Hydrothermal chemistry of vanadium oxides with aromatic di- and tri-phosphonates in the presence of secondary metal copper(II) cationic complex subunits

CrystEngComm ◽  
2010 ◽  
Vol 12 (2) ◽  
pp. 446-469 ◽  
Author(s):  
Paul DeBurgomaster ◽  
Wayne Ouellette ◽  
Hongxue Liu ◽  
Charles J. O'Connor ◽  
Jon Zubieta
Keyword(s):  
Vanadium Oxides ◽  
Cationic Complex ◽  
Hydrothermal Chemistry

scholarly journals Using a Battery to Synthesize New Vanadium Oxides

2017 ◽  
Vol 2 (20) ◽  
pp. 5800-5804 ◽  
Author(s):  
Marie Guignard ◽  
Claude Delmas
Keyword(s):  
Vanadium Oxides

Synthesis, structural characterization and catalytic activity of chlororuthenium(II) complexes with substituted Schiff base/phosphine ancillary ligands

2020 ◽  
Vol 75 (9-10) ◽  
pp. 851-857
Author(s):  
Chong Chen ◽  
Fule Wu ◽  
Jiao Ji ◽  
Ai-Quan Jia ◽  
Qian-Feng Zhang
Keyword(s):  
Schiff Base ◽  
Catalytic Activity ◽  
Structural Characterization ◽  
Room Temperature ◽  
Molecular Structures ◽  
Cationic Complex ◽  
Neutral Complex ◽  
Ancillary Ligands ◽  
X Ray ◽  
X Ray Crystallography

AbstractTreatment of [(η6-p-cymene)RuCl2]2 with one equivalent of chlorodiphenylphosphine in tetrahydrofuran at reflux afforded a neutral complex [(η6-p-cymene)RuCl2(κ1-P-PPh2OH)] (1). Similarly, the reaction of [Ru(bpy)2Cl2·2H2O] (bpy = 2,2′-bipyridine) and chlorodiphenylphosphine in methanol gave a cationic complex [Ru(bpy)2Cl(κ1-P-PPh2OCH3)](PF6) (2), while treatment of [RuCl2(PPh3)3] with [2-(C5H4N)CH=N(CH2)2N(CH3)2] (L1) in tetrahydrofuran at room temperature afforded a ruthenium(II) complex [Ru(PPh3)Cl2(κ3-N,N,N-L1)] (3). Interaction of the chloro-bridged complex [Ru(CO)2Cl2]n with one equivalent of [Ph2P(o-C6H4)CH=N(CH2)2N(CH3)2] (L2) led to the isolation of [Ru(CO)Cl2(κ3-P,N,N-L2)] (4). The molecular structures of the ruthenium(II) complexes 1–4 have been determined by single-crystal X-ray crystallography. The properties of the ruthenium(II) complex 4 as a hydrogenation catalyst for acetophenone were also tested.

Reactivities of m-xylene, phenol and benzene on vanadium oxides layered on TiO2 and ZrO2

1991 ◽  
Vol 45 (2) ◽  
pp. 265-269 ◽  
Author(s):  
F. Hatayama ◽  
T. Ohno ◽  
T. Maruoka ◽  
H. Miyata
Keyword(s):  
Vanadium Oxides

Synthesis of Novel Vanadium Oxide Nanotubes and Nanofibers

2002 ◽  
Vol 740 ◽  
Author(s):  
Samuel T. Lutta ◽  
Hong Dong ◽  
Peter Y. Zavalij ◽  
M. Stanley Whittingham
Keyword(s):  
Thermal Analysis ◽  
Vanadium Oxide ◽  
Electrochemical Behavior ◽  
Redox Reactions ◽  
Sol Gel ◽  
Vanadium Oxides ◽  
Organic Polymer ◽  
Fibrous Morphology ◽  
Surfactant Templates ◽  
Vanadium Oxide Nanotubes

ABSTRACTWe are exploring the synthesis and properties of structured vanadium oxides mainly nanotubes and nanorods. Nanotubes initially formed with surfactant templates have been readily exchanged with simple cations without change of the basal-plane structure. These compounds contain d-like vanadium oxide layers with the vanadium in VO6 octahedra. This structure is particularly suitable for redox reactions. In this paper we report on synthesis of vanadium oxide, (NH4)xV2O5-d·nH2O rods using organic polymer as template. This compound has been synthesized by sol-gel reaction and subsequent hydrothermal treatment. TGA, SEM, XRD and FTIR were used to characterize this compound. Thermal analysis of this compound shows that the fibrous morphology is maintained when it is heated in nitrogen and oxygen above 300 °C. However, in both cases the size of the fibers decreases. Performance of this compound as cathode material in secondary electrolyte has been investigated using LiPF6 as electrolyte. A capacity of 140 mAh/g was obtained which remained fairly constant with up to at least 10 cycles. We also investigated electrochemical behavior of thermal products.

