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Temperature control and solvent specification are used to reduce aromatic aldehydes and ketones to intermediate alcohols rather than methylene derivatives using HCO2NH4 as a catalytic hydrogen transfer agent. A mechanism for the catalytic reduction is proposed. 相似文献
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Jessica Cid Dr. Jorge J. Carbó Dr. Elena Fernández 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(40):12794-12802
Most trivalent boron reagents are electrophiles owing to the vacancy for two electrons to fill the outer orbital of boron; however, interestingly, trivalent boron compounds can change their electrophilic character to a nucleophilic character by only changing the nature of the substituents on the boron atoms. With the help of computational tools, we have analyzed the structural‐ and electronic properties of boryl fragments that were either bonded to main‐group metals or coordinated to transition‐metals/rare‐earth‐metals and we have designed a map that might help to identify certain trends. This trend map will be useful for selecting an appropriate trivalent boron compound, depending on the sought reactivity. 相似文献
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Navarrete-Astorga Elena Rodríguez-Moreno Jorge Dalchiele Enrique A. Schrebler Ricardo Leyton Patricio Ramos-Barrado José R. Martín Francisco 《Journal of Solid State Electrochemistry》2017,21(5):1431-1444
Journal of Solid State Electrochemistry - A feasibility study of the synthesis of gel polymer electrolytes based in methyl methacrylate (MMA) and 1-vinyl-2-pyrrolidone (VP) using [HEMIm][BF4] as... 相似文献
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Hsu‐Feng Lee Po‐Hsun Wang Yi‐Chiang Huang Wen‐Hung Su Ram Gopal Chun Che Lee Steven Holdcroft Wen‐Yao Huang 《Journal of polymer science. Part A, Polymer chemistry》2014,52(18):2579-2587
A series of sterically‐encumbered, sulfonated, poly(arylene ether) copolymers were synthesized and their proton conductivity examined. The series was prepared by copolymerizing a novel monomer, 2″,3″,5″,6″‐tetraphenyl‐[1,1′:4',1″:4″,1″':4″',1″″‐quinquephenyl]‐4,4″″‐diol, with 4,4'‐difluorobenzophenone and bisphenol A. Subsequent sulfonation and solution casting provided membranes possessing ion exchange capacities of 1.9 to 2.7 mmol/g and excellent mechanical properties (Young's modulus, 0.2–1.2 GPa; tensile strength, 35–70 MPa; elongation at break, 62–231%). Water uptake ranged from 34 to 98 wt% at 80 °C/100% RH. Proton conductivities ranged between 0.24 to 16 mS/cm at 80 °C/60% RH, and 3 to 167 mS/cm at 80 °C/95% RH. TEM analysis of the polymers, in the dehydrated state, revealed isolated spherical aggregates of ions, which presumably coalesce when hydrated to provide highly conductive pathways. The strategy of using highly‐encumbered polymer frameworks for the design of mechanically‐robust and dimensionally‐stable proton conducting membranes is demonstrated. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 2579‐2587 相似文献
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In a recent paper in this Journal, one of us argued against placing He above Be in Mendeleiev’s system of the elements. In it the goal was to dispute the notion that in Mendeleiev’s system of the elements the location of He should in fact lie above Be, which has a very similar electronic configuration, rather than above the noble gas column. That paper was based on rather old, Hartree–Fock limit studies on the strikingly limited non-additive contributions in the He3 and He4 systems in contrast with the much larger non-additivity obtained for the Be3, Be4 and Be5 oligomers. In a recent benchmark multireference Averaged Quadratic Coupled Cluster results on Be2 and Be3 we showed that the delocalized non-additive contribution comprises 94 % of the binding energy of Be3. Here we use this and other pertinent information (drawn from the same paper) to conclude that He may not be associated with Be in Mendeleiev’s Table, despite their quite similar spectroscopic ground states. Furthermore, we use the new results to show that the large non-additivity implies that less than 2 % of the Be3 binding is located in each Be pair contained within the Be trimer. The rest of the interaction energy is necessarily delocalized over all three Be atoms. This might actually announce the bulk properties (i.e. “the electron gas”) that in solid-state physics explain the large electric and heat conduction for the solid Be metal. Thus, in the case of beryllium the metallic characteristics are already evident in Be3, a far cry from the monoatomic helium gas. 相似文献
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