scholarly journals Mechanochemical synthesis ofN-salicylideneaniline: thermosalient effect of polymorphic crystals

IUCrJ ◽  
2017 ◽  
Vol 4 (3) ◽  
pp. 243-250 ◽  
Author(s):  
Sudhir Mittapalli ◽  
D. Sravanakumar Perumalla ◽  
Ashwini Nangia

Polymorphs of the dichloro derivative ofN-salicylideneaniline exhibit mechanical responses such as jumping (Forms I and III) and exploding (Form II) in its three polymorphs. The molecules are connectedviathe amide N—H...O dimer synthon and C—Cl...O halogen bond in the three crystal structures. A fourth high-temperature Form IV was confirmed by variable-temperature single-crystal X-ray diffraction at 180°C. The behaviour of jumping exhibited by the polymorphic crystals of Forms I and III is due to the layered sheet morphology and the transmission of thermal stress in a single direction, compared with the corrugated sheet structure of Form II such that heat dissipation is more isotropic causing blasting. The role of weak C—Cl...O interactions in the thermal response of molecular crystals is discussed.

2017 ◽  
Vol 32 (1) ◽  
pp. 15-22
Author(s):  
Weicai Ju ◽  
Simin Qiu ◽  
Yaqiu Tao ◽  
Xiaodong Shen ◽  
Zhigang Pan

An organic polar hydrate was obtained through cocrystallization of 2,4-diaminotoluene (2,4-DAT) and L(+)-tartaric acid (TA) from ethanol. Dehydration behavior of the obtained hydrate was investigated using variable temperature powder X-ray diffraction (PXRD) and thermal analysis. Proton transfer from L(+)-TA to 2,4-DAT in both hydrate and dehydrated form was revealed via Fourier transform infrared spectroscopy. The crystal structures of both forms were determined using PXRD techniques. The similarities and differences between two crystal structures were analyzed and the role of water in the hydrate crystal structure was demonstrated.


2002 ◽  
Vol 750 ◽  
Author(s):  
B. L. French ◽  
J. C. Bilello

ABSTRACTIn this study the stress and morphology of Ta coatings sputtered on Si (100) substrates were monitored in situ and in real-time during thermal testing to allow interruptions at critical events in the coatings' stress evolution. These observations were carried out using white beam Laue transmission diffraction topography/radiography and a high-temperature sample stage at the Stanford Synchrotron Radiation Laboratory (SSRL). The structure of specimens from interrupted thermal tests was then analyzed using x-ray diffraction θ-2θ scans. The structure and phases present in the film at different stages of the thermal test were correlated with specific mechanical responses in the coating such as stress generation. This information was employed to elucidate the role of phase evolution in the respective stress responses of films deposited in high and low-pressure regimes.


2014 ◽  
Vol 70 (a1) ◽  
pp. C896-C896 ◽  
Author(s):  
Paul Coster ◽  
Craig Henderson ◽  
Steven Hunter ◽  
William Marshall ◽  
Colin Pulham

2,4-dinitroanisole (DNAN) is an energetic material, developed as an insensitive replacement for TNT in melt-cast explosive formulations. While DNAN-based formulations demonstrate greatly reduced sensitivity to accidental initiation compared to those using TNT, issues remain with the replacement of TNT with DNAN. For instance, DNAN based formulations have demonstrated catastrophic levels of irreversible growth during heat-cycling, with volume increases of up to 15% reported. [1] In order to investigate the role of polymorphism in the irreversible growth of DNAN, high-pressure and variable-temperature neutron and x-ray diffraction studies have been performed. Two polymorphs of DNAN have been found to exist at ambient temperature and pressure, the thermodynamic form, DNAN-I, and the kinetic form, DNAN-II.[2,3] The phase diagrams of both form-I and -II of DNAN have been explored for the first time. In the case of DNAN-II, two high-pressure phase transitions were found. DNAN-II initially transformed to DNAN-III, which at higher pressures transformed to DNAN-IV. In addition, variable temperature studies demonstrated that the DNAN-II to DNAN-III transition also occurs when DNAN-II is cooled below room temperature. The thermal expansion of the DNAN-II/III lattice was investigated from 150K to 363K, demonstrating that an abrupt change in the thermal behaviour of lattice parameters occurs at the DNAN-II/III transition. From these combined crystallographic studies, the structure of DNAN-III has been solved, showing it is closely related to DNAN-II. In the case of DNAN-I, high-pressure neutron powder diffraction studies demonstrated that it transforms to a new form (DNAN-V) that is distinct from DNAN-II,-III or -IV. Rietveld refinement of the high-pressure DNAN-I data also determined that the material exhibits negative linear compressibility, which is of interest given the use of DNAN as a shock-insensitive energetic material. Comparison of the behaviour of DNAN-I and –II under variable temperature and high-pressure conditions indicates that the kinetic form, DNAN-II, is the denser phase under all conditions studied. This work highlights the importance of crystallographic techniques in order to understand the polymorphism of energetic materials.


