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11.
Teréz Balogh 《Tetrahedron》2004,60(3):679-682
Our studies are presented to replace alcohols as solvents in reverse hydrolytic reactions catalyzed by immobilized β-glucosidase to synthesize O-substituted β-d-glucopyranosides in preparative-scale. We found that 1,2-diacetoxyethane is a suitable solvent and O-alkyl or aryl β-d-glucosides were synthesized in moderate yields (after isolation 12-19%). In these reactions proportion of glucose and glucosyl acceptor hydroxy compounds was 1:20. We suggest that 1,2-diacetoxyethane can be useful not only for alcohols but for other glucosyl donor compounds unsuitable for the role of solvent (e.g., phenols) in the synthesis of O-β-d-glucosides by reverse hydrolysis. 相似文献
12.
Hydrogen desorption exceeding ten weight percent from the new quaternary hydride Li3BN2H8 总被引:3,自引:0,他引:3
Pinkerton FE Meisner GP Meyer MS Balogh MP Kundrat MD 《The journal of physical chemistry. B》2005,109(1):6-8
Mobile applications of hydrogen power have long demanded new solid hydride materials with large hydrogen storage capacities. We report synthesis of a new quaternary hydride having the approximate composition Li(3)BN(2)H(8) with 11.9 wt % theoretical hydrogen capacity. It forms by reacting LiNH(2) and LiBH(4) powders in a 2:1 molar ratio either by ball milling or by heating the mixed powders above 95 degrees C. This new quaternary hydride melts at approximately 190 degrees C and releases > or =10 wt % hydrogen above approximately 250 degrees C. A small amount of ammonia (2-3 mol % of the generated gas) is released simultaneously. Preliminary calorimetric measurements suggest that hydrogen release is exothermic and, hence, not easily reversible. 相似文献
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Ferenc Faigl Ervin Kovács Dóra Balogh Tamás Holczbauer Mátyás Czugler Béla Simándi 《Central European Journal of Chemistry》2014,12(1):25-32
The first enzyme-catalyzed kinetic resolution of tert-butyl-3-hydroxy-4-phenylpyrrolidine-1-carboxylate is presented. Enzyme, solvent and temperature optimization resulted in a new resolution method with E = 40 enantioselectivity. The acetate derivative of the (+)-(3S,4R) enantiomer formed while the (?)-(3R,4S) isomer remained intact. Very good enantioselectivities (E > 200) were achieved in the enzyme-catalyzed alcoholysis of the racemic acetate in i-propanol and t-butanol where the (+)-(3S,4R) enantiomer was prepared in pure form (ee > 99.7%). Absolute configuration of the (?)-(3R,4S)-enantiomer was determined by single crystal X-ray diffraction method. 相似文献
16.
Dr. Aleksandra Mitrović Stefan Wild Vicent Lloret Michael Fickert Dr. Mhamed Assebban Dr. Bence G. Márkus Prof. Ferenc Simon Dr. Frank Hauke Dr. Gonzalo Abellán Prof. Andreas Hirsch 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(10):3361-3366
Two-dimensional (2D) black phosphorus (BP) represents one of the most appealing 2D materials due to its electronic, optical, and chemical properties. Many strategies have been pursued to face its environmental instability, covalent functionalization being one of the most promising. However, the extremely low functionalization degrees and the limitations in proving the nature of the covalent functionalization still represent challenges in many of these sheet architectures reported to date. Here we shine light on the structural evolution of 2D-BP upon the addition of electrophilic diazonium salts. We demonstrated the absence of covalent functionalization in both the neutral and the reductive routes, observing in the latter case an unexpected interface conversion of BP to red phosphorus (RP), as characterized by Raman, 31P-MAS NMR, and X-ray photoelectron spectroscopies (XPS). Furthermore, thermogravimetric analysis coupled to gas chromatography and mass spectrometry (TG-GC-MS), as well as electron paramagnetic resonance (EPR) gave insights into the potential underlying radical mechanism, suggesting a Sandmeyer-like reaction. 相似文献
17.
Strong Asymptotics of the Orthogonal Polynomials with Respect to a Measure Supported on the Plane 下载免费PDF全文
We consider the orthogonal polynomials with respect to the measure over the whole complex plane. We obtain the strong asymptotic of the orthogonal polynomials in the complex plane and the location of their zeros in a scaling limit where n grows to infinity with N . The asymptotics are described in terms of three (probability) measures associated with the problem. The first measure is the limit of the counting measure of zeros of the polynomials, which is captured by the g‐function much in the spirit of ordinary orthogonal polynomials on the real line. The second measure is the equilibrium measure that minimizes a certain logarithmic potential energy, supported on a region K of the complex plane. The third measure is the harmonic measure of K c with a pole at ∞ . This appears as the limit of the probability measure given (up to the normalization constant) by the squared modulus of the nth orthogonal polynomial times the orthogonality measure, i.e., The compact region K that is the support of the second measure undergoes a topological transition under the variation of the parameter in a double scaling limit near the critical point given by we observe the Hastings‐McLeod solution to Painlevé II in the asymptotics of the orthogonal polynomials. © 2014 Wiley Periodicals, Inc. 相似文献
18.
Dr. Bence Kutus Jun Zhu Dr. Jian Luo Prof. Dr. Qi-Qiang Wang Dr. Alexandru Lupan Dr. Amr A. A. Attia Prof. Dr. De-Xian Wang Dr. Johannes Hunger 《Chemphyschem》2020,21(17):1957-1965
Tritopic ion-pair receptors can bind bivalent salts in solution; yet, these salts have a tendency to form ion-pairs even in the absence of receptors. The extent to which such receptors can enhance ion pairing has however remained elusive. Here, we study ion pairing of M2+ (Ba2+, Sr2+) and X− (I−, ClO4−) in acetonitrile with and without a dichlorooxacalix[2]arene[2]triazine-related receptor containing a pentaethylene-glycol moiety. We find marked ion association already in receptor-free solutions. When present, most of the MX+ ion-pairs are bound to the receptor and the overall degree of ion association is enhanced due to coordinative, hydrogen-bonding, and anion-π interactions. The receptor shows higher selectivity for iodides but also stabilizes perchlorates, despite the latter are often considered as weakly coordinating anions. Our results show that ion-pair binding is strongly correlated to ion pairing in these solutions, thereby highlighting the importance of taking ion association in organic solvents into account. 相似文献
19.
Zoltán M. Balogh Katrin Fässler Ioannis D. Platis 《Journal d'Analyse Mathématique》2011,113(1):265-291
We develop a method using the modulus of curve families to study minimisation problems for the mean distortion functional
in the class of finite distortion homeomorphisms. We apply our method to prove extremality of the spiral-stretch mappings
defined on annuli in the complex plane. This generalises results of Gutlyanskiĭ and Martio [12] and Strebel [23]. 相似文献
20.
Corrigendum: Effect of hexyl substituent groups on photophysical and electrochemical properties of the poly[(9,9‐dioctyfluorene)‐2,7‐Diyl‐alt‐(4,7‐bis (3‐hexylthien‐5‐Yl)‐2,1,3‐benzothiadiazole)‐2′,2″‐diyl] 下载免费PDF全文