Relevant bibliographies by topics / V(CO)6

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Academic literature on the topic 'V(CO)6'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "V(CO)6"

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Charland, J. P., E. J. Gabe, J. M. McCall, J. R. Morton, and K. F. Preston. "Structure of [V(CO)3(PMe3)4][V(CO)6]." Acta Crystallographica Section C Crystal Structure Communications 43, no. 1 (1987): 48–50. http://dx.doi.org/10.1107/s010827018709704x.

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Spears, Kenneth G., and Hairong Shang. "Models for Quantum Effects in Electron Transfer: Co(Cp)2+|V(CO)6-." Journal of Physical Chemistry A 104, no. 12 (2000): 2668–80. http://dx.doi.org/10.1021/jp993405i.

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Marin, Timothy W., Bradley J. Homoelle, and Kenneth G. Spears. "Ultrafast Electron Transfer in the [Co(Cp)2|V(CO)6] Radical Pair." Journal of Physical Chemistry A 106, no. 7 (2002): 1152–66. http://dx.doi.org/10.1021/jp012934v.

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Churchill, Melvyn Rowen, and Thomas S. Janik. "Crystal structure of hexakis(tetrahydrofuran)sodium hexacarbonylvanadate(−I), [Na(THF)6 +][V(CO)6 −]." Journal of Chemical Crystallography 25, no. 9 (1995): 597–99. http://dx.doi.org/10.1007/bf01667030.

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Vasilyeva, L., E. Nikitina, S. Tsarova, L. Gulyaeva, and V. Werbitzky. "SARS Co-V-2 CORONAVIRAL INFECTION IN PREGNANT WOMEN (CLINICAL DATA USE "6 City Clinical Hospital")." Emergency Cardiology and Cardiovascular Risks 5, no. 1 (2021): 1190–94. http://dx.doi.org/10.51922/2616-633x.2021.5.2.1190.

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The article analyzes the features of the course of pregnancy in 110 women hospitalized in the Healthcare Institution “6th City Clinical Hospital” of Minsk for SARS CoV-2 coronavirus infection in April-October 2020. The authors studied the anamnestic data of pregnant women, analyzed the clinical data and the data from the instrumental and laboratory examinations of pregnant women with SARS CoV-2 coronavirus infection in the Republic of Belarus. A comparative analysis was carried out dealing with the treatment of pregnant women for coronavirus infection with SARS CoV-2 in a hospital setting.
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McCall, J. M., J. R. Morton, and K. F. Preston. "The EPR spectra and structures of V(CO)6 and certain derivatives." Journal of Magnetic Resonance (1969) 64, no. 3 (1985): 414–19. http://dx.doi.org/10.1016/0022-2364(85)90103-9.

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Sievers, Michael R., and P. B. Armentrout. "Collision-Induced Dissociation Studies of V(CO)x+, x = 1-7: Sequential Bond Energies and the Heat of Formation of V(CO)6." Journal of Physical Chemistry 99, no. 20 (1995): 8135–41. http://dx.doi.org/10.1021/j100020a041.

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Scheuermann, Barry W., John M. Kowalchuk, Donald H. Paterson, and David A. Cunningham. "V˙co 2 andV˙e kinetics during moderate- and heavyintensity exercise after acetazolamide administration." Journal of Applied Physiology 86, no. 5 (1999): 1534–43. http://dx.doi.org/10.1152/jappl.1999.86.5.1534.

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The effect of carbonic anhydrase inhibition with acetazolamide (Acz) on CO2 output (V˙co 2) and ventilation (V˙e) kinetics was examined during moderate- and heavy-intensity exercise. Seven men [24 ± 1 (SE) yr] performed cycling exercise during control (Con) and Acz (10 mg/kg body wt iv) sessions. Each subject performed step transitions (6 min) in work rate from 0 to 100 W [below ventilatory threshold (<V˙eT)] and to an O2 uptake corresponding to ∼50% of the difference between the work rate atV˙eT and peak O2 uptake [above ventilatory threshold (>V˙eT)].V˙e and gas exchange were measured
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Herberhold, Max, Silke Köppl та Wolfgang Milius. "Mixed-Sandwich η5/η7 Vanadium Complexes. The Molecular Structure of (η5-2-Methyl-indenyl)-(η7-cycloheptatrienyl)-vanadium". Zeitschrift für Naturforschung B 54, № 7 (1999): 899–903. http://dx.doi.org/10.1515/znb-1999-0713.

