Search results for "physical chemistry"
showing 10 items of 1199 documents
Elektrooptische Emissionsuntersuchungen, III. Das Dipolmoment von trans-p-Dimethylamino-p′-nitrostilben im ersten angeregten Singulettzustand
1977
Aus elektrooptischen Emissions- und Absorptionsuntersuchungen in flussigen und glasig erstarrten Losungen kombiniert mit dielektrischen Untersuchungen konnten u. a. das Dipolmoment und die Polarisierbarkeitskomponente in Richtung des Dipolmoments von trans-p-Dimethylamino-p′-nitrostilben (DMANS) im ersten angeregten Singulettzustand bestimmt werden zu μ0a = (63 ± 5) · 10−30 Cm und α0az = (442 ± 65) · 10−40 CV−1 m2. Es zeigte sich, das die elektrooptischen Absorptions- und Emissionsuntersuchungen an DMANS in unpolaren Losungen zu einem konsistenten Satz von Dipolmomenten fuhren, das also die Aquilibrierung mit der Umgebung nach Anre-gung im unpolaren Cyclohexan keinen Einflus auf das permane…
Thermometric study of the dissociation equilibria of the maleinimidodioxime
1982
The values of the dissociation constants of the maleinimidodioxime are potentiometrically determined at various ionic strengths, and extrapolated to zero ionic strength (pK1T=10.41;pk2T=11.60). From these values and from the thermometric titration curves the enthalpies of neutralization (ΔHN1=−21.76,ΔHN2=−23.77 kJ/mol) and the thermodynamic parameters of dissociation of this substance at 25.0 °C are determined (ΔG1θ=59.41,ΔG2θ=66.23,ΔH1θ=34.06,ΔH2θ=32.05 kJ/mol;ΔS1θ=−85.06,ΔS2θ=−114.64 J/(K mol)).
Leitfahigkeitsmessungen an Polystyrylnatrium in Dimethoxiäthan (DME) und Tetrahydrofuran (THF)
1971
An Polystyrylnatrium werden in zwei polaren organischen Losungsmitteln Leitfahigkeitsmessungen uber einen groseren Temperaturbereich ausgefuhrt. Aus der Temperaturabhangigkeit der Dissoziationskonstante ergibt sich, das die undissoziierte Verbindung in zwei Formen, dem Kontaktionenpaar (I) und dem solvatgetrennten Ionenpaar (II), vorkommt. Enthalpie- und Entropiedifferenz beim ubergang von I nach II, sowie die entsprechenden thermodynamischen Parameter der Dissoziation von II werden ermittelt. Der effektive Ladungsabstand im solvatgetrennten Ionenpaar betragt etwa 7 A. Conductivity measurements were carried out with polystyryl sodium in two polar solvents within a large temperature range. T…
Determination of New Radical Species in Ammonium Tartrate Dosimeters by CW- and Pulsed-EPR Techniques
2015
Samples of ammonium tartrate irradiated with doses of about 0.1–1 kGy by different beams of ionizing radiation (60Co–γ, 19 MeV protons and 62 MeV per nucleon carbon ions) were studied by continuous-wave electron paramagnetic resonance (cw-EPR) and by pulse-EPR techniques. Careful analysis of the cw-EPR and of the echo-detected EPR spectra allowed the identification of a second radical in the system besides the already known radical formed at high temperature by an hydrogen elimination at C(2) position [M. Brustolon et al., Res. Chem. Int 4:359, 1996]. The spectrum of the radical is compatible with that of a radical obtained by hydroxyl elimination.
Intramolecular charge transfer and dual fluorescence of 4-(dimethylamino)benzonitrile: ultrafast branching followed by a two-fold decay mechanism.
2011
International audience; In this contribution we present new experimental and theoretical results for the intramolecular charge transfer (ICT) reaction underlying the dual fluorescence of 4-(dimethylamino) benzonitrile ( DMABN), which indicate that the fully twisted ICT (TICT) state is responsible for the time-resolved transient absorption spectrum while a distinct partially twisted ICT (pTICT) structure is suggested for the fluorescent ICT state.
Hexafluoro complex of rutherfordium in mixed HF/HNO3 solutions
2008
Formation of anionic fluoride-complexes of element 104, rutherfordium, produced in the 248 Cm( 18 O, 5n) 261 Rf reaction was studied by anion-exchange on an atom-at-a-time scale. It was found that the hexafluoro complex of Rf, [RfF 6 ] 2- , was formed in the studied fluoride ion concentrations of 0.0005-0.013 M. Formation of [RfF 6 ] 2- was significantly different from that of the homologues Zr and Hf, [ZrF 6 ] 2- and [HfF 6 ] 2- ; the evaluated formation constant of [RfF 6 ] 2- is at least one-order of magnitude smaller than those of [ZrF 6 ] 2- and [HfF 6 ] 2- .
Anionic Fluoro Complex of Element 105, Db
2009
We report on the characteristic anion-exchange behavior of the superheavy element dubnium (Db) with atomic number Z=105 in HF/HNO3 solution at the fluoride ion concentration [F−]=0.003 M. The resul...
Study of the high temperature behaviour of titanium alloy Ti6242S under complex atmospheres : aeronautical applications
2018
The use of titanium alloys in many applications (transport, energy, chemistry,...) allows significant weight savings in relation to the good mechanical properties/density ratio of these materials. Since titanium alloys are employed at high temperatures (T>500°C), their behavior in such conditions has to be studied in severe conditions in order to understand degradation mechanisms. Moreover, some specific conditions can be met during application, like thermal cycling, water vapour or presence of salts. These parameters are known to influence oxidation behavior of titanium alloys.In this thesis work, oxidation behavior of an aeronautics titanium alloy (Ti6242S) has been studied in air and moi…
Photophysical Properties of Charged Cyclometalated Ir(III) Complexes: A Joint Theoretical and Experimental Study
2011
The photophysical properties of a series of charged biscyclometalated [Ir(ppy)(2)(N boolean AND N)](1+) complexes, where ppyH is 2-phenylpyridine and N boolean AND N is 2,2'-bipyridine (bpy), 6-phenyl-2,2'-bipyridine (pbpy), and 6,6'-dipheny1-2,2'-bipyridine (dpbpy) for complexes 1, 2, and 3, respectively, have been investigated in detail. The photoluminescence performance in solution decreases from 1 to 3 upon attachment of phenyl groups to the ancillary ligand. The absorption spectra recorded over time suggest that complex 3 is less stable compared to complexes 1 and 2 likely due to a nucleophilic-assisted ancillary ligand-exchange reaction. To clarify this behavior, the temperature depen…
The electromigration and diffusion of hydrogen in molybdenum
1990
Abstract The electromigration and diffusion of hydrogen atoms in molybdenum were investigated using the resistance method in the temperature range 293–773 K. The following dependence of the diffusion coefficient D and electrical mobility vE on temperature were obtained: D = (5.3 ± 1.53) × 10 −10 exp {− (0.8 ± 0.01) eV kT } { m 2 s −1 } v E = (1.24 ± 0.19) × 10 −8 exp {− (0.9 ± 0.01) eV kT }{ m 2 ( V s ) −1 } . The hydrogen migrates towards the cathode and the effective valency grows with temperature, fulfilling the relation Z eff = (1.42 ± 0.03) − (5.0 ± 0.2) × 10 −8 (Ω m ) ρ ; where ρ is the specific electric resistance.