Academic literature on the topic '5-trans THF'

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Journal articles on the topic "5-trans THF"

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Willey, Gerald R., Paul R. Meehan, Timothy J. Woodman, and Michael G. B. Drew. "Identification of the dysprosium(III) chloride solvate DyCl3(THF)3.5: crystal structure of the ion pair [trans-DyCl2(THF)5] [trans-DyCl4(THF)2]." Polyhedron 16, no. 4 (January 1997): 623–27. http://dx.doi.org/10.1016/0277-5387(96)00315-4.

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Sobota, Piotr, Jozef Utko, and Slawomir Szafert. "Ionization of YCl3 in Tetrahydrofuran. Crystal Structures of the [trans-YCl2(THF)5][trans-YCl4(THF)2] Salt and Polymeric [YCl3.cntdot.2THF].infin. Compounds." Inorganic Chemistry 33, no. 23 (November 1994): 5203–6. http://dx.doi.org/10.1021/ic00101a011.

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Phuphuak, Y., F. Bonnet, G. Stoclet, M. Bria, and P. Zinck. "Isoprene chain shuttling polymerisation between cis and trans regulating catalysts: straightforward access to a new material." Chemical Communications 53, no. 38 (2017): 5330–33. http://dx.doi.org/10.1039/c7cc01016h.

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Isoprene chain shuttling polymerisation between the 1,4-trans regulating Cp*La(BH4)2(THF)2/MgnBuEt (Cp* = C5Me5) and the 1,4-cis regulating NdCl3(THF)2/AlR3 (R = Et or iBu) systems provides access to stereoblock polyisoprene.
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Anfang, Stefan, Kurt Dehnicke, and Jörg Magull. "Die Kristallstrukturen der Dysprosium-Komplexe [DyCl3(DME)2] und [DyCl2(THF)5]+[DyCl4(THF)2]- / Crystal Structures of the Dysprosium Complexes [DyCl3(DME)2] and [DyCl2(THF)5]+[DyCl4(THF)2]-." Zeitschrift für Naturforschung B 51, no. 4 (April 1, 1996): 531–35. http://dx.doi.org/10.1515/znb-1996-0416.

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Abstract [DyCl3(DME)2] (DME = 1,2-dimethoxyethane) has been prepared from the known tetrahy-drofuran complex [Dy2Cl6(THF)7] in boiling DME. Both complexes were characterized by structure determinations. [DyCl3(DME)2]: Space group P21/c, Z = 4, lattice dimensions at -70 °C: a = 1141.9(6), b = 884.2(4), c = 1558.3(6) pm, β = 104.83(4)°. The complex has a molecular structure with a distorted pentagonal bipyramidal geometry in which the oxygen atoms of the chelating DME molecules and one chlorine atom occupy the pentagonal plane. [DyCl2(THF)5]+[DyCl4(THF)2]-: Space group C2/c, Z = 4, lattice dimensions at -70 °C: a -1241.4(9), b = 1139.4(6), c = 2735.1(19) pm, β = 91.19(4)°. The complex contains a seven-coordinate cation with axial chloride ligands in a pentagonal bipyramidal structure and a six-coordinate anion with a trans octahedral geometry.
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Siewert, Birgit, and Ulrich Müller. "Die Kristallstrukturen von PPh4[AsCl4(THF)2] und PPh4[AsBr4(THF)2] / The Crystal Structures of PPh4[AsCl4(THF)2] and PPh4[AsBr4(THF)2]." Zeitschrift für Naturforschung B 47, no. 5 (May 1, 1992): 680–84. http://dx.doi.org/10.1515/znb-1992-0512.

