The Mass Spectra of Phenoxaphosphine Derivatives
العنوان: | The Mass Spectra of Phenoxaphosphine Derivatives |
---|---|
المؤلفون: | A. Kalir, Itshak Granoth, Ernst D. Bergmann, Z. Pelah |
المصدر: | Israel Journal of Chemistry. 8:621-632 |
بيانات النشر: | Wiley, 1970. |
سنة النشر: | 1970 |
مصطلحات موضوعية: | Group (periodic table), Chemistry, Stereochemistry, Phosphorus atom, Halogen, Mass spectrum, General Chemistry, Medicinal chemistry, Electron ionization, Ion |
الوصف: | Derivatives of phenoxaphosphine (I) do not behave under electron impact like diphenyl ethers: they do not lose CO, while loss of CHO was observed. The first step is the breakage of the P-R bond, followed by elimination of the phosphorus atom or—after rearrangement — a PO group. Methyl groups are either eliminated or cause the formation of tropylium structures. In halogen derivatives of I, not only the elimination of CHO, but also of COHal has been observed. In phenyl-di-(o-phenoxyphenyl)-phosphine (XXVI), a C-O bond is broken in preference to a C-P bond, and the 10,10-diphenylphenoxaphosphonium ion (XXVIII) is formed. |
تدمد: | 0021-2148 |
DOI: | 10.1002/ijch.197000074 |
URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_________::83ce36bddaf24e2570e729a79050df5c https://doi.org/10.1002/ijch.197000074 |
Rights: | CLOSED |
رقم الانضمام: | edsair.doi...........83ce36bddaf24e2570e729a79050df5c |
قاعدة البيانات: | OpenAIRE |
ResultId |
1 |
---|---|
Header |
edsair OpenAIRE edsair.doi...........83ce36bddaf24e2570e729a79050df5c 704 3 unknown 703.574829101563 |
PLink |
https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi...........83ce36bddaf24e2570e729a79050df5c&custid=s6537998&authtype=sso |
FullText |
Array
(
[Availability] => 0
)
Array ( [0] => Array ( [Url] => https://explore.openaire.eu/search/publication?articleId=doi_________::83ce36bddaf24e2570e729a79050df5c# [Name] => EDS - OpenAIRE [Category] => fullText [Text] => View record in OpenAIRE [MouseOverText] => View record in OpenAIRE ) ) |
Items |
Array
(
[Name] => Title
[Label] => Title
[Group] => Ti
[Data] => The Mass Spectra of Phenoxaphosphine Derivatives
)
Array ( [Name] => Author [Label] => Authors [Group] => Au [Data] => <searchLink fieldCode="AR" term="%22A%2E+Kalir%22">A. Kalir</searchLink><br /><searchLink fieldCode="AR" term="%22Itshak+Granoth%22">Itshak Granoth</searchLink><br /><searchLink fieldCode="AR" term="%22Ernst+D%2E+Bergmann%22">Ernst D. Bergmann</searchLink><br /><searchLink fieldCode="AR" term="%22Z%2E+Pelah%22">Z. Pelah</searchLink> ) Array ( [Name] => TitleSource [Label] => Source [Group] => Src [Data] => <i>Israel Journal of Chemistry</i>. 8:621-632 ) Array ( [Name] => Publisher [Label] => Publisher Information [Group] => PubInfo [Data] => Wiley, 1970. ) Array ( [Name] => DatePubCY [Label] => Publication Year [Group] => Date [Data] => 1970 ) Array ( [Name] => Subject [Label] => Subject Terms [Group] => Su [Data] => <searchLink fieldCode="DE" term="%22Group+%28periodic+table%29%22">Group (periodic table)</searchLink><br /><searchLink fieldCode="DE" term="%22Chemistry%22">Chemistry</searchLink><br /><searchLink fieldCode="DE" term="%22Stereochemistry%22">Stereochemistry</searchLink><br /><searchLink fieldCode="DE" term="%22Phosphorus+atom%22">Phosphorus atom</searchLink><br /><searchLink fieldCode="DE" term="%22Halogen%22">Halogen</searchLink><br /><searchLink fieldCode="DE" term="%22Mass+spectrum%22">Mass spectrum</searchLink><br /><searchLink fieldCode="DE" term="%22General+Chemistry%22">General Chemistry</searchLink><br /><searchLink fieldCode="DE" term="%22Medicinal+chemistry%22">Medicinal chemistry</searchLink><br /><searchLink fieldCode="DE" term="%22Electron+ionization%22">Electron