SOLID-STATE 13C AND 45Sc NMR STUDIES ON ENDOHEDRAL SCANDIUM-CARBIDE METALLOFULLERENES: A MOTIONAL DYNAMICS OF Sc ATOMS IN FULLERENES

NANO ◽  
2008 ◽  
Vol 03 (01) ◽  
pp. 21-25 ◽  
Author(s):  
HARUYA OKIMOTO ◽  
WILHELM HEMME ◽  
YASUHIRO ITO ◽  
TOSHIKI SUGAI ◽  
RYO KITAURA ◽  
...  

Sc 2 C 2@ C 82( II ) and Sc 2 C 2@ C 82( III ) have been synthesized and chromatographically isolated and characterized by using UV-Vis-NIR absorption spectroscopy. Solid-state 13 C and 45 Sc NMR on Sc 2 C 2@ C 82 metallofullerenes provide the rotational activation energy of Sc atoms encapsulated in C 82 fullerenes which is lower than that in solution due to crystal field effects on the rate of the rotation.

2017 ◽  
Vol 53 (71) ◽  
pp. 9930-9933 ◽  
Author(s):  
Yijue Xu ◽  
Lysiane Champion ◽  
Bulat Gabidullin ◽  
David L. Bryce

In situ 31P solid-state NMR studies of mechanochemical halogen bond formation provide insights into the cocrystallisation process and an estimate of the activation energy.


1978 ◽  
Vol 33 (8) ◽  
pp. 896-898 ◽  
Author(s):  
Paul K. Burkert ◽  
Frank M. Hutter

The first Re NQR spectra of rhenium oxygen compounds with rhenium atoms in the pseudo-octahedral environment of Re2O7(H2O)2 and Re2O7(H2O)2 · 2(1,4)-dioxane were found. The values of the Re NQR coupling constants of these rhenium atoms are the highest measured until now. They show, that the gradient of the electrical field is much more sensitive to distortions of an octahedral crystal field than to distortions of a tetrahedral field.


2004 ◽  
Vol 835 ◽  
Author(s):  
A. R. Czardybon ◽  
K. Sivasubramaniam ◽  
G.R. Goward

ABSTRACTThis study aims to develop novel polyelectrolytes including lithiated imidazole heterocycles for use in lithium ion rechargeable batteries. Lithium ion local mobility in these materials is characterized by 6, 7Li solid-state NMR. By comparing these results with macroscopic ionic conductivity, measured by impedance spectroscopy, we will be able to develop a picture of the ionic conductivity at the microscopic level. Multinuclear solid state NMR provides information on microscopic interactions including ionic mobility and ring reorientations which govern the efficiency of conductivity. Our research includes 6, 7Li variable MAS NMR studies at intermediate spinning speeds, relaxation investigations to determine spin-lattice relaxation times (T1) of lithium ion hopping, and 2D exchange spectroscopy to determine possible chemical exchange processes. A very long T1 (135 s at ambient temperature) and an activation energy Ea = 17.2 kJ/mol suggests rigid molecule structure and the absence of the ring reorientation of the model compound, lithium imidazolium (LiIm). We compare this to the behavior of LiIm doped with lithium methanesulfonate, which we show to form a new ionic complex with lower T1 and corresponding lower activation energy. With the goal of creating new polyelectrolytes, we have synthesized electrolytes incorporating lithiated imidazole rings, where lithium transport may be independent of polymer-backbone flexibility, and thus polymers with high Tg may be viable. Such materials are highly desirable for secondary lithium polymer battery applications.


2020 ◽  
Vol 22 (32) ◽  
pp. 18050-18059
Author(s):  
Carlos O. Amorim ◽  
João N. Gonçalves ◽  
João S. Amaral ◽  
Vítor S. Amaral

The search for better and inexpensive magnetoelectric materials is now commonplace in solid state physics, using electric field induced strain to change the multiferroic magnetic state.


Langmuir ◽  
2000 ◽  
Vol 16 (17) ◽  
pp. 7066-7069 ◽  
Author(s):  
L. Soriano ◽  
G. G. Fuentes ◽  
C. Quirós ◽  
J. F. Trigo ◽  
J. M. Sanz ◽  
...  

1989 ◽  
Vol 111 (15) ◽  
pp. 5658-5660 ◽  
Author(s):  
P. Popelier ◽  
A. T. H. Lenstra ◽  
C. Van Alsenoy ◽  
H. J. Geise

1979 ◽  
Vol 40 (C5) ◽  
pp. C5-180-C5-182 ◽  
Author(s):  
J. X. Boucherle ◽  
D. Givord ◽  
J. Laforest ◽  
J. Schweizer ◽  
F. Tasset

2019 ◽  
Vol 15 (8) ◽  
pp. 850-862
Author(s):  
Mirthala Flores-García ◽  
Juan Manuel Fernández-G. ◽  
Cristina Busqueta-Griera ◽  
Elizabeth Gómez ◽  
Simón Hernández-Ortega ◽  
...  

Background: Ischemic heart disease, cerebrovascular accident, and venous thromboembolism have the presence of a thrombotic event in common and represent the most common causes of death within the population. Objective: Since Schiff base copper(II) complexes are able to interact with polyphosphates (PolyP), a procoagulant and potentially prothrombotic platelet agent, we investigated the antiplatelet aggregating properties of two novel tridentate Schiff base ligands and their corresponding copper( II) complexes. Methods: The Schiff base ligands (L1) and (L2), as well as their corresponding copper(II) complexes (C1) and (C2), were synthesized and characterized by chemical analysis, X-ray diffraction, mass spectrometry, and UV-Visible, IR and far IR spectroscopy. In addition, EPR studies were carried out for (C1) and (C2), while (L1) and (L2) were further analyzed by 1H and 13C NMR. Tests for antiplatelet aggregation activities of all of the four compounds were conducted. Results: X-ray diffraction studies show that (L1) and (L2) exist in the enol-imine tautomeric form with a strong intramolecular hydrogen bond. NMR studies show that both ligands are found as enol-imine tautomers in CDCl3 solution. In the solid state, the geometry around the copper(II) ion in both (C1) and (C2) is square planar. EPR spectra suggest that the geometry of the complexes is similar to that observed in the solid state by X-ray crystallography. Compound (C2) exhibited the strongest antiplatelet aggregation activity. Conclusion: Schiff base copper(II) complexes, which are attracting increasing interest, could represent a new approach to treat thrombosis by blocking the activity of PolyP with a potential anticoagulant activity and, most importantly, demonstrating no adverse bleeding events.


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