
Functional Theory ◽  
Molecular Weights ◽  
Monomer Structure ◽  
The Density Functional Theory

In this study, poly(oxyethyl propiolate)s (POP)s featuring various oxyethylene derivatives are synthesized using a [Rh(norbornadiene)Cl]2 catalyst. In particular, POPs featuring the normal oxyethylene chain in the side-chain exhibit excellent yields and high molecular weights in methanol and N,N-dimethylformamide at 40 °C, compared with poly(n-alkyl propiolate)s (PnAP)s. The high reactivity of the oxyethyl propiolate (OP) monomers is clarified by considering the time dependences of the polymerization yields of OPs and alkyl propiolates (Aps). Furthermore, the monomer structure and intermediate conformation of the Rh complex are optimized using Density Function theory (DFT) methods (B3LYP/6-31G** and B3LYP/LANL2DZ) and a polymerization mechanism is proposed.

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