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1Author    Peter Remmert, Edmund Fischer, Hans-Ulrich HummelRequires cookie*
 Title    Phasenuntersuchungen im System 2 H a -T a S 2-2 H c -M o S 2 Investigations on Phases in the System 2 H a -T a S 2-2 H c -M o S 2  
 Abstract    Ternary phases in the system TaS2-M o S 2 have been obtained by thermal reactions at 1050 °C of binary layered disulfides and N H 4C1 as promotor. Ternary phases Taj_*Mo*S2 exist in the range 0.5 < jc< 0.9. In the range of 0.25 < * < 0.55 the reactions are quantitative and the phase-compositions are determined by the amounts of the starting materials. For x < 0 .2 lT -T a S 2 and for jc> 0.60 2 H c -M o S 2 are contaminating the resulting ternary phases. Ternary phases have been characterized by X-ray powder diffraction and are indexed rhombohedrally on the basis o f a 3 R-structure with metals in trigonal-prismatic coordination. The phases Tal jcMo*S2 with 0.25 < * < 0.55 show a reversible transition of higher order asso­ ciated with a change in the electrical conductivity mechanism. B elow 420 K the phases show semiconductivity while above 460 K metallic conductivity is observed. 
  Reference    Z. Naturforsch. 49b, 1175—1178 (1994); eingegangen am 15. April 1994 
  Published    1994 
  Keywords    Ternary Phases, Preparation, Phase Transition 
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 TEI-XML for    default:Reihe_B/49/ZNB-1994-49b-1175.pdf 
 Identifier    ZNB-1994-49b-1175 
 Volume    49 
2Author    S. Lewicki, B. Szafrańska, Z. PająkRequires cookie*
 Title    Molecular Motion in Solid Tetrapropylammonium Bromide and Iodide  
 Abstract    The proton NMR second moment and spin-lattice relaxation time for tetrapropylammonium bromide and iodide have been measured over a wide temperature range. A solid-solid phase transition related to the onset of cation tumbling was found for both salts and confirmed by DTA. In the low temperature phases methyl group reorientation was evidenced. For iodide a dynamic nonequivalence of the methyl groups and the onset of ethyl groups motion was also discovered. 
  Reference    Z. Naturforsch. 47a, 1115—1118 (1992); received July 14 1992 
  Published    1992 
  Keywords    NMR, Molecular motions, Phase transitions 
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 TEI-XML for    default:Reihe_A/47/ZNA-1992-47a-1115.pdf 
 Identifier    ZNA-1992-47a-1115 
 Volume    47 
3Author    Barbara Szafrańska, Zdzisław PająkRequires cookie*
 Abstract    o le c u la r M o tio n in S o lid T e tr a e th y l-a n d T e tra p ro p y la m m o n iu m T e tr a f lu o r o b o r a te s Proton and fluorine NMR second moments and spin-lattice relaxation times for polycrystalline tetraethyl-and tetrapropylammonium tetrafluoroborates have been measured over a wide range of temperatures. Solid-solid phase transitions were found for both compounds and confirmed by DSC. Methyl group C3 reorientation followed by more complex cation motions was evidenced in the low temperature phases. Overall cation reorientation characterises the high temperature phases of both compounds. Isotropic anion reorientation was found in both salts in both phases. 
  Reference    Z. Naturforsch. 50a, 584—588 (1995); received August 15 1994 
  Published    1995 
  Keywords    NMR, Molecular motions, Phase transitions 
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 TEI-XML for    default:Reihe_A/50/ZNA-1995-50a-0584.pdf 
 Identifier    ZNA-1995-50a-0584 
 Volume    50 
4Author    M. Grottel3, A. Kozakb, Z. PająkRequires cookie*
 Title    l H a n  
 Abstract    d 19F N M R S tu d y o f C a tio n a n d A n io n M o tio n s in G u a n id in iu m F lu o r o a n tim o n a te s Proton and fluorine NMR linewidths, second moments, and spin-lattice relaxation times of polycrystalline [C(NH2)3]2SbF5 and C(NH2)3SbF6 were studied in a wide temperature range. For the pentafluoroantimonate, C3-reorientation of the guanidinium cation and C4-reorientation of the SbF5 anion were revealed and their activation parameters determined. The dynamical inequivalence of the two guanidinium cations was evidenced. For the hexafluoroantimonate, two solid-solid phase transitions were found. In the low temperature phase the guanidinium cation undergoes C3 reorien­ tation while the SbF6 anion reorients isotropically. The respective activation parameters were derived. At high temperatures new ionic plastic phases were evidenced. 
