scholarly journals Three colour solid-state luminescence from positional isomers of facilely modified thiophosphoranyl anthracenes

2020 ◽  
Vol 56 (54) ◽  
pp. 7479-7482
Author(s):  
Timo Schillmöller ◽  
Paul Niklas Ruth ◽  
Regine Herbst-Irmer ◽  
Dietmar Stalke

Three positional isomers of thiophosphoranyl anthracene were synthesized and their divers photophysical properties were investigated.


2014 ◽  
Vol 106 ◽  
pp. 197-204 ◽  
Author(s):  
Weibo Yan ◽  
Chenming Hong ◽  
Guankui Long ◽  
Yang Yang ◽  
Zhiwei Liu ◽  
...  


2015 ◽  
Vol 44 (17) ◽  
pp. 7991-8000 ◽  
Author(s):  
Yan Suffren ◽  
Niall O'Toole ◽  
Andreas Hauser ◽  
Erwann Jeanneau ◽  
Arnaud Brioude ◽  
...  

The solid state luminescence of [Mn4(ThiaSO2)2F]X (X = K+ and [K(18-crown-6)]+, ThiaSO2 = p-tert-butylsulphonylcalix[4]arene) compounds show a strong O2 pressure dependence.



2020 ◽  
Vol 49 (34) ◽  
pp. 11997-12008
Author(s):  
Aliia V. Shamsieva ◽  
Elvira I. Musina ◽  
Tatiana P. Gerasimova ◽  
Igor D. Strelnik ◽  
Anna G. Strelnik ◽  
...  

The current work presents novel dinuclear Cu(i) complexes bearing P,N-ligands. Their structures, isomerization, and photophysical properties are discussed in detail.



2003 ◽  
Vol 32 (11) ◽  
pp. 1002-1003 ◽  
Author(s):  
Seiji Watase ◽  
Takayuki Kitamura ◽  
Nobuko Kanehisa ◽  
Masami Nakamoto ◽  
Yasushi Kai ◽  
...  




2019 ◽  
Vol 15 ◽  
pp. 2013-2019 ◽  
Author(s):  
Esther Nieland ◽  
Oliver Weingart ◽  
Bernd M Schmidt

ortho-Fluoroazobenzenes are a remarkable example of bistable photoswitches, addressable by visible light. Symmetrical, highly fluorinated azobenzenes bearing an iodine substituent in para-position were shown to be suitable supramolecular building blocks both in solution and in the solid state in combination with neutral halogen bonding acceptors, such as lutidines. Therefore, we investigate the photochemistry of a series of azobenzene photoswitches. Upon introduction of iodoethynyl groups, the halogen bonding donor properties are significantly strengthened in solution. However, the bathochromic shift of the π→π* band leads to a partial overlap with the n→π* band, making it slightly more difficult to address. The introduction of iodine substituents is furthermore accompanied with a diminishing thermal half-life. A series of three azobenzenes with different halogen bonding donor properties are discussed in relation to their changing photophysical properties, rationalized by DFT calculations.



2016 ◽  
Vol 12 ◽  
pp. 825-834 ◽  
Author(s):  
Andreea Petronela Diac ◽  
Ana-Maria Ţepeş ◽  
Albert Soran ◽  
Ion Grosu ◽  
Anamaria Terec ◽  
...  

New indeno[1,2-c]pyran-3-ones bearing different substituents at the pyran moiety were synthesized and their photophysical properties were investigated. In solution all compounds were found to be blue emitters and the trans isomers exhibited significantly higher fluorescence quantum yields (relative to 9,10-diphenylanthracene) as compared to the corresponding cis isomers. The solid-state fluorescence spectra revealed an important red shift of λmax due to intermolecular interactions in the lattice, along with an emission-band broadening, as compared to the solution fluorescence spectra.



2016 ◽  
Vol 128 ◽  
pp. 271-278 ◽  
Author(s):  
Mingyang Liu ◽  
Lu Zhai ◽  
Jingbo Sun ◽  
Pengchong Xue ◽  
Peng Gong ◽  
...  


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