X-Ray Spectroscopic Analysis of Electronic Properties of One-Dimensional Nanostructured Materials

Author(s):  
Han-Wei Chang ◽  
Chi Liang Chen ◽  
Sofia Ya Hsuan Liou ◽  
Chung-Li Dong
2013 ◽  
Vol 750-752 ◽  
pp. 1104-1108 ◽  
Author(s):  
Feng Rao Lang ◽  
Li Yan You

The Zn (II) complex [Zn (O2CFcCO2)(H2O)2]H2O was synthesized with ferrocenedicarboxylic acid under mild conditions. Its crystal structure was characterized by elemental analysis, IR data and X-ray diffraction single crystal structure analyses. The Zn (II) coordination units are connected, forming one-dimensional chain. At the meanwhile, the luminescence properties and the electronic properties were determined.


2004 ◽  
Vol 69 (6) ◽  
pp. 1292-1300 ◽  
Author(s):  
Tahahiro Tani ◽  
Kazuki Sada ◽  
Masatsugu Ayabe ◽  
Yuya Iwashita ◽  
Takanori Kishida ◽  
...  

Crystal structure of hexylammonium anthracene-9-carboxylate was investigated. The salt was arranged by a one-dimensional hydrogen bond network to form a columnar structure in the crystalline state. This columnar structure should be the model of fibrous assemblies in the organogels of anthracene-9-carboxylate alkylammonium salts having a long alkyl chain.


2013 ◽  
Vol 121 (1411) ◽  
pp. 287-290 ◽  
Author(s):  
Masahiko TANAKA ◽  
Yoshio KATSUYA ◽  
Yoshitaka MATSUSHITA ◽  
Osami SAKATA

Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1771
Author(s):  
Fei Wang ◽  
Kejiang Liang ◽  
Mads Christian Larsen ◽  
Steffen Bähring ◽  
Masatoshi Ishida ◽  
...  

We report a fully organic pyridine-tetrapyrrolic U-shaped acyclic receptor 10, which prefers a supramolecular pseudo-macrocyclic dimeric structure (10)2 in a less polar, non-coordinating solvent (e.g., CHCl3). Conversely, when it is crystalized from a polar, coordinating solvent (e.g., N,N-dimethylformamide, DMF), it exhibited an infinite supramolecular one-dimensional (1D) “zig-zag” polymeric chain, as inferred from the single-crystal X-ray structures. This supramolecular system acts as a potential receptor for strong acids, e.g., p-toluenesulfonic acid (PTSA), methane sulfonic acid (MSA), H2SO4, HNO3, and HCl, with a prominent colorimetric response from pale yellow to deep red. The receptor can easily be recovered from the organic solution of the host–guest complex by simple aqueous washing. It was observed that relatively stronger acids with pKa < −1.92 in water were able to interact with the receptor, as inferred from 1H NMR titration in tetrahydrofuran-d8 (THF-d8) and ultraviolet–visible (UV–vis) spectroscopic titrations in anhydrous THF at 298 K. Therefore, this new dynamic supramolecular receptor system may have potentiality in materials science research.


Small ◽  
2021 ◽  
pp. 2005162
Author(s):  
Ziyi Chen ◽  
Andrew G. Walsh ◽  
Xiao Wei ◽  
Manzhou Zhu ◽  
Peng Zhang

1983 ◽  
Vol 208 (1-3) ◽  
pp. 427-433 ◽  
Author(s):  
M.G. Fedotov ◽  
E.A. Kuper ◽  
V.N. Litvinenko ◽  
V.E. Panchenko ◽  
V.A. Ushakov

2021 ◽  
pp. 1-3
Author(s):  
Carina Schlesinger ◽  
Edith Alig ◽  
Martin U. Schmidt

The structure of the anticancer drug carmustine (1,3-bis(2-chloroethyl)-1-nitrosourea, C5H9Cl2N3O2) was successfully determined from laboratory X-ray powder diffraction data recorded at 278 K and at 153 K. Carmustine crystallizes in the orthorhombic space group P212121 with Z = 4. The lattice parameters are a = 19.6935(2) Å, b = 9.8338(14) Å, c = 4.63542(6) Å, V = 897.71(2) ų at 153 K, and a = 19.8522(2) Å, b = 9.8843(15) Å, c = 4.69793(6) Å, V = 921.85(2) ų at 278 K. The Rietveld fits are very good, with low R-values and smooth difference curves of calculated and experimental powder data. The molecules form a one-dimensional hydrogen bond pattern. At room temperature, the investigated commercial sample of carmustine was amorphous.


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