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The behavior of group-4 homologs Zr and Hf on extraction-chromatographic sorbents LN resin and TRU resin in mixtures of HF and HNO3 is considered. Distribution coefficients of the elements in the mixtures of 5·10−4 M–1 M HF and 0.01 M–5 M HNO3 are determined. Strong retention of both elements was found on LN resin in the range of concentrations c(HF) ≤ 0.01 M for all concentrations of HNO3. Retention tends to gradually disappear while increasing c(HF) to 0.5 M. On TRU resin retention is observed only in solutions with c(HNO3) ≥ 2 M and c(HF) ≤ 0.01 M. The possibility of separating Zr(IV) and Hf(IV) on LN resin is illustrated in two different acid mixtures, whereas their separation on TRU resin under the conditions studied in this work is difficult. The results obtained can be used to isolate analytes from multicomponent mixtures during analytical tasks, as well as to separate them from each other.

  相似文献   
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Development of supramolecular methods to further activate a highly reactive intermediate is a fascinating strategy to create novel potent catalysts for activation of inert chemicals. Herein, a supramolecular approach to enhance the oxidizing ability of a high-valent oxo species of a nitrido-bridged iron porphyrinoid dimer that is a known potent molecular catalyst for light alkane oxidation is reported. For this purpose, a nitrido-bridged dinuclear iron complex of porphyrin-phthalocyanine heterodimer 3 5+, which is connected through a fourfold rotaxane, was prepared. Heterodimer 3 5+ catalyzed ethane oxidation in the presence of H2O2 at a relatively low temperature. The site-selective complexation of 3 5+ with an additional anionic porphyrin (TPPS4−) through π–π stacking and electrostatic interactions afforded a stable 1:1 complex. It was demonstrated that the supramolecular post-synthetic modification of 3 5+ enhances its catalytic activity efficiently. Moreover, supramolecular conjugates achieved higher catalytic ethane oxidation activity than nitrido-bridged iron phthalocyanine dimer, which is the most potent iron-oxo-based molecular catalyst for light-alkane oxidation reported so far. Electrochemical measurements proved that the electronic perturbation from TPPS4− to 3 5+ enhanced the catalytic activity.  相似文献   
806.
The Mills reaction and cyclization of readily available 2-aminobenzyl alcohols and nitrosobenzenes using thionyl bromide provided 2H-indazoles in up to 88 % yields. In the metal-free process, acetic acid played a crucial role for the both Mills reaction and cyclization. A brominated 2H-indazole could also be obtained through the one-pot sequence.  相似文献   
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Hyper-parallel quantum information processing is a promising and beneficial research field. Herein, a method to implement a hyper-parallel controlled-phase-flip (hyper-CPF) gate for frequency-, spatial-, and time-bin-encoded qubits by coupling flying photons to trapped nitrogen vacancy (NV) defect centers is presented. The scheme, which differs from their conventional parallel counterparts, is specifically advantageous in decreasing against the dissipate noise, increasing the quantum channel capacity, and reducing the quantum resource overhead. The gate qubits with frequency, spatial, and time-bin degrees of freedom (DOF) are immune to quantum decoherence in optical fibers, whereas the polarization photons are easily disturbed by the ambient noise.  相似文献   
809.
Lipina  T. I. 《Mathematical Notes》2020,108(5-6):721-726
Mathematical Notes - An algorithm is presented which determines in a finite number of steps whether an initial finite binary automaton is spherically transitive. Since the class of deterministic...  相似文献   
810.
Dudkin  F.A. 《Archiv der Mathematik》2020,114(2):129-134
Archiv der Mathematik - A generalized Baumslag–Solitar group is a finitely generated group that acts on a tree with infinite cyclic edge and vertex stabilizers. A group G is residually a...  相似文献   
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