  Reference    Z. Naturforsch. 50a, 742—748 (1995); received March 2 1995 
  Published    1995 
  Keywords    NMR, Molecular Motions, Phase transitions 
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 TEI-XML for    default:Reihe_A/50/ZNA-1995-50a-0742.pdf 
 Identifier    ZNA-1995-50a-0742 
 Volume    50 
5Author    M. Grottel, M. Szafrański, Z. PająkRequires cookie*
 Title    NMR Study of Cation Motion in Guanidinium Iodoplumbates  
 Abstract    Proton NMR second moments and spin-lattice relaxation times of polycrystalline C(NH 2) 3 PbI 3 and [C(NH 2) 3 ]2PbI 4 were studied in a wide temperature range. The order-disorder character of the existing solid-solid phase transitions was confirmed and for tetraiodoplumbate a new phase transition at 170 K was discovered. For both compounds a dynamical inequivalence and unusual high mobility of the guanidinium cations were revealed. For the reorientations discovered (NH 2 group flipping, C 3 in-plane reorientation and a tumbling) the activation parameters were determined. 
  Reference    Z. Naturforsch. 52a, 783—788 (1997); received October 6 1997 
  Published    1997 
  Keywords    NMR, Molecular Motions, Phase Transitions 
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 TEI-XML for    default:Reihe_A/52/ZNA-1997-52a-0783.pdf 
 Identifier    ZNA-1997-52a-0783 
 Volume    52 
6Author    R. Tchukvinskyi, R. Cach, Z. CzaplaRequires cookie*
 Title    Dielectric Study of the Ferroelectric Phase Transition in DMAGaS Crystal  
 Abstract    Electric permittivity measurments as functions of temperature at constant dc electric field and as func-tions of the dc electric field at constant temperatures in the paraelectric phase have been performed for DMAGaS crystal. The changes of the permittivity maximum with the electric field intensity evidence the first-order character of the ferroelectric phase transition at T cX . The field dependence of the permit-tivity e(E) in the paraelectric phase is discussed, using the classical electric equation of state. A meth-od for the determination of the corresponding coefficients is proposed. The obtained B and C coeffi-cients, together with double hysteresis loop observed above T cl prove the first-order character of the ferroelectric phase transition in DMAGaS crystal. 
  Reference    Z. Naturforsch. 53a, 105—111 (1998); received October 15 1998 
  Published    1998 
  Keywords    Ferroelectricity, Phase Transition, Dielectric Properties 
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 TEI-XML for    default:Reihe_A/53/ZNA-1998-53a-0105.pdf 
 Identifier    ZNA-1998-53a-0105 
 Volume    53 
7Author    M. Arietta, S. Schriewer-Pöttgen, Wolfgang JeitschkoRequires cookie*
 Title    Two Modifications of Hg5Re2O 10  
 Abstract    The previously reported mercury perrhenate Hg5 Re2O 10, prepared hydrothermally, has now been obtained by reaction of HgO with the mercury(II) metaperrhenate H g (R e 0 4)2 in sealed silica tubes. A second modification o f this compound can be obtained by reaction of elem ental mercury with H g (R e 0 4)2 also in sealed silica tubes. Its crystal structure has been determined from single-crystal X-ray data: P 2 x/c, a -861.5(1), b = 1200.9(2), c = 1203.9(2) pm, ß = 97.15(1)°, Z = 4, R = 0.024 for 1733 structure factors and 105 variables. Both modifi­ cations may be represented by the formula H g2+-2H g20 -2 R e 0 4_, indicating that mercury occurs in oxidation states I and II. In both modifications the mercury and some oxygen atoms form two-dimensionally infinte, puckered, cationic nets of the composition (H g2+-2H g20)" , which are separated by the R e 0 4~ tetrahedra. In the modification reported earlier the mer­ cury oxygen nets consist of condensed 16-membered rings, while the nets of the present modification contain 10-and 22-membered rings. 
