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131.
Internal waves from a body accelerating in a thermocline 总被引:1,自引:0,他引:1
Many papers study the steady wave system around bodies moving in thermoclines but little attention has been given to unsteady wave systems. This paper concentrates on the unsteady wave systems around accelerating bodies in thermoclines. The wave shapes are calculated using a theory derived from a dispersion relation based on an exp-tanh density profile. All modes of oscillation can be determined and it is shown that for the lowest mode both oblique and transverse waves occur whereas for the higher modes the presence of transverse waves depends on the background conditions and on the speed of the body. Cauchy-Poisson impulsive start waves are included. The theoretical wave shapes compare quite well with those calculated using finite-difference formulations of the full Navier-Stokes equations when a body accelerates from rest.It is also shown how the dispersion relation =N sin together with the WKB approximation can produce the same plan-view wave forms as those obtained using the thermocline wave dispersion relation given by [17, 30]. 相似文献
132.
Lewis Acid Catalyzed Condensation–Cyclization Cascade: Direct Synthesis of Di/Trifluoromethyl‐1,2,3,4‐tetrahydroquinazolines
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Prof. Dr. G. K. Surya Prakash Dr. Attila Papp Socrates B. Munoz Nathan May John‐Paul Jones Prof. Dr. Ralf Haiges Prof. Dr. Pierre Mothé Esteves Dr. Thomas Mathew 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(28):10170-10178
Condensed heterocycles such as quinazolines constitute the framework of many promising drugs. The great impact of the dramatic fluorine effect in pharmaceuticals prompted a great surge in the quest for fluorinated drug design resulting in over 20 % fluorine‐containing drugs in the market today. Therefore, finding an efficient and cost‐effective method for the direct synthesis of fluorine‐tagged quinazoline systems is of great significance in the pharmaceutical arena. For the first time, a one‐pot sequential condensation–cyclization reaction to form selectively the difluoro/trifluoromethylated tetrahydroquinazolines from simple components difluoro/trifluoroacetaldehyde hemiacetal and aromatic amines is reported. Our recent studies using difluoro/trifluoroacetaldehyde hemiacetal as simple and elegant difluoro/trifluoromethyl synthons and metal triflates such as gallium triflate as safe and stable Lewis acid catalysts led us to this direct synthesis protocol for the expedient and convenient synthesis of fluorinated quinazolines. DFT calculations at PCM/B3LYP/6‐31++G** were carried out for evaluating a possible reaction mechanism for this cyclization. According to the DFT calculations, product stereochemistry is thermodynamically driven, favoring the cis isomer as the major product, which is also confirmed experimentally. 相似文献
133.
Rory Campbell Dr. Martin F. Davis Mathew Fazakerley Dr. Peter Portius 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(51):18690-18698
The first charge‐neutral Lewis base adducts of tin(IV) tetraazide, [Sn(N3)4(bpy)], [Sn(N3)4(phen)] and [Sn(N3)4(py)2], and the salt bis{bis(triphenylphosphine)iminium} hexa(azido)stannate [(PPN)2Sn(N3)6] (bpy = 2,2′‐bipyridine; phen = 1,10‐phenanthroline; py = pyridine; PPN = N(PPh3)2) have been prepared using covalent or ionic azide‐transfer reagents and ligand‐exchange reactions. The azides were isolated on the 0.3 to 1 g scale and characterized by IR and NMR spectroscopies, microanalytical and thermal methods and their molecular structures determined by single‐crystal XRD. All complexes have a distorted octahedral Sn[N]6 coordination geometry and possess greater thermal stability than their Si and Ge homologues. The nitrogen content of the adducts of up to 44 % exceed any SnIV compound known hitherto. 相似文献
134.
Inside Back Cover: Isolation of CeLu2N@Ih‐C80 through a Non‐Chromatographic,Two‐Step Chemical Process and Crystallographic Characterization of the Pyramidalized CeLu2N within the Icosahedral Cage (Chem. Eur. J. 29/2015)
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135.
A three-dimensional ray theory is presented for calculating the phase configuration of internal waves around a moving disturbance
in a flow with arbitrary stratification and background shear. The theory is applied to two-dimensional stratified shear flows
which have been produced in the laboratory and good agreement is shown between the theoretical and experimental phase configurations.
Good agreement is also shown when caustics and critical levels are present. This paper includes the wave systems arising from
a combined translation and oscillatory motion of a source and it shows how distinct systems of waves arise from each, type
of motion under different background conditions. This paper shows that for two-dimensional steady wave systems the critical
level is at a well defined height which is independent of wavenumber but in three dimensions the critical height can in general
vary with wavenumber. 相似文献
136.
The phase configuration of trapped internal waves from a body moving in a thermocline 总被引:1,自引:0,他引:1
Some two-dimensional internal wave systems are generated experimentally by a cylinder moving with constant velocity in a thermocline modelled with stratified brine. The phase configuration of the waves is shown to compare quite well with ray theory, and the phase changes which result from energy reflections are well defined in some of the schlieren photographs. 相似文献
137.
