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

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

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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2

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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3

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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4

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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5

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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6

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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7

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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8

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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9

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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10

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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11

Nuber, B., W. Schatz та M. L. Ziegler. "Darstellung und Charakterisierung der μ3-Oxo-Cluster [Cp3Mo3(CO)4µ-Cl)(µ3-O)] und [Cp3Mo3(µ-CO)3(CO)3(µ3-O)]+ / Synthesis and Characterization of the µ3-Oxo Clusters [Cp3Mo3(CO)4μ-Cl)(μ3-O)] and [Cp3Mo3(μ-CO)3(CO)3(μ3-O)]+". Zeitschrift für Naturforschung B 45, № 4 (1990): 508–14. http://dx.doi.org/10.1515/znb-1990-0416.

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[CpMo(CO)3]2 (1) (Cp = cyclopentadienyl) reacts with InCl3 in diglyme to yield the oxo-cluster [Cp3Mo3(CO)4(μ-Cl)(μ3-O)] (2) and the cationic oxo-cluster [Cp3Mo3(μ-CO)3(CO)3(μ3-O)]+ as the salt [Cp3Mo3(μ-CO)3(CO)3(μ3-O)][CpMo(CO)3InCl3] (3). The compounds were characterized by elemental analysis, spectroscopic data and X-ray structure analysis. Compound 2 crystallizes in the orthorhombic space group P212121 with a = 1006.0(3), b = 1244.6(4) and c = 1600.8(5) pm, V = 2004.3 x 106 pm3, Z = 4. Compound 3 crystallizes in the monoclinic space group P 21/m with a = 874.4(8), b = 1407(1) and c = 1500

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12

Charushnikova, I. A., N. N. Krot, and I. N. Polyakova. "Crystal Structure of Double Co(NH3)63+Np(V) Malonates Co(NH3)6(NpO2C3H2O4)2A·H2O (A = OH and NO3)." Radiochemistry 46, no. 4 (2004): 347–50. http://dx.doi.org/10.1023/b:rach.0000039110.79156.ac.

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13

Graf, Marion, Kurt Merzweiler, Clemens Bruhn та Hans-Christian Böttcher. "Reaktion von [Co(But2PH)2I2] mit [Ru3(CO)12]: Synthese und Röntgenkristallstrukturanalyse von [Ru3(CO)6(μ-H)(μ-I)2(μ-PBut2)(But2PH)]/ Reaction of [Co(But2PH)2I2] with [Ru3(CO)12]: Synthesis and X-Ray Crystal Structure of [Ru3(CO)6(μ-H)(μ-I)2(μ-PBut2)(But2PH)]". Zeitschrift für Naturforschung B 53, № 8 (1998): 865–70. http://dx.doi.org/10.1515/znb-1998-0815.

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Abstract [Co(But2PH)2I2] (1) reacts with [Ru3(CO)12] in refluxing toluene to give a mixture of products including the novel metal clusters [Ru3(CO)6(μ-H)(μ-I)2(μ-PBut2)(But2PH)] (2) and [Ru3(CO)7(μ-H)(μ-I)(μ-PBut2)2] (3) besides the known complex [Ru3(CO)8(μ-H)2(μ3- PBut)(But2PH)] (4). No cluster expansion products could be observed. Thus the cobalt compound acts merely as a phosphine and iodine transfer reagent. The molecular structures of the metal complexes 1 and 2 were determined by single-crystal X-ray structure analyses. 1 crystallizes in the tetragonal space group P4̄21c with a = 13.230

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14

Boeré, René T., Klaus H. Moock, Vicki Klassen, Joel Weaver, Dieter Lentz, and Heike Michael-Schulz. "Electrochemistry of methylidyne and 1,2,3,5-dithiadiazole complexes of iron and nickel and a reinterpretation of the composition of "PhCN2S2Fe2(CO)6"." Canadian Journal of Chemistry 73, no. 9 (1995): 1444–53. http://dx.doi.org/10.1139/v95-179.