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The diamagnetic halfsandwich complexes [V(η7-C7H7)(CO)3] and [V(η5-L5)(CO)4] have been used as intermediates in the conversion of hexcarbonylvanadium, V(CO)6, to the paramagnetic trovacene derivatives, [V(η5-L5)(η7-C7H7)] [L5 = cyclopentadienyl ligand, C5H4-R (R = H (1), Me (1a), tBu (1b)) and C5Me5 (1c); indenyl (2) and 2-methylindenyl (2a)]. The molecular structure of 2a has been determined: the distances between vanadium and the center Z of the (nearly parallel) ring ligands are 193.0 pm (V-Z5) and 146.2 pm (V-Z7).
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Mantra, I. Nyoman. "Meningkatkan Prestasi Belajar Agama Hindu Melalui Pelaksanaan Model Pembelajaran Kooperatif Co-Op Co-Op." Journal of Education Action Research 3, no. 4 (2019): 382. http://dx.doi.org/10.23887/jear.v3i4.21866.

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Penelitian ini dilaksanakan di SD Negeri 6 Ketewel di Kelas V yang kemampuan siswanya untuk materi Pelajaran Agama Hindu masih tergolong rendah. Tujuan penelitian tindakan kelas ini adalah untuk meningkatkan prestasi belajar Agama Hindu siswa kelas V SD Negeri 6 Ketewel tahun pelajaran 2017/2018 melalui pelaksanaan model pembelajaran Kooperatif Co-Op Co-Op. Rancangan penelitian pada penelitian ini adalah penelitian tindakan kelas dua siklus. Metode pengumpulan datanya adalah tes prestasi belajar. Metode analisis datanya adalah deskriptif kuantitatif. Hasil yang diperoleh dari penelitian ini ad
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Dissertations / Theses on the topic "V(CO)6"

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Rey, Michaël. "Théorie des spectres rovibroniques des molécules octaédriques : Hamiltonien et moments de transition." Phd thesis, Université de Bourgogne, 2002. http://tel.archives-ouvertes.fr/tel-00004623.

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Cette thèse est consacrée à l'étude des interactions rovibroniques au sein de complexes octaédriques pour lesquels l'approximation de Born-Oppenheimer n'est plus valide. Pour la première fois, un modèle rovibronique tensoriel effectif complet a été développé à partir des travaux portant sur les toupies sphériques dans un état électronique non dégénéré. Ce modèle inclut le cas de systèmes moléculaires possédant un nombre pair ou impair d'électrons et sa validité a pu être testée sur deux molécules, toutes deux octaédriques : V(CO)6 et ReF6. Pour ces deux systèmes, nous avons alors considéré qua
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Kováč, Michal. "Modulátor OFDM v obvodu FPGA." Master's thesis, Vysoké učení technické v Brně. Fakulta elektrotechniky a komunikačních technologií, 2015. http://www.nusl.cz/ntk/nusl-221112.

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The master’s thesis deals with the design of modulator OFDM in the FPGA circuit. The thesis describes basic attributes of modulation OFDM, its pros and cons. With the help of created block level scheme, it describes all the components of the processing of the data signal on its way from the transmitter to the receiver. The Atlys Spartan-6 Development Board has been chosen for the implementation of the modulator. The other part of thesis is the design and realization of the analog-digital interface for the modulator OFDM. The interface consists of PCB, which is connected to the development boar
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Books on the topic "V(CO)6"

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Gerlach, Peter K. Build a Co-Parenting Team: After Divorce or Remarriage (Stepfamily Information Series, V. 6). Xlibris Corporation, 2003.

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Build a Co-Parenting Team: After Divorce or Remarriage (Stepfamily Information Series, V. 6). Xlibris Corporation, 2003.

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Aloysius P, Llamzon. Part II The Jurisprudence on Corruption in International Investment Arbitration: Case and Trend Analysis, 6 The Cases. Oxford University Press, 2014. http://dx.doi.org/10.1093/law/9780198714262.003.0006.

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This chapter discusses the decisions and awards in nineteen cases identified as significant for the study of corruption in international investment arbitration. It covers the following: cases where corruption was outcome-determinative; [e.g. World Duty Free Company Ltd. v. Republic of Kenya, Metal-Tech v. Khazakhstan, and Siemens v. Argentina] and cases where corruption allegations did not prosper [e.g. Southern Pacific Properties v. Arab Republic of Egypt, Wena Hotels Ltd. v. Arab Republic of Egypt, and Tanzania Electric Supply Co. v. Independent Power Tanzania Ltd].
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Book chapters on the topic "V(CO)6"

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Schweitzer, George K., and Lester L. Pesterfield. "The Fe–Co–Ni Group." In The Aqueous Chemistry of the Elements. Oxford University Press, 2010. http://dx.doi.org/10.1093/oso/9780195393354.003.0017.