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In the effort to react W(CO)6 with (PPh4)2[As2Cl8] and Cr(CO)6 with PPh4[As2SBr5] in tetrahydrofurane under UV irradiation the title compounds were obtained as main products. Their crystal structures were determined by X-ray diffraction. PPh4[AsCl4(THF)2], monoclinic, P2/c, Z = 2, a = 881.6(3), b = 809.0(6), c = 2418.6(9) pm, β = 99.44(4)°, R = 0.086 for 1619 observed unique reflexions. PPh4[AsBr4(THF)2], monoclinic, C 2/c, Z = 4, a = 2459.2(5), b = 748.2(3), c = 1784.3(4) pm, β = 94.02(2)°, R = 0.080 for 1513 reflexions. In both compounds ions [AsX4(THF)2]- are located on inversion centers; they have octahedral coordination with trans configuration; the stereochemical activity of the lone electron pairs does not show up in deviations of the bond angles, but in increased bond lengths. The PPh4+ ions are stacked to columns in the b direction.
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Morra, Barbora, Nicholas A. Morra, Daniel G. MacDonald, and Brian L. Pagenkopf. "Gram-Scale Synthesis of the Co(nmp)2 Catalyst to Prepare trans-2,5-Disubstituted Tetrahydrofurans by the Aerobic Oxidative Cyclization of Pent-4-en-1-ols." Synthesis 52, no. 06 (January 8, 2020): 847–52. http://dx.doi.org/10.1055/s-0039-1690730.

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Co(nmp)2 is an efficient catalyst for the aerobic oxidative cyclization of pent-4-en-1-ols to give 5-hydroxymethyl trans-tetrahydrofurans (THFs) as single diastereomers in high yield. The trans-THF pharmacophore is of interest because it is found in many biologically active natural products. The three-step synthesis of Co(nmp)2 described here gives the catalyst as a fine powder in 80–85% overall yield on 10-gram scale. The use of the catalyst in a representative oxidative cyclization is also described.
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Lindner, Ekkehard, and Berthold Andres. "Notizen: Neuartige basische Liganden für die homogenkatalytische Methanolcarbonylierung, XV [1]. (Ether-Phosphan)-stabilisierter cis-Dihydrido-Rhodium(III)-Komplex / Novel Basic Ligands for the Homogenous Catalytic Methanolcarbonylation, XV [1]. (Ether-Phosphane)-Stabilized cis-Dihydrido-rhodium(III) Complex." Zeitschrift für Naturforschung B 43, no. 3 (March 1, 1988): 369–70. http://dx.doi.org/10.1515/znb-1988-0321.

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Reaction of [Rh(NBD)(P∼O)2][SbF6] (1) (NBD = norbornadiene) with hydrogen results in the formation of the stable dihydrido rhodium complex [cis- (2). Rh - O bond cleavage in 2 by carbon monoxide or NaBH4 affords the products [trans-(P∼O)2Rh(CO)3][SbF6] (3) and [trans-H2Rh((P∼O)2(η2-H2BH2)] (5), respectively. Upon treating a THF solution of 3 with argon, 3 eliminates CO to give the complex (4) with a mono- and bidentate (ether-phosphane) ligand.
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Trifonov, Alexander A., Mikhail N. Bochkarev, Herbert Schumann, and Sebastian Dechert. "On Attempts to Synthesize Lanthanide Complexes of the Dianionic Fluorenyl-alkoxo Ligand [C13H8-cyclo-C6H10-O]2-. Crystal Structure of (C13H9-cyclo-C6H10-O)LaI2(DME)2." Zeitschrift für Naturforschung B 58, no. 5 (May 1, 2003): 389–94. http://dx.doi.org/10.1515/znb-2003-0506.

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Racemic trans-2-(9(H)-fluoren-9-yl)cyclohexanol, C13H9-cyclo-C6H10-OH (1), reacts with two equivalents of potassium naphthalenide in THF to give the dipotassium salt [C13H8-cyclo-C6H10-O]- K2(THF) (2). Recrystallization of 2 from pyridine affords the solvent free salt [C13H8-cyclo-C6H10- O]K2 (3). The reactions of LaI3(THF)4 with one equivalent of 2 or of YbI2(THF)2 with equimolar amounts of 2 produce the alkoxolanthanum diiodide (C13H9-cyclo-C6H10-O)LaI2(DME)2 (4) and the ytterbium dialkoxide (C13H9-cyclo-C6H10-O)2Yb(THF)0.5(5), respectively. [(Me3Si)2N]3Y reacts with three equivalents of 1 with elimination of hexamethyldisilazane and formation of the yttrium trialkoxide (C13H9-cyclo-C6H10-O)3Y (6). The compounds 2 to 5 were characterized by elemental analyses, 1H NMR, 13C NMR and IR spectra. The molecular structure of 4 was determined by single crystal X-ray diffraction.
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Wiberg, Nils, Angelika Wörner, Hans-Wolfram Lerner, Konstantin Karaghiosoff, and Heinrich Nöth. "Supersilylverbindungen des Phosphors, V [1]. Darstellung, Struktur und Reaktivität des Pentaphosphids (tBu3Si)3P5Na2 und des Pentaphosphans (tBu3Si)3P5[2] / Supersilyl Compounds of Phosphorus, V [1]. Preparation, Structure, and Reactivity of the Pentaphosphide (tBu3Si)3P5Na2 and the Pentaphosphane (tBu3Si)3P5 [2]." Zeitschrift für Naturforschung B 53, no. 9 (September 1, 1998): 1004–14. http://dx.doi.org/10.1515/znb-1998-0912.

