Dergi makalesi Açık Erişim
Tarakci, Deniz Kutlu; Gurol, Ilke
<?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">Synthesis and characterization of tetra-substituted titanium(IV) phthalocyanines with axial ligand</subfield> </datafield> <datafield tag="909" ind1="C" ind2="4"> <subfield code="p">TURKISH JOURNAL OF CHEMISTRY</subfield> <subfield code="v">38</subfield> <subfield code="n">6</subfield> <subfield code="c">1056-1063</subfield> </datafield> <controlfield tag="001">90519</controlfield> <datafield tag="980" ind1=" " ind2=" "> <subfield code="a">user-tubitak-adresli-yayinlar</subfield> </datafield> <datafield tag="980" ind1=" " ind2=" "> <subfield code="a">user-tubitak-destekli-proje-yayinlari</subfield> </datafield> <datafield tag="520" ind1=" " ind2=" "> <subfield code="a">In this paper, the synthesis and characterization of peripheral tetra-2-(2-ethyloxyethyloxy)ethyloxy substituted oxo-titanium phthalocyanines (TiOPcs) are reported. The reaction of 2,2,3,3-tetrafluoropropoxy substituted and [2-(2-ethoxyethoxy) ethoxy] substituted TiOPcs (1 and 3) with 4-[(6-hydroxyhexyl)oxy]benzene-1,2-diol as a strongly chelating oxygen donor ligand is described. Compounds 1 a and 3 a bearing the hydroxyl group as an axial ligand of the bulky group are converted into a thiol group (1c and 3c). The new compounds are characterized by elemental analysis, FT-IR, (1) H NMR, and mass spectrometry. While the fluoropropoxy substituted TiOPc has good solubility in polar solvents such as acetone and THF, the other TiOPc is soluble in chloroform.</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="u">Tubitak Marmara Res Ctr, Mat Inst, Gebze, Kocaeli, Turkey</subfield> <subfield code="a">Gurol, Ilke</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="u">Gebze Inst Technol, Dept Chem, TR-41400 Gebze, Kocaeli, Turkey</subfield> <subfield code="a">Tarakci, Deniz Kutlu</subfield> </datafield> <datafield tag="260" ind1=" " ind2=" "> <subfield code="c">2014-01-01</subfield> </datafield> <controlfield tag="005">20210316115335.0</controlfield> <datafield tag="909" ind1="C" ind2="O"> <subfield code="o">oai:zenodo.org:90519</subfield> <subfield code="p">user-tubitak-adresli-yayinlar</subfield> <subfield code="p">user-tubitak-destekli-proje-yayinlari</subfield> </datafield> <datafield tag="856" ind1="4" ind2=" "> <subfield code="z">md5:9c501e447f61eb18e2aa482f2acf8739</subfield> <subfield code="s">1356191</subfield> <subfield code="u">https://aperta.ulakbim.gov.trrecord/90519/files/10-3906-kim-1406-46.pdf</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">10.3906/kim-1406-46</subfield> <subfield code="2">doi</subfield> </datafield> </record>
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