Results 11 to 20 of about 925 (184)
Two in one: the bismuth bromido clusters in [Bi6Cp*6Br9][Bi7Br24]
The reaction of [FeCp*(CO)2]2 in CH2Cl2 with BiBr3 in a 1:1 molar ratio gave the novel bismuth compound [Bi6Cp*6Br9][Bi7Br24] (1), which is composed of a cationic and an anionic bismuth bromido cluster: the cation is based on a hexanuclear bismuth {Bi6 ...
Wójcik Katarzyna +4 more
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Crystal structure of di-n-butylbis(η5-pentamethylcyclopentadienyl)hafnium(IV)
The crystal structure of the title compound, [Hf(C10H15)2(C4H9)2], reveals two independent molecules in the asymmetric unit. The diffraction experiment was performed with a racemically twinned crystal showing a 0.529 (5):0.471 (5) component ratio.
Perdita Arndt +4 more
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An NHC‐Coordinated Silicon/Sulfur Analogue of an Acyl Carbene
An NHC complex of an Si/S analogue of an acyl carbene is synthesized by the reaction of a disilyne with a cyclic thiourea. The observed Si2S three‐membered ring with unsymmetrical Si─S distances and a Si─Si single bond is consistent with intramolecular coordination of the silathioacyl sulfur to the silylene center.
Takuto Toyooka +2 more
wiley +2 more sources
In the molecular structure of the dinuclear title compound [η5-(C5(CH3)5)(CO)Fe{(μ-BCl)(μ-CO)}PtCl(P(C6H11)3)]·C6H6, the two metal atoms, iron(II) and platinum(II), are bridged by one carbonyl (μ-CO) and one chloridoborylene ligand (μ-BCl). The PtII atom
Holger Braunschweig, Thomas Kramer
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Protic molecules containing strong O─H or N─H bonds typically resist hydrogen‐atom abstraction because of the high reactivity of the resulting heteroatom‐centered radicals. However, association of the protic molecules with redox‐active Lewis acids can provide powerful hydrogen‐atom donors or proton‐coupled‐electron‐transfer reagents.
Petra Vojáčková, Armido Studer
wiley +2 more sources
Crystal structures of titanium–aluminium and –gallium complexes bearing two μ2-CH3 units
The isotypic crystal structures of two titanocene complexes containing an EMe3 unit (E = Al, Ga; Me = methyl) with two μ2-coordinating methyl groups, namely [μ-1(η5)-(adamantan-1-yl-2κC1)cycylopentadienyl]di-μ2-methyl-methyl-2κC-[1(η5 ...
Tim Oswald +4 more
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(Glycol-κ2O,O′)nitrosyl(η5-pentamethylcyclopentadienyl)ruthenium(II) bis(trifluoromethanesulfonate)
The title compound, [Ru(C10H15)(NO)(HOCH2CH2OH)](CF3SO3)2, possesses a three-legged piano-stool geometry around the Ru atom, with an average Ru—O distance of 2.120 (6) Å and an Ru—N—O angle of 159.45 (14)° ...
Milan Gembicky +2 more
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Iodidobis(η5-pentamethylcyclopentadienyl)titanium(III)
In the title complex molecule, [Ti(C10H15)2I], the paramagnetic Ti(III) atom is coordinated by two pentamethylcyclopentadienyl (Cp*) ligands and one iodide ligand. The two Cp* ligands are in a staggered orientation.
Monty Kessler +2 more
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The title compound, (1,4,7,10,13,16-hexaoxacyclooctadecane-κ6O)potassium dicarbonyl(η5-pentamethylcyclopentadienyl)ferrate(II), [K(C12H24O6)][Fe(C10H15)(CO)2], consists of K+ cations embedded in 18-crown-6 molecules and [FeCp*(CO)2]− anions.
Yoshiyuki Mizuhata +3 more
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Rh(III)-catalyzed directed C–H bond amidation of ferrocenes with isocyanates
[RhCp*(OAc)2(H2O)] [Cp* = pentamethylcyclopentadienyl] catalyzed the C–H bond amidation of ferrocenes possessing directing groups with isocyanates in the presence of 2 equiv/Rh of HBF4·OEt2.
Satoshi Takebayashi +3 more
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