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The orange THF adduct (tBu3Si)3P5Na2 (THF)4 of the pentaphosphide (tBu3Si)3P5Na2 (3) has been prepared, (i) by protolysis of the tetraphosphide (tBu3Si)2P4Na2(THF)n (2) with CF3CO2H in THF (molar ratio 2 : 1 ) , (ii) by dissolving crystalline 2 in toluene, and (iii) by the reaction of P4 with tBu3SiNa(THF)2 in benzene (molar ratio 1 : 4). According to an X-ray structural analysis, the THF adduct of 3 contains a P3 ring with two PNa(SitBu3) substituents in cis position and one SitBu3 substituent in trans position to the former groups. The protolysis of 3 with CF3CO2H leads to the pentaphosphane P5H2(SitBu3)3 (9), the silylation of 3 with Me2SiCl2 to the pentaphosphane P5 (SiMe2)(SitBu3)3 (10), and the oxidation of 3 with C2(CN)4 to the pentaphosphane P5(SitBu3)3 (5). The structures of 3,5,9, and 10 have been assigned from 31P and 29Si NMR data. The pentaphosphane 5 contains a hitherto unknown P5 backbone of a P3 ring anellated with a P4 ring.
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Paul, Ratan Kumar, Md Faruak Ahmad, Mohammad Mizanur Rahman Khan, and Muhammad Younus. "Synthesis and Antibacterial Activities of Sugar-containing Platinum Ethynyl Complexes." Journal of Bangladesh Academy of Sciences 40, no. 1 (June 22, 2016): 65–77. http://dx.doi.org/10.3329/jbas.v40i1.28326.

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New sugar-containing aryl ethynyl ligand [N-(4-trimethylsilylethynylphenyl)-?-D-glucopyranosylamine] 2 has been prepared by the reaction of [N-(4-iodophenyl)-?-D-glucopyranosylamine] 1 with trimethysilylacetylene in the presence of Pd(OAc)2/CuI catalyst, in iPr2NH and DMF solvent mixture. The trimethylsilyl group of compound 2 was deprotected using K2CO3 in methanol to form terminal ethynylene ligand [N-(?-D-glucopyranosyl)aniline-4-ethyne] 3. Novel platinum mono-ethynyl complex trans-[(P(Bu)3)2PtCl(C?C-4-C6H4-NH-D-glocose)] 4 and bis-ethynyl complex trans-[(P(Bu)3)2PtCl(C?C-4-C6H4-NH-D-glocose)2] 5 were formed by the dehydrohalogenation reaction of trans-[Pt(P(Bu)3)2Cl2] with terminal ethynyl ligand 3 in iPr2NH/THF, in the presence of CuI, at 65ºC. The complexes are hygroscopic in air, and are fairly soluble in methanol and CH2Cl2. The new compound 2 - 5 were characterized by FTIR and UV-Vis spectroscopy and elemental analysis. The compounds were tested for antibacterial activity using disk diffusion technique. The platinum complexes 4 and 5 displayed good resistivity against the following bacteria: Escherichia coli, Proteus penneri, Klebsiella oxytoca and Pseudomonas aeruginosa.Journal of Bangladesh Academy of Sciences, Vol. 40, No. 1, 65-77, 2016New sugar-containing aryl ethynyl ligand [N-(4-trimethylsilylethynylphenyl)-?-D-glucopyranosylamine] 2 has been prepared by the reaction of [N-(4-iodophenyl)-?-D-glucopyranosylamine] 1 with trimethysilylacetylene in the presence of Pd(OAc)2/CuI catalyst, in iPr2NH and DMF solvent mixture. The trimethylsilyl group of compound 2 was deprotected using K2CO3in methanol to form terminal ethynylene ligand [N-(?-D-glucopyranosyl)aniline-4-ethyne] 3. Novel platinum mono-ethynyl complex trans-[(P(Bu)3)2PtCl(C?C-4-C6H4-NH-D-glocose)] 4 and bis-ethynyl complex trans-[(P(Bu)3)2PtCl(C?C-4-C6H4-NH-D-glocose)2] 5 were formed by the dehydrohalogenation reaction of trans-[Pt(P(Bu)3)2Cl2] with terminal ethynyl ligand 3 in iPr2NH/THF, in the presence of CuI, at 65ºC. The complexes are hygroscopic in air, and are fairly soluble in methanol and CH2Cl2. The new compound 2 - 5 were characterized by FTIR and UV-Vis spectroscopy and elemental analysis. The compounds were tested for antibacterial activity using disk diffusion technique. The platinum complexes 4 and 5 displayed good resistivity against the following bacteria: Escherichia coli, Proteus penneri, Klebsiella oxytoca and Pseudomonas aeruginosa.Journal of Bangladesh Academy of Sciences, Vol. 40, No. 1, 65-77, 2016
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Dissertations / Theses on the topic "5-trans THF"