  Reference    Z. Naturforsch. 50b, 1335—1339 (1995); received February 27 1995 
  Published    1995 
  Keywords    Crystal Structure, Mercury Perrhenates, Phase Transitions 
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 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-1335.pdf 
 Identifier    ZNB-1995-50b-1335 
 Volume    50 
8Author    G. W. PohlRequires cookie*
 Title    Spectral Properties of Fluorescent Dyes in Lecithin Vesicles Probes for the Structure of Lipid Bilayer Membranes and for Membrane Potentials  
 Abstract    Three fluorescent dyes (a merocyanin, a cyanin and a modified umbelliferon) have been in­ corporated into vesicles from three different lecithins. Their absorption spectrum, emission spectrum and fluorescence polarization in the lipid vesicles has been studied and compared with the spectral properties in homogeneous organic solutions. The reactivity of lipid bound dyes with reagents in the aqueous phase was investigated. The location use as indicators of phase transitions or membrane 
  Reference    (Z. Naturforsch. 31c, 575 [1976]; received May 10 1976) 
  Published    1976 
  Keywords    Lecithin Vesicles, Fluorescent Probes, Phase Transitions, Membrane Potentials 
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 TEI-XML for    default:Reihe_C/31/ZNC-1976-31c-0575.pdf 
 Identifier    ZNC-1976-31c-0575 
 Volume    31 
9Author    H. Heithier, H.-J Galla, H. MöhwaldRequires cookie*
 Title    Fluorescence Spectroscopic and Thermodynamic Studies of Chlorophyll Containing Monolayers and Vesicles. Part I: Mixed Monolayers of Pheophytin A and Lecithin  
 Abstract    Mixed monolayers of pheophytin a and a-L-dimyristoyl lecithin (DML) are investigated on the water surface. The studies gain their special value from the simultaneous measurement of surface pressure and fluorescence intensity as a function of the covered area per molecule. A phase separation in the liquid state of the monolayer is established. Phase 1 exists almost exclusively of pheophytin molecules. Phase 2 exists essentially of D M L domains solubilizing pheo­ phytin in a concentration of 15 mol%. During the D M L main transition the pheophytin solubility decreases to about 2 mol%, the excess pheophytin being precipitated within the surface layer. During the pheophytin main transition an ordered structure below the surface layer is formed. A stabilizing interaction between the pheophytin domains and their environment is observed and discussed. A sharp fluorescence change at a pressure below 0.5 dyn/cm indicates another phase transition. It very probably involves an unwrapping of pheophytin from water molecules. 
  Reference    Z. Naturforsch. 33c, 382 (1978); received March 15/April 3 1978 
  Published    1978 
  Keywords    Monolayers, Chlorophyll, Energy Transfer, Fluorescence Spectroscopy, Phase Transitions 
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 TEI-XML for    default:Reihe_C/33/ZNC-1978-33c-0382.pdf 
 Identifier    ZNC-1978-33c-0382 
 Volume    33 
10Author    Srabani Banerjee, S. N. ChatterjeeRequires cookie*
 Title    Effect of Sodium Cholate on the Phase Transition Temperature of Dipalmitoyl Phosphatidylcholine  
 Abstract    On treatm ent with sodium cholate, the phase transition tem perature (Tc) of m ultilam ellar liposomes derived from dipalm itoyl phosphatidylcholine (DPPC) progressively decreased with increasing cholate: lipid-P m olar ratio. A molar ratio of 4.5 caused a one degree depression in Tc. The unilamellar cholate vesicles o f DPPC exhibited the same Tc as that o f the m ultilam ellar ones. The formation of unilam ellar vesicles from the m ultilam ellar ones by cholate treatm ent was in­ vestigated by electron microscopy. 
