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Bridged cyclophosphazenes resulting from deprotonation reactions of cyclotriphophazenes bearing a P-NH group

Besli, Serap; Coles, Simon J.; Davies, David B.; Kilic, Adem; Shaw, Robert A.


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  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/18643</identifier>
  <creators>
    <creator>
      <creatorName>Besli, Serap</creatorName>
      <givenName>Serap</givenName>
      <familyName>Besli</familyName>
      <affiliation>Gebze Inst Technol, Dept Chem, Gebze, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Coles, Simon J.</creatorName>
      <givenName>Simon J.</givenName>
      <familyName>Coles</familyName>
      <affiliation>Univ Southampton, Dept Chem, Southampton SO17 1BJ, Hants, England</affiliation>
    </creator>
    <creator>
      <creatorName>Davies, David B.</creatorName>
      <givenName>David B.</givenName>
      <familyName>Davies</familyName>
      <affiliation>Univ London Birkbeck Coll, Sch Biol &amp; Chem Sci, London WC1E 7HX, England</affiliation>
    </creator>
    <creator>
      <creatorName>Kilic, Adem</creatorName>
      <givenName>Adem</givenName>
      <familyName>Kilic</familyName>
      <affiliation>Gebze Inst Technol, Dept Chem, Gebze, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Shaw, Robert A.</creatorName>
      <givenName>Robert A.</givenName>
      <familyName>Shaw</familyName>
      <affiliation>Univ London Birkbeck Coll, Sch Biol &amp; Chem Sci, London WC1E 7HX, England</affiliation>
    </creator>
  </creators>
  <titles>
    <title>Bridged Cyclophosphazenes Resulting From Deprotonation Reactions Of Cyclotriphophazenes Bearing A P-Nh Group</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>2011</publicationYear>
  <dates>
    <date dateType="Issued">2011-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/18643</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1039/c1dt10073d</relatedIdentifier>
  </relatedIdentifiers>
  <rightsList>
    <rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights>
    <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights>
  </rightsList>
  <descriptions>
    <description descriptionType="Abstract">Cyclotriphosphazene derivatives containing a P-NHR group in the side-chain react in the presence of a strong base to form stable intermolecular bridged products. Reaction of sodium hydride with mono-spiro cyclophosphazene derivatives having a P-NH group, N3P3Cl4[O(CH2)(3)NH], (1a) or N3P3Cl4[CH3N(CH2)(3)NH], (1b) leads to formation of bis-cyclophosphazenes bridged with an eight-membered cyclophosphazene ring in an ansa arrangement (2a, 2b) whereas reaction of sodium hydride with mono-amino cyclophosphazene derivatives [N3P3Cl5(NHR), R = n-hexyl, 3a; i-Pr, 3b; Ph, 3c] give bis-cyclophosphazenes bridged with a four-membered cyclophosphazane ring in a spiro arrangement (4a-c). In the latter reaction P-O-P bridged compounds (5a-c) were also obtained as a result of hydrolysis reactions associated with the amount of moisture in the solvent tetrahydrofuran. In addition, it was found that reaction of a mixture of cyclotriphosphazene with either mono spiro compound, (1a) or (1b), in the presence of sodium hydride lead to formation of the first examples of asymmetrically-bridged cyclophosphazenes (6a-b).</description>
  </descriptions>
</resource>
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