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Garside, Paul. "Analysis of the canonical initiation and trans-acting factor requirements of 5'TOP containing mRNAs." Thesis, University of Nottingham, 2010. http://eprints.nottingham.ac.uk/14089/.

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All eukaryotic mRNAs process a cap structure (m7G(5')ppp(5')N) at the S' end of their message and most have an A as the first nucleotide after the cap. However, 30% of messages within eukaryotic cells have a C (m7G(t')ppp(5')C) as the first nucleotide followed by a short polypyrimidine tract. These mRNAs are termed TOP (Tenninal Oligopyrimidine tract) messages and are co-ordinately regulated by mitogenic, growth and nutritional stimuli. This work describes the construction of a reporter vector that encodes mRNA containing the TOP motif, and its use in a series of systematic experiments to further investigate the translational regulation of TOP messages. Given that TOP containing mRNAs are known to encode proteins involved in the translational machinery, these findings have important implications with regard to translational control and translation related disease. In this study, reporter vectors have been used to investigate the role of the mTOR and PI3K signalling pathways, which have previously been implicated in the translational regulation of TOP containing mRNAs. The data obtained suggests that the mTOR signalling pathway may be involved in the regulation of TOP containing mRNAs. The canonical initiation and frans-acting factor requirements of TOP mRNAs were also investigated using a combination of protein over-expression and affinity purification of TOP-containing-mRNA:protein complexes. The data obtained raises the possibility that eIF4E may not be required in the initiation of TOP containing mRNA translation. The candidate trans-acting factors that were identified include La, ILF2 and EBPl, the latter of which has previously been shown to associate with mature ribosomes in the cytoplasm. Finally, affinity purification of TOP-containing-mRNA:microRNA complexes was carried out. Candidate microRNAs which may be involved in the regulation of TOP containing mRNAs were identified. The data obtained was consistent with a previous study, which suggested that microRNA-IOa may bind to the S'UTR of TOP containing mRNAs.
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Timmerman, Stephanie Lynn. "Characterization of the internal ribosomal entry sites located in the 5' leader of the mouse TRKB MRNA /." Connect to full text via ProQuest. IP filtered, 2006.

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Thesis (Ph.D. in Biochemistry & Molecular Genetics) -- University of Colorado at Denver and Health Sciences Center, 2006.
Typescript. Includes bibliographical references (leaves 119-131). Free to UCDHSC affiliates. Online version available via ProQuest Digital Dissertations;
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Vandenberghe, Amanda. "Characterization of the troponin I gene of the ascidian Ciona intestinalis, evidence for mRNA 5' leader trans-splicing in the chordates." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape2/PQDD_0032/MQ64472.pdf.