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The title compounds have been studied in CH2Cl2 by cyclic voltammetry. Nonacarbonyldi(μ3-methylidyne)triiron, [Fe3(CO)9(μ3-CX)2] (X = F, Cl, Br, H), undergo chemically reversible 1e− reduction (−0.72 to −0.88 V vs. SCE) and irreversible oxidation (+1.59 to +1.72 V); the compound for which X = F displays a second, irreversible reduction (−1.96 V). Using reduction potentials of comparable μ3-E (E = S, Se, NPh, PPh) clusters, μ3-methylidyne ligands are shown to be strongly basic, comparable to PPh and NPh and more basic than S or Se. The methylidyne clusters are both more difficult to oxidize and

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15

Abul-Futouh, Hassan, Wolfgang Imhof, Wolfgang Weigand, and Laith R. Almazahreh. "Electrochemical and Computational Insights into the Reduction of [Fe2(CO)6{µ-(SCH2)2GeMe2}] Hydrogenase H-Cluster Mimic." Inorganics 7, no. 4 (2019): 50. http://dx.doi.org/10.3390/inorganics7040050.

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The electrochemical reduction of the complex [Fe2(CO)6{µ-(SCH2)2GeMe2}] (1) under N2 and CO is reported applying cyclic voltammetry. Reduction of complex 1 in CO saturated solutions prevents the possible release of CO from the dianion 12−, while the latter reacts with additional CO forming a spectroscopically uncharacterized product P1. This product undergoes a reversible redox process at E1/2 = −0.70 V (0.2 V∙s−1). In this report, the structure of the neutral complex 1, isomers of dianionic form of 1, and P1 are described applying DFT computations. Furthermore, we propose reaction pathways fo

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16

Bröchler, Raimund, Iona H. T. Sham, Matthias Bodenbinder, et al. "The Synthesis and the Molecular Structure of Hexakis(carbonyl)hexafluoroantimonato(V)tungsten(II) Undecafluorodiantimonate(V), [W(CO)6(FSbF5)][Sb2F11]." Inorganic Chemistry 39, no. 10 (2000): 2172–77. http://dx.doi.org/10.1021/ic991331j.

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17

Grigor'ev, M. S., M. Yu Antipin, N. N. Krot, and A. A. Bessonov. "Synthesis of New Crystalline Pu(V) Compounds from Solutions: V. Crystal Structure of [Co(NH3)6][PuO2(C2O4)2] · 3H2O." Radiochemistry 47, no. 5 (2005): 460–63. http://dx.doi.org/10.1007/s11137-005-0118-2.

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18

Minyaev, Mikhail E., та John E. Ellis. "Crystal structure of heptakis(2,6-dimethylphenyl isocyanide-κC)vanadium(I) iodide". Acta Crystallographica Section E Crystallographic Communications 71, № 4 (2015): 431–34. http://dx.doi.org/10.1107/s2056989015006015.

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The title salt, [V(C9H9N)7]+I−or [V(CNXyl)7]+I−(Xyl is 2,6-dimethylphenyl), crystallized from tetrahydrofuran at low temperatures after reacting (Et4N)+[V(CO)6]−, excess of CNXyl and iodine. The complex cation and the two crystallographically different iodide anions, each located on a different glide plane, are well separated in the crystal structure. The V(CN)7core of the cation has the form of a distorted monocapped trigonal prism. This compound is of interest as the first isolable homoleptic seven-coordinate vanadium analog of the 18-electron [V(CO)7]+monocation.

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19

Barybin, Mikhail V., Marie K. Pomije, and John E. Ellis. "Highly reduced organometallics 42. A new method for the syntheses of [V(CO)6]− and [V(PF3)6]− involving anthracenide mediated reductions of VCl3(THF)3." Inorganica Chimica Acta 269, no. 1 (1998): 58–62. http://dx.doi.org/10.1016/s0020-1693(97)05771-x.

