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1.
The synthesis and complexation properties of 1,4-dimethyl-8-[2-(2-pyridyl)ethyl]-1,4,8,11-tetraazacyclotetra-decane ( 2 ) are described. This ligand forms with Cu2+ two complexes, one of which has been characterized by X-ray structure analysis. The structural, spectral, and kinetic studies indicate that the two Cu2+ complexes are isomers with the macrocycle in the trans-III and trans-I configuration. The rate of the interconversion of the trans-I isomer to the thermodynamically more stable trans-III species is proportional to [OH?]. A mechanism for this reaction is proposed.  相似文献   
2.
The two bis-macrocycles 4 and 5 in which the tetraaza units are separated by a chain of different length, have been synthesized using 1,4,7-tritosyl-1,4,7,11-tetraazacyclotetradecane as starting compound and bifunctional alkylating agents. The bis-macrocycles give binuclear complexes with Ni2+ and Cu2+, the properties of which have been studied to obtain information about the interaction of the two subunits as a function of the distance. The VIS spectra of the Ni2+ and Cu2+ complexes indicate that both metal ions are in a square-planar geometry as expected from the results of the analogous complexes with 1,4,7,11-tetraazacyclotetradecane 7 . Cyclic voltammetry and differential pulse polarography of the binuclear Ni2+complexes in CH3CN show a single two-electron step for ligand 5 , whereas two distinct one-electron redox processes can be observed for ligand 4 , indicating that the two metal ions interact with each other when the chain length is shorter. Similarly, the EPR studies of frozen solutions of the binuclear Cu2+ complexes clearly show that a magnetic dipolar interaction between the two paramagnetic centers exists, and that the strength of it depends upon the length of the bridge. Finally, from the X-ray structures of the binuclear Ni2+ complexes with 4 and 5 , it is seen that the two rings are kept apart as far as possible, the distances between the two metal ions determined in the solid correlate well with the observations in solution.  相似文献   
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After a brief introduction of the terms supercooling, amorphous solid state, glass transition and devitrification, the known ways of production of amorphous solid water are discussed. DSC experiments with quench cooled aqueous solutions show the phenomenon of glass transition and devitrification.This revised version was published online in November 2005 with corrections to the Cover Date.  相似文献   
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Riesen H  Dubicki L 《Inorganic chemistry》2000,39(10):2206-2211
Zeeman and site selective luminescence and excitation spectra in the region of the 2E<--4A2 transition are reported for the hexaaquachromium(III) complex in the trigonal ferroelectric guanidinium aluminum sulfate hexahydrate. The two prominent transitions are due to the R1 lines of the two sites of C3 and C3v point symmetry. The two R1 lines display g parallel = -3.1 and g parallel = -3.2, respectively, and show no measurable Zeeman shift or splitting with B perpendicular c. This behavior is consistent with the presence of a very large trigonal field. A peculiar feature of the present system is the conspicuous absence of any prominent R2 line. From the Zeeman data with B perpendicular c and a comparison of vibrational sidelines in excitation and luminescence it is concluded that the R2 level strongly interacts with vibrational levels.  相似文献   
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Saponification of homodiazepine 1a and 1b , in the absence of any proton donors, led to the formation of the 6π electron anionic species A which, by virtue of a 1,5-electrocyclization, is in equilibrium with the allylic anion B . This latter tricyclic species is thermodynamically less favoured than its bicyclic isomer A . Nevertheless, B could be trapped by acylation and led tupe- 2 compounds which are the major reaction products. This is due to the fact that B is more nucleophilic and, therefore, much more reactive than A . The transoid topology of the tricyclic products 2 was demonstrated by 1H-NMR and by an X-ray diagram of 2d . The transoid geometry of 2 is a consequence of a torquospecific 1,5-electrocyclization (of A ), which is due to a steric, and possibly even to an electronic factor.  相似文献   
9.
We report time-resolved transient spectral hole burning of Verneuil-grown 20 ppm and ca. 0.6 ppm ruby (Al2O3:Cr3+) in zero field and low magnetic fields B∥c at 4 K. The hole-burning spectroscopy of the 20 ppm sample implies relatively rapid cross relaxation in the 4A2 ground state on the ∼1 ms timescale both in zero field and in low magnetic fields, B∥c, up to 0.2 T. In the 0.6 ppm sample, side-hole to anti-hole conversion is observed both in zero field and in low magnetic fields. This conversion is caused by population storage in 4A2 ground state levels. Spin-lattice relaxation, on the 200 ms timescale, is directly observed from the time dependence of the resonant hole and anti holes in B∥c, consistent with a very low cross-relaxation rate. However, in zero field cross relaxation in the 4A2 ground state is still a significant relaxation mechanism for the 0.6 ppm sample resulting in hole decay in ∼50 ms.  相似文献   
10.
Wavelength-selective excited-state lifetime measurements and absorption, luminescence, and hole-burning spectra of a natural African emerald crystal are reported. The (2)E excited-state lifetime displays an extreme wavelength dependence, varying from 190 to 37 μs within 1.8 nm of the R(1)-line. Overall, the excited state is strongly quenched, in comparison to laboratory-created emerald (τ=1.3 ms), with an average quenching rate of ~6 × 10(3) s(-1) at 2.5 K. This quenching is attributed to photoinduced electron transfer caused by a relatively high concentration of Fe(2+) ions. The forward electron-transfer rate, k(f), from the nearest possible Fe(2+) sites at around 5 ? is estimated to be ~20 × 10(3) s(-1) at 2.5 K. The photoreductive quenching of the excited Cr(3+) ions by Fe(2+) is followed by rapid electron back-transfer in the ground state upon deactivation. The exchange interaction based quenching can be modeled by assuming a random quencher distribution within the possible Fe(2+) sites with the forward electron-transfer rate, k(f), given as a function of acceptor-donor separation R by exp[(R(f)-R)/a(f)]; R(f) and a(f) values of 13.5 and 2.7 ? are obtained at 2.5 K. The electron transfer/back-transfer reorganizes the local crystal lattice, occasionally leading to a minor variation of the short-range structure around the Cr(3+) ions. This provides a mechanism for spectral hole-burning for which a moderately high quantum efficiency of about ~0.005% is observed. Spectral holes are subject to spontaneous hole-filling and spectral diffusion, and both effects can be quantified within the standard two-level systems for non-photochemical hole-burning. Importantly, the absorbance increases on both sides of broad spectral holes, and isosbestic points are observed, in accord with the expected distribution of the "photoproduct" in a non-photochemical hole-burning process.  相似文献   
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