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Park, Youngwoo. "Selective translation of influenza viral messenger RNAs mediated by trans-acting factor(s) through an interaction with the sequence element in the 5'-untranslated region /." Thesis, Connect to this title online; UW restricted, 1999. http://hdl.handle.net/1773/11496.

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Lai, Chi-Jung, and 賴啟榮. "(一)Studies of the Structure of Vanadium Species in VAPO-5 Molecular Sieves via Density Function Theory(二)Bifurcation Analysis of the Trans←→Cis Rotation." Thesis, 2003. http://ndltd.ncl.edu.tw/handle/42696312785312865530.

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碩士
東海大學
化學系
91
(1)Theoretical calculation using density functional B3LYP correlation- exchange is employed to study the structure of different sizes of the VAPO-5 clusters. The results indicate that the substitution of either the phosphorus site or aluminum site of the AFI framework by vanadium is in general not feasible. The isolates vanadium was found to exist as a mono-oxo(V4+=O)(Of)4 species for reduced, dehydrated VAPO-5 and as di-oxo V5+O4 species for calcined, dehydrated VAPO-5. (2)The topological analyses of the internal rotation of three different series of monorotor molecules are investigated in this paper. The bifurcation descriptions indicate that the types of catastrophe and topological regions are related to the generic form of potential energy function , and the critical points. When the double-barrier energy functions are represented as the third-order generic polynomial of the reduced reaction corrdinate, the process is isomorphic to the elementary fold catastrophe. Similarly, when the triple-barrier energy functions are represented as the fourth-order generic polynomial of the reduced reaction coordinate, the process is isomorphic to the elementary cusp catastrophe.
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Books on the topic "5-trans THF"

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Chalifman, Aleksandr. Opening for white according to Anand 1.e4: 1.e4 c5 2. Nf3 Nc6 3.d4 cxd4 4. Nxd4 Nf6 5. Nc3, Chelyabinsk variation / [transl. from the Russian by Evgeny Ermenkov]. Sofia: Chess stars, 2007.

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Lorino, Philippe. Pragmatism, a process perspective on organizations. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198753216.003.0009.

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Mainstream organization studies have long conceptualized organizations as structures imposing order on individual and collective practices. Many organization scholars see organizing as an ongoing process, given the ceaseless adaptative experience of organizations. After an account of the “process turn” in organization studies, this chapter identifies six key questions about the characteristics of organizing processes and analyzes the process orientation of pragmatism and the specific contribution of the main pragmatist thinkers to process thought. It clarifies the pragmatist responses to the six key issues: (1) Organizing is an intrinsic dimension of ordinary activity rather than a specific process reflexively examining activity; (2) organizing is a relational/trans-actional rather than (inter-)subjective process; (3) organizing is a teleological rather than self-contained and autopoietic process; (4) organizing operates segmentation and unification, spatializing and temporalizing at the same time; (5) organizing is both experience-based and creative, it entangles cognition and intuition; (6) organizing is ediated by signs.
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Hutchison, Alastair J., and Michael L. Picton. Fractures in patients with chronic kidney disease. Edited by David J. Goldsmith. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0121.

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Patients with any degree of chronic kidney disease (CKD) have a much higher risk of fractures than the general population, and the risk of death at 1 year post hip fracture in a dialysis patient is over 60%, compared to less than 20% for a non-CKD patient. The assessment of fracture risk and diagnosis of the underlying skeletal pathology in CKD patients is a significant clinical challenge. Non-invasive imaging techniques are not totally reliable in the general population, and the presence of advanced CKD (stages 4, 5, and 5D) renders them largely useless. Bone strength is not determined only by quantity of bone, and renal osteodystrophy can significantly affect bone quality, rendering it liable to fracture even in the presence of a normal bone density measurement. Currently, the only reliable method of assessing both quantity and quality of bone is the examination of trans-iliac bone biopsy, which is generally, but probably incorrectly, perceived to be overly invasive. However, identifying the cause of reduced bone strength and fractures may influence the choice of therapy. For example, in the presence of low-turnover states such as adynamic bone, antiresorptive agents may be ineffective. Pharmaceuticals licensed for the treatment of osteoporosis in the general population can be used similarly in patients with CKD 1–3 without dosage alteration. In CKD 4, post-hoc analyses suggest denosumab is effective and safe, based on a 3-year study that included 73 such patients. In CKD 5 and 5D no dependable data exists to guide therapy, and it should probably be reserved for patients who have already suffered and survived a fracture, and are therefore at high risk of death from a second event.
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Book chapters on the topic "5-trans THF"

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Cibulka, I., J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture Cyclohexane C6H12 + C12H18 trans-1,trans-5,cis-9-Cyclododecatriene (VMSD1111, LB3228_V)." In Binary Liquid Systems of Nonelectrolytes I, 760–61. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-02935-6_285.