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20

Tachibana, Kazuya, Hideaki Imanaka, Hiroshi Miyano, Muneyuki Takeuchi, Keiji Kumon, and Masaji Nishimura. "Effect of Ventilatory Settings on Accuracy of Cardiac Output Measurement Using Partial CO2Rebreathing." Anesthesiology 96, no. 1 (2002): 96–102. http://dx.doi.org/10.1097/00000542-200201000-00021.

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Background Recently, a new device has been developed to measure cardiac output noninvasively using partial carbon dioxide (CO(2)) rebreathing. Because this technique uses CO(2) rebreathing, the authors suspected that ventilatory settings, such as tidal volume and ventilatory mode, would affect its accuracy: they conducted this study to investigate which parameters affect the accuracy of the measurement. Methods The authors enrolled 25 pharmacologically paralyzed adult post-cardiac surgery patients. They applied six ventilatory settings in random order: (1) volume-controlled ventilation with in

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21

Charushnikova, I. A., N. N. Krot, and I. N. Polyakova. "Crystal Structure of a Double Oxalate of Np(V) and Co(NH3) 6 3+ , Co(NH3)6NpO2(C2O4)2·1.5H2O." Radiochemistry 47, no. 6 (2005): 540–44. http://dx.doi.org/10.1007/s11137-006-0003-7.

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22

Hoch, Martin, and Dieter Rehder. "Isotope effects and coupling constants in [CpV(CO)3(1,2H)]− and the 13CO and C18O isotopomers of CpV(CO)4 and [V(CO)6]−." Inorganica Chimica Acta 111, no. 1 (1986): L13—L15. http://dx.doi.org/10.1016/s0020-1693(00)82204-5.

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23

Minkwitz, Rolf, Horst Borrmann та Joachim Nowicki. "Darstellung und Kristallstruktur von [Co2(CO)6(μ-S2)]2+(AsF6-)2 · 1/2 SO2Preparation and Crystal Structure of [Co2(CO)6(μ-S2)]2+(AsF6-)2 · 1/2SO2". Zeitschrift für Naturforschung B 47, № 7 (1992): 915–18. http://dx.doi.org/10.1515/znb-1992-0703.

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[Co2(CO)6(μ-S2)]2+(AsF6-)2· 1/2SO2 is formed in the reaction of S82+(AsF6-)2 with Co2(CO)8 in SO2 at R.T.. The complex crystallizes in the orthorhombic space group Pbcn (No. 60) with a = 1508.0(9), b = 1642.7(8), c = 871.3(6) pm, V = 2158(2)•106 pm3, Z = 4. In the tetrahedral Co2S2 unit a short S–S distance (198 pm) is observed.

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24

Pizarro, Sebastián, Guillermo Saá, Francisco Gajardo, and Alvaro Delgadillo. "Synthesis and Characterization of Chloridobis(dimethylglyoximato)4-(2-ferrocenylvinyl)pyridinecobalt(III): A New Heterobinuclear Cobaloxime." Journal of Chemistry 2016 (2016): 1–5. http://dx.doi.org/10.1155/2016/1385236.

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The synthesis of a new heterobinuclear cobaloxime with 4-(2-ferrocenylvinyl)pyridine, fcvpy, is reported. The complex [CoCl(dmgH)2(fcvpy)], where dmgH2is dimethylglyoxime and dmgH is dimethylglyoximato, has been characterized by1H-NMR, UV-Vis, cyclic voltammetry, and elemental analysis. The cyclic voltammogram of this complex shows a fc/fc+reversible wave at +0.58 V versus Ag/AgCl, one irreversible wave,Epc= −0.54 V versus Ag/AgCl, assigned to the reduction of Co(III) to Co(II), and two quasireversible processes at −1.02 V and −1.10 V versus Ag/AgCl associated with the reduction of Co(II). The

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25

Chao, Lisa C. F., Andreas Decken, James F. Britten, and Michael J. McGlinchey. "Organic and inorganic templates bearing CCo3(CO)9 cluster fragments: X-ray crystal structures of C(CH2OCOCCl3)4 and of CH3C(O)CHC(OH)MLn where MLn = CCo3(CO)9 or (C6H5)Cr(CO)3." Canadian Journal of Chemistry 73, no. 7 (1995): 1196–205. http://dx.doi.org/10.1139/v95-147.

