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Synthesis, Characterization and Decomposition of 4‐Diazo‐2,6‐dinitrophenol
A high energetic compound 4‐diazo‐2,6‐dinitrophenol was synthesized by employing one‐pot facile method from 4‐chloro‐3,5‐dinitroaniline. Its structure was characterized by Fourier transform infrared spectroscopy (FT‐IR), elemental analysis (EA), and nuclear magnetic resonance spectroscopy (1H NMR, 1...
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Published in: | Propellants, explosives, pyrotechnics explosives, pyrotechnics, 2021-09, Vol.46 (9), p.1388-1396 |
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container_title | Propellants, explosives, pyrotechnics |
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creator | Wang, Jian‐long Cao, Cai Cao, Jun‐yan Yan, Yu‐min Chen, Li‐zhen Cao, Duan‐lin |
description | A high energetic compound 4‐diazo‐2,6‐dinitrophenol was synthesized by employing one‐pot facile method from 4‐chloro‐3,5‐dinitroaniline. Its structure was characterized by Fourier transform infrared spectroscopy (FT‐IR), elemental analysis (EA), and nuclear magnetic resonance spectroscopy (1H NMR, 13C NMR and 15N NMR). The crystal structure was determined using an X‐ray single crystal diffractometer. The detonation properties of 4‐diazo‐2,6‐dinitrophenol and 6‐diazo‐3,5‐dichloro‐2,4‐dinitrophenol were compared by using Kamlet formula. Besides, the thermal behavior of 4‐diazo‐2,6‐dinitrophenol was analyzed by differential scanning calorimetry (DSC) and accelerating rate calorimeter (ARC), then according to the thermal analysis data, the thermal decomposition kinetics parameters were calculated using the thermal analysis data based on Kissinger method and Flynn‐Wall‐Ozawa method. |
doi_str_mv | 10.1002/prep.202100005 |
format | article |
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Its structure was characterized by Fourier transform infrared spectroscopy (FT‐IR), elemental analysis (EA), and nuclear magnetic resonance spectroscopy (1H NMR, 13C NMR and 15N NMR). The crystal structure was determined using an X‐ray single crystal diffractometer. The detonation properties of 4‐diazo‐2,6‐dinitrophenol and 6‐diazo‐3,5‐dichloro‐2,4‐dinitrophenol were compared by using Kamlet formula. Besides, the thermal behavior of 4‐diazo‐2,6‐dinitrophenol was analyzed by differential scanning calorimetry (DSC) and accelerating rate calorimeter (ARC), then according to the thermal analysis data, the thermal decomposition kinetics parameters were calculated using the thermal analysis data based on Kissinger method and Flynn‐Wall‐Ozawa method.</description><identifier>ISSN: 0721-3115</identifier><identifier>EISSN: 1521-4087</identifier><identifier>DOI: 10.1002/prep.202100005</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>4-Diazo-2,6-dinitrophenol ; Chemical analysis ; Crystal structure ; Crystals ; Data analysis ; Detonation ; Detonation velocity ; Fourier transforms ; Infrared analysis ; Infrared spectroscopy ; NMR ; NMR spectroscopy ; Nuclear magnetic resonance ; Single crystals ; Spectrum analysis ; Thermal analysis ; Thermal Decomposition ; Thermodynamic properties</subject><ispartof>Propellants, explosives, pyrotechnics, 2021-09, Vol.46 (9), p.1388-1396</ispartof><rights>2021 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3175-b03d0343e777e05308ae277aedce38285271469552e02c2957bd03152935b9a03</citedby><cites>FETCH-LOGICAL-c3175-b03d0343e777e05308ae277aedce38285271469552e02c2957bd03152935b9a03</cites><orcidid>0000-0003-4432-3701</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Wang, Jian‐long</creatorcontrib><creatorcontrib>Cao, Cai</creatorcontrib><creatorcontrib>Cao, Jun‐yan</creatorcontrib><creatorcontrib>Yan, Yu‐min</creatorcontrib><creatorcontrib>Chen, Li‐zhen</creatorcontrib><creatorcontrib>Cao, Duan‐lin</creatorcontrib><title>Synthesis, Characterization and Decomposition of 4‐Diazo‐2,6‐dinitrophenol</title><title>Propellants, explosives, pyrotechnics</title><description>A high energetic compound 4‐diazo‐2,6‐dinitrophenol was synthesized by employing one‐pot facile method from 4‐chloro‐3,5‐dinitroaniline. Its structure was characterized by Fourier transform infrared spectroscopy (FT‐IR), elemental analysis (EA), and nuclear magnetic resonance spectroscopy (1H NMR, 13C NMR and 15N NMR). The crystal structure was determined using an X‐ray single crystal diffractometer. The detonation properties of 4‐diazo‐2,6‐dinitrophenol and 6‐diazo‐3,5‐dichloro‐2,4‐dinitrophenol were compared by using Kamlet formula. Besides, the thermal behavior of 4‐diazo‐2,6‐dinitrophenol was analyzed by differential scanning calorimetry (DSC) and accelerating rate calorimeter (ARC), then according to the thermal analysis data, the thermal decomposition kinetics parameters were calculated using the thermal analysis data based on Kissinger method and Flynn‐Wall‐Ozawa method.