том 48 издание 5 страницы 765-767

Dual-mode fluorescence switching of photochromic bisthiazolylcoumarin

Тип публикацииJournal Article
Дата публикации2012-01-01
scimago Q1
wos Q2
БС1
SJR1.037
CiteScore7.4
Impact factor4.2
ISSN13597345, 1364548X
Materials Chemistry
Metals and Alloys
Surfaces, Coatings and Films
General Chemistry
Ceramics and Composites
Electronic, Optical and Magnetic Materials
Catalysis
Краткое описание
Three new photochromic coumarins were synthesized. Fluorescence of the open form of 7-hydroxy-3,4-bisthiazolyl-coumarin increased to 1400% by changing the pH only slightly from 6.05 to 7.58. This was subsequently quenched to 1.5% of the maximum intensity at the UV photostationary state in water-methanol media.
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ГОСТ |
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Suzuki K., Ubukata T., YOKOYAMA Y. Dual-mode fluorescence switching of photochromic bisthiazolylcoumarin // Chemical Communications. 2012. Vol. 48. No. 5. pp. 765-767.
ГОСТ со всеми авторами (до 50) Скопировать
Suzuki K., Ubukata T., YOKOYAMA Y. Dual-mode fluorescence switching of photochromic bisthiazolylcoumarin // Chemical Communications. 2012. Vol. 48. No. 5. pp. 765-767.
RIS |
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TY - JOUR
DO - 10.1039/c1cc16516j
UR - https://doi.org/10.1039/c1cc16516j
TI - Dual-mode fluorescence switching of photochromic bisthiazolylcoumarin
T2 - Chemical Communications
AU - Suzuki, Kazushi
AU - Ubukata, Takashi
AU - YOKOYAMA, Yasushi
PY - 2012
DA - 2012/01/01
PB - Royal Society of Chemistry (RSC)
SP - 765-767
IS - 5
VL - 48
PMID - 22134671
SN - 1359-7345
SN - 1364-548X
ER -
BibTex |
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BibTex (до 50 авторов) Скопировать
@article{2012_Suzuki,
author = {Kazushi Suzuki and Takashi Ubukata and Yasushi YOKOYAMA},
title = {Dual-mode fluorescence switching of photochromic bisthiazolylcoumarin},
journal = {Chemical Communications},
year = {2012},
volume = {48},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/c1cc16516j},
number = {5},
pages = {765--767},
doi = {10.1039/c1cc16516j}
}
MLA
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Suzuki, Kazushi, et al. “Dual-mode fluorescence switching of photochromic bisthiazolylcoumarin.” Chemical Communications, vol. 48, no. 5, Jan. 2012, pp. 765-767. https://doi.org/10.1039/c1cc16516j.