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dc.contributor.authorYilmaz, Nurdane
dc.contributor.authorOz, Sevi
dc.contributor.authorAtakol, Arda
dc.contributor.authorSvoboda, Ingrid
dc.contributor.authorAydiner, Burcu
dc.contributor.authorAkay, M. Abdulkadir
dc.contributor.authorAtakol, Orhan
dc.date.accessioned2019-11-24T20:38:32Z
dc.date.available2019-11-24T20:38:32Z
dc.date.issued2015
dc.identifier.issn1388-6150
dc.identifier.issn1588-2926
dc.identifier.urihttps://dx.doi.org/10.1007/s10973-014-4243-z
dc.identifier.urihttps://hdl.handle.net/20.500.12513/2539
dc.descriptionWOS: 000350225500083en_US
dc.description.abstract1-phenyl-1H-tetrazole (I), 1(2-chlorophenyl)-1H-tetrazole (II), 1(4-chlorophenyl)-1H-tetrazole (III), 1(4-hydroxyphenyl)-1H-tetrazole (IV), 1(4-methoxyphenyl)-1H-tetrazole (V), 1(4-nitrophenyl)-1H-tetrazole (VI), 1(2-pyridyl)-1H-tetrazole (VII), and bis-1,4-tetrazol-1-yl benzene (VIII) were prepared from aniline, 2-chloro aniline, 4-chloro aniline, 4-hydroxy aniline, 4-methoxy aniline, 4-nitro aniline, 2-aminopyridine, and 1,4-phenylendiamine and characterized by Infrared spectroscopy, elemental analysis, mass spectrometry, H-1 Nuclear Magnetic Resonance, and C-13 Nuclear Magnetic Resonance spectroscopy. Suitable crystals of compounds I, II, IV, V, and VI were obtained and their molecular structures were determined using single crystal X-ray Diffraction. All tetrazole compounds were also investigated using Thermogravimetry-Differential Thermal Analysis. At temperatures between 190-240 A degrees C, the tetrazole ring decomposed exothermically. The decomposition products were estimated by relating the mass loss data and IR spectroscopy results of the residue with N-2 release and isonitrile formation as outcome of thermal decomposition. The heat of the exothermic decomposition was measured by Differential Scanning Calorimetry. Optimizations and frequency analyses of all tetrazole compounds were performed at the B3LYP/cc-pVDZ level of theory which are DFT-based structures. The optimum geometries of tetrazole compounds were enlightened with the help of Gaussian 09 pocket program. The enthalpies of formation for solid state were calculated theoretically by CBS-4 M algorithm. The calculated results were compared with the experimental data obtained from DSC study. It was seen that the enthalpies of decomposition of compounds II, III, IV, and V were in good agreement with the theoretical values. However, decomposition of compounds I, VI, VII, and VIII showed significant variation from the theoretical calculations.en_US
dc.description.sponsorshipUniversity of Ankara Scientific Research FundAnkara University [12B4240003]; Ahi Evran University Scientific Research FundAhi Evran University [4001.12.014]en_US
dc.description.sponsorshipFinancial support of this work by the University of Ankara Scientific Research Fund under contract no. 12B4240003 and Ahi Evran University Scientific Research Fund under contract no. 4001.12.014 are gratefully acknowledged. We are indebted to and thank Prof. Dr. Wolfgang Donner for providing laboratory facilities at TU Darmstadt.en_US
dc.language.isoengen_US
dc.publisherSPRINGERen_US
dc.relation.isversionof10.1007/s10973-014-4243-zen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectSubstituted-1H-tetrazolesen_US
dc.subjectTGen_US
dc.subjectDSCen_US
dc.subjectEnergetic materialsen_US
dc.subjectThermal decompositionen_US
dc.subjectCBS-4Men_US
dc.titleAn experimental and theoretical study toward the synthesis, structure and thermal decomposition of some phenyl tetrazolesen_US
dc.typearticleen_US
dc.relation.journalJOURNAL OF THERMAL ANALYSIS AND CALORIMETRYen_US
dc.contributor.departmentKırşehir Ahi Evran Üniversitesi, Fen-Edebiyat Fakültesi, Kimya Bölümüen_US
dc.identifier.volume119en_US
dc.identifier.issue3en_US
dc.identifier.startpage2321en_US
dc.identifier.endpage2328en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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