  Reference    Z. Naturforsch. 38c, 302—306 (1983); received Septem ber 20/N ovem ber 15 1982 
  Published    1983 
  Keywords    Liposomes, DPPC, Sodium Cholate, Phase Transition, Electron Microscopy 
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 TEI-XML for    default:Reihe_C/38/ZNC-1983-38c-0302.pdf 
 Identifier    ZNC-1983-38c-0302 
 Volume    38 
11Author    Akinobu Sasane, Hisanori Shinohara, Yoshihiro Mori, Yoshio Kume, Tetsuo Asaji, Daiyu NakamuraRequires cookie*
 Title    A Temperature Dependence Study of 35 C1 Nuclear Quadrupole Resonance Frequencies in Some Hexachloroplatinate(IV) Hexahydrates  
 Abstract    The temperature dependence of 35 C1 NQR frequencies was investigated in various hexachloro-platinate(IV) hexahydrates containing the following divalent ions as counter cations: Mn(II), Fe(II), Co(II), Ni(II), Cu(II), Zn(II), Cd(II), and Ba(II). All of the compounds except the Cu(II) and Ba(II) salts yield a single 35 C1 NQR line at all temperatures studied. For the Mn(II), Cu(II), and Ba(II) salts, the NQR frequencies are considerably shifted by deuteration. For the deuterated Mn(II) salt, two 35 C1 NQR lines were observed whose relative peak-height intensities vary in dependence on the history of the thermal treatment of the sample. The very broad higher frequency line could be observed for a sample which had been at 77 K or below. It could not be observed for a sample which was cooled slowly to room temperature after it had been heated up to ca. 420 K. A structural phase transition was located at 135. 6 and 129. 4 K for the Cu(II) salt and its deuterated analog, respectively. The frequency shift by deuteration is discussed in relation to the strength of O-H ... CI type hydrogen bonds. 
  Reference    Z. Naturforsch. 42a, 611—616 (1987); received February 171987 
  Published    1987 
  Keywords    Magnetic resonance (NQR), hydrogen bonding, phase transition 
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 TEI-XML for    default:Reihe_A/42/ZNA-1987-42a-0611.pdf 
 Identifier    ZNA-1987-42a-0611 
 Volume    42 
12Author    J. Wąsicki, Z. Pająk, A. KozakRequires cookie*
 Title    Cation and Anion Reorientation at Phase Transition in Pyridinium Tetrafluoroborate  
 Abstract    Temperature dependences of and 19 F second moment and spin-lattice relaxation times for polycrystalline pyridinium tetrafluoroborate were measured. A phase transition was discovered at 202 K. A model of cation reorientation between inequivalent (low-temperature phase) and equiva-lent (high-temperature phase) equilibrium positions is proposed. Whether the anion reorients isotropically or about a symmetry axis cannot be decided. An analysis of cross-relaxation effects yielded activation parameters for cation and anion reorientation. The rotational correlation times for both ions converge just at the phase transition reaching the value of 10~ 10 s. 
  Reference    Z. Naturforsch. 45a, 33—36 (1990); received August 5 1989 
  Published    1990 
  Keywords    NMR, cross-relaxation, molecular motions, phase transitions 
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 TEI-XML for    default:Reihe_A/45/ZNA-1990-45a-0033.pdf 
 Identifier    ZNA-1990-45a-0033 
 Volume    45 
13Author    Masao Hashimoto, Akiko Shono, Yoshiyuki Mido, Haruo Niki, Hiroshi Hentona, Koichi ManoRequires cookie*
 Title    Narrowing of the 3 5 CI NQR Lines of Trichloroacetamide Caused by Its Ferroelectric Phase Transition  
 Abstract    Dielectric measurements on single crystals and DSC of the title compound (monoclinic, space group P2 X) revealed a ferroelectric transition at ca. 355 K (AH xs 0.5 kJ mol"Powder x-ray diffraction indicated that the high temperature phase is also monoclinic and the change in volume at the transition is very small. A displacement of hydrogen atoms is considered as responsible for the appearance of ferroelectricity. The 35 C1 NQR signals at ca. 77 K were considerably broad, but a drastic narrowing took place after the compound had once experienced the phase transition. A tentative assignment of the NQR spectrum was made from a calculation of the NQR frequencies based on the CNDO/2 method. Another phase transition was evidenced by a small drift of the DSC curve and a slight anomaly of the dielectric behavior around 358 K. The present *H NMR experi-ments gave no indication of the onset of torsional motion of the NH 2 group reported to occur at ca. 210 K. 
