{"title":"Synthesis of halogen analogues of sulfur mustard","authors":"Paweł Sura, S. Popiel, J. Nawała","doi":"10.5604/01.3001.0015.8773","DOIUrl":null,"url":null,"abstract":"Bis(2-chloroethyl) sulfide, known as mustard gas (HD), is a well-known, poisonous warfare\nagent whose first use on the battlefield dates back to the First World War. However, there are halogen\nanalogues which, instead of two chlorine atoms bonded to carbon atoms in the beta position, have\nbromine, iodine, or fluorine atoms. These compounds were not used for military purposes and they\nwere not covered by the Chemical Weapons Convention (CWC). Moreover, these are the substances\nthat are very poorly described in the literature. However, due to their chemical structure and properties,\nthey can be excellent imitators of sulfur mustard, used to carry out a number of tests without the need\nto use the above-mentioned chemical warfare agent. Halogen analogues of sulfur mustard can be used\nto study the course and kinetics of electrophilic and nucleophilic reactions, as well as to conduct the\ndecontamination process, including its effectiveness, in much safer conditions, while maintaining the\ncredibility of the results. The article reviews the literature data on the properties of halogen analogues\nof sulfur mustard and it presents descriptions of the synthesis of these compounds. Then, their analysis\nwas carried out using gas chromatography coupled with an atomic emission detector (GC-AED) and\ngas chromatography with a mass spectrometer (GC-MS). As a result of the performed syntheses and\nanalyses, it was possible to obtain the assumed chemicals and to collect their mass spectra, while the\nspectra of bis (2-iodoethyl) sulfide and bis (2-fluoroethyl) sulfide are not available in commercial\nmass libraries.\n\n","PeriodicalId":232579,"journal":{"name":"Bulletin of the Military University of Technology","volume":"98 3 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bulletin of the Military University of Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5604/01.3001.0015.8773","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Bis(2-chloroethyl) sulfide, known as mustard gas (HD), is a well-known, poisonous warfare
agent whose first use on the battlefield dates back to the First World War. However, there are halogen
analogues which, instead of two chlorine atoms bonded to carbon atoms in the beta position, have
bromine, iodine, or fluorine atoms. These compounds were not used for military purposes and they
were not covered by the Chemical Weapons Convention (CWC). Moreover, these are the substances
that are very poorly described in the literature. However, due to their chemical structure and properties,
they can be excellent imitators of sulfur mustard, used to carry out a number of tests without the need
to use the above-mentioned chemical warfare agent. Halogen analogues of sulfur mustard can be used
to study the course and kinetics of electrophilic and nucleophilic reactions, as well as to conduct the
decontamination process, including its effectiveness, in much safer conditions, while maintaining the
credibility of the results. The article reviews the literature data on the properties of halogen analogues
of sulfur mustard and it presents descriptions of the synthesis of these compounds. Then, their analysis
was carried out using gas chromatography coupled with an atomic emission detector (GC-AED) and
gas chromatography with a mass spectrometer (GC-MS). As a result of the performed syntheses and
analyses, it was possible to obtain the assumed chemicals and to collect their mass spectra, while the
spectra of bis (2-iodoethyl) sulfide and bis (2-fluoroethyl) sulfide are not available in commercial
mass libraries.