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Pentaerythritol and trichloroacetyl chloride react to yield the tetrakis-trichloroacetate ester C(CH2-O2C-CCl3)4, 5, which crystallizes in the triclinic space group [Formula: see text] with a = 9.874(2) Å, b = 11.811(2) Å, c = 12.858(3) Å, α = 114.35(3)°, β = 95.63(3)°, γ = 99.11 (3)°, and V = 1326.5(5) Å3 for Z = 2. The molecule adopts a geometry in which the trichloroacetate chains fold to produce a flattened tetrahedron, giving a molecule of approximate D2d symmetry. Treatment of 5 with CO2(CO)8 gave, as the highest molecular weight product, the tris-cluster complex C[CH2-O2C-CCo3(CO)9]3(CH

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26

Wang, Lijuan, Huitao Fan, Chaojun Du, et al. "Synthesis, structure and properties of a Co-crystallized complex based on polyoxovanadate [V IV 12 V V 6 O 42 ] 6− and a mononuclear vanadium complex [VON(CH 2 CH 2 O) 3 ]." Inorganic Chemistry Communications 63 (January 2016): 39–41. http://dx.doi.org/10.1016/j.inoche.2015.11.011.

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27

Bi, Yan Hong, Zhao Yu Wang, and Xi Rong Zhao. "Enhanced Performance of Thermomyces lanuginosus Lipase-Catalyzed Regioselective Acylation of 6-Azauridine by a Co-Solvent Approach." Advanced Materials Research 550-553 (July 2012): 1395–99. http://dx.doi.org/10.4028/www.scientific.net/amr.550-553.1395.

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A comparative study was made of lipozyme TL IM-catalyzed regioselective acylation of 6-azauridine with vinyl palmitate for the preparation of the 5'-O-monoester in co-solvent mixtures and pure polar solvents. Among the solvent systems investigated, a co-solvent mixture of anhydrous acetone/isooctane was found to be the best reaction medium, in which Lipozyme TL IM also exhibited good thermal and operational stability. It was also found that the acylation was dependent on the hydrophobic solvent content. The most suitable co-solvent was anhydrous acetone/isooctane (90:10, v/v). Under the optima

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28

Wait, Michael. "The Slumbering Sovereign: Sir Owen Dixon's Common Law Constitution Revisited." Federal Law Review 29, no. 1 (2001): 57–74. http://dx.doi.org/10.1177/0067205x0102900103.

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29

Bley, Bianca, Helge Willner, and Friedhelm Aubke. "Synthesis and Spectroscopic Characterization of Hexakis(carbonyl)iron(II) Undecafluorodiantimonate(V), [Fe(CO)6][Sb2F11]2." Inorganic Chemistry 36, no. 2 (1997): 158–60. http://dx.doi.org/10.1021/ic9608105.

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30

Cao, Hong-Xia, Jun Zhang, Cheng-Long Guo, Jingguang G. Chen, and Xiang-Kun Ren. "Modifying surface properties of KIT-6 zeolite with Ni and V for enhancing catalytic CO methanation." Applied Surface Science 426 (December 2017): 40–49. http://dx.doi.org/10.1016/j.apsusc.2017.07.138.

