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171.
Aequationes mathematicae - 相似文献
172.
Aequationes mathematicae - Assume that $$\Omega \subset \mathbb {R}^k$$ is an open set, V is a real separable Banach space and $$f_1,\ldots ,f_N :\Omega \rightarrow \Omega $$ , $$g_1,\ldots ,... 相似文献
173.
Aequationes mathematicae - Let $$I\subset {\mathbb {R}}$$ be an interval that is closed under addition, and $$ k\in {\mathbb {N}}$$ , $$k\ge 2\,$$ . For a function $$f:I\rightarrow \left( 0,\infty... 相似文献
174.
Dr. Łukasz Mąkolski Vadim Szejko Dr. Karolina Zelga Dr. Adam Tulewicz Dr. Piotr Bernatowicz Dr. Iwona Justyniak Prof. Janusz Lewiński 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(18):5666-5674
Simple RZnOR’ alkoxides are among the first known organozinc compounds, and widespread interest in their multifaced chemistry has been driven by their fundamental significance and potential applications including various catalytic reactions. Nevertheless, their chemistry in solution and in the solid state remains both relatively poorly understood and a subject of constant debate. Herein, the synthesis and structural characterization of long-sought structural forms, a roof-like trimer [(tBuZn)3(μ-OC(H)Ph2)2(μ3-OC(H)Ph2)] and a ladder-type tetramer [(PhZn)4(μ-OC(H)Ph2)2(μ3-OC(H)Ph2)2], incorporating diphenylmethanolate as a model alkoxide ligand, are reported. Both novel aggregates are robust in the solid state and resistant towards mechanical force. By using 1H NMR and diffusion-order spectroscopy, it is demonstrated that new RZnOR’ alkoxides are kinetically labile in solution and readily undergo ligand scrambling, such as in the case of Schlenk equilibrium. The elucidated key structural issues, which have remained undiscovered for decades, significantly advance the chemistry of RZnOR’ alkoxides and should support the rational design of zinc alkoxide-based applications. 相似文献
175.
Dr. Karolina Zelga Dr. Tomasz Pietrzak Dr. Tomasz Han Dr. Iwona Justyniak Dr. Elżbieta Chwojnowska Prof. Piotr Sobota Prof. Janusz Lewiński 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(57):14234-14239
Alkylzinc aminoalcoholates have emerged as powerful catalysts in organic synthesis and polymerization processes. Despite extensive research, difficulties in the rational design of these catalytic systems and in-depth understanding of their modes of action have hitherto been encountered. Most of the major obstacles stem largely from the relatively limited knowledge of the structure-activity relationship of zinc catalysts. In fact, the key active species are often generated in situ via the protonolysis of the alkylzinc precursors, which precludes their isolation and detailed characterization. Herein, the effectiveness of the oxygenation over the classical protonolysis in the synthesis of zinc alkylperoxides stabilized by an aminoalcoholate ligand is demonstrated. The controlled oxygenation of a tert-butylzinc complex incorporating a pridinolum (prinol) ligand leads to well-defined a dinuclear adduct of a (prinol)ZnOOtBu moiety with the parent tBuZn(prinol) complex and a novel dimer [tBuOOZn(prinol)]2 with terminal alkylperoxide groups. The observed reaction outcomes strongly depend on the reaction conditions. Although sparse examples of heteroleptic adducts of the [RZn(L)]x[ROOZn(L)]y-type are known, the herein reported homoleptic [ROOZn(L)]x aggregate is unprecedented. Strikingly, comparative studies involving reactions between tBuZn(prinol) and tert-butylhydroperoxide or ethanol revealed that the respective seemingly simple zinc alkylperoxides, or zinc alkoxides, respectively, are not accessible via the classical alcoholysis. We believe that these game-changing results concerning multifaceted chemistry of organozinc aminoalcoholates should pave the way for more rational development of various Zn-based catalytic systems. 相似文献
176.
Anna Jurowska Janusz Szklarzewicz Maciej Hodorowicz Wiktoria Serafin Ennio Zangrando Ghodrat Mahmoudi 《Molecules (Basel, Switzerland)》2022,27(20)
Four dioxidovanadium(V) complexes with Schiff-base ligands based on 2-hydroxybenzhydrazide with four different substituted salicylaldehydes (5-chlorosalicylaldehyde, 3,5-dichlorosalicylaldehyde, 5-nitrosalicylaldehyde, 3-bromo-5-chlorosalicylaldehyde) were synthesized and described, by using V2O5 and triethylamine. The single crystal X-ray structure measurements as well as elemental analyses and IR spectra confirmed the formulas of the ionic complexes with a protonated triethylamine acting as counterion, HTEA[VO2(L)] (HL = Schiff-base ligand). The kinetic stability of the complexes at pH = 2 and 7 was discussed with respect to the neutral vanadium(V) complexes previously studied as potential insulin-mimetic agents. A correlation between the substituents in an aromatic ring of the Schiff-base ligands with crystal packing, and also with the stability of the compounds, was presented. 相似文献
177.
Artificial Neural Networks for Guest Chirality Classification through Supramolecular Interactions 下载免费PDF全文
Jarosław M. Granda Prof. Janusz Jurczak 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(39):12368-12372
A novel strategy for classification of guest chirality based on the combination of artificial neural networks and anion‐receptor chemistry is reported. The receptor reported herein forms supramolecular complexes with a variety of biologically important carboxylates, in which the chemical shift changes during addition of anions result in complex guest‐stereochemistry‐dependent patterns as followed by 1H NMR spectroscopy. The neural network had learnt these patterns from a training set of 12 anions, and successfully identified the “unknown” chirality of 14 guests present in the test set. Additionally, principal component analysis could discriminate most of the guests studied (26) and allowed for identification of the receptor protons, which are responsible for information transfer of guest chirality. 相似文献
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180.
Diastereoselective C2-elongation processes of N-mono- 1a-c and N,N-diprotected 1d-fl-alaninals, using vinylmagnesium bromide and chloride, are described. A substantial difference between effects of the N-protecting groups replacing either one or two amino protons was observed. 相似文献