2006 ◽  
Vol 6 (1) ◽  
pp. 274-282 ◽  
Author(s):  
Grażyna Wójcik ◽  
Jolanta Holband ◽  
Jarosław J. Szymczak ◽  
Szczepan Roszak ◽  
Jerzy Leszczynski

2013 ◽  
Vol 69 (11) ◽  
pp. 1234-1237 ◽  
Author(s):  
Heidi Lopez de Diego ◽  
Vishal Koradia ◽  
Andrew D. Bond

Gaboxadol hydrochloride, also known as THIP hydrochloride (systematic name: 3-hydroxy-4,5,6,7-tetrahydro-1,2-oxazolo[5,4-c]pyridin-6-ium chloride), C6H9N2O2+·Cl−, exists as two enantiotropically related polymorphs. Transformation between the polymorphs occurs in a single-crystal-to-single-crystal manner at 221 K, and the enthalpy of transformation from the high-temperature form to the low-temperature form is −0.7 kJ mol−1. Single-crystal structures have been determined at 298 and 220 K. At 298 K, the structure is triclinic (space groupP\overline{1}), with two formula units in the crystallographic asymmetric unit. At 220 K, the structure is monoclinic (space groupI2/a), with one formula unit in the asymmetric unit. The structures contain identical hydrogen-bonded layers and the transformation between the polymorphs corresponds to a shift of adjacent layers relative to each other. The transformation is shown to be reversible by differential scanning calorimetry and variable-temperature powder X-ray diffraction.


Molecules ◽  
2019 ◽  
Vol 24 (9) ◽  
pp. 1840
Author(s):  
Laura Bravo-García ◽  
Edurne S. Larrea ◽  
Beñat Artetxe ◽  
Luis Lezama ◽  
Juan M. Gutiérrez-Zorrilla ◽  
...  

Reactions between pyridinic ligands such as 1,2-bis(4-pyridyl)ethane (bpa) and transition metal cations are a very widespread technique to produce extended coordination polymers such as Metal-Organic Frameworks. In combination with a second ligand these systems could present different topologies and behaviors. In this context, the use of 1,2,4,5-benzenetetracarboxylic acid (H4btec) gave us a novel 2D compound, [Cu2(bpa)(btec)(H2O)4]n (1), which was prepared by microwave-assisted synthesis and structurally characterized by means of single crystal X-ray diffraction. Its thermal behavior was analyzed through thermogravimetric analysis and variable temperature powder X-ray diffraction, concluding that thermal stability is influenced by the coordination water molecules, allowing two sequential thermochromic phase transformations to take place. These transformations were monitored by electronic paramagnetic resonance spectroscopy and magnetic susceptibility measurements. In addition, the crystal structure of the anhydrous compound [Cu2(bpa)(btec)]n (1.ah) was determined. Finally, a topological study was carried out for the bpa ligand considering all the structures deposited in the Cambridge Structural Databased. More than 1000 structures were analyzed and classified into 17 different topologies, according to the role of the ligand.


1993 ◽  
Vol 58 (7) ◽  
pp. 1591-1599 ◽  
Author(s):  
Abd El-Aziz A. Said

Molybdenum oxide catalyst doped or mixed with (1 - 50) mole % Fe3+ ions were prepared. The structure of the original samples and the samples calcined at 400 °C were characterized using DTA, X-ray diffraction and IR spectra. Measurements of the electrical conductivity of calcined samples with and without isopropyl alcohol revealed that the conductance increases on increasing the content of Fe3+ ions up to 50 mole %. The activation energies of charge carriers were determined in presence and absence of the alcohol. The catalytic dehydration of isopropyl alcohol was carried out at 250 °C using a flow system. The results obtained showed that the doped or mixed catalysts are active and selective towards propene formation. However, the catalyst containing 40 mole % Fe3+ ions exhibited the highest activity and selectivity. Correlations were attempted to the catalyst composition with their electronic and catalytic properties. Probable mechanism for the dehydration process is proposed in terms of surface active sites.


2019 ◽  
Vol 4 (1) ◽  
pp. 91-102 ◽  
Author(s):  
Ryan T. Shafranek ◽  
Joel D. Leger ◽  
Song Zhang ◽  
Munira Khalil ◽  
Xiaodan Gu ◽  
...  

Directed self-assembly in polymeric hydrogels allows tunability of thermal response and viscoelastic properties.


1961 ◽  
Vol 5 ◽  
pp. 276-284
Author(s):  
E. L. Moore ◽  
J. S. Metcalf

AbstractHigh-temperature X-ray diffraction techniques were employed to study the condensation reactions which occur when sodium orthophosphates are heated to 380°C. Crystalline Na4P2O7 and an amorphous phase were formed first from an equimolar mixture of Na2HPO4·NaH2PO4 and Na2HPO4 at temperatures above 150°C. Further heating resulted in the formation of Na5P3O10-I (high-temperature form) at the expense of the crystalline Na4P4O7 and amorphous phase. Crystalline Na5P3O10-II (low-temperature form) appears after Na5P3O10-I.Conditions which affect the yield of crystalline Na4P2O7 and amorphous phase as intermediates and their effect on the yield of Na5P3O10 are also presented.


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