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Iodidobis(≠5-penta-methyl-cyclo-penta-dien-yl)titanium(III)
In the title complex mol-ecule, [Ti(C10H15) 2I], the paramagnetic Ti(III) atom is coordinated by two penta-methyl-cyclo-penta-dienyl (Cp*) ligands and one iodide ligand. The two Cp*ligands are in a staggered orientation. The coordination geometry at the titanium atom can be described as distorted trigonal-planar.
(tert-Butylimido)bis(η5-cyclopenta-dienyl) pyridinezirconium(IV)
The title compound, [Zr(C5H5)2(C 4H9N)(C5H5N)], was obtained from the reaction of (C5H5)2Zr(py)(η2- Me3SiC2SiMe3) (py is pyridine) and tBuN=C=NtBu alongside the formation of (C 5H5)2Zr(CNtBu)(2-Me 3SiC2SiMe3). The zirconium atom is coordinated in a distorted tetrahedral geometry by two cyclopentadienyl ligands, a pyridine ligand, and a tertbutylimido ligand via a Zr=N double bond. The tertbutyl group is disordered over two positions in a 0.634 (5):0.366 (5) ratio.
Crystal structure of 1-bis(((1R,2S,5R)-2-isopropyl-5-methylcyclohexyl) cyclopentadienyl)-1-trimethylphosphine-2,3-bis(trimethylsilyl) -1-hafnacycloprop-2-ene-hexane (1:0.5), (HfC8H18Si 2)(C15H22)2(PC3H 9) · 0.5C6H14
C44H78HfPSi2, tetragonal, P4 1212 (no. 92), a = 14.9634(2) Å, c = 44.9270(8) Å, V = 10059.3 Å3, Z = 8, Rgt(F) = 0.026, wRref(F2) = 0.073, T = 200 K. © by Oldenbourg Wissenschaftsverlag, München.
Intermolecular hydrogen bonding in isostructural pincer complexes [OH-(t-BuPOCOPt-Bu)MCl] (M = Pd and Pt)
In the crystal structure of the isostructural title compounds, namely {2,6-bis[(di-tert-butylphosphanyl)oxy]-4-hydroxyphenyl}chloridopalladium(II), [Pd(C22H39O3P2)Cl], 1, and {2,6-bis[(di-tert-butylphosphanyl)oxy]-4-hydroxyphenyl}chloridoplatinum(II), [Pt(C22H39O3P2)Cl], 2, the metal centres are coordinated in a distorted square-planar fashion by the POCOP pincer fragment and the chloride ligand. Both complexes form strong hydrogen-bonded chain structures through an interaction of the OH group in the 4-position of the aromatic POCOP backbone with the halide ligand.
[Bis(diphenylphosphanyl)dimethylsilane κ2P,P′] tetracarbonylchromium(0)
The title compound, [Cr(C26H26P2Si)(CO) 4], was obtained by the reaction of Ph2PSiMe 2PPh2 with Cr(CO)6 in refluxing toluene by ligand exchange. The CrC4P2 coordination geometry at the Cr atom is distorted octa-hedral, with a P - Cr - P bite angle of 80.27 (1)°.
Crystal structure of bis(pentamethylcyclopentadienyl)(1-tert- butylisocyanido)-2-trimethylsilyl-3-[(trimethylsilyl)ethynyl]-hafnacyclopropene, (C10H15)2(C5H9N) Hf(C10H18Si2)
C35H57HfNSi2, monoclinic, P121/c1 (no. 14), a = 10.7410(3) Å, b = 16.2302(5) Å, c = 21.6945(7) Å, β = 104.512(2)°, V = 3661.3 Å3, Z = 4, R gt(F) = 0.049, wRref(F2) = 0.138, T = 200 K. © 2014 Oldenbourg Wissenschaftsverlag, München.
[2,2-Bis(diphenylphosphanyl)propane κ2P,P0] tetracarbonylchromium(0)dichloromethane monosolvate
The title compound, [Cr(C27H26P2)(CO) 4]·CH2Cl2, was obtained by the reaction of Ph2PCMe2PPh2 with Cr(CO)6 in refluxing toluene by substitution of two carbonyl ligands. The CrC 4P2 coordination geometry at the Cr atom is distorted octa-hedral, with a P - Cr - P bite angle of 70.27 (2)°.
Crystal structure of bis(pentamethylcyclopentadienyl)-(4,4′-di-tert- butylbipyridyl)hafnium(IV)-hexane (1:0.5), Hf(C10H15) 2(C18H24N2) · 0.5C 6H14
C41H61HfN2, monoclinic, P21/n (no. 14), a = 13.4410(4) Å, b = 13.9983(6) Å, c = 21.1996(8) Å, β = 98.144(3)°, V = 3948.5 Å3, Z = 4, Rgt(F) = 0.051, wRref(F2) = 0.121,T = 200 K. © 2014 Oldenbourg Wissenschaftsverlag, München.
Bis(dimethyl sulfoxide)hydridobis(triphenylphosphane)cobalt(I)
The title compound, [CoH(C18H15P)2(C 2H6OS)2], was synthesized by the reaction of chloridotris(triphenyl-phosphane)cobalt(I), [ClCo(PPh3)3], in the presence of one equivalent potassium hydridotris(pyrazol-yl)borate in dimethyl sulfoxide. The structure displays a distorted trigonal-pyramidally coordinated cobalt(I) atom, with two phosphane ligands and one DMSO ligand in the equatorial plane. The coordination is completed by one further DMSO ligand and the anionic hydride in the axial positions.