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31

Bernhardt, Eduard, Bianca Bley, Rudolf Wartchow, et al. "Hexakis(carbonyl)iron(II) Undecafluorodiantimonate(V), [Fe(CO)6][Sb2F11]2, and -Hexafluoroantimonate(V), [Fe(CO)6][SbF6]2, Their Syntheses, and Spectroscopic and Structural Characterization by Single Crystal X-ray Diffraction and Normal Coordinate Analysis." Journal of the American Chemical Society 121, no. 31 (1999): 7188–200. http://dx.doi.org/10.1021/ja990958y.

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32

Li, Hongqi, and Ian S. Butler. "Solid-State Infrared Photoacoustic Spectra of Group 6B Metal Mixed Carbonyl-t-Butylisocyanide Complexes, M(CO)6-n(CNtBu)n(M = Cr, Mo, W; n = 1–3)." Applied Spectroscopy 47, no. 2 (1993): 218–21. http://dx.doi.org/10.1366/0003702934048244.

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Solid-state mid- and near-IR photoacoustic (PA) spectra have been measured at room temperature for the group 6B metal(0) mixed carbonyl- t-butylisocyanide complexes M(CO)6- n(CN tBu) n ( M = Cr, Mo, W; n = 1-3). Vibrational assignments are proposed for many of the observed bands. The PA spectra in the near-IR region (4600-3600 cm−1), where the binary v(CN) and v(CO) overtones and combinations absorb, are useful spectral fingerprints for these organometallic complexes.

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33

Zhang, C., X. Lin, Z. Zhang, L. S. Long, C. Wang, and W. Lin. "A hybrid polyoxometalate–organic molecular catalyst for visible light driven water oxidation." Chem. Commun. 50, no. 78 (2014): 11591–94. http://dx.doi.org/10.1039/c4cc03487b.

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A novel organic–inorganic hybrid monocapped/bicapped Keggin structure [Co<sup>II</sup>(bpy)<sub>3</sub>]<sub>6</sub>(H<sub>2</sub>bpy)[(Co<sup>II</sup>bpy)<sub>2</sub>(PMo<sub>8</sub><sup>VI</sup>Mo<sub>4</sub><sup>V</sup>O<sub>40</sub>)]3 [(Co<sup>II</sup>bpy)(PMo<sub>8</sub><sup>VI</sup>Mo<sub>4</sub><sup>V</sup>O<sub>40</sub>)]·16H<sub>2</sub>O (bpy = 2,2′-bipyridine) was synthesized and shown to be an efficient visible light-driven catalyst for water oxidation.

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34

Charushnikova, I. A., N. N. Krot, and Z. A. Starikova. "Crystal structure of a double Np(V) and Co(NH3) 6 3+ maleate, Co(NH3)6[NpO2(HL)2(H2O)3](HL)2?H2O [L = OOC(HC)2COO]." Radiochemistry 46, no. 6 (2004): 565–69. http://dx.doi.org/10.1007/s11137-005-0028-3.

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35

Brownlee, Robert T. C., and B. Philip Shehan. "NMR relaxation times and quadrupole coupling constants in [M(CO)6] (M  Cr, Mo, W) and [V(CO)6]−. Transition-metal quadrupole moments. 17O relaxation times and bonding." Journal of Magnetic Resonance (1969) 66, no. 3 (1986): 503–10. http://dx.doi.org/10.1016/0022-2364(86)90193-9.

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36

Grigor'ev, M. S., I. A. Charushnikova, Z. A. Starikova, N. N. Krot, and I. N. Polyakova***. "Crystal Structure of Double Np(V) Malonate with Co(NH3)63+in the Outer Sphere, [Co(NH3)6][NpO2L]2HL (L = OOCCH2COO)." Radiochemistry 46, no. 3 (2004): 232–35. http://dx.doi.org/10.1023/b:rach.0000031677.66293.4d.