Paramagnetic Centers Created Under Mechanochemical Treatment of Mixed Molybdenum-Vanadium Oxides

2016 ◽  
Vol 47 (6) ◽  
pp. 575-588 ◽  
Author(s):  
I. V. Kolbanev ◽  
E. N. Degtyarev ◽  
A. N. Streletskii ◽  
A. I. Kokorin
Keyword(s):  
Vanadium Oxides ◽  
Mechanochemical Treatment ◽  
Paramagnetic Centers

scholarly journals Crystal structures of [Mn(bdc)(Hspar)2(H2O)0.25]·2H2O containing MnO6+1capped trigonal prisms and [Cu(Hspar)2](bdc)·2H2O containing CuO4squares (Hspar = sparfloxacin and bdc = benzene-1,4-dicarboxylate)

2016 ◽  
Vol 72 (1) ◽  
pp. 96-101
Author(s):  
Zhe An ◽  
Jing Gao ◽  
William T. A. Harrison
Keyword(s):  
Hydrogen Bonds ◽  
Water Molecule ◽  
Crystal Structures ◽  
Metal Ion ◽  
Three Dimensional ◽  
Trigonal Prism ◽  
Planar Geometry ◽  
Cationic Complex ◽  
Counter Ion ◽  
Square Planar

The syntheses and crystal structures of 0.25-aqua(benzene-1,4-dicarboxylato-κ2O,O′)bis(sparfloxacin-κ2O,O′)manganese(II) dihydrate, [Mn(C8H4O4)(C19H22F2N4O3)2(H2O)0.25]·2H2O or [Mn(bdc)(Hspar)2(H2O)0.25]·2H2O, (I), and bis(sparfloxacin-κ2O,O′)copper(II) benzene-1,4-dicarboxylate dihydrate, [Cu(C19H22F2N4O3)2](C8H4O4)·2H2O or [Cu(Hspar)2](bdc)·2H2O, (II), are reported (Hspar = sparfloxacin and bdc = benzene-1,4-dicarboxylate). The Mn2+ion in (I) is coordinated by twoO,O′-bidentate Hspar neutral molecules (which exist as zwitterions) and anO,O′-bidentate bdc dianion to generate a distorted MnO6trigonal prism. A very long bond [2.580 (12) Å] from the Mn2+ion to a 0.25-occupied water molecule projects through a square face of the prism. In (II), the Cu2+ion lies on a crystallographic inversion centre and a CuO4square-planar geometry arises from its coordination by twoO,O′-bidentate Hspar molecules. The bdc dianion acts as a counter-ion to the cationic complex and does not bond to the metal ion. The Hspar ligands in both (I) and (II) feature intramolecular N—H...O hydrogen bonds, which closeS(6) rings. In the crystals of both (I) and (II), the components are linked by N—H...O, O—H...O and C—H...O hydrogen bonds, generating three-dimensional networks.

scholarly journals Structure, properties, and MEMS and microelectronic applications of vanadium oxides

Sadhana ◽  
2009 ◽  
Vol 34 (4) ◽  
pp. 531-542 ◽  
Author(s):  
Robert B. Darling ◽  
Shiho Iwanaga
Keyword(s):  
Vanadium Oxides ◽  
Structure Properties

Solvent, coordination and hydrogen-bond effects on the chromic luminescence of the cationic complex [(phen)(H2O)Re(CO)3]+

2016 ◽  
Vol 40 (7) ◽  
pp. 6451-6459 ◽  
Author(s):  
Pablo Mella ◽  
Karina Cabezas ◽  
Carla Cerda ◽  
Marjorie Cepeda-Plaza ◽  
German Günther ◽  
...  
Keyword(s):  
Hydrogen Bond ◽  
Hydrogen Bonding ◽  
Solvent Polarity ◽  
Cationic Complex ◽  
Unusual Behavior ◽  
Luminescence Emission

The unusual behavior of the solution luminescence emission of [(phen)(H2O)Re(CO)3]+(CF3SO3)− depends on the solvent polarity, and coordinating and hydrogen bonding ability.

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