  Reference    Z. Naturforsch. 45a, 327—333 (1990); received August 26 1989 in revised form November 1 1989 
  Published    1990 
  Keywords    NQR, Phase transition, Ferroelectricity, Hydrogen bond, Disordered structure 
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 TEI-XML for    default:Reihe_A/45/ZNA-1990-45a-0327.pdf 
 Identifier    ZNA-1990-45a-0327 
 Volume    45 
14Author    J. Pirnat, J. Lužnik, Z. Trontelj, P. K. KadabaRequires cookie*
 Title    Iodine NQR and Phase Transitions in [N(CH 3 ) 4 ] 2 ZnI 4 * a  
 Abstract    Using a superregenerative NQR spectrometer, the temperature dependence of 127 I NQR spectra in [N(CH 3) 4 ] 2 ZnI 4 was measured between 167 and 335 K. The measurements confirm two known structural phase transitions at 219 and 257.5 K. The correspondence between the distinct regions of iodine NQR spectra and the crystal structure is discussed. The relation of [N(CH 3) 4 ] 2 ZnI 4 to the incommensurate family with the general formula X 2 YZ 4 and the high temperature (paraphase) crystal space group D^ (Pmcn) is studied. 
  Reference    Z. Naturforsch. 45a, 349—352 (1990); received August 23 1989 in revised form 25 November 1989 
  Published    1990 
  Keywords    NQR, phase transitions, ferroelectric, crystal structure, displacement modulation 
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 TEI-XML for    default:Reihe_A/45/ZNA-1990-45a-0349.pdf 
 Identifier    ZNA-1990-45a-0349 
 Volume    45 
15Author    Juan Murgich, Ismardo Bonalde, JoseA. AbaneroRequires cookie*
 Title    N Nuclear Quadrupole Resonance Study of the Phase Transitions of Ba[Fe(CN) 5 N0] -3H 2 0  
 Abstract    The 14 N nuclear quadrupole resonance (NQR) of the cyanides in Ba[Fe(CN) s NO] • 3H 2 0 (BNP) was observed between 77 and 293 K. Phase transitions exist at 118,131 (both weakly first order) and 233 K (second order). Most of the cyanides were perturbed by the structural changes except for one of the trans cyanides that was only affected by the transition at 131 K. The mechanism of the phase transitions is interpreted in terms of soft modes resulting from the ion rearrangement produced by the slowing down of the water molecules upon cooling. A comparison of the NQR spectrum of BNP with that of Na ? [Fe(CN) 5 NO] • 3H 2 0 showed that the substitution of Na + by Ba 2 produced only minor changes in the charge distribution of the nitroprusside ion. 
  Reference    Z. Naturforsch. 45a, 353—356 (1990); received August 25 1989 
  Published    1990 
  Keywords    Magnetic Resonance (NQR), Nitroprussides, Phase Transitions 
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 TEI-XML for    default:Reihe_A/45/ZNA-1990-45a-0353.pdf 
 Identifier    ZNA-1990-45a-0353 
 Volume    45 
16Author    J. Von CieminskiRequires cookie*
 Title    Modeling of High-Signal Electrostriction. I  
 Abstract    A thermodynamical calculation of high-signal electrostriction, especially of ferroelectric materials, is proposed. It permits to model the high-signal electrostriction of the paraelectric and the funda-mental switching behaviour of the ferroelectric phase. Extraordinary high-signal deformation curves can be explained, the influence of the thermodynamical coefficients can be estimated and the order of phase transitions can be determined experimentally from the high-signal deformation curves. 
  Reference    Z. Naturforsch. 45a, 1090—1094 (1990); received May 8 1990 
  Published    1990 
  Keywords    Electromechanical properties, Electrostriction, Ferroelectrics, Thermodynamic, Phase transition 
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 TEI-XML for    default:Reihe_A/45/ZNA-1990-45a-1090.pdf 
 Identifier    ZNA-1990-45a-1090 
 Volume    45 
17Author    J. Von CieminskiRequires cookie*
 Title    Modeling of High-Signal Electrostriction. II  
 Abstract    The predictions obtained with a thermodynamical method are compared with experimental results. Several materials which pass a ferroelectric phase transition of first or second order are investigated. The predictions correspond well with the experimentaly determined qualitative and quantitative features as to the field and temperature dependence. Finally, extraordinary strain-field curves are predicted and proved. 