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37

Alt, Helmut G., Heidi E. Engelhardt, Abbas Razavi, Marvin D. Rausch, and Robin D. Rogers. "Pentamethylcyclopentadienyl-, Acetylcyclopentadienyl- und Indenyl-dicarbonyl-AcetylenkompIexe des Vanadiums. Molekülstruktur von C9H7V(CO)2PhC2H / Pentamethylcyclopentadienyl, Acetylcyclopentadienyl and Indenyl Dicarbonyl Acetylene Complexes of Vanadium. Molecular Structure of C9H7V(CO)2PhC2H." Zeitschrift für Naturforschung B 43, no. 4 (1988): 438–44. http://dx.doi.org/10.1515/znb-1988-0409.

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AbstractThe photo-induced reaction of C5Me5V(CO)4 (1). (C5H4COMe)V(CO)4 (2) and C9H7V(CO)4 (3) with acetylenes R1C2R2 (R1, R2 = H. Me, Ph) yields the substitution products C5Me5V(CO)2R1C2R2 (4), (C5H4COMe)V(CO)2R1C2R2 (6) and C9H7V(CO)2R1C2R2 (7). One CO ligand of complexes 4 can be substituted by PMe3 affording complexes of the type C5Me5V(CO)(PMe3)R1C2R2 (5). The acetylene complexes 4-7 are characterized by their IR. 1H, 13C and 51V NMR as well as their mass spectra. In these compounds the alkyne ligand shows a hindered rotation around the metal alkyne bond axis. The rotation barrier (ΔG≠ =

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38

Fraser JA, Hugh B. "2017 WA Lee Lecture: The Australian Law of Contractual Penalties." QUT Law Review 18, no. 2 (2019): 111. http://dx.doi.org/10.5204/qutlr.v18i2.763.

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In 2005, in Ringrow Pty Ltd v BP Australia Pty Ltd,[1] the High Court (Gleeson CJ, Gummow, Kirby, Hayne, Callinan and Heydon JJ) observed that Lord Dunedin’s formulation in Dunlop Pneumatic Tyre Co Ltd v New Garage & Motor Co Ltd,[2] of the principles governing the identification, proof and consequences of penalties in contractual stipulations had endured for 90 years and had been applied countless times in the High Court and other courts. (The Court cited, as examples, O’Dea v Allstates Leasing System (WA) Pty Ltd,[3] Acron Pacific Ltd v Offshore Oil NL,[4] AMEV-UDC Finance Ltd v Austin,[

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Asemi, Zatollah, Fariba Raygan, Fereshteh Bahmani, et al. "The effects of vitamin D, K and calcium co-supplementation on carotid intima-media thickness and metabolic status in overweight type 2 diabetic patients with CHD." British Journal of Nutrition 116, no. 2 (2016): 286–93. http://dx.doi.org/10.1017/s0007114516001847.

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AbstractThis study was conducted to examine the effects of vitamin D, K and Ca co-supplementation on carotid intima-media thickness (CIMT) and metabolic status in overweight diabetic patients with CHD. This randomised, double-blind, placebo-controlled trial was conducted among sixty-six diabetic patients with CHD. Participants were randomly allocated into two groups to take either 5µg vitamin D, 90 µg vitamin K plus 500 mg Ca supplements (n 33) or placebo (n 33) twice a day for 12 weeks. Fasting blood samples were obtained at the beginning of the study and after the 12-week intervention period

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Qiao, Yu, Jin Yi, Shaohua Guo, et al. "Li2CO3-free Li–O2/CO2 battery with peroxide discharge product." Energy & Environmental Science 11, no. 5 (2018): 1211–17. http://dx.doi.org/10.1039/c7ee03341a.

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We demonstrate that a Li–O<sub>2</sub>/CO<sub>2</sub> battery cycles via formation of peroxodicarbonate (C<sub>2</sub>O<sub>6</sub><sup>2−</sup>) but not Li<sub>2</sub>CO<sub>3</sub>, and operates with a low charge potential of 3.5 V.

