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S K Hoffmann

Publications and source records attributed to S K Hoffmann.

7 recordsLinked to original sources
PubMed2003

Water and lipid relations in beech (Fagus sylvatica L.) seeds and its effect on storage behaviour.

Beech (Fagus sylvatica L.) seeds indicate intermediate storage behaviour. Properties of water in seed tissues were studied to understand their requirements during storage conditions. Water sorption isotherms showed that at the same relative humidity (RH) the water content is significantly higher in embryo axes than cotyledons. This tendency maintains also after recalculating the water content for zero amount of lipids in tissues. Differential thermal analysis (DTA) indicated water crystallization exotherms in the embryo axes at moisture content (MC) higher than 29% and 16% in the cotyledons. In order to examine the occurrence of glassy state in the cytoplasm of beech embryos as a function of water content, isolated embryo axes were examined using electron spin resonance (ESR) of nitroxide TEMPO probe located inside axes cells. TEMPO molecules undergo fast reorientations with correlation time varied from 2 x 10(-9) s at 180 K to 2 x 10(-11) s at 315 K. Although the TEMPO molecules label mainly the lipid bilayers of cell membranes, they are sensitive to the dynamics and phase transformation of the cytoplasmic cell interior. The label motion is clearly affected by a transition between liquid and glassy state of the cytoplasm. The glass transition temperature (T(g)) raises from 253 to 293 K when water content decreases from 18% to 8%. Far from T(g) the motion is described by Arrhenius equation with very small activation energy E(a) in the liquid state and is relatively small in the glassy state where E(a)=1.5 kJ/mol for 28% H(2)O and E(a)=4.7 kJ/mol for 8% H(2)O or less. The optimal storage conditions of beech seeds are proposed in the range from 255 K for 15% H(2)O to 280 K for 9% H(2)O.

Cyclic N-Oxides↗
PubMed2001

Flexibility of CuCl4-tetrahedra in bis[cinchoninium tetrachlorocuprate(II)]trihydrate single crystals. X-ray diffraction and EPR studies.

Crystal structure of bis[cinchoninium tetrachlorocuprate(II)] trihydrate, [(C19H24N2O)CuCl4]2-3H2O, has been determined by X-ray diffraction at 100 K and reexamined at 293 K. The compound crystallizes in orthorhombic system with a P2(1)2(1)2(1) space group and unit cell parameters a = 15.3031(14), b = 36.415(3), and c = 7.8341(5) A at 100 K, and Z = 4. The asymmetric unit consists of two (CuCl4)(2-) tetrahedral anions linked by hydrogen bonds to two doubly protonated cinchonine molecules and three water molecules. The tetrahedra are strongly flattened, to approximately D(2d) symmetry, with different deformation for two inequivalent (CuCl4)(2-) -ions in the asymmetric unit. The deformation of (CuCl4)(2-) and cinchoninium cations varies with temperature due to a rearrangement of the bifurcated hydrogen bond network. This is a continuous process observed as a monotonic variation of the EPR spectral parameters and the unit cell dimensions. EPR spectra show that very weak exchange coupling J(12) = 0.0030 cm(-1) operates between Cu(2+) ions within asymmetric units, corresponding to the general formula of the compound, as well as between equivalent Cu(2+) sites of different molecules, whereas the coupling is negligible between inequivalent sites. The intermolecular J(12) coupling is temperature-independent indicating that the whole asymmetric unit behaves as a magnetic unit (pseudodimer) in the whole temperature range.

Cinchona Alkaloids↗
PubMed2001

Dephasing relaxation of the electron spin echo of the vibronic Cu(H(2)O)(6) complexes in Tutton salt crystals at low temperatures.

Two-pulse electron spin echo (ESE) measurements of the phase relaxation (phase memory time T(M)) were performed in a series of Tutton salt crystals M(I)(2)M(II)(SO(4))(2).6X(2)O (M(I)=NH(4), K, Cs; M(II)=Zn, Mg; X=H, D) weakly doped with Cu(2+) ions (c approximately equal to 10(18) ions/cm(3)) in temperature range 4-60 K where ESE signals were detectable. The ESE decay was strongly modulated with proton (or deuteron) frequencies and described by the decay function V(2tau)=V(0)exp(-btau-mtau(2)) with the mtau(2) term being temperature independent and negligible above 20 K. Various mechanisms leading to the tau- or tau(2)-type ESE decay are reviewed. The m and b coefficients for nuclear spectral diffusion (NSD), electron spectral diffusion (SD), and instantaneous diffusion (ID) were calculated in terms of existing theories and the resulting rigid lattice T(0)(M) times were found to be close one to another within the crystal family with average values: 17.5 micros (NSD protons), 200 micros (NSD deuterons), 8 micros (SD), and 5 micros (ID). The ID dominates but the calculated effective T(M)(0) is longer than the experimental T(M)(0)=2 micros. This is due to a nonuniform distribution of the Cu(2+) ions with a various degree of the disorder in the studied crystals. The acceleration of the dephasing rate 1/T(M) with temperature is due to the mechanisms producing exp(-btau) decay. They are reviewed and two of them were found to be operative in Tutton salt crystals: (a) Excitations to the vibronic levels of energy Delta leading to the temperature dependence 1/T(M)=B exp(-Delta/kT), with the vibronic levels produced by strong Jahn-Teller effect, and (b) spin-lattice relaxation processes being effective above 50 K. Based on the Delta values being on the order of 100 cm(-1), the scheme of vibronic levels in the Tutton salts is presented, and the independence of the Delta on temperature proves that the adiabatic potential surface shape of Jahn-Teller active Cu(H(2)O)(6) complexes is not affected by temperature below 65 K.

