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Gas-phase reactions of alcohols with hexamethylene triperoxide diamine (HMTD) under atmospheric pressure chemical ionization conditions
RATIONALE Hexamethylene triperoxide diamine (HMTD) is a sensitive peroxide explosive first synthesized in 1885. HMTD exhibits an unusual gas‐phase phenomenon in the presence of alcohols that has been previously observed, but incorrectly resolved. We are attempting to determine this specific mechanis...
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Published in: | Rapid communications in mass spectrometry 2015-01, Vol.29 (1), p.74-80 |
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creator | Colizza, Kevin Porter, Matthew Smith, James L. Oxley, Jimmie C. |
description | RATIONALE
Hexamethylene triperoxide diamine (HMTD) is a sensitive peroxide explosive first synthesized in 1885. HMTD exhibits an unusual gas‐phase phenomenon in the presence of alcohols that has been previously observed, but incorrectly resolved. We are attempting to determine this specific mechanism.
METHODS
We used positive ion mode atmospheric pressure chemical ionization (APCI) as the interface to the mass spectrometer. HMTD was infused with various solvents including 18O‐ and 2H‐labeled methanol in order to determine gas‐phase reaction mechanisms.
RESULTS
Based on these labeled experiments, it was determined that, under APCI conditions, the alcohol oxygen attacks a methylene carbon of HMTD and releases H2O2. This was attempted with nine different alcohols and, in each case, the alcohol is fully incorporated into the molecule with the peroxide release. A mechanism for this reaction has been proposed.
CONCLUSIONS
This work appears to have confirmed the gas‐phase reaction mechanism of HMTD with alcohols. As we continue efforts to characterize this unusual molecule, the information may prove useful in determining formation and degradation mechanism(s). In addition, this property of HMTD may find use in other fields of science. Copyright © 2014 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/rcm.7084 |
format | article |
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Hexamethylene triperoxide diamine (HMTD) is a sensitive peroxide explosive first synthesized in 1885. HMTD exhibits an unusual gas‐phase phenomenon in the presence of alcohols that has been previously observed, but incorrectly resolved. We are attempting to determine this specific mechanism.
METHODS
We used positive ion mode atmospheric pressure chemical ionization (APCI) as the interface to the mass spectrometer. HMTD was infused with various solvents including 18O‐ and 2H‐labeled methanol in order to determine gas‐phase reaction mechanisms.
RESULTS
Based on these labeled experiments, it was determined that, under APCI conditions, the alcohol oxygen attacks a methylene carbon of HMTD and releases H2O2. This was attempted with nine different alcohols and, in each case, the alcohol is fully incorporated into the molecule with the peroxide release. A mechanism for this reaction has been proposed.
CONCLUSIONS
This work appears to have confirmed the gas‐phase reaction mechanism of HMTD with alcohols. As we continue efforts to characterize this unusual molecule, the information may prove useful in determining formation and degradation mechanism(s). In addition, this property of HMTD may find use in other fields of science. Copyright © 2014 John Wiley & Sons, Ltd.</description><identifier>ISSN: 0951-4198</identifier><identifier>EISSN: 1097-0231</identifier><identifier>DOI: 10.1002/rcm.7084</identifier><identifier>PMID: 25462366</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Alcohols ; Atmospheric pressure ; Barometric pressure ; Diamines ; Ionization ; Methyl alcohol ; Peroxides ; Reaction mechanisms</subject><ispartof>Rapid communications in mass spectrometry, 2015-01, Vol.29 (1), p.74-80</ispartof><rights>Copyright © 2014 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4204-4731ef5c0da7aa7752431b5d0a12ddce7c3683abf2a727d0b6ea9414a530e5553</citedby><cites>FETCH-LOGICAL-c4204-4731ef5c0da7aa7752431b5d0a12ddce7c3683abf2a727d0b6ea9414a530e5553</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25462366$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Colizza, Kevin</creatorcontrib><creatorcontrib>Porter, Matthew</creatorcontrib><creatorcontrib>Smith, James L.</creatorcontrib><creatorcontrib>Oxley, Jimmie C.</creatorcontrib><title>Gas-phase reactions of alcohols with hexamethylene triperoxide diamine (HMTD) under atmospheric pressure chemical ionization conditions</title><title>Rapid communications in mass spectrometry</title><addtitle>Rapid Commun. Mass Spectrom</addtitle><description>RATIONALE
Hexamethylene triperoxide diamine (HMTD) is a sensitive peroxide explosive first synthesized in 1885. HMTD exhibits an unusual gas‐phase phenomenon in the presence of alcohols that has been previously observed, but incorrectly resolved. We are attempting to determine this specific mechanism.
METHODS
We used positive ion mode atmospheric pressure chemical ionization (APCI) as the interface to the mass spectrometer. HMTD was infused with various solvents including 18O‐ and 2H‐labeled methanol in order to determine gas‐phase reaction mechanisms.
RESULTS
Based on these labeled experiments, it was determined that, under APCI conditions, the alcohol oxygen attacks a methylene carbon of HMTD and releases H2O2. This was attempted with nine different alcohols and, in each case, the alcohol is fully incorporated into the molecule with the peroxide release. A mechanism for this reaction has been proposed.
