Clarification of Cross-Linkage Structure in Boric Acid Doped Poly(vinyl alcohol) and Its Model Compound As Studied by an Organized Combination of X-ray Single-Crystal Structure Analysis, Raman Spectroscopy, and Density Functional Theoretical Calculation

2014 ◽  
Vol 118 (22) ◽  
pp. 6032-6037 ◽  
Author(s):  
Takahiko Itou ◽  
Hideyuki Kitai ◽  
Akira Shimazu ◽  
Tsukasa Miyazaki ◽  
Kohji Tashiro

ChemInform ◽  
1987 ◽  
Vol 18 (22) ◽  
Author(s):  
G. ADMIRAAL ◽  
J. L. VAN DER VEER ◽  
R. A. G. DE GRAAFF ◽  
J. H. J. DEN HARTOG ◽  
J. REEDIJK




2000 ◽  
Vol 55 (2) ◽  
pp. 213-221 ◽  
Author(s):  
Jürgen Schatz ◽  
Frank Schildbach ◽  
Axel Lentz ◽  
Sylvia Rastätter ◽  
Joachim Schilling ◽  
...  

The inclusion complexes formed from carbon disulfide and p-tert-butylcalix[4]arene ( 1·CS2) or p-tert-butylcalix[6]arene (2·CS2) were investigated by X-ray crystal structure analysis, infrared (IR) and Raman spectroscopy. The complex 1·CS2 crystallises in the space group P4/n, 2·CS2 in the space group P21/n. In case of p-tert-butylcalix[4]arene as host the carbon disulfide molecule is included in the cavity. In the crystal structure of p-tert-butylcalix[ 6]arene clathrate, self-complexation of one tert-butyl group in the cavity of another calix[ 6]arene can be observed. Due to inclusion, the symmetry of CS2 is lowered both in the p-tert- butylcalix[4]arene and p-tert-butylcalix[6]arene case causing significant shifts in the fully assigned infrared and Raman spectra.



2005 ◽  
Vol 60 (5) ◽  
pp. 569-571 ◽  
Author(s):  
Ali Ramazani ◽  
Ali Morsali ◽  
Bijan Ganjeie ◽  
Ali Reza Kazemizadeh ◽  
Ebrahim Ahmadi ◽  
...  

Selenourea reacts with dialkyl acetylenedicarboxylates under solvent-free conditions to form 1:1 adducts, which undergo a cyclization reaction to produce alkyl Z-2-(2-amino-4-oxo-1,3-selenazol- 5(4H)-ylidene)acetates, in good yields. The stereochemistry of the ethyl Z-2-(2-amino-4-oxo-1,3- selenazol-5(4H)-ylidene)acetate was established by X-ray single crystal structure analysis. The reaction is completely stereoselective.





Author(s):  
H. J. Berthold ◽  
E. Vonholdt ◽  
R. Wartchow ◽  
T. Vogt

AbstractNHA single crystal structure analysis of NThe deuterated compound NThe structures of the ordered low temperature phases will be reported separately.



Synlett ◽  
2021 ◽  
Author(s):  
Hong-Wu Zhao ◽  
Xiao-Fan Bi ◽  
Hai-Liang Pang ◽  
Zhe Tang ◽  
Heng Zhang ◽  
...  

In the presence of Na2CO3, the conjugate addition between α-halogeno hydrazones and nitroso compounds proceeded readily, thus delivering multifunctionalized nitrones in the reasonable chemical yields with excellent strereoselectivities. The chemical structure and stereochemical configuration of title chemical entities were unambiguously identified by an X-ray single crystal structure analysis.



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