New Complexes of Molybdenum(II) and Tungsten(II) with a C,N-Chelated Stannylene

2007 ◽  
Vol 72 (5-6) ◽  
pp. 629-636 ◽  
Author(s):  
Zdeňka Padělková ◽  
Ivana Císařová ◽  
Karla Fejfarová ◽  
Jana Holubová ◽  
Aleš Růžička ◽  
...  
Keyword(s):  
Transition Metal ◽  
Equatorial Plane ◽  
X Ray Diffraction ◽  
X Ray ◽  
Bond Forming ◽  
Nitrogen Donor ◽  
And Tungsten

Two new complexes of [Sn{2-[(CH3)2NCH2]C6H4}2] with [Mo(η5-C5H5)(CO)3Cl] and [W(η5-C5H5)(CO)3Cl], respectively, were prepared via insertion of stannylene into the Mo-Cl or W-Cl bond forming thus the transition metal-tin bond. These complexes were studied by IR, NMR and X-ray diffraction techniques. The tin atom in these complexes is five-coordinated with the carbon atoms of ligands and transition metal in equatorial plane and the chlorine and the nitrogen donor atoms in axial positions. The attempts to photolyse, reduce or fluorinate the prepared complexes and characterize the products of these reactions failed.

Preparation, properties and structure of some intermediate nido- and arachno-monocarbaboranes

1981 ◽  
Vol 46 (10) ◽  
pp. 2345-2353 ◽  
Author(s):  
Karel Baše ◽  
Bohumil Štíbr ◽  
Jiří Dolanský ◽  
Josef Duben
Keyword(s):  
Transition Metal ◽  
Metal Complexes ◽  
Transition Metal Complexes ◽  
Nmr Spectra ◽  
Liquid Ammonia ◽  
X Ray Diffraction ◽  
X Ray ◽  
H Nmr ◽  
Starting Compound

The 6-N(CH3)3-6-CB9H11 carbaborane reacts with sodium in liquid ammonia with the formation of 6-CB9H12- which was used as a starting compound for preparing the 4-CB8H14, 9-L-6-CB9H13 (L = (CH3)2S, CH3CN and P(C6H5)3), 1-(η5-C5H5)-1,2-FeCB9H10-, and 2,3-(η5-C5H5)2-2,31-Co2CB9H10- carboranes. The 4-CB8H14 compound was dehydrogenated at 623 K to give 4-(7)-CB8H12 carborane. Base degradation of 6-N(CH3)3-6-CB9H11 in methanol resulted in the formation of 3,4-μ-N(CH3)3CH-B5H10. The structure of all compounds was proposed on the basis of their 11B and 1H NMR spectra and X-ray diffraction was used in the case of the transition metal complexes.

Characterization on the Microstructures and Optical Performances of TiO2 Doped with Transition Metals

2014 ◽  
Vol 887-888 ◽  
pp. 388-394 ◽  
Author(s):  
Xin Hua Liu ◽  
Yi Deng ◽  
Yu Chuan Zhang ◽  
Yin Hang Zhou
Keyword(s):  
Transition Metal ◽  
Metal Ions ◽  
Photoelectron Spectroscopy ◽  
Transition Metal Ions ◽  
Ultraviolet Region ◽  
Visible Light Region ◽  
X Ray Diffraction ◽  
X Ray ◽  
Light Region ◽  
Cu Ions

The structures and optical performances of TiO2doped with 4thperiodic transition metal ions were investigated in this paper. The characterization results of X-ray photoelectron spectroscopy and X-ray diffraction showed that the transition metal ions existed in oxidative states, and composites formed because of the reaction between doped metal ions and TiO2. The absorption spectroscopy of TiO2doped with zinc was mainly in ultraviolet region, close to that of the pure TiO2. While for TiO2doped with other transition metal ions including V, Cr, Mn, Fe, Co, Ni and Cu ions, the absorption spectroscopies covered ultraviolet region and visible light region, much broader than that of the pure TiO2.

