Dergi makalesi Açık Erişim

Phenylene-2,5-dimethylpyrazine co-oligomers: synthesis by Suzuki couplings, X-ray structures of neutral and diprotonated teraryl species and efficient blue emission

Turksoy, F; Hughes, G; Batsanov, AS; Bryce, MR


MARC21 XML

<?xml version='1.0' encoding='UTF-8'?>
<record xmlns="http://www.loc.gov/MARC21/slim">
  <leader>00000nam##2200000uu#4500</leader>
  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Phenylene-2,5-dimethylpyrazine co-oligomers: synthesis by Suzuki couplings, X-ray structures of neutral and diprotonated teraryl species and efficient blue emission</subfield>
  </datafield>
  <datafield tag="909" ind1="C" ind2="4">
    <subfield code="p">JOURNAL OF MATERIALS CHEMISTRY</subfield>
    <subfield code="v">13</subfield>
    <subfield code="n">7</subfield>
    <subfield code="c">1554-1557</subfield>
  </datafield>
  <controlfield tag="001">95503</controlfield>
  <datafield tag="980" ind1=" " ind2=" ">
    <subfield code="a">user-tubitak-adresli-yayinlar</subfield>
  </datafield>
  <datafield tag="520" ind1=" " ind2=" ">
    <subfield code="a">Phenylene-2,5-dimethylpyrazinyl co-oligomers and a dipyridylpyrazine derivative have been synthesised by Suzuki cross-coupling reactions starting from 2,5-dibromo-3,6-dimethylpyrazine. X-Ray crystal structures are reported for two teraryl derivatives, viz. 2,5-bis(2-methoxyphenyl)-3,6-dimethylpyrazine 2 and 2,5-bis(6-methoxypyridin-3-yl)-3,6-dimethylpyrazine 6, and a diprotonated pyrazinyl dication salt, viz. 2,5-bis(2-methoxyphenyl)-3,6-dimethylpyrazinium bis(tetrafluoroborate) salt 3. Compounds 2 and 6 and the dication in 3 have crystallographic C-i symmetry and adopt twisted conformations: dihedral angles between the aryl and pyrazine rings are 74.0degrees (2), 56.4degrees (3) and 44.6degrees (6). Violet-blue photoluminescence is seen for 2 lambda(max) 372 nm, 5 lambda(max) 418 nm and 6 lambda(max) 387 nm in ethanol solution. [Compound 5 is 1,4-dimethoxy-2,5-bis{2-(5-tertbutylphenyl-3,6-dimethylpyrazinyl)benzene}]. Blue electroluminescence, lambda(max) 444 nm, is observed for the device structure ITO/PEDOT/5/Ca with no long-wavelength emission from pi-aggregates or exciton states.</subfield>
  </datafield>
  <datafield tag="650" ind1="1" ind2="7">
    <subfield code="2">opendefinition.org</subfield>
    <subfield code="a">cc-by</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Hughes, G</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Batsanov, AS</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Bryce, MR</subfield>
  </datafield>
  <datafield tag="980" ind1=" " ind2=" ">
    <subfield code="b">article</subfield>
    <subfield code="a">publication</subfield>
  </datafield>
  <datafield tag="542" ind1=" " ind2=" ">
    <subfield code="l">open</subfield>
  </datafield>
  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Turksoy, F</subfield>
  </datafield>
  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2003-01-01</subfield>
  </datafield>
  <controlfield tag="005">20210316131647.0</controlfield>
  <datafield tag="909" ind1="C" ind2="O">
    <subfield code="o">oai:zenodo.org:95503</subfield>
    <subfield code="p">user-tubitak-adresli-yayinlar</subfield>
  </datafield>
  <datafield tag="856" ind1="4" ind2=" ">
    <subfield code="z">md5:9c6d557b0e44a0d8098a1c2a0e439745</subfield>
    <subfield code="s">273</subfield>
    <subfield code="u">https://aperta.ulakbim.gov.trrecord/95503/files/bib-b46ac4aa-ef9d-42cc-b3d7-0396d481883b.txt</subfield>
  </datafield>
  <datafield tag="540" ind1=" " ind2=" ">
    <subfield code="u">http://www.opendefinition.org/licenses/cc-by</subfield>
    <subfield code="a">Creative Commons Attribution</subfield>
  </datafield>
  <datafield tag="024" ind1=" " ind2=" ">
    <subfield code="a">10.1039/b303472k</subfield>
    <subfield code="2">doi</subfield>
  </datafield>
</record>
37
8
görüntülenme
indirilme
Görüntülenme 37
İndirme 8
Veri hacmi 2.2 kB
Tekil görüntülenme 37
Tekil indirme 8

Alıntı yap