2007 ◽  
Vol 15 (19) ◽  
pp. 12240 ◽  
Author(s):  
Emir Karamehmedovic ◽  
Christian Pedersen ◽  
Martin T. Andersen ◽  
Peter Tidemand-Lichtenberg

1996 ◽  
Vol 24 (Supplement) ◽  
pp. 85-88
Author(s):  
H. Kan ◽  
T. Kanzaki ◽  
H. Miyajima ◽  
Y. Ito ◽  
K. Matsui ◽  
...  

2021 ◽  
Vol 53 (1) ◽  
Author(s):  
Huamao Huang ◽  
Tianxiang Lan ◽  
Cheng Huang ◽  
Chao Wang ◽  
Chukun Huang ◽  
...  

CrystEngComm ◽  
2021 ◽  
Vol 23 (7) ◽  
pp. 1657-1662
Author(s):  
Na Zhang ◽  
Yuqing Yin ◽  
Jian Zhang ◽  
Tao Wang ◽  
Siyuan Wang ◽  
...  

Lu2O3 crystals have attracted intense attention due to their great potential in the field of high power solid-state lasers.


ACS Omega ◽  
2021 ◽  
Vol 6 (12) ◽  
pp. 8717-8725
Author(s):  
Maha Alhaddad ◽  
Reda M. Mohamed ◽  
Mohamed H. H. Mahmoud

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.


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