Journal Article↗
PubMed2001

Electron spin relaxation in pseudo-Jahn-Teller low-symmetry Cu(II) complexes in diaqua(L-aspartate)Zn(II).H(2)O crystals.

Low-temperature (4-55 K) pulsed EPR measurements were performed with the magnetic field directed along the z-axis of the g-factor of the low-symmetry octahedral complex [(63)Cu(L-aspartate)(2)(H2O)2] undergoing dynamic Jahn-Teller effect in diaqua(L-aspartate)Zn(II) hydrate single crystals. Spin-lattice relaxation time T(1) and phase memory time T(M) were determined by the electron spin echo (ESE) method. The relaxation rate 1/T(1) increases strongly over 5 decades in the temperature range 4-55 K. Various processes and mechanisms of T(1)-relaxation are discussed, and it is shown that the relaxation is governed mainly by Raman relaxation processes with the Debye temperature Theta(D)=204 K, with a detectable contribution from disorder in the doped Cu(2+) ions system below 12 K. An analytical approximation of the transport integral I(8) is given in temperature range T=0.025-10Theta(D) and applied for computer fitting procedures. Since the Jahn-Teller distorted configurations differ strongly in energy (delta(12)=240 cm(-1)), there is no influence of the classical vibronic dynamics mechanism on T(1). Dephasing of the ESE (phase relaxation) is governed by instantaneous diffusion and spectral diffusion below 20 K with resulting rigid lattice value 1/T(0)(M)=1.88 MHz. Above this temperature the relaxation rate 1/T(M) increases upon heating due to two mechanisms. The first is the phonon-controlled excitation to the first excited vibronic level of energy Delta=243 cm(-1), with subsequent tunneling to the neighbor potential well. This vibronic-type dynamics also produces a temperature-dependent broadening of lines in the ESEEM spectra. The second mechanism is produced by the spin-lattice relaxation. The increase in T(M) is described in terms of the spin packets forming inhomogeneously broadened EPR lines.

Aspartic Acid↗
PubMed1990

Carriers of ataxia-telangiectasia gene display additional protein fraction and changes in the environment of SH groups in erythrocyte membrane.

Additional protein fraction migrating slower than spectrin has been detected in erythrocyte membranes from an ataxia-telangiectasia (A-T) patient and from his mother (A-T heterozygote). In erythrocyte membranes labelled with maleimide spin label changes in signal of the weakly immobilized spin label as related to that of strongly immobilized one (w/s) were noted. In comparison to age-matched control groups the values of w/s were lower in A-T heterozygotes (ten persons) and higher in A-T homozygotes (four persons). In control persons the values of w/s increased with age, whereas in families with A-T no significant differences in this parameter were noted between children and parents. The presence of additional protein fraction in erythrocytes membranes of A-T patient and A-T heterozygote indicates that these phenotypes can be differentiated from the healthy control persons for the first time on the basis of changes detected in the erythrocytes. This change in erythrocyte membrane may explain the decrease in the w/s parameter of electron spin resonance in A-T heterozygotes. On the other hand increased values of w/s in A-T patients may be caused by disease process.

Adult↗
PubMedDate not supplied

Molecular changes in erythrocyte membranes induced by nitroimidazoles and radiation.

A damage of erythrocyte membranes by gamma-irradiation in the presence of nitroimidazole derivatives was shown by the demonstration of their effect on lipid peroxidation and SDS-PAGE protein pattern (1000 Gy) as well as on electron spin resonance (ESR) spectra of maleimide spin-labels attached to the membrane (for doses < or = 300 Gy). Erythrocyte membranes were labeled with two maleimide labels MAL-6 and MAL-M-3-PROXYL under strictly controlled and reproducible conditions with incubation at physiological temperature of 37 degrees C. The labels were bound to SH groups on the protein surface (weakly immobilized W-sites) as well as to internal SH-groups (strongly immobilized S-sites). The amplitude ratio W/S of the ESR signals was used for a monitoring of an influence of nitroimidazole drugs and gamma-irradiation. The influence appeared, even for the lowest doses, only when nitroimidazole drug was attached to the membrane. It was due to a destruction of spin-label paramagnetic centre both at W and S-sites and was related to the recombination processes during radiolysis connected with nitroimidazoles. It indicated a radiosensitivity of the nitroimidazoles. However, the persistent degradation of the membranes by the oxidative stress appeared above the threshold dose of 300 Gy determined from transformation of the W-sites into S-sites in ESR spectra. For the higher dose (1000 Gy) a fragmentation of the band 3 proteins was clearly seen as well as a partial damage of higher molecular-weight proteins with a simultaneous formation of much higher molecular-weight polymers.

Cyclic N-Oxides↗