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Cibulka, I., J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture Cyclohexane C6H12 + C12H18 trans-1,trans-5,cis-9-Cyclododecatriene (VMSD1212, LB3222_V)." In Binary Liquid Systems of Nonelectrolytes I, 762–63. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-02935-6_286.

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Cibulka, I., J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture Tetrachloromethane CCl4 + C12H18 trans-1,trans-5,cis-9-Cyclododecatriene (VMSD1111, LB3230_V)." In Binary Liquid Systems of Nonelectrolytes II, 2293–94. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-23277-0_1033.

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Cibulka, I., J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture Tetrachloromethane CCl4 + C12H18 trans-1,trans-5,cis-9-Cyclododecatriene (VMSD1212, LB3224_V)." In Binary Liquid Systems of Nonelectrolytes II, 2295–96. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-23277-0_1034.

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Cibulka, I., J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture Heptane C7H16 + C12H18 trans-1,trans-5,cis-9-Cyclododecatriene (VMSD1111, LB3225_V)." In Binary Liquid Systems of Nonelectrolytes II, 444–45. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-23277-0_190.

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Cibulka, I., J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture Heptane C7H16 + C12H18 trans-1,trans-5,cis-9-Cyclododecatriene (VMSD1212, LB3219_V)." In Binary Liquid Systems of Nonelectrolytes II, 446–47. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-23277-0_191.

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Cibulka, I., J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture trans-1,trans-5,cis-9-Cyclododecatriene C12H18 + C12H26 Dodecane (VMSD1111, LB3226_V)." In Binary Liquid Systems of Nonelectrolytes II, 448–49. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-23277-0_192.

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Cibulka, I., J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture trans-1,trans-5,cis-9-Cyclododecatriene C12H18 + C12H26 Dodecane (VMSD1212, LB3220_V)." In Binary Liquid Systems of Nonelectrolytes II, 450–51. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-23277-0_193.

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Cibulka, I., J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture trans-1,trans-5,cis-9-Cyclododecatriene C12H18 + C16H34 Hexadecane (VMSD1111, LB3227_V)." In Binary Liquid Systems of Nonelectrolytes II, 452–53. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-23277-0_194.

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Cibulka, I., J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture trans-1,trans-5,cis-9-Cyclododecatriene C12H18 + C16H34 Hexadecane (VMSD1212, LB3221_V)." In Binary Liquid Systems of Nonelectrolytes II, 454–55. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-23277-0_195.

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Conference papers on the topic "5-trans THF"

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Epimakhov, Andrey. "Bronze age cemetery of Kamenny ambar-5 in the Southern Trans-Urals (typology, chronology, genetics)." In Antiquities of East Europe, South Asia and South Siberia in the context of connections and interactions within the Eurasian cultural space (new data and concepts). Institute for the History of Material Culture Russian Academy of Sciences, 2019. http://dx.doi.org/10.31600/978-5-907053-35-9-246-247.

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2

Cavalli, Stefano, Silvia Cantoni, Alessandro Accetta, Fiorella Pastore, Gessica Marchini, Serena Bertolini, Gino Villetti, and Fabrizio Facchinetti. "The selective Rho kinase inhibitor trans-6-((4-aminocyclohexyl)amino)-5-fluoro-2-methoxynicotinamide ameliorates experimental pulmonary hypertension." In ERS International Congress 2017 abstracts. European Respiratory Society, 2017. http://dx.doi.org/10.1183/1393003.congress-2017.pa2379.

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3

Zhongwei, Yuan, Wang Runci, Yan Taihong, and Zheng Weifang. "The Removal of Uranium From Simulated Ammonium Diuranate Filtrate by Nanofiltration." In 2017 25th International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/icone25-67899.