ionization</searchLink><br /><searchLink fieldCode="DE" term="%22Ion%22">Ion</searchLink> ) Array ( [Name] => Abstract [Label] => Description [Group] => Ab [Data] => Derivatives of phenoxaphosphine (I) do not behave under electron impact like diphenyl ethers: they do not lose CO, while loss of CHO was observed. The first step is the breakage of the P-R bond, followed by elimination of the phosphorus atom or—after rearrangement — a PO group. Methyl groups are either eliminated or cause the formation of tropylium structures. In halogen derivatives of I, not only the elimination of CHO, but also of COHal has been observed. In phenyl-di-(o-phenoxyphenyl)-phosphine (XXVI), a C-O bond is broken in preference to a C-P bond, and the 10,10-diphenylphenoxaphosphonium ion (XXVIII) is formed. ) Array ( [Name] => ISSN [Label] => ISSN [Group] => ISSN [Data] => 0021-2148 ) Array ( [Name] => DOI [Label] => DOI [Group] => ID [Data] => 10.1002/ijch.197000074 ) Array ( [Name] => URL [Label] => Access URL [Group] => URL [Data] => <link linkTarget="URL" linkTerm="https://explore.openaire.eu/search/publication?articleId=doi_________::83ce36bddaf24e2570e729a79050df5c" linkWindow="_blank">https://explore.openaire.eu/search/publication?articleId=doi_________::83ce36bddaf24e2570e729a79050df5c</link><br /><link linkTarget="URL" linkTerm="https://doi.org/10.1002/ijch.197000074" linkWindow="_blank">https://doi.org/10.1002/ijch.197000074</link> ) Array ( [Name] => Copyright [Label] => Rights [Group] => Cpyrght [Data] => CLOSED ) Array ( [Name] => AN [Label] => Accession Number [Group] => ID [Data] => edsair.doi...........83ce36bddaf24e2570e729a79050df5c ) |
RecordInfo |
Array
(
[BibEntity] => Array
(
[Identifiers] => Array
(
[0] => Array
(
[Type] => doi
[Value] => 10.1002/ijch.197000074
)
)
[Languages] => Array
(
[0] => Array
(
[Text] => Undetermined
)
)
[PhysicalDescription] => Array
(
[Pagination] => Array
(
[PageCount] => 12
[StartPage] => 621
)
)
[Subjects] => Array
(
[0] => Array
(
[SubjectFull] => Group (periodic table)
[Type] => general
)
[1] => Array
(
[SubjectFull] => Chemistry
[Type] => general
)
[2] => Array
(
[SubjectFull] => Stereochemistry
[Type] => general
)
[3] => Array
(
[SubjectFull] => Phosphorus atom
[Type] => general
)
[4] => Array
(
[SubjectFull] => Halogen
[Type] => general
)
[5] => Array
(
[SubjectFull] => Mass spectrum
[Type] => general
)
[6] => Array
(
[SubjectFull] => General Chemistry
[Type] => general
)
[7] => Array
(
[SubjectFull] => Medicinal chemistry
[Type] => general
)
[8] => Array
(
[SubjectFull] => Electron ionization
[Type] => general
)
[9] => Array
(
[SubjectFull] => Ion
[Type] => general
)
)
[Titles] => Array
(
[0] => Array
(
[TitleFull] => The Mass Spectra of Phenoxaphosphine Derivatives
[Type] => main
)
)
)
[BibRelationships] => Array
(
[HasContributorRelationships] => Array
(
[0] => Array
(
[PersonEntity] => Array
(
[Name] => Array
(
[NameFull] => A. Kalir
)
)
)
[1] => Array
(
[PersonEntity] => Array
(
[Name] => Array
(
[NameFull] => Itshak Granoth
)
)
)
[2] => Array
(
[PersonEntity] => Array
(
[Name] => Array
(
[NameFull] => Ernst D. Bergmann
)
)
)
[3] => Array
(
[PersonEntity] => Array
(
[Name] => Array
(
[NameFull] => Z. Pelah
)
)
)
)
[IsPartOfRelationships] => Array
(
[0] => Array
(
[BibEntity] => Array
(
[Dates] => Array
(
[0] => Array
(
[D] => 01
[M] => 01
[Type] => published
[Y] => 1970
)
)
[Identifiers] => Array
(
[0] => Array
(
[Type] => issn-print
[Value] => 00212148
)
[1] => Array
(
[Type] => issn-locals
[Value] => edsair
)
)
[Numbering] => Array
(
[0] => Array
(
[Type] => volume
[Value] => 8
)
)
[Titles] => Array
(
[0] => Array
(
[TitleFull] => Israel Journal of Chemistry
[Type] => main
)
)
)
)
)
)
)
|
IllustrationInfo |