STUDIES ON THE CONFORMATIONS OF 4-N,N-DIMETHYLAMINOTHIANES AND THE CORRESPONDING METHIODIDES. EVIDENCE FROM A SINGLE CRYSTAL X-RAY DIFFRACTION ANALYSIS THAT A TWIST-BOAT CONFORMER EXISTS IN THE SOLID STATE FOR TRIMETHYL-[2,2-DIMETHYL-trans−6-PHENYLTHIAN-r-4-YL]-AMMONIUM IODIDE

1983 ◽  
Vol 17 (3) ◽  
pp. 343-365 ◽  
Author(s):  
Pullachipatti K. Subramanian ◽  
Kondareddiar Ramalingam ◽  
Nantelle S. Pantaleo ◽  
Dick Van Der Helm ◽  
Nagichettiar Satyamurthy ◽  
...  
2016 ◽  
Vol 20 (01n04) ◽  
pp. 245-253 ◽  
Author(s):  
Hirotaka Mori ◽  
Atsuhiro Osuka

meso–meso Directly-linked trimeric and pentameric porphyrin–hexaphyrin hybrid arrays 5 and 6 comprising of electron-deficient porphyrin units were prepared by cross-condensation of monomeric and dimeric electron-deficient meso-formyl porphyrins with a tripyrrane. The solid-state structures of 5 and 6 have been determined by single crystal X-ray diffraction analysis. The latter is the largest crystal structure of meso–meso linked multiporphyrinic array analogues reported to date.


CrystEngComm ◽  
2021 ◽  
Author(s):  
Kousik Ghosh ◽  
Antonio Frontera ◽  
Shouvik Chattopadhyay

A heteronuclear cobalt(III)/potassium complex, [(L1)2Co2K(L2)2], {Where, H2L1 = N,N-bis(3-ethoxysalicylidene)2,2-dimethyl-1,3-propanediamine and HL2 = 3-ethoxysalicylaldehyde}, has been synthesized and characterized by several analytical techniques including single crystal X-ray diffraction analysis. The energetic...


2019 ◽  
Vol 42 (1) ◽  
pp. 46-50
Author(s):  
Felix Roschke ◽  
Günther Thiele ◽  
Stefanie Dehnen ◽  
Michael Mehring

Abstract We report on the synthesis of a new bismuth aryloxide molecule Bi[OC6H4(CH2C6H5)-2]3 (1), which was characterized by NMR and IR spectroscopy as well as single-crystal X-ray diffraction analysis. A characteristic structural feature is the dimeric unit with a central Bi2O2 core resulting from μ-binding phenolates. In addition, both bismuth atoms show a Bi⋅⋅⋅π arene interaction with a quite short Bi⋅⋅⋅πcentroid distance of 3.11 Å in the solid state.


1990 ◽  
Vol 04 (06) ◽  
pp. 423-431 ◽  
Author(s):  
P. Y. HSIEH ◽  
JAMES YE ◽  
Z. SHI ◽  
W. K. CHU

Results from the study of highly structure-confined YBa 2 Cu 3 O 7−x superconductors synthesized by different coprecipitation processes are presented, with the superconducting samples made from oxalic-nitrate salts demonstrating higher critical temperature and critical current in comparison with solid reaction oxides. Among the measured samples, the critical temperature, T c , is typically 90–95 K (T c (maximum)=105 K) and the critical current is 1.2 – 1.9 × 104 A/cm 2 at 4.5 K and 1200 A/cm 2 at 78 K. Peak patterns similar to those of solid-state reactions by X-ray diffraction analysis have also been found although these spectra show considerably broadness. Superconductors resulted from coprecipitation techniques with no calcining (heat-treatment) processing can be attained. Further studies on producing single-crystal with increasing critical current and temperature are discussed.


Synlett ◽  
2017 ◽  
Vol 28 (19) ◽  
pp. 2609-2613 ◽  
Author(s):  
Fumitoshi Kakiuchi ◽  
Akiko Izumoto ◽  
Hikaru Kondo ◽  
Takuya Kochi

Tetraarylanthracenes containing several fluoro groups were synthesized using the ruthenium-catalyzed C–O or C–F arylation with arylboronates and their structural and spectroscopic studies were conducted. The RuH2(CO)(PPh3)3-catalyzed C–O arylation of aromatic ketones was found to be effective for the introduction of aryl groups containing multiple fluoro groups. Anthracenes possessing fluorinated aryl groups were prepared in two steps from 1,4,5,8-tetramethoxyanthraquinone by C–O arylation and reduction of the carbonyl groups. A tetraphenylanthracene containing a fluorinated anthracene moiety was also prepared using C–F phenylation of octafluoroanthraquinone. Single-crystal X-ray diffraction analysis showed that the positions of fluoro groups on the tetraarylanthracenes lead to notable difference in the crystal packing structures. The larger difference between the tetraarylanthracenes was observed in the fluorescence spectra in the solid state than those in chloroform.


Symmetry ◽  
2021 ◽  
Vol 13 (12) ◽  
pp. 2350
Author(s):  
Ivan V. Buslov ◽  
Alexander S. Novikov ◽  
Victor N. Khrustalev ◽  
Mariya V. Grudova ◽  
Alexey S. Kubasov ◽  
...  

The synthesis of 2-pyridyltellurenyl bromide via Br2 oxidative cleavage of the Te–Te bond of dipyridylditelluride is reported. Single-crystal X-ray diffraction analysis of 2-pyridyltellurenyl bromide demonstrated that the Te atom of 2-pyridyltellurenyl bromide was involved in four different noncovalent contacts: Te⋯Te interactions, two Te⋯Br ChB, and one Te⋯N ChB contact forming 3D supramolecular symmetrical framework. In contrast to 2-pyridylselenenyl halides, the Te congener does not react with nitriles furnishing cyclization products. 2-Pyridylselenenyl chloride was demonstrated to easily form the corresponding adduct with benzonitrile. The cyclization product was studied by the single-crystal X-ray diffraction analysis, which revealed that in contrast to earlier studied cationic 1,2,4-selenadiazoles, here we observed that the adduct with benzonitrile formed supramolecular dimers via Se⋯Se interactions in the solid state, which were never observed before for 1,2,4-selenadiazoles.


Author(s):  
Süheyla Özbey ◽  
Nilgün Karalı ◽  
Aysel Gürsoy

AbstractIn this study 4-(3-coumarinyl)-3-benzyl-4-thi azolin-2-one 4-methylbenzylidenehydrazone 3 was synthesised. An independent proof of the thiazolylhydrazone structure of 3 was achieved by single crystal X-ray diffraction analysis. Elemental analyses and spectral data (IR,


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