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Che, Chi-Ming, Yu-Pey Wang, Kap-Sun Yeung, Kwok-Yin Wong, and Shie-Ming Peng. "Synthesis and molecular structures of novel seven-co-ordinated oxo- and nitrido-rhenium(V) complexes of 2,2′ : 6′,2″ : 6″,2‴-quaterpyridine." J. Chem. Soc., Dalton Trans., no. 18 (1992): 2675–77. http://dx.doi.org/10.1039/dt9920002675.

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Elliot, David J., Sanna Haukilahti, David G. Holah, et al. "Reactions between Co(II), 1,2-bis(diphenylphosphino)ethane, and NaBH3CN in the presence and absence of CO. The crystal structure of bis(cyanotrihydroborato)tetrakis(N,N-dimethylformamide)cobalt(II)." Canadian Journal of Chemistry 66, no. 7 (1988): 1770–75. http://dx.doi.org/10.1139/v88-285.

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Reactions between Co(II), Diphos, and NaBH3CN lead to Co(BH3CN)2(Diphos)2, 1, or [Co(BH3CN)(Diphos)2]X, 2 (X = ClO4 or BPh4), and, in certain solvents, 2 reacts to produce [Co(CN)(Diphos)2](ClO4). Compound 1 can be reversibly converted to Co(BH3CN)2(DMF)4, 4, via Co(BH3CN)2(Diphos)(DMF). In addition, 1 reacts with CO to form the Co(I) and Co(III) compounds [Co(Diphos)2](CO)]X and [Co(Diphos)2(CN)2]X (X = BH3CN or BPh4). Single crystal X-ray diffraction studies of 4 show that the compound crystallizes in the triclinic space group [Formula: see text], with unit cell parameters a = 7.572(6), b =

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Moreno, C. M., G. Artola, and J. M. Sanchez. "Interaction between Ti-6%Al-4%V Alloys and Hardmetals Coated by Cathodic-Arc Technology." Materials Science Forum 492-493 (August 2005): 353–58. http://dx.doi.org/10.4028/www.scientific.net/msf.492-493.353.

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At present, milling of titanium based alloys for aerospace applications is mainly carried out with un-coated WC-Co carbide tools. The present work evaluates the chemical interaction of the Ti-6%Al-4%V alloy with these WC-Co commercial hardmetals. Strong decarburation induced by carbon diffusion to the Ti based alloy is observed at temperatures ranging from 750-1000°C. This reaction is responsible for the high adhesion found at the alloy-carbide interface. Different cathodic arc coatings have proved efficient in inhibiting such reaction and the associated adhesion to the Ti-6%Al-4%V alloy. Dela

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Kulkarni, Manasi B., Anagha M. Joshi та Rohini V. Patil. "A NOVEL HPTLC METHOD FOR SIMULTANEOUS DETERMINATION OF CO-ENZYME Q10 AND α-TOCOPHEROL IN BULK AND PHARMACEUTICAL FORMULATION". International Journal of Pharmacy and Pharmaceutical Sciences 10, № 10 (2018): 134. http://dx.doi.org/10.22159/ijpps.2018v10i10.28828.

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Objective: HPTLC Method for Simultaneous quantification of co-enzyme Q10 and α-tocopherol in bulk and capsule dosage form was developed and validated as per International Conference on Harmonization [(ICH) Q2 (R1)] guideline.Methods: The chromatograms were developed using a mobile phase of Toluene: ethyl acetate: chloroform (10:1:2 v/v/v) on Pre-coated silica 60F 254 plates and quantified by densitometric absorbance mode at 280 nm.Results: The Rf values were 0.77 and 0.87 for co-enzyme Q10 and α-tocopherol, respectively. The linearity of the method was found to be in the concentration range of

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Yan, Yabin, Yanlong Yu, Di Wu, Yajun Yang, and Yaan Cao. "Correction: TiO2/vanadate (Sr10V6O25, Ni3V2O8, Zn2V2O7) heterostructured photocatalysts with enhanced photocatalytic activity for photoreduction of CO2 into CH4." Nanoscale 10, no. 5 (2018): 2659. http://dx.doi.org/10.1039/c8nr90017e.