  Reference    Z. Naturforsch. 45a, 1095—1101 (1990); received May 8 1990 
  Published    1990 
  Keywords    Electromechanical properties, Electrostriction, Ferroelectrics, Thermodynamic, Phase transition 
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 TEI-XML for    default:Reihe_A/45/ZNA-1990-45a-1095.pdf 
 Identifier    ZNA-1990-45a-1095 
 Volume    45 
18Author    Z. Szafrańska, A. Pająk, KozakRequires cookie*
 Abstract    Proton and fluorine NMR second moments and spin-lattice relaxation times for polycrystalline tetrabutylammonium tetrafluoroborate have been measured over a wide range of temperatures at several Larmor frequencies. An analysis of cross-relaxation effects results in a determination of activation parameters for anion and cation reorientations. Three solid phases characterized by different ion dynamics are evidenced. M o le c u la r M o tio n in S o lid T e tra b u ty la m m o n iu m T e tr a f lu o r o b o r a te 
  Reference    Z. Naturforsch. 46a, 545—550 (1991); received March 14 1991 
  Published    1991 
  Keywords    NMR, Cross-relaxation, Molecular motions, Phase transitions 
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 TEI-XML for    default:Reihe_A/46/ZNA-1991-46a-0545.pdf 
 Identifier    ZNA-1991-46a-0545 
 Volume    46 
19Author    MarcoL H Gruwel1, RoderickE. WasylishenRequires cookie*
 Abstract    e u te riu m N M R S tu d y o f th e S o lid -S o lid P h a s e T ra n s itio n in P h e n e th y la m m o n iu m B ro m id e 30, 1991 Using 2H NMR, the dynamics of the cation in phenethylammonium bromide were studied in the two solid phases. Line shape and spin-lattice relaxation rate studies of the ammonium headgroups and the adajacent methylene groups indicate the onset of alkyl-chain motion prior to the first order phase transition. In the low-temperature phase the line shape and the spin-lattice relaxation rates of the -ND3 groups are consistent with C3 jumps and an activation energy of 54±4 kJ mol"1. However, in the high-temperature phase the spin-lattice relaxation studies indicate the presence of small-angle diffusion of the -ND3 groups around the C3 symmetry axis. In this phase the -CD2-groups show line shapes typical of large-amplitude two-site jumps occurring at a rate > 107 s~ l. In the low-temperature phase, at temperatures below 295 K, the -CD2-2H NMR line shapes indicate that the C-D bonds are essentially static. 
  Reference    Z. Naturforsch. 46a, 691 (1991); received March 
  Published    1991 
  Keywords    2H NMR, Phase transition, Relaxation, Molecular jumps 
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 TEI-XML for    default:Reihe_A/46/ZNA-1991-46a-0691.pdf 
 Identifier    ZNA-1991-46a-0691 
 Volume    46 
20Author    S. Torre, P. FerloniRequires cookie*
 Title    Molecular Motion in Solid Tetramethylammonium Tetrafluoroborate  
 Abstract    Measurements of n B and NMR relaxation times, differential scanning calorimetry and thermomechanical analysis, carried out on polycrystalline (CH 3) 4 NBF 4 from room temperature to about 100 K, have permitted to discuss the crystal dynamics of this salt and to analyze the nature of the phase transition occurring at «150K. Moreover, by means of an evaluation of the n B quadrupole coupling constant, information about the position of the F atoms has been obtained. An explanation of the NMR data in terms of an order-disorder phase transition involving the F~ ions is given. 
  Reference    Z. Naturforsch. 47a, 721—727 (1992); received March 24 1992 
  Published    1992 
  Keywords    (CH 3 ) 4 NBF 4, Molecular motion, Phase transition 
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 TEI-XML for    default:Reihe_A/47/ZNA-1992-47a-0721.pdf 
 Identifier    ZNA-1992-47a-0721 
 Volume    47