Organic Crystals with Tunable Emission Colors Based on a Single Organic Molecule and Different Molecular Packing Structures

2006 ◽  
Vol 18 (18) ◽  
pp. 2369-2372 ◽  
Author(s):  
H. Y. Zhang ◽  
Z. L. Zhang ◽  
K. Q. Ye ◽  
J. Y. Zhang ◽  
Y. Wang
Author(s):  
Daiki Ito ◽  
Raku Shirasawa ◽  
Shinnosuke Hattori ◽  
Shigetaka Tomiya ◽  
Gouhei Tanaka

2009 ◽  
Vol 9 (11) ◽  
pp. 4945-4950 ◽  
Author(s):  
Huan Wang ◽  
Feng Li ◽  
Bingrong Gao ◽  
Zengqi Xie ◽  
Suijun Liu ◽  
...  

Author(s):  
C. E. Leslie ◽  
J. R. Fryer ◽  
C. J. Gilmore ◽  
W. Nicolson

Imaging of organic crystals in the electron microscope is limited by their sensitivity to the electron beam, with even the most stable molecules only giving a resolution of ~3Å. By contrast, electron diffraction requires a lower beam intensity, and so can give much better resolution, down to ~lÅ under favourable conditions. Intensities may be measured directly from the diffraction pattern, and the phase determination problem can be surmounted by applying the maximum entropy method, which chooses phases by likelihood estimation.It was decided to apply this method to the organic molecule anthanthrene, C22H12 (fig. 1), since x-ray studies found that the crystals were monoclinic with a = 12.10Å, b = 10.34Å, c = 10.74Å, β = 92.2°, space group P21/a and Z = 4, but no details of the atomic co-ordinates were given in the literature. A previous study of the molecule, using KC1 as the substrate, produced epitaxial layers showing the acprojection being most common at room temperature.


2015 ◽  
Vol 3 (22) ◽  
pp. 5764-5768 ◽  
Author(s):  
Juan F. Galisteo-López ◽  
Sandra Gómez-Esteban ◽  
Berta Gómez-Lor ◽  
Cefe López

A novel organic system with tunable emission is demonstrated comprising a truxene-based organogel which resonantly transfers energy to a dopant organic molecule.


2014 ◽  
Vol 38 (8) ◽  
pp. 3429 ◽  
Author(s):  
Hongbo Lu ◽  
Shanna Zhang ◽  
Aixiang Ding ◽  
Miao Yuan ◽  
Guiyu Zhang ◽  
...  

2000 ◽  
Vol 56 (6) ◽  
pp. 1035-1045 ◽  
Author(s):  
E. V. Peresypkina ◽  
V. A. Blatov

Using the methods of coordination sequences and of molecular Voronoi–Dirichlet polyhedra, the topological properties of molecular packings and molecular coordination numbers (MCNs) were determined in the crystal structures of 33 575 monosystem organic compounds within the first three coordination spheres. Numerous examples of disagreement between the topology of molecular packing and the system of intermolecular contacts in a crystal structure were found. It is concluded that within the first coordination sphere most of the molecules tend to arrange with MCN = 14, obeying the model of the thinnest covering of space, but molecular packings as a whole tend to be constructed according to one of the close packings.


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