CONCLUSIONS
This work appears to have confirmed the gas‐phase reaction mechanism of HMTD with alcohols. As we continue efforts to characterize this unusual molecule, the information may prove useful in determining formation and degradation mechanism(s). In addition, this property of HMTD may find use in other fields of science. Copyright © 2014 John Wiley & Sons, Ltd.</description><subject>Alcohols</subject><subject>Atmospheric pressure</subject><subject>Barometric pressure</subject><subject>Diamines</subject><subject>Ionization</subject><subject>Methyl alcohol</subject><subject>Peroxides</subject><subject>Reaction mechanisms</subject><issn>0951-4198</issn><issn>1097-0231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqNkV9r1EAUR4Modq2Cn0AGfKkPqfM3kzzqVneFVkUqgi_D3ZkbMjXJxJmE7voF_Npm27WCIPg0cDmcH8PJsqeMnjJK-ctou1NNS3kvWzBa6Zxywe5nC1oplktWlUfZo5SuKGVMcfowO-JKFlwUxSL7uYKUDw0kJBHBjj70iYSaQGtDE9pErv3YkAa30OHY7FrskYzRDxjD1jskzkPn59vJ-uLy7AWZeoeRwNiFNDQYvSVDxJSmiMQ22HkLLZkn_A_YLxEbeudvNh9nD2poEz45vMfZ57dvLpfr_PzD6t3y1XluJacyl1owrJWlDjSA1opLwTbKUWDcOYvaiqIUsKk5aK4d3RQIlWQSlKColBLH2cmtd4jh-4RpNJ1PFtsWegxTMqxQTHKlqPwPlFfV7KRiRp__hV6FKfbzR24owZRm1R-hjSGliLUZou8g7gyjZt_RzB3NvuOMPjsIp02H7g78HW4G8lvg2re4-6fIfFpeHIQH3qcRt3c8xG-m0EIr8-X9yqzPPpavuSjNV_ELUsS23g</recordid><startdate>20150115</startdate><enddate>20150115</enddate><creator>Colizza, Kevin</creator><creator>Porter, Matthew</creator><creator>Smith, James L.</creator><creator>Oxley, Jimmie C.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>JQ2</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>20150115</creationdate><title>Gas-phase reactions of alcohols with hexamethylene triperoxide diamine (HMTD) under atmospheric pressure chemical ionization conditions</title><author>Colizza, Kevin ; Porter, Matthew ; Smith, James L. ; Oxley, Jimmie C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4204-4731ef5c0da7aa7752431b5d0a12ddce7c3683abf2a727d0b6ea9414a530e5553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Alcohols</topic><topic>Atmospheric pressure</topic><topic>Barometric pressure</topic><topic>Diamines</topic><topic>Ionization</topic><topic>Methyl alcohol</topic><topic>Peroxides</topic><topic>Reaction mechanisms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Colizza, Kevin</creatorcontrib><creatorcontrib>Porter, Matthew</creatorcontrib><creatorcontrib>Smith, James L.</creatorcontrib><creatorcontrib>Oxley, Jimmie C.</creatorcontrib><collection>Istex</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Rapid communications in mass spectrometry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Colizza, Kevin</au><au>Porter, Matthew</au><au>Smith, James L.</au><au>Oxley, Jimmie C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gas-phase reactions of alcohols with hexamethylene triperoxide diamine (HMTD) under atmospheric pressure chemical ionization conditions</atitle><jtitle>Rapid communications in mass spectrometry</jtitle><addtitle>Rapid Commun. Mass Spectrom</addtitle><date>2015-01-15</date><risdate>2015</risdate><volume>29</volume><issue>1</issue><spage>74</spage><epage>80</epage><pages>74-80</pages><issn>0951-4198</issn><eissn>1097-0231</eissn><abstract>RATIONALE
Hexamethylene triperoxide diamine (HMTD) is a sensitive peroxide explosive first synthesized in 1885. HMTD exhibits an unusual gas‐phase phenomenon in the presence of alcohols that has been previously observed, but incorrectly resolved. We are attempting to determine this specific mechanism.
METHODS
We used positive ion mode atmospheric pressure chemical ionization (APCI) as the interface to the mass spectrometer. HMTD was infused with various solvents including 18O‐ and 2H‐labeled methanol in order to determine gas‐phase reaction mechanisms.
RESULTS
Based on these labeled experiments, it was determined that, under APCI conditions, the alcohol oxygen attacks a methylene carbon of HMTD and releases H2O2. This was attempted with nine different alcohols and, in each case, the alcohol is fully incorporated into the molecule with the peroxide release. A mechanism for this reaction has been proposed.
CONCLUSIONS
This work appears to have confirmed the gas‐phase reaction mechanism of HMTD with alcohols. As we continue efforts to characterize this unusual molecule, the information may prove useful in determining formation and degradation mechanism(s). In addition, this property of HMTD may find use in other fields of science. Copyright © 2014 John Wiley & Sons, Ltd.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>25462366</pmid><doi>10.1002/rcm.7084</doi><tpages>7</tpages></addata></record> |
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source | Wiley-Blackwell Read & Publish Collection |
subjects | Alcohols Atmospheric pressure Barometric pressure Diamines Ionization Methyl alcohol Peroxides Reaction mechanisms |
title | Gas-phase reactions of alcohols with hexamethylene triperoxide diamine (HMTD) under atmospheric pressure chemical ionization conditions |
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