</description><subject>4-Diazo-2,6-dinitrophenol</subject><subject>Chemical analysis</subject><subject>Crystal structure</subject><subject>Crystals</subject><subject>Data analysis</subject><subject>Detonation</subject><subject>Detonation velocity</subject><subject>Fourier transforms</subject><subject>Infrared analysis</subject><subject>Infrared spectroscopy</subject><subject>NMR</subject><subject>NMR spectroscopy</subject><subject>Nuclear magnetic resonance</subject><subject>Single crystals</subject><subject>Spectrum analysis</subject><subject>Thermal analysis</subject><subject>Thermal Decomposition</subject><subject>Thermodynamic properties</subject><issn>0721-3115</issn><issn>1521-4087</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkMtOwzAQRS0EEqWwZR2JbVPGdhwnS9QHIFWi4rG2nGSiumrjYKdC7YpP4Bv5ElyKYMlmXjp3RnMJuaQwpADsunXYDhmw0ACII9KjgtE4gUwekx7IUHNKxSk5834JsKdoj8yftk23QG_8IBottNNlh87sdGdsE-mmisZY2nVrvfme2DpKPt8_xkbvbMhskIZYmcZ0zrYLbOzqnJzUeuXx4if3yct08jy6i2cPt_ejm1lccipFXACvgCccpZQIgkOmkUmpsSqRZywTTNIkzYVgCKxkuZBF4MNHORdFroH3ydVhb-vs6wZ9p5Z245pwUjGR5mmSAcsCNTxQpbPeO6xV68xau62ioPauqb1r6te1IMgPgjezwu0_tJo_TuZ_2i9DOXIq</recordid><startdate>202109</startdate><enddate>202109</enddate><creator>Wang, Jian‐long</creator><creator>Cao, Cai</creator><creator>Cao, Jun‐yan</creator><creator>Yan, Yu‐min</creator><creator>Chen, Li‐zhen</creator><creator>Cao, Duan‐lin</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7TB</scope><scope>8FD</scope><scope>FR3</scope><scope>H8D</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0003-4432-3701</orcidid></search><sort><creationdate>202109</creationdate><title>Synthesis, Characterization and Decomposition of 4‐Diazo‐2,6‐dinitrophenol</title><author>Wang, Jian‐long ; Cao, Cai ; Cao, Jun‐yan ; Yan, Yu‐min ; Chen, Li‐zhen ; Cao, Duan‐lin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3175-b03d0343e777e05308ae277aedce38285271469552e02c2957bd03152935b9a03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>4-Diazo-2,6-dinitrophenol</topic><topic>Chemical analysis</topic><topic>Crystal structure</topic><topic>Crystals</topic><topic>Data analysis</topic><topic>Detonation</topic><topic>Detonation velocity</topic><topic>Fourier transforms</topic><topic>Infrared analysis</topic><topic>Infrared spectroscopy</topic><topic>NMR</topic><topic>NMR spectroscopy</topic><topic>Nuclear magnetic resonance</topic><topic>Single crystals</topic><topic>Spectrum analysis</topic><topic>Thermal analysis</topic><topic>Thermal Decomposition</topic><topic>Thermodynamic properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Jian‐long</creatorcontrib><creatorcontrib>Cao, Cai</creatorcontrib><creatorcontrib>Cao, Jun‐yan</creatorcontrib><creatorcontrib>Yan, Yu‐min</creatorcontrib><creatorcontrib>Chen, Li‐zhen</creatorcontrib><creatorcontrib>Cao, Duan‐lin</creatorcontrib><collection>CrossRef</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Propellants, explosives, pyrotechnics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Jian‐long</au><au>Cao, Cai</au><au>Cao, Jun‐yan</au><au>Yan, Yu‐min</au><au>Chen, Li‐zhen</au><au>Cao, Duan‐lin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis, Characterization and Decomposition of 4‐Diazo‐2,6‐dinitrophenol</atitle><jtitle>Propellants, explosives, pyrotechnics</jtitle><date>2021-09</date><risdate>2021</risdate><volume>46</volume><issue>9</issue><spage>1388</spage><epage>1396</epage><pages>1388-1396</pages><issn>0721-3115</issn><eissn>1521-4087</eissn><abstract>A high energetic compound 4‐diazo‐2,6‐dinitrophenol was synthesized by employing one‐pot facile method from 4‐chloro‐3,5‐dinitroaniline. Its structure was characterized by Fourier transform infrared spectroscopy (FT‐IR), elemental analysis (EA), and nuclear magnetic resonance spectroscopy (1H NMR, 13C NMR and 15N NMR). The crystal structure was determined using an X‐ray single crystal diffractometer. The detonation properties of 4‐diazo‐2,6‐dinitrophenol and 6‐diazo‐3,5‐dichloro‐2,4‐dinitrophenol were compared by using Kamlet formula. Besides, the thermal behavior of 4‐diazo‐2,6‐dinitrophenol was analyzed by differential scanning calorimetry (DSC) and accelerating rate calorimeter (ARC), then according to the thermal analysis data, the thermal decomposition kinetics parameters were calculated using the thermal analysis data based on Kissinger method and Flynn‐Wall‐Ozawa method.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/prep.202100005</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-4432-3701</orcidid></addata></record> |
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subjects | 4-Diazo-2,6-dinitrophenol Chemical analysis Crystal structure Crystals Data analysis Detonation Detonation velocity Fourier transforms Infrared analysis Infrared spectroscopy NMR NMR spectroscopy Nuclear magnetic resonance Single crystals Spectrum analysis Thermal analysis Thermal Decomposition Thermodynamic properties |
title | Synthesis, Characterization and Decomposition of 4‐Diazo‐2,6‐dinitrophenol |
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