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In this study, a simulated ammonium diuranate filtrate (ADUF) which was obtained by adding uranyl nitrate to a 35 g/L ammonium nitrate solution to adjust the uranium concentration to about 50 mg/L was treated by a nanofiltration process. Experiments were carried out on a plate membrane testing device with a trans-membrane pressure (TMP) range of 0.5 ∼ 3.0 MPa, a crossflow velocity range of 10 ∼ 50 cm/s and a temperature range of 5 ∼ 35 °C. The results show that NF270 membrane has good rejection property for uranium and excellent permeability for ammonium nitrate. The ammonium nitrate concentration in the permeate is about 32 g/L which means the reject ratio of ammonium nitrate is only about 10%. Though NF270 membrane shows good uranium rejection property, the corresponding permeate flux is very high. When the trans-membrane pressure is 1.5 MPa, the uranium reject ratio is 96.8% and the the corresponding permeate flux is about 80 L/(m2·h). It indicates a bright application prospect of nanofiltration process in the treatment of ADUF.
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4

Hosmane, Ramachandra, and Saika Siddiqui. "Novel Imidazole Analogues of Stilbene: Synthesis and Characterization of Cis- and Trans-1,2-bis(4-nitro-1-p-methoxybenzylimidazol-5-yl)ethene." In The 3rd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1999. http://dx.doi.org/10.3390/ecsoc-3-01741.

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5

Osawa, Naoki, Yoshinobu Yamamoto, and Tomoaki Kunugi. "Investigation of MHD RANS Modeling Base on DNS Database Under the Advanced Blanket Design Conditions Utilized Molten Salt." In 2014 22nd International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/icone22-30653.

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In this study, validations of Reynolds Averaged Navier-Stokes Simulation (RANS) based on Kenjeres & Hanjalic MHD turbulence model (Int. J. Heat & Fluid Flow, 21, 2000) coupled with the low-Reynolds number k-epsilon model have been conducted with the usage of Direct Numerical Simulation (DNS) database. DNS database of turbulent channel flow imposed wall-normal magnetic field on, are established in condition of bulk Reynolds number 40000, Hartmann number 24, and Prandtl number 5. As the results, the Nagano & Shimada model (Trans. JSME series B. 59, 1993) coupled with Kenjeres & Hanjalic MHD turbulence model has the better availability compared with Myong & Kasagi model (Int. Fluid Eng, 109, 1990) in estimation of the heat transfer degradation in MHD turbulent heat transfer.
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Osawa, Naoki, Yoshinobu Yamamoto, and Tomoaki Kunugi. "Investigation of MHD RANS Modeling Base on DNS Database Under the Advanced Blanket Design Conditions Utilized Molten Salt." In 2014 22nd International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/icone22-30712.

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In this study, validations of Reynolds Averaged Navier-Stokes Simulation (RANS) based on Kenjeres & Hanjalic MHD turbulence model (Int. J. Heat & Fluid Flow, 21, 2000) coupled with the low-Reynolds number k-epsilon model have been conducted with the usage of Direct Numerical Simulation (DNS) database. DNS database of turbulent channel flow imposed wall-normal magnetic field on, are established in condition of bulk Reynolds number 40000, Hartmann number 24, and Prandtl number 5. As the results, the Nagano & Shimada model (Trans. JSME series B. 59, 1993) coupled with Kenjeres & Hanjalic MHD turbulence model has the better availability compared with Myong & Kasagi model (Int. Fluid Eng, 109, 1990) in estimation of the heat transfer degradation in MHD turbulent heat transfer.
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7

Kumar, Parvesh, Tarun Chaudhary, and Vijay Kumar Ram. "Design of Constant Transconductance Operational Amplifier By CMOS With High Gain And Low Operational Power." In International Conference on Women Researchers in Electronics and Computing. AIJR Publisher, 2021. http://dx.doi.org/10.21467/proceedings.114.64.

