High pressure NQR study of hydrogen bonds in ferroelectric N(CH3)4H(Cl3CCOO)2

1988 ◽  
Vol 77 (1) ◽  
pp. 145-151 ◽  
Author(s):  
M. Zdanowska-Fráczek ◽  
M. Maćakowiak ◽  
R. Jakubas
Keyword(s):  
2003 ◽  
Vol 125 (40) ◽  
pp. 12358-12364 ◽  
Author(s):  
Kwang Ming Lee ◽  
Hai-Chou Chang ◽  
Jyh-Chiang Jiang ◽  
Jack C. C. Chen ◽  
Hsiang-En Kao ◽  
...  

2016 ◽  
Vol 2 (1) ◽  
Author(s):  
Annette Bussmann-Holder ◽  
Jürgen Köhler ◽  
M.-H. Whangbo ◽  
Antonio Bianconi ◽  
Arndt Simon

AbstractThe recent report of superconductivity under high pressure at the record transition temperature of Tc =203 K in pressurized H2S has been identified as conventional in view of the observation of an isotope effect upon deuteration. Here it is demonstrated that conventional theories of superconductivity in the sense of BCS or Eliashberg formalisms cannot account for the pressure dependence of the isotope coefficient. The only way out of the dilemma is a multi-band approach of superconductivity where already small interband coupling suffices to achieve the high values of Tc together with the anomalous pressure dependent isotope coefficient. In addition, it is shown that anharmonicity of the hydrogen bonds vanishes under pressure whereas anharmonic phonon modes related to sulfur are still active.


2014 ◽  
Vol 70 (a1) ◽  
pp. C988-C988
Author(s):  
Sergey Arkhipov ◽  
Boris Zakharov ◽  
Elena Boldyreva

"Experiments for studying crystalline materials under extreme conditions are a powerful tool for investigating ""structure-property"" relationships. They also give information on the behavior of hydrogen bonds and are important both for materials science and crystal engineering. In addition, many processes in the living organisms are also related to mechanical stress. One of the most interesting tasks is to identify factors which influence the stability of a structure, or a part of the structure, at high pressure. Experiments on the systematic study of compounds in a wide range of pressures allow us to accumulate data that can be used to solve this problem. For a more complete picture, the mixed crystals of the selected compound are studied. Investigation of mixed crystals and cocrystals of interest can be compared with the crystals of individual compounds. We have chosen the structure of L-serine - L-ascorbic acid to be compared with those of L-serine and L-ascorbic acids for such a study. Phase transitions were previously reported to be induced by increasing pressure in both L-serine [1] and L-ascorbic acid [2]; moreover, the structure of L-serine was followed at multiple pressures by single-crystal and powder X-ray diffraction[3]. L-serine – L-ascorbic acid co-crystal was studied in the pressure range 0-5.4 GPa (at multiple points at every 0.5-0.7 GPa) by single-crystal X-ray diffraction and Raman spectroscopy. A phase transition has been detected and some rearrangement in the network of hydrogen bonds was observed. The high pressure data were compared with those for the individual structures of the L-serine and L-ascorbic acid. This work was supported by RFBR (grants 12–03-31541, 14-03-31866, 13-03-92704, 14-03-00902 ), Ministry of Science and Education of Russia and Russian Academy of Sciences."


1976 ◽  
Vol 29 (3) ◽  
pp. 479 ◽  
Author(s):  
SD Hamann ◽  
M Linton

Infrared measurements have been made of the influence of pressures between 0 and 40 kbar on the asymmetrical stretching frequencies v3 and bending frequencies v2 of the hydrogen-bonded ions FHF- and ClHCl- in the solid salts NaHF2, KHF2, NH4HF2, (CH3)4NHCl2 and (C2H5)4NHCl2 at 25�C. The behaviour of the symmetrical stretching frequency v1 for FHF- in KHF2 has been deduced indirectly from the shifts of combination bands. Contrary to the behaviour of compounds with weaker, 'normal', hydrogen bonds, the v3 bands shift to higher frequencies and the v2 bands shift to lower frequencies with increasing pressure. The vl band of KHF2 shifts to higher frequencies. These trends are all in agreement with predictions made in Part I for a simple model of hydrogen bonds. A new high-pressure phase transition has been found to occur in NaHF2 at about 40 kbar.


1986 ◽  
Vol 41 (1-2) ◽  
pp. 290-293
Author(s):  
Mariusz Maćkowiak ◽  
Maria Zdanowska-Fra̧zek ◽  
Piotr Kozioł ◽  
Jan Stankowski ◽  
Alarich Weiss

The 127I NQR frequency in anilinium iodide C6H5NH3⊕I⊖ was studied at pressures up to 300 MPa and within the temperature range 77 K - 290 K. With increasing pressure the order-disorder transition point Tc is shifted to higher temperatures. The pressure coefficient of the phase transition temperature amounts to dTc/dp = 4.2 x 10-2 deg MPa-1. The pressure coefficient of the NQR frequency is negative. In addition, the 12'I nuclear quadrupole coupling constants and the respective asymmetry parameters η were evaluated as a function of pressure. The results confirm the close connection between the mechanism of the phase transition and the dynamics of the N - H⊕ ...I⊖ hydrogen bonds.


Author(s):  
Ewa Patyk-Kaźmierczak ◽  
Michał Kaźmierczak

Benzocaine (BZC), an efficient and highly permeable anaesthetic and an active pharmaceutical ingredient of many commercially available drugs, was studied under high pressure up to 0.78 GPa. As a result, new BZC polymorph (IV) was discovered. The crystallization of polymorph (IV) can be initiated by heating crystals of polymorph (I) at a pressure of at least 0.45 GPa or by their compression to 0.60 GPa. However, no phase transition from polymorph (I) to (IV) was observed. Although polymorph (IV) exhibits the same main aggregation motif as in previously reported BZC polymorphs (I)–(III), i.e. a hydrogen-bonded ribbon, its molecular packing and hydrogen-bonding pattern differ considerably. The N—H...N hydrogen bonds joining parallel BZC ribbons in crystals at ambient pressure are eliminated in polymorph (IV), and BZC ribbons become positioned at an angle of about 80°. Unfortunately, crystals of polymorph (IV) were not preserved on pressure release, and depending on the decompression protocol they transformed into polymorph (II) or (I).


1994 ◽  
Vol 376 ◽  
Author(s):  
A.I. KOLESNIKOV

ABSTRACTInelastic incoherent neutron scattering measurements on the hdaice, ice Ih and high-pressure phases ice VI and ice VIII revealed similarity between the amorphous phase and crystalline ice VI and led to the new proposition that hda ice consists of two interpenetrating hydrogen-bonded networks with no hydrogen bonds between “sublattices”.


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