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The three elements to be treated in this chapter (Fe, Co, Ni) are the sixth, seventh, and eighth members of the first transition series. The first five members (Sc, Ti, V, Cr, Mn) have been treated in previous chapters (Chapters 12, 13, and 14). The ten elements of this first transition series (Sc through Zn) are characterized by electron activity in the 4s–3d levels. All elements in the 3d transition series are metals, and many of their compounds tend to be colored as a result of unpaired electrons. Most of the elements have a strong tendency to form complex ions due to participation of the d electrons in bonding. Unlike the previous three elements (V, Cr, Mn), these three do not show a variety of oxidation states. The higher oxidation states are almost absent in compounds, Fe showing principally the II and III, Co the II and III, and Ni only the II. The III states are less stable than the II states unless they are stabilized by complex formation. The resemblance of these three elements is notable, they being more like each other than they are to the elements below them. a. E–pH diagram. The E–pH diagram in Figure 15.1 shows Fe in oxidation states of 0, II, and III. This diagram, which involves iron at 10−1.0 M is oversimplified in several ways. The Fe(II) and Fe(III) cations are more properly designated as Fe(HOH)6+2 and Fe(HOH)6+3, reflecting the coordination number of 6. The region just to the left of the Fe+2/Fe(OH)2 line involves Fe(OH)+, and the region just to the left of the Fe+3/FeO(OH) line involves numerous hydroxo complexes such as Fe(HOH)5OH+2 and Fe(HOH)4(OH)2+. At very high pH values, there is a tendency for Fe(OH)2 to be converted to HFeO2−, and at very high E values, the powerful oxidant, red-purple FeO4−2 can be produced. When these latter five species are introduced, Figure 15.2 results. This, too, is probably simplified since it is known that other species are present, such as Fe2(OH)4+4 and Fe3(OH)4+5. The species FeO4−2 can only be prepared in a very strong base.
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Jordan, Robert B. "Reaction Mechanisms of Organometallic Systems." In Reaction Mechanisms of Inorganic and Organometallic Systems. Oxford University Press, 2007. http://dx.doi.org/10.1093/oso/9780195301007.003.0007.

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The general principles discussed in Chapter 3 also apply to reactions of organometallic complexes. Because these systems do not have a wide range of structurally similar complexes with different metal atoms for comparative studies across the Periodic Table, comparisons are usually made down a particular group. However, there is a wide range of ligands available for studies of entering and leaving group effects. This area has been the subject of several recent reviews. A major difference from the systems discussed in Chapter 3 is that many of these complexes are soluble in organic solvents, including hydrocarbons. This can minimize the complicating factor of solvent coordination, but these solvents often have quite low dielectric constants so that various types of preassociation are more probable. The metal carbonyl family of compounds is typical of the range of structures and reactivities of organometallic complexes. The rate of CO exchange was examined in early studies, and this work is the subject of a recent review. The order of reaction rates is as follows: Where the rate law has been determined, the reaction is first-order in [M(CO)R] and zero-order in [CO]. This implies a D mechanism, since a solvent intermediate is unlikely for the "noncoordinating" solvents. This mechanism also is probable for other ligand substitutions. The main mechanistic exception to the above generalizations is V(CO)6, which has an Ia mechanism for PR3 substitution reactions. This compound is unique in that it is the only 17-electron metal carbonyl and also is by far the most labile. Some kinetic results for substitution on V(CO)6 in hexane are given in Table 5.1. The substitution rates have rather low ΔH* values, and the negative ΔS* values are typical of an associative process. The rates for various entering groups correlate with the basicity rather than the size, as measured by the cone angle. It has been suggested that formation of a 19-electron associative intermediate from a 17-electron reactant is much more favorable than a 20-electron intermediate from an 18-electron reactant.
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Gurney, Peter. "Co-operation v. Socialism: Being a Report of a Debate between Mr H.H. Champion and Mr Ben Jones (Manchester: Central Co-op Board, 1887), 6–23." In Contemporary Thought on Nineteenth Century Socialism. Routledge, 2020. http://dx.doi.org/10.4324/9780429452352-21.

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Habashi, F. "Transition Metals Production: V, Cr, Mn, Co, Ni." In Encyclopedia of Materials: Science and Technology. Elsevier, 2002. http://dx.doi.org/10.1016/b0-08-043152-6/01849-0.

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McFarland, Ben. "Unfolding the Periodic Table." In A World From Dust. Oxford University Press, 2016. http://dx.doi.org/10.1093/oso/9780190275013.003.0007.