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In the following paper, there is a presentation of a small potential, small capacity CMOS which programs numerically working trans conductance circuit of an amplifier (OTA). A constant transconductance up to (7% of max variation) secures the whole usual-mode of the input range. The circuit process and it can also be operated on a voltage supply of 3.3V with a common-mode range of input from 0.3 to 1.6V. A constant-current is maintained by the designed OTA and also provide a continuous transmission capacity for varying burden capacitors with no increase in consumption of capacity. Simulation of the circuit works upon T-SPICE .5 µm level 49 sub-micron technology.
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8

Idrisov, R. А. "POTENTIAL PRODUCTIVITY ADAPTIVE AGROPHUTOCENOZIS ON SLOPING LANDS OF THE STEPPE TRANS-URALS." In STATE AND DEVELOPMENT PROSPECTS OF AGRIBUSINESS. DSTU-PRINT, 2020. http://dx.doi.org/10.23947/interagro.2020.1.125-128.

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The correct construction of agrophytocenoses on the slopes of the steppe trans-Urals helped to create maximum productivity. In the arid climate, the most productive were the double mixtures of alfalfa with brittle sitnik, wheatgrass is syd, providing an average of 41.6 and 40.2 quintals per hectare (c/ha) of hay, 32.1 and 31.0 GJ/ha OE (exchange energy per hectare), 4.5 and 4.3 quintals per hectare of boiled protein (c/ha) over 5 years. Single-species steppe ecotypes, brittle sieve and wheatgrass sieve in productivity slightly gave way to double components, providing respectively hay- 32.2 and 37.2 cents per hectare, exchange energy 22.2 and 25.7 GJ/ha, digested protein 1.93 and 2.53 c/ha. The enrichment of agrophytocense by the legume component allowed to increase the metabolic energy content to the level of 32.1 and 31.0-GJ/ha, digested protein to 4.5 and 4.3 quintals per hectare, which is 14 times the nutritional value of the metabolic energy, the digested protein is 10 times higher than the natural herb.
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9

Terao, Yutaka, and Norimitsu Sakagami. "Application of Wave Devouring Propulsion System for Ocean Engineering." In ASME 2013 32nd International Conference on Ocean, Offshore and Arctic Engineering. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/omae2013-10691.

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A Wave Devouring Propulsion System (WDPS) generates thrust directly from wave power while simultaneously generating a strong damping force. A simple WDPS design consists of hydrofoils mounted below the bow of a vessel. If a WDPS is integrated with the hull of a vessel, then it can power the vessel forward, even against the wave direction itself. One example of a successful WDPS was installed on the vessel named Mermaid II, which completed a trans-Pacific voyage in 2008, traveling approximately 7,800 km from Hawaii to Japan using wave power alone. This success indicates that the WDPS has potential for use in the field of ocean engineering. As described in this paper, we intend to apply the WDPS to the small autonomous boat and to conduct sea trials. We designed and built an autonomous WDPS boat, developed a data acquisition system, and experimentally investigated its performance in Orida Bay. The experimentally obtained results indicate that the autonomous navigation of the WDPS boat is possible when the wave height is greater than 5–10 cm.
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10

Parsoya, Vaibhav, Thomas Ward, and Jonathan Bailey. "Effect of Forecastle, Bulwark and Sheer on Probabilities of Green Sea Occurrence on Deck of a Typical Aframax and Suezmax Sized Hulls." In ASME 2014 33rd International Conference on Ocean, Offshore and Arctic Engineering. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/omae2014-23011.

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A study resulting in qualitative and quantitative information about the effect of forecastle and sheer is presented in this paper. This is based on a linear direct calculation and extends the work of the JIP on F(P)SO Green water loading described in Buchner (2002) by including forward speed effects. The approach calculates Relative Wave Elevation (RWE) from a linear 3D diffraction analysis and adds nonlinear corrections by way of non-linear response spectra of RWE. The probabilities of green sea occurrence are calculated for variable heights of forecastle/sheer, vessel draft, vessel speed and sea depth for relative heading and mean zero upcrossing wave period for sea states on typical tanker routes (Arabian Gulf to Bass Strait (South East Australia), North East (Global Wave Statistics European Data set Areas 5 and 15 with 90m water depth), IACS Common Structural Rules North Atlantic, Lloyds Register 100A1 and Alaska (Trans-Alaska Pipeline System) to Long Beach). This comparison is done on one typical sized Aframax and Suezmax hull. A downtime in hours over 25 years of design life in 3 hours sea state is also computed which can be a direct input to the risk matrix analysis.
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