1H nuclear magnetic resonance, differential scanning calorimetry, and electrical conductivity studies on the phase transitions of pentylammonium chloride and the cationic self-diffusion in its rotator phase

1988 ◽  
Vol 66 (8) ◽  
pp. 1961-1969 ◽  
Author(s):  
Shigehiko Iwai ◽  
Ryuichi Ikeda ◽  
Daiyu Nakamura

Measurements of 1H nmr, differential thermal analysis, and differential scanning calorimetry have revealed that solid pentylammonium chloride, cooled rapidly from room temperature, forms a mixture of the stable and metastable low-temperature phases below the phase transition temperature, Ttr (238 K). The sample annealed just below Ttr for 3 h was shown to consist of a single stable phase down to about 100 K, indicating the existence of a time-consuming phase transition taking place successively just below the normal transition. In the rotator phase obtainable above Ttr (257 K), 1H nmr studies proved the presence of axial rotation of the whole cation about the long axis, similar to n-paraffins in their rotator phase. Above room temperature, the onset of the translational self-diffusion of the cations within 2D planes in the layer structure of the rotator phase was detected by measuring the temperature dependence of electrical conductivity as well as 1H T1 and T1p. 2D self-diffusion constants and diffusional correlation times evaluated from the electrical conductivity observed between room and the melting temperatures indicate that the 2D cationic diffusion near the melting point is as fast as 3D self-diffusion in usual plastic crystals. Cationic motions in the two different rotator phases α and α′ are compared.

1980 ◽  
Vol 35 (1) ◽  
pp. 98-102 ◽  
Author(s):  
P. Franzosini ◽  
M. Sanesi ◽  
A. Cingolani ◽  
P. Ferloni

Abstract The phase transition temperatures and enthalpies were determined by differential scanning calorimetry between room temperature and the isotropic liquid region for the lithium n.alkanoates from tridecanoate to eicosanoate. The number and nature of the phases involved were discussed in comparison with the literature data available for some of the homologues concerned. For diffe-rent kinds of transitions, the significant features of the plots AS vs. number of carbon atoms were put into evidence.


2018 ◽  
Vol 12 (1) ◽  
pp. 134-139
Author(s):  
S.M. Van Der Merwe ◽  
N. Bouropoulos ◽  
D.A. Katsamenis ◽  
O.L. Lampou ◽  
D.G. Fatouros

Background: The effect of different concentrations of the absorption enhancer Trimethyl Chitosan (TMC) to the physicochemical properties of Large Unilamellar Vesicles (LUV) comprised of L-a-Phospahtidyl Choline (PC) were investigated in the current study. Methods: The Degree of Quartenization (DQ) of trimethylchitosan was assessed with nuclear magnetic resonance (1H NMR). The vesicles were characterized by means of Dynamic Light Scattering (DLS), ζ-potential, Differential Scanning Calorimetry (DSC) and Contact Angle Goniometry (CAG) measurements. Results: The data showed that the surface charge of the PC liposomes was significantly altered as a function of the TMC concentration, giving evidence of presence of the polyelectrolyte to the liposome’s membrane. Varying the concentration of TMC affected the phase Transition Temperature (Tm) of the lipid, verifying the miscibility of the polyelectrolyte with the lipid bilayer. The association of the polymer with the liposomes was related to the amount of the polyelectrolyte present, reflecting changes to the wettability of the dispersion as measured by CAG. Conclusion: The results demonstrated that presence of TMC significantly modified the physical properties of liposomes. Such systems might have a potential use for mucosal delivery (e.g. nasal route of administration).


1999 ◽  
Vol 19 (2) ◽  
pp. 95-108 ◽  
Author(s):  
Todorka G. Vladkova ◽  
Alexander Chr. Alaminov ◽  
Milka G. Pankova

Abstract The possible interactions between oligoamidephosphate (OAPli) and the curatives of a sulphenamide-accelerated sulphur vulcanizing system were studied by differential scanning calorimetry, IR-spectroscopy, and X-ray analysis. The interactions in double mixtures were between OAPh and zinc oxide (ZnO) and OAPh and sulphur. The OAPh/ZnO interaction that starts at room temperature seems to be the key for understanding the peculiarities of sulphenamide-accelerated sulphur vulcanization in the presence of OAPh.


Energies ◽  
2021 ◽  
Vol 14 (19) ◽  
pp. 6344
Author(s):  
Philipp S. Borchers ◽  
Patrick Gerlach ◽  
Yihan Liu ◽  
Martin D. Hager ◽  
Andrea Balducci ◽  
...  

In this work, two new redox-active ionic liquids, one based on 2,2,6,6-tetramethylpiperidine-N-oxide and the other based on 4,4′-bipyridine, are synthesized and characterized. A ferrocene-based redox-active ionic liquid is used for referencing the results. All ionic liquids are formed via salt-metathesis from halogenate to bis(trifluoromethylsulfonyl)imide. Their fundamental thermal characteristics are assessed with differential scanning calorimetry. While the imidazolium ionic liquids show no melting point, the phase transition is well observable for the viologen-based ionic liquid. The properties of the neat redox-active ionic liquids and of binary mixtures containing these ionic liquids (0.1 m) and 1-butyl-1-methyl pyrrolidinium-bis(trifluoromethylsulfonyl)imide have been investigated. Finally, the use of these binary mixtures in combination with activated carbon-based electrodes has been considered in view of the use of these redox-active electrolytes in supercapacitors.


2009 ◽  
Vol 108 (1) ◽  
pp. 106-115 ◽  
Author(s):  
B. GARBARZ-GLOS ◽  
R. BUJAKIEWICZ-KOROŃSKA ◽  
D. MAJDA ◽  
M. ANTONOVA ◽  
A. KALVANE ◽  
...  

2012 ◽  
Vol 535-537 ◽  
pp. 950-953
Author(s):  
Li Na Bai ◽  
Gui Xing Zheng ◽  
Zhi Jian Duan ◽  
Jian Jun Zhang

The influences of Gd concentration on martensitic transformation and magnetic properties of NiMnIn alloys were investigated by differential scanning calorimetry (DSC) , vibrating sample magnetometry (VSM), X-ray diffraction (XRD) and etc. It is Observed through the experiment: the addition of Gd enhances martensite transition temperature;X-ray diffraction analysis of experimental alloys is revealed that to the mixture is martensite and austenite at room temperature; content of Gd is not proportional to the improvement of magnetic property.


2010 ◽  
Vol 14 (07) ◽  
pp. 646-659 ◽  
Author(s):  
Eric Rose ◽  
Emma Gallo ◽  
Nicolas Raoul ◽  
Léa Bouché ◽  
Ariane Pille ◽  
...  

Three "basket handle" porphyrins have been prepared by condensation of tetrakis-(α,β,α,β-2-aminophenyl)porphyrin atropoisomer with 1,1′-binaphthyl, 2,2′-dimethoxy, -3,3′-dicarbonylchloride, -3,3′-diacetylchloride and -3,3′-dipropanoylchloride. The epoxidation of styrene with the three iron catalysts, obtained after metalation of the free porphyrins, occurs with good yields and moderate ee up to 54%. These porphyrins showed unexpected conformational differences, as revealed by NMR spectroscopy. In particular, variable temperature NMR studies showed that the methoxy group in one of them undergoes intermediate conformational exchange on the 1H NMR time scale at room temperature. Lowering the temperature to -50 °C revealed the presence of four states in slow exchange on the NMR time scale. These results evidence a dynamic conformational equilibrium of the binaphthyl handles that adopt different, asymmetric positions with respect to the porphyrin plane.


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