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Synthesis and chemosensing properties of cinnolinecontaining poly(arylene ethynylene)s. / Danilkina, N.A.; Vlasov, P.S.; Vodianik, S.M.; Kruchinin, A.A.; Vlasov, Y.G.; Balova, I.A.

в: Beilstein Journal of Organic Chemistry, Том 11, 2015, стр. 373-384.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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Author

Danilkina, N.A. ; Vlasov, P.S. ; Vodianik, S.M. ; Kruchinin, A.A. ; Vlasov, Y.G. ; Balova, I.A. / Synthesis and chemosensing properties of cinnolinecontaining poly(arylene ethynylene)s. в: Beilstein Journal of Organic Chemistry. 2015 ; Том 11. стр. 373-384.

BibTeX

@article{d6eb3888b8234073a21db9b22f0107c7,
title = "Synthesis and chemosensing properties of cinnolinecontaining poly(arylene ethynylene)s",
abstract = "Novel poly(arylene ethynylene)s comprising a cinnoline core were prepared in high yields via a three-step methodology. A Richtertypecyclization of 2-ethynyl- and 2-(buta-1,3-diynyl)aryltriazenes was used for cinnoline ring formation, followed by a Sonogashiracoupling for the introduction of trimethylsilylethynyl moieties and a sila-Sonogashira coupling as the polycondensationtechnique. The fluorescence of the cinnoline-containing polymers in THF was highly sensitive to quenching by Pd2+ ions.",
author = "N.A. Danilkina and P.S. Vlasov and S.M. Vodianik and A.A. Kruchinin and Y.G. Vlasov and I.A. Balova",
year = "2015",
doi = "10.3762/bjoc.11.43",
language = "English",
volume = "11",
pages = "373--384",
journal = "Beilstein Journal of Organic Chemistry",
issn = "1860-5397",
publisher = "Beilstein-Institut Zur Forderung der Chemischen Wissenschaften",

}

RIS

TY - JOUR

T1 - Synthesis and chemosensing properties of cinnolinecontaining poly(arylene ethynylene)s

AU - Danilkina, N.A.

AU - Vlasov, P.S.

AU - Vodianik, S.M.

AU - Kruchinin, A.A.

AU - Vlasov, Y.G.

AU - Balova, I.A.

PY - 2015

Y1 - 2015

N2 - Novel poly(arylene ethynylene)s comprising a cinnoline core were prepared in high yields via a three-step methodology. A Richtertypecyclization of 2-ethynyl- and 2-(buta-1,3-diynyl)aryltriazenes was used for cinnoline ring formation, followed by a Sonogashiracoupling for the introduction of trimethylsilylethynyl moieties and a sila-Sonogashira coupling as the polycondensationtechnique. The fluorescence of the cinnoline-containing polymers in THF was highly sensitive to quenching by Pd2+ ions.

AB - Novel poly(arylene ethynylene)s comprising a cinnoline core were prepared in high yields via a three-step methodology. A Richtertypecyclization of 2-ethynyl- and 2-(buta-1,3-diynyl)aryltriazenes was used for cinnoline ring formation, followed by a Sonogashiracoupling for the introduction of trimethylsilylethynyl moieties and a sila-Sonogashira coupling as the polycondensationtechnique. The fluorescence of the cinnoline-containing polymers in THF was highly sensitive to quenching by Pd2+ ions.

U2 - 10.3762/bjoc.11.43

DO - 10.3762/bjoc.11.43

M3 - Article

VL - 11

SP - 373

EP - 384

JO - Beilstein Journal of Organic Chemistry

JF - Beilstein Journal of Organic Chemistry

SN - 1860-5397

ER -

ID: 3939898