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121.
122.
This work is concerned with the design of a leading edge for a flat-plate model used to study laminar and transitional boundary layers. For this study, the flow over the complete boundary-layer model, including leading edge, flat section, and trailing-edge flap, is modeled. The effect of important geometrical features of the leading edge on the resulting pressure distribution, starting from the well-known symmetric modified super ellipse, is investigated. A minimal pressure gradient on the measurement side of the plate is achieved using an asymmetrical configuration of modified super ellipses, with a thickness ratio of 7/24. An aerodynamic shape optimization is performed to obtain a novel leading edge shape that greatly reduces the length of the non-zero pressure gradient region and the adverse pressure gradient region compared to geometries defined by ellipses. Wind tunnel testing is used to validate the numerical solutions. 相似文献
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124.
Howard C. Johnson 《International Journal of Mathematical Education in Science & Technology》2013,44(5):741-743
The purpose of this article is to delineate procedures for viewing education software intended for use in a mathematics classroom. These procedures are applicable at all levels. 相似文献
125.
Elisabet Öberg Andreas Orthaber Marie-Pierre Santoni Fredrick Howard Sascha Ott 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-3):152-158
Abstract Attempts to utilize C-ethylenic phosphaalkenes in metathesis reactions are discussed. Unprecedented reactivity is observed where the vinylphosphaalkene undergoes the first step of the catalytic cycle and cross-metathesis with the phenylmethylene moiety of Grubbs 2nd generation catalyst. However, homo-metathesis reaction to form 1,6-diphosphahexa-1,3,5-triene is not observed, presumably due to steric constraints. 相似文献
126.
A series of predominately hydroxyl-ended polyesters were made from tridecanedioic acid derived from crambe oil. Comparison materials with sebacic and adipic acids were also prepared. Suitable polyesters were converted into polyurethane elastomers by chain extension and cross-linking with a diisocyanate and further diol. Polyesters based on ethandiol were unsuitable for the production of flexible urethanes as a slow crystallization occurred on standing; this did not happen when mixed ethane- and propan-diols were employed in polyesterification. Polyurethanes based on diphenylmethane diisocyanate are stronger than those made with the mixed isomers of toluene diisocyanate. Polyurethane networks based on brassylic acid have a lower 相似文献
127.
Victor Z. Sun Uh‐Joo Choe April R. Rodriguez Howard Dai Timothy J. Deming Daniel T. Kamei 《Macromolecular bioscience》2013,13(5):539-550
An arginine‐leucine block copolypeptide (R60L20) is synthesized, which is capable of forming vesicles with controllable sizes, able to transport hydrophilic cargo across the cell membrane, and exhibit relatively low cytotoxicity. The R60L20 vesicles also possess the ability to deliver DNA into mammalian cells for transfection. Although the transfection efficiency is lower than that of the commercially available transfection agent Lipofectamine 2000, the R60L20 vesicles are able to achieve transfection with significantly lower cytotoxicity and immunogenicity. This behavior is potentially due to its stronger interaction with DNA which subsequently provides better protection against anionic heparin.
128.
As a result of a continuing study utilizing nitrogenous bases2–6, we now wish to report that the base 3-quinuclidinol (13) is useful for the cleavage of β-keto and vinylogous β-keto esters. 相似文献
129.
Dr. Andrey Y. Khalimon Prof. Dr. Stanislav K. Ignatov Andrey I. Okhapkin Dipl.‐Ing. Razvan Simionescu Prof. Dr. Lyudmila G. Kuzmina Prof. Dr. Judith A. K. Howard Dr. Georgii I. Nikonov 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(26):8573-8590
The reactions of bis(borohydride) complexes [(RN?)Mo(BH4)2(PMe3)2] ( 4 : R=2,6‐Me2C6H3; 5 : R=2,6‐iPr2C6H3) with hydrosilanes afford new silyl hydride derivatives [(RN?)Mo(H)(SiR′3)(PMe3)3] ( 3 : R=Ar, R′3=H2Ph; 8 : R=Ar′, R′3=H2Ph; 9 : R=Ar, R′3=(OEt)3; 10 : R=Ar, R′3=HMePh). These compounds can also be conveniently prepared by reacting [(RN?)Mo(H)(Cl)(PMe3)3] with one equivalent of LiBH4 in the presence of a silane. Complex 3 undergoes intramolecular and intermolecular phosphine exchange, as well as exchange between the silyl ligand and the free silane. Kinetic and DFT studies show that the intermolecular phosphine exchange occurs through the predissociation of a PMe3 group, which, surprisingly, is facilitated by the silane. The intramolecular exchange proceeds through a new non‐Bailar‐twist pathway. The silyl/silane exchange proceeds through an unusual MoVI intermediate, [(ArN?)Mo(H)2(SiH2Ph)2(PMe3)2] ( 19 ). Complex 3 was found to be the catalyst of a variety of hydrosilylation reactions of carbonyl compounds (aldehydes and ketones) and nitriles, as well as of silane alcoholysis. Stoichiometric mechanistic studies of the hydrosilylation of acetone, supported by DFT calculations, suggest the operation of an unexpected mechanism, in that the silyl ligand of compound 3 plays an unusual role as a spectator ligand. The addition of acetone to compound 3 leads to the formation of [trans‐(ArN)Mo(OiPr)(SiH2Ph)(PMe3)2] ( 18 ). This latter species does not undergo the elimination of a Si? O group (which corresponds to the conventional Ojima′s mechanism of hydrosilylation). Rather, complex 18 undergoes unusual reversible β‐CH activation of the isopropoxy ligand. In the hydrosilylation of benzaldehyde, the reaction proceeds through the formation of a new intermediate bis(benzaldehyde) adduct, [(ArN?)Mo(η2‐PhC(O)H)2(PMe3)], which reacts further with hydrosilane through a η1‐silane complex, as studied by DFT calculations. 相似文献
130.
Nikhil Reddy Madadi Narsimha Reddy PenthalaLin Song Howard P. HendricksonPeter A. Crooks 《Tetrahedron letters》2014
2H-1,2,3-Triazoles (2) were synthesized by [3+2] cycloaddition of (Z)-2,3-diaryl substituted acrylonitriles (1) with sodium azide and ammonium chloride in DMF/water. This method represents a facile and efficient reaction procedure for the synthesis of 4,5-diaryl-2H-1,2,3-triazoles in modest to good yields. 相似文献