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Correction for ‘TiO<sub>2</sub>/vanadate (Sr<sub>10</sub>V<sub>6</sub>O<sub>25</sub>, Ni<sub>3</sub>V<sub>2</sub>O<sub>8</sub>, Zn<sub>2</sub>V<sub>2</sub>O<sub>7</sub>) heterostructured photocatalysts with enhanced photocatalytic activity for photoreduction of CO<sub>2</sub> into CH<sub>4</sub>′ by Yabin Yan et al., Nanoscale, 2016, 8, 949–958.

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Bond, Alan M., Ray Colton, Peter J. Mahon, Graeme A. Snook, and Wee T. Tan. "Voltammetric Oxidation of Solution and Solid Phases of Salts of [V(CO)6]-in Aqueous (Electrolyte) Media." Journal of Physical Chemistry B 102, no. 7 (1998): 1229–34. http://dx.doi.org/10.1021/jp972830d.

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Piron, J., P. Piret, J. Meunier-Piret, and M. van Meerssche. "Complexes du Fer-Carbonyle Avec L'acétylène et ses Dérivés. V. Structure de Fe2(CO)6 · (CH3C2CH3)2CO." Bulletin des Sociétés Chimiques Belges 78, no. 1-2 (2010): 121–30. http://dx.doi.org/10.1002/bscb.19690780115.

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Jong-Ho, Shinn, Seon Kwang-Il, Lee Dae-Hee, and Min Kyoung-Wook. "CO-to-H2 Abundance Ratio of the Foreground Gas of the Carina Nebula." Symposium - International Astronomical Union 217 (2004): 192–93. http://dx.doi.org/10.1017/s0074180900197438.

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We analyze CO and H2 absorption lines of the foreground molecular cloud in the Carina nebula. We use HST-STIS (Hubble Space Telescope - Space Telescope Imaging Spectrograph) & IUE (International Ultraviolet Explorer) INES data to analyze the A-X (v=0→2) absorption band of CO for several hot stars toward the Carina nebula, while 9 stars of them have FUSE (Far Ultraviolet Spectroscopic Explorer) spectra to analyze the (v=0→4) vibrational band in the Lyman series of H2. The column densities of CO and H2 varies in the vicinity of N(CO) ~ 1013cm−2 and N(H2) ~ 1019cm−2, respectively. The resulta

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Bruce, MI, DN Duffy та MG Humphrey. "Reactions of Transition-Metal Sigma-Acetylides. V. Synthesis and X-Ray Structure of Co2(µ-η2-PhC2Fe(Co)2(η-C5h5))(Co)6". Australian Journal of Chemistry 39, № 1 (1986): 159. http://dx.doi.org/10.1071/ch9860159.

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The reaction between Co2(CO)8 and Fe(C2Ph)(CO)2(η-C5H5) gave the title complex in 44% yield. The molecular structure was determined from a single-crystal X-ray diffraction study, and consists of the transition metal acetylide acting as a conventional μ- alkyne ligand to a Co2(CO)6 unit. Crystals are monoclinic, space group P21/n, with a 11.610(8), b 14.657(4), c 12.526(6)Ǻ, β 90.30(5)°, and Z 4; 1683 independent data were refined to R 0.080, Rw 0.087.

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Xing, Tian, Zhong‐Yu Wang, Yong‐Chang Sun, et al. "Co‐polymerization of propylene oxide and CO 2 using early transition metal (groups IV and V) metallocalix[ n ]arenes (n = 4, 6, 8)." Journal of Applied Polymer Science 138, no. 22 (2021): 50513. http://dx.doi.org/10.1002/app.50513.

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