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Our starting point is not hidden, nor is it far off. It is not an extreme place like Mono Lake or Freswick Castle, but it is a central concept expressed on a single page. The periodic table is the center of chemistry, and therefore of this book. You can spot it at a distance from its vaguely cathedral-like shape. You can see the chemical symbols that it contains on magnets and T-shirts and restaurant signs. Its regular columns are not quite symmetric, but that is because it has been twisted out of its natural shape by the contingencies of history. Rearrange it just a little and a simple mathematical pattern appears. To see this pattern, imagine that the periodic table is made out of beads on an abacus, arranged in the familiar U shape. Then push all the beads to the left: … Row 1 = H- He Row 2 = Li- Be- B- C- N- O- F- Ne Row 3 = Na- Mg- Al- Si- P- S- Cl- Ar Row 4 = K- Ca- Sc- Ti- V- Cr- Mn- Fe- Co- Ni- Cu- Zn- Ga- Ge- As- Se- Br- Kr Row 5 = Rb- Sr- Y- Zr- Nb- Mo- Tc- Ru- Rh- Pd- Ag- Cd- In- Sn- Sb- Te- I- Xe … By row, there are 2, 8, 8, 18, and 18 elements. The pattern continues in the rows below, but it is obscured by the fact that on most tables 14 elements have been moved out of the sixth and seventh rows. On the table here I have put them where they belong. These rows have 32 elements each. This can be simplified even more. The rows increase, first by 2, then by 6 more (2 + 6 = 8), then by 10 more (2 + 6 + 10 = 18), then by 14 (2 + 6 + 10 + 18 = 32). The series 2, 6, 10, 14 is the doubles of counting up by odd numbers: 1, 3, 5, 7. Put another way, each row is equal to 2n + 1 with n = integers from 0.
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"The Alliance Spring Co Ltd v First Secretary of State (Admin)." In PLR 2005. Estates Gazette, 2012. http://dx.doi.org/10.4324/9780080937298-6.

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Bianchi, C. L., S. Vitali, and V. Ragaini. "Comparison between Co and Co(Ru-promoted)-ETS-10 catalysts prepared in different ways for Fischer-Tropsch Synthesis." In Natural Gas Conversion V, Proceedings ofthe 5th International Natural Gas Conversion Symposium,. Elsevier, 1998. http://dx.doi.org/10.1016/s0167-2991(98)80426-6.

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Tiwari, Vivek, Sharad Malik, and Andrew Wolfe. "Power Analysis of Embedded Software: A First Step Towards Software Power Minimization Manuscript received June 15, 1994; revised August 23, 1994. The work of V. Tiwari was supported by an IBM Graduate Fellowship. The work of S. Malik was supported by an IBM Faculty Development Award. IEEE Log Number 9406371." In Readings in Hardware/Software Co-Design. Elsevier, 2002. http://dx.doi.org/10.1016/b978-155860702-6/50019-3.

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"CREATING A NEW FIRST AMENDMENT RIGHT: MIAMI HERALD PUBLISHING CO. V. TORNILLO AND THE STORY OF ACCESS TO THE MEDIA." In Defending the First. Routledge, 2006. http://dx.doi.org/10.4324/9781410613509-6.

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ZEHRINGER, R., P. OELHAFEN, H. J. GÜNTHERODT, Y. YAMADA, and U. MIZUTANI. "Electronic Structure of (Ni33Zr67)85X15 (X ≡ Ti, V, Cr, Mn, Fe, Co and Cu) Metallic Glasses Studied by Photoelectron Spectroscopy." In Rapidly Quenched Metals 6. Elsevier, 1988. http://dx.doi.org/10.1016/b978-1-85166-973-8.50075-6.

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Conference papers on the topic "V(CO)6"

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Liu, Jinhe, and Jing Chen. "Design and study on weld protection drag cover as welding Ti 6 A 14 V by CO 2 laser." In Photonics China '98, edited by ShuShen Deng and S. C. Wang. SPIE, 1998. http://dx.doi.org/10.1117/12.317916.

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Bardin, Yves-Vincent, Christophe Pierre, and Johan Boullet. "Ultra-high brightness, low insertion loss, kW-class co and contra propagative 6+1:1 combiner (Conference Presentation)." In Components and Packaging for Laser Systems V, edited by Alexei L. Glebov and Paul O. Leisher. SPIE, 2019. http://dx.doi.org/10.1117/12.2511275.

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Huth, M., A. Heilos, G. Gaio, and J. Karg. "Operation Experiences of Siemens IGCC Gas Turbines Using Gasification Products From Coal and Refinery Residues." In ASME Turbo Expo 2000: Power for Land, Sea, and Air. American Society of Mechanical Engineers, 2000. http://dx.doi.org/10.1115/2000-gt-0026.

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The Integrated Gasification Combined Cycle concept is an emerging technology that enables an efficient and clean use of coal as well as residuals in power generation. After several years of development and demonstration operation, now the technology has reached the status for commercial operation. SIEMENS is engaged in 3 IGCC plants in Europe which are currently in operation. Each of these plants has specific characteristics leading to a wide range of experiences in development and operation of IGCC gas turbines fired with low to medium LHV syngases. The worlds first IGCC plant of commercial s
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