Photoluminescence of Pharmaceutical Materials in the Solid State. 4. Fluorescence Studies of Various Solvated and Desolvated Solvatomorphs of Erythromycin A

Author(s):  
Harry G. Brittain
2005 ◽  
Vol 22 (6) ◽  
pp. 999-1006 ◽  
Author(s):  
Harry G. Brittain ◽  
Bruce J. Elder ◽  
Paul K. Isbester ◽  
Allen H. Salerno

2014 ◽  
Vol 25 (1) ◽  
pp. 59-68 ◽  
Author(s):  
Na’il Saleh ◽  
Salah Al-Trawneh ◽  
Hmoud Al-Dmour ◽  
Samir Al-Taweel ◽  
John P. Graham

Author(s):  
Huey Chong Kwong ◽  
Ai Jia Sim ◽  
C. S. Chidan Kumar ◽  
Ching Kheng Quah ◽  
Suchada Chantrapromma ◽  
...  

In the bischalcone molecule of the title compound, C24H18O4·2C3H7NO, the central benzene and terminal hydroxyphenyl rings form a dihedral angle of 14.28 (11)° and the central C=C double bond adopts a trans configuration. In the crystal, the bischalcone and solvate molecules are interconnected via O—H...O hydrogen bonds, which were investigated by Hirshfeld surface analysis. Solid-state fluorescence was measured at λex = 4400 Å. The emission wavelength appeared at 5510 Å, which corresponds to yellow light and the solid-state fluorescence quantum yield (F f) is 0.18.


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