Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Nusrallah Jubran"'
Autor:
Jonas Sidaravicius, Jolita Ostrauskaite, Vygintas Jankauskas, Valentas Gaidelis, J.V. Grazulevicius, Zbigniew Tokarski, A. Dzena, A. Danilevicius, Nusrallah Jubran, S. Grevys
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 163:523-528
The synthesis and optical, thermal as well as photoelectrical properties of a series of glass-forming phenothiazine-based mono- and dihydrazones are reported. The ionization potentials of the phenothiazine-based hydrazones measured by electron photoe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b6a2ecb147693e8eef377ce0517c815
https://doi.org/10.1016/j.jphotochem.2004.02.009
https://doi.org/10.1016/j.jphotochem.2004.02.009
Autor:
Dale D. Russell, Ryan L Meyer, Nathan G. Davis, Ron Moudry, Nusrallah Jubran, Zbigniew Tokarski, Hwan-Koo Lee
Publikováno v:
NIP & Digital Fabrication Conference. 20:538-542
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2046a69c392480718faf1568dff617d5
https://doi.org/10.2352/issn.2169-4451.2004.20.1.art00006_2
https://doi.org/10.2352/issn.2169-4451.2004.20.1.art00006_2
Autor:
Nusrallah Jubran, Kam Law, Zbig Tokarski, Ron Moudry, James Baker, Hwan-Koo Lee, Valentas Gaidelis, Jonas Sidaravicius, Edmundas Montrimas
Publikováno v:
NIP & Digital Fabrication Conference. 18:674-677
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0778dc8189f6fbf7dd20a6d056c96f9
https://doi.org/10.2352/issn.2169-4451.2002.18.1.art00060_2
https://doi.org/10.2352/issn.2169-4451.2002.18.1.art00060_2
Autor:
Louis M. Leichter, Zhongxing Zhang, Hengyuan Lang, Alan R. Katritzky, Norman P Sweeny, Nusrallah Jubran
Publikováno v:
Journal of Heterocyclic Chemistry. 34:561-565
2-Mono- and 2,5-bis[bis[(4-dimethylamino)phenyl]hydroxymethyl]substituted furan, thiophene and N-methylpyrrole were synthesized by mono- and dilithiation of furan, thiophene and N-methylpyrrole, respectively, and subsequent reaction with Michler's ke
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::681a9dee88b73636483a98c695758eeb
https://doi.org/10.1002/jhet.5570340236
https://doi.org/10.1002/jhet.5570340236
Autor:
Nusrallah Jubran, Hengyuan Lang, Louis M. Leichter, Zhongxing Zhang, Alan R. Katritzky, Norman P Sweeny
Publikováno v:
Journal of Materials Chemistry. 7:1399-1404
Lithiations ofN-phenylbenzenesulfinamides followed by treatment with Michler’s ketone and subsequent cyclizations during acidic workup provide 3,3-diaryl-3H-2,1-benzoxathiole 1-oxides in reasonable to good yields. The title compounds 11a, c–e, h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b81fa135c66dd36eee98783d673f5123
https://doi.org/10.1039/a608290d
https://doi.org/10.1039/a608290d
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84c6b101c00e7155a86bcf39120df6b0
https://doi.org/10.1002/chin.199922166
https://doi.org/10.1002/chin.199922166
Publikováno v:
Thermochimica Acta. 167:111-121
The thermal behavior of substituted dithiooxamide ligands and their nickel complexes has been studied with differential scanning calorimetry and thermogravimetry. The thermal products were analyzed by mass spectral and IR techniques. The mechanism of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ec0b5a15b00b85c28f6d84ffbb343cc
https://doi.org/10.1016/0040-6031(90)80470-j
https://doi.org/10.1016/0040-6031(90)80470-j
Autor:
Tadas Malinauskas, Vygintas Jankauskas, Vytautas Getautis, Juozas V. Grazulevicius, Zbig Tokarski, Nusrallah Jubran
Publikováno v:
Chemistry Letters. 33:1336-1337
The novel families of hole transporting monomers and polymers containing hydrazone moieties are reported. The polymers were prepared in polyaddition reaction of hydrazone-containing diepoxides with 4,4'-thiobisbenzenethiol. The hole drift mobilities
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57a2dc7f7909e537c5abdd0065239423
https://doi.org/10.1246/cl.2004.1336
https://doi.org/10.1246/cl.2004.1336
Autor:
Edmundas Montrimas, Nusrallah Jubran, Valentas Gaidelis, Vygintas Jankauskas, Ausra Matoliukstyte, Juozas V. Grazulevicius, Ramunas Lygaitis, Zbig Tokarski
Publikováno v:
Molecular Crystals and Liquid Crystals. 427:107/[419]-116/[428]
9-(4-methoxyphenyl)carbazolyl-containing hydrazones were prepared by multi-step synthetic route including Ullmann coupling of carbazole with 4-iodoanisole, formylation of 9-(4-methoxyphenyl)carbazole by Vilsmeier reaction and the condensation of mono
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ac13528c3ca0d6bf1daa4413d41544b
https://doi.org/10.1080/15421400590892082
https://doi.org/10.1080/15421400590892082
Autor:
Valentas Gaidelis, Juozas V. Grazulevicius, Jonas Sidaravicius, Nusrallah Jubran, Vygintas Jankauskas, Ramunas Lygaitis, Zbig Tokarski
Publikováno v:
Molecular Crystals and Liquid Crystals. 427:95/[407]-106/[418]
3,3′-Di(9-(4-butylphenyl)carbazyl) and 3,3′-di(9-ethylcarbazyl)-based hydrazones were synthesized by the multi-step synthetic route including oxidative dimerization of 9-(4-butylphenyl)carbazole and 9-ethylcarbazole, formylation of the dimmers ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5033accd77732ecc6836eac8c5769d3f
https://doi.org/10.1080/15421400590892064
https://doi.org/10.1080/15421400590892064