Synthesis, crystallization and Hirshfeld surface analysis of transition metal carboxylate pentapyridines

CrystEngComm ◽  
2021 ◽  
Author(s):  
Marissa K. Melvin ◽  
Brian W. Skelton ◽  
Paul K. Eggers ◽  
Colin L. Raston
Keyword(s):  
Transition Metal ◽  
Surface Analysis ◽  
Coordination Complexes ◽  
Hirshfeld Surface ◽  
Hirshfeld Surface Analysis ◽  
Metal Coordination ◽  
Metal Carboxylate ◽  
X Ray Diffraction ◽  
X Ray ◽  
Directing Effect

Single X-ray diffraction studies and Hirshfeld surface analysis of three transition metal coordination complexes of Py5Me2COOH reveals the ligand's diverse coordination utility and the structure directing effect of the carboxylate moiety.

scholarly journals Bis(dicarbollide) Complexes of Transition Metals as a Platform for Molecular Switches. Study of Complexation of 8,8′-Bis(methylsulfanyl) Derivatives of Cobalt and Iron Bis(dicarbollides)

Molecules ◽  
2020 ◽  
Vol 25 (23) ◽  
pp. 5745
Author(s):  
Sergey A. Anufriev ◽  
Sergey V. Timofeev ◽  
Alexei A. Anisimov ◽  
Kyrill Yu. Suponitsky ◽  
Igor B. Sivaev
Keyword(s):  
Solid State ◽  
Transition Metal ◽  
Molecular Switches ◽  
X Ray Diffraction ◽  
Chelate Complexes ◽  
X Ray ◽  
Complexes Of Transition Metals ◽  
Silver Palladium ◽  
Solid State Structures ◽  
Derivatives Of

Complexation of the 8,8′-bis(methylsulfanyl) derivatives of cobalt and iron bis(dicarbollides) [8,8′-(MeS)2-3,3′-M(1,2-C2B9H10)2]− (M = Co, Fe) with copper, silver, palladium and rhodium leads to the formation of the corresponding chelate complexes, which is accompanied by a transition from the transoid to the cisoid conformation of the bis(dicarbollide) complex. This transition is reversible and can be used in design of coordination-driven molecular switches based on transition metal bis(dicarbollide) complexes. The solid-state structures of {(Ph3P)ClPd[8,8′- (MeS)2-3,3′-Co(1,2-C2B9H10)2-κ2-S,S′]} and {(COD)Rh[8,8′-(MeS)2-3,3′-Co(1,2-C2B9H10)2-κ2-S,S′]} were determined by single crystal X-ray diffraction.

scholarly journals Radial X‐Ray Diffraction Study of Superhard Early Transition Metal Dodecaborides under High Pressure

2019 ◽  
Vol 29 (22) ◽  
pp. 1900293 ◽  
Author(s):  
Jialin Lei ◽  
Georgiy Akopov ◽  
Michael T. Yeung ◽  
Jinyuan Yan ◽  
Richard B. Kaner ◽  
...  
Keyword(s):  
High Pressure ◽  
Transition Metal ◽  
Diffraction Study ◽  
X Ray Diffraction ◽  
X Ray ◽  
Early Transition Metal ◽  
Early Transition

Transition Metal-Gallium Ordering In HfCoGa2 And HfNiGa2

2003 ◽  
Vol 58 (1) ◽  
pp. 16-21 ◽  
Author(s):  
Martin Schlüter ◽  
Birgit Heying ◽  
Rainer Pöttgen
Keyword(s):  
Transition Metal ◽  
Single Crystals ◽  
Crystal Chemistry ◽  
Glassy Carbon ◽  
Previous Investigation ◽  
Subsequent Annealing ◽  
X Ray Diffraction ◽  
X Ray ◽  
Arc Melting

Abstract The gallides HfCoGa2 and HfNiGa2 were synthesized by arc-melting of the elements and subsequent annealing in glassy carbon crucibles. Their structures have been reinvestigated by X-ray diffraction on powders and single crystals: I4mm, a = 1222.4(1), c = 812.0(1) pm, wR2 = 0.0766, 1464 F2 values, 64 variables, BASF = 0.41(2) for HfCoGa2 and a = 1224.0(2), c = 809.3(2) pm, wR2 = 0.0609, 1499 F2 values, 63 variables for HfNiGa2. In contrast to a previous investigation (Dopov. Akad. Nauk Ukr. RSR, Ser. A, 51 (1988)) we observe a fully ordered arrangement of the transition metal and gallium atoms. The crystal chemistry of these gallides is briefly discussed.

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