Arianne Soliven Gary R. Dennis Emily F. Hilder R. Andrew Shalliker Paul G. Stevenson 《Chromatographia》2014,77(9-10):663-671
Analytical scale silica monoliths are commercially limited to three column selectivities (bare silica, C8 and C18). An in situ modification is reported in detail to overcome this barrier and allow for any functionality of choice to be bonded to the silica surface of the monolithic stationary phase support. The modification method was conducted on a commercial bare silica column to bond the C18 moiety to the silica surface through a silylation reaction. The C18 type of stationary phase was chosen, as this is the most commonly bonded functionality for the majority of stationary phases used for high-performance liquid chromatography (HPLC) separations. The C18-modified monolith’s performance was compared to a commercial C18 monolithic and a particle packed column of the same analytical scale column dimensions (100 × 4.6 mm). The modified C18 monolith proved to be of high quality with an efficiency of 73,267 N m?1, fast analysis times (operated at flow rates up to 3 mL min?1 using a conventional 400 bar HPLC system) and improved resolution of a set of polar and non-polar substituted aromatics in comparison to a commercial C18 monolith. 相似文献
138.
139.
Chen M Dong C Penfold J Thomas RK Smyth TJ Perfumo A Marchant R Banat IM Stevenson P Parry A Tucker I Campbell RA 《Langmuir : the ACS journal of surfaces and colloids》2011,27(14):8854-8866
The adsorption of the lactonic (LS) and acidic (AS) forms of sophorolipid and their mixtures with the anionic surfactant sodium dodecyl benzene sulfonate (LAS) has been measured at the air/water interface by neutron reflectivity, NR. The AS and LS sophorolipids adsorb with Langmuir-like adsorption isotherms. The more hydrophobic LS is more surface active than the AS, with a lower critical micellar concentration, CMC, and stronger surface adsorption, with an area/molecule ~70 ?(2) compared with 85 ?(2) for the AS. The acidic sophorolipid shows a maximum in its adsorption at the CMC which appears to be associated with a mixture of different isomeric forms. The binary LS/AS and LS/LAS mixtures show a strong surface partitioning in favor of the more surface active and hydrophobic LS component but are nevertheless consistent with ideal mixing at the interface. In contrast, the surface composition of the AS/LAS mixture is much closer to the solution composition, but the surface mixing is nonideal and can be accounted for by regular solution theory, RST. In the AS/LS/LAS ternary mixtures, the surface adsorption is dominated by the sophorolipid, and especially the LS component, in a way that is not consistent with the observations for the binary mixtures. The extreme partitioning in favor of the sophorolipid for the LAS/LS/AS (1:2) mixtures is attributed to a reduction in the packing constraints at the surface due to the AS component. Measurements of the surface structure reveal a compact monolayer for LS and a narrow solvent region for LS, LS/AS, and LS/LAS mixtures, consistent with the more hydrophobic nature of the LS component. The results highlight the importance of the relative packing constraints on the adsorption of multicomponent mixtures, and the impact of the lactonic form of the sophorolipid on the adsorption of the sophorolipid/LAS mixtures. 相似文献
140.
Brayshaw SK Schiffers S Stevenson AJ Teat SJ Warren MR Bennett RD Sazanovich IV Buckley AR Weinstein JA Raithby PR 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(16):4385-4395
We introduce a new highly efficient photochromic organometallic dithienylethene (DTE) complex, the first instance of a DTE core symmetrically modified by two Pt(II) chromophores [Pt(PEt(3))(2)(C≡C)(DTE)(C≡C)Pt(PEt(3))(2)Ph] (1), which undergoes ring-closure when activated by visible light in solvents of different polarity, in thin films and even in the solid state. Complex 1 has been synthesised and fully photophysically characterised by (resonance) Raman and transient absorption spectroscopy complemented by calculations. The ring-closing photoconversion in a single crystal of 1 has been followed by X-ray crystallography. This process occurs with the extremely high yield of 80%--considerably outperforming the other DTE derivatives. Remarkably, the photocyclisation of 1 occurs even under visible light (>400 nm), which is not absorbed by the non-metallated DTE core HC≡C(DTE)C≡CH (2) itself. This unusual behaviour and the high photocyclisation yields in solution are attributed to the presence of a heavy atom in 1 that enables a triplet-sensitised photocyclisation pathway, elucidated by transient absorption spectroscopy and DFT calculations. The results of resonance Raman investigation confirm the involvement of the alkynyl unit in the frontier orbitals of both closed and open forms of 1 in the photocyclisation process. The changes in the Raman spectra upon cyclisation have permitted the identification of Raman marker bands, which include the acetylide stretching vibration. Importantly, these bands occur in the spectral region unobstructed by other vibrations and can be used for non-destructive monitoring of photocyclisation/photoreversion processes and for optical readout in this type of efficiently photochromic thermally stable systems. This study indicates a strategy for generating efficient solid-state photoswitches in which modification of the Pt(II) units has the potential to tune absorption properties and hence operational wavelength across the visible range. 相似文献