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Akademický článek
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Publikováno v:
Journal of Fluorescence. 27:537-549
Newly synthesized, differently substituted chalcones (1,3-diaryl-2-propen-1-ones) have been studied using steady-state and time-resolved techniques combined with quantum-chemical modelling. To explore spectroscopic structure - property relationships
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a72f16e424846c9eb1adfea03873e5d8
https://doi.org/10.1007/s10895-016-1981-2
https://doi.org/10.1007/s10895-016-1981-2
Publikováno v:
Journal of Luminescence. 153:152-161
In this article, we report the photophysical properties of six, newly synthesized donor-substituted 2-amino-1,3-dicyano-5,6,7,8-tetrahydronaphthalene fluorophores. The steady-state and time-resolved spectroscopic experiments have been used to investi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96ae31ba83f14e5e5ff64cc8f20b5c2a
https://doi.org/10.1016/j.jlumin.2014.03.019
https://doi.org/10.1016/j.jlumin.2014.03.019
Publikováno v:
The European Physical Journal Special Topics. 222:2373-2379
The absorption and fluorescence transition dipole moments ( $$\hat M_{ge}$$ and $$\hat M_{eg}$$ ) for ethyl 5-(4-aminophenyl)-3-amino-2, 4-dicyanobenzoate (EAADCy) and ethyl 5-(4-dimethylaminophenyl)-3-amino-2, 4-dicyanobenzoate (EDMAADCy) have been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6de85c827c1d466e63258f27ee3fc603
https://doi.org/10.1140/epjst/e2013-02019-6
https://doi.org/10.1140/epjst/e2013-02019-6
Autor:
V. Drozdowska, J. R. Heldt, Henryk Toczek, K. Rudź, Mirosław Darecki, Włodzimierz Freda, Emilia Baszanowska
Publikováno v:
The European Physical Journal Special Topics. 222:2157-2170
Seawater in addition to natural components such as living and non-living organic matter contains also components artificially introduced into the marine environment, such as oil substances. These components, present in the surface layer of the sea, c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f41c48a7fcc54a75b7a58c593c48b2f2
https://doi.org/10.1140/epjst/e2013-01992-x
https://doi.org/10.1140/epjst/e2013-01992-x
Autor:
Marek Józefowicz, Marek Pietrzak, Agnieszka Bajorek, Beata Jędrzejewska, Janina R. Heldt, Józef Heldt
Publikováno v:
Journal of Luminescence. 134:414-422
The influence of degree of methyl methacrylate (MM) polymerization on the both emission modes (LE—locally excited and ICT—intramolecular charge transfer) of the fluorescence spectrum of ethyl 5-(4-aminophenyl)-3-amino-2,4-dicyanobenzoate (EAADCy)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e0d1d6f0a84cf7361b8fba62432c3d9
https://doi.org/10.1016/j.jlumin.2012.08.009
https://doi.org/10.1016/j.jlumin.2012.08.009
Publikováno v:
Journal of Luminescence. 132:755-764
The absorption and fluorescence transition dipole moments ( M ˆ g e and M ˆ e g ) for methyl benzoate and its eight ortho and para substituted derivatives have been investigated using steady-state and time-resolved fluorescence techniques and semie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0fa2446f9a625845173a8f6d40cc35dc
https://doi.org/10.1016/j.jlumin.2011.10.024
https://doi.org/10.1016/j.jlumin.2011.10.024
Publikováno v:
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 86:481-489
The effects of α- and β-cyclodextrins (CDs) on the both emission modes (LE – locally excited and TICT – twisted intramolecular charge transfer) of the fluorescence spectrum of methyl-p-dimethylaminobenzoate (I) and its o-methoxy (II) derivative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::899c2f2deaac0acd1512f75bb1e21f88
https://doi.org/10.1016/j.saa.2011.10.072
https://doi.org/10.1016/j.saa.2011.10.072
Publikováno v:
Journal of Molecular Liquids. 157:61-66
Steady-state spectroscopic studies of ortho (–OCH3 and –OH) derivatives of methyl p-dimethylaminobenzoate indicate that molecules under study are capable of simultaneously creating locally excited (LE) and intramolecular charge transfer (ICT) exc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e48fc8a9bc6ed58b99257d94c7320fb7
https://doi.org/10.1016/j.molliq.2010.08.010
https://doi.org/10.1016/j.molliq.2010.08.010