✦ LIBER ✦

Vibration Spectra of 1,3,5-Triamino-2,4,6-trinitrobenzene

✍ Scribed by Deopura, B. L.

Book ID: 118126372
Publisher: American Institute of Physics
Year: 1971
Tongue: English
Weight: 644 KB
Volume: 54
Category: Article
ISSN: 0021-9606
DOI: 10.1063/1.1675458

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Vibrational spectrum of 1,3,5-triamino-2

Vibrational spectrum of 1,3,5-triamino-2,4,6-trinitrobenzene

✍ Theodore G. Towns 📂 Article 📅 1983 🏛 Elsevier Science 🌐 English ⚖ 376 KB

The mid-infrared (4-00 cm-I) spectra in KBr matrix of the title compound (TATB) and four of its isotopic derivatives have been analysed for the purpose of vibrational assignments. The relative simplicity of the spectra, in conjunction with the various isotopic shifts, indicates that thirteen of the

Thermal decomposition of 1,3,5-triamino-

Thermal decomposition of 1,3,5-triamino-2,4,6-trinitrobenzene

✍ Milton Farber; R.D. Srivastava 📂 Article 📅 1981 🏛 Elsevier Science 🌐 English ⚖ 411 KB

The products of sublimation and thermal decomposition of 1,3,5-triamino-2,4,6-trinitmbenzene have been determined mass spectrometrically in the temperature range 200-300°C employing both the effusion and Langmuir evaporation methods. Electron impact ionization energies 1-2 eV above appearance potent

ChemInform Abstract: Synthesis of 2,4,6-

ChemInform Abstract: Synthesis of 2,4,6-Triamino-1,3,5-trinitrobenzene

✍ Gilson da Silva; Elizabeth da Costa Mattos 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 18 KB 👁 1 views

UV-Induced Degradation Rates of 1,3,5-Tr

UV-Induced Degradation Rates of 1,3,5-Triamino-2,4,6-Trinitrobenzene (TATB)

✍ Williams, Darren L.; Timmons, James C.; Woodyard, James D.; Rainwater, Ken A.; L 📂 Article 📅 2003 🏛 American Chemical Society 🌐 English ⚖ 54 KB

A New Synthetic Route to 1,3,5-Triamino-

A New Synthetic Route to 1,3,5-Triamino-2,4,6-Trinitrobenzene (TATB)

✍ Anthony J. Bellamy; Simon J. Ward; Peter Golding 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 378 KB 👁 2 views

A new, three-stage synthesis of 1,3,5-triamino-2,4,6-trinitrobenzene (TATB) has been developed which avoids the use of halogenated precursors or reagents. The starting material, 1,3,5trihydroxy-benzene, is converted via the sequence nitrationalkylation-amination to TATB in an overall yield of 87%. T

Growth of 1,3,5-Triamino-2,4,6-trinitrob

Growth of 1,3,5-Triamino-2,4,6-trinitrobenzene (TATB) I. Anisotropic thermal expansion

✍ John R. Kolb; H. F. Rizzo 📂 Article 📅 1979 🏛 John Wiley and Sons 🌐 English ⚖ 734 KB

## Abstract Expansion of TATB is studied on a molecular level by means of x‐ray crystallography. Continuous monitoring of the cell constants of TATB between 214 K and 377 K allows calculation of a volume change of +5.1% for this molecular system. Expansion of the pure material is almost exclusively