SiO in a complex: The first silanone that is stable at room temperature (3) is reported. The two-step synthesis involves carbonylation of the silylidyne complex 1 to give the chromiosilylene 2, followed by oxidation of 2 with N2 O. Silanone 3 features a polar, short SiO bond (1.526(3) Å) to a trigonal-planar-coordinated silicon center and reacts with water to give the dihydroxysilyl complex.
Azurin*, a by-product of heterologous expression of the gene encoding the blue copper protein azurin from Pseudomonas aeruginosa in Escherichia coli, was characterized by chemical analysis and electrospray ionization mass spectrometry, and its structure determined by X-ray crystallography. It was shown that azurin* is native azurin with its copper atom replaced by zinc in the metal binding site. Zinc is probably incorporated in the apo-protein after its expression and transport into the periplasm. Holo-azurin can be reconstituted from azurin* by prolonged exposure of the protein to high copper ion concentrations or unfolding of the protein and refolding in the presence of copperions.An X-ray crystallographic analysis of azurin* at 0.21-nm resolution revealed that the overall structure of azurin is not perturbed by the metal exchange. However, the geometry of the co-ordination sphere changes from trigonal bipyramidal in the case of copper azurin to distorted tetrahedral for the zinc protein. The copper ligand Met121 is no longer co-ordinated to zinc which adopts a position close to the carbonyl oxygen atom from residue Gly45.The polypeptide structure surrounding the metal site undergoes moderate reorganization upon zinc binding. The largest displacement observed is for the carbonyl oxygen from residue Gly45, whch is involved in copper and zinc binding. It moves by 0.03 nm towards the zinc, thereby reducing its distance to the metal from 0.29 nm in the copper protein to 0.23 nm in the derivative.
Silylene with a carbene carabiner: The synthesis, structure, and some reactions of a stable carbene adduct of dibromosilylene, SiBr2(Idipp) (see picture; Idipp=1,3‐bis(2,6‐diisopropylphenyl)‐ imidazol‐2‐ylidene), are described. SiBr2(Idipp) was characterized by X‐ray crystallography, NMR spectroscopy, and theoretical methods.
The reaction of SiCl4 with an excess of (PPN)N3 (PPN+ = [(Ph3P)2N]+) affords selectively (PPN)2[Si(N3)6] (1). Simultaneous thermal analysis (TG-DTA) shows that the hexaazidosilicate salt is remarkably stable, melting at Tonex = 214 degrees C. Melting of 1 is followed by two distinct exothermic decomposition processes at Ton = 256 and 321 degrees C, the first one involving elimination of N2 and the second one degradation of the PPN cations and evolution of Si(N3)4, N2, and some HN3. The crystal structure of 1 consists of discrete PPN+ cations and S2 symmetric [Si(N3)6]2- anions, which have a very rare, octahedral SiN6 framework and the highest nitrogen content (90%) among the hexaazidometallates reported so far. The IR, Raman, 29Si, and 14N NMR spectra of 1 in CH3CN suggest in combination with the calculated spectra the presence of intact [Si(N3)6]2--anions of S6 symmetry in solution. Geometry optimizations with various methods and basis sets show an S6 symmetric structure to be the most stable [Si(N3)6]2- isomer, the calculated bonding parameters comparing well with the experimental values.
The first N-heterocyclic carbene adducts of arylchlorosilylenes are reported and compared with the homologous germanium compounds. The arylsilicon(II) chlorides SiArCl(Im-Me(4)) [Ar=C(6)H(3)-2,6-Mes(2) (Mes=C(6)H(2)-2,4,6-Me(3)), C(6)H(3)-2,6-Trip(2) (Trip=C(6)H(2)-2,4,6-iPr(3))] were obtained selectively on dehydrochlorination of the arylchlorosilanes SiArHCl(2) with 1,3,4,5-tetramethylimidazol-2-ylidene (Im-Me(4)). The analogous arylgermanium(II) chlorides GeArCl(Im-Me(4)) were prepared by metathetical exchange of GeCl(2)(Im-Me(4)) with LiC(6)H(3)-2,6-Mes(2) or addition of Im-Me(4) to GeCl(C(6)H(3)-2,6-Trip(2)). All compounds were fully characterized. Density functional calculations on ECl(C(6)H(3)-2,6-Trip(2))(Im-Me(4)), where E=Si, Ge, at different levels of theory show very good agreement between calculated and experimental bonding parameters, and NBO analyses reveal similar electronic structures of the two aryltetrel(II) chlorides. The low gas-phase Gibbs free energy of bond dissociation of SiCl(C(6)H(3)-2,6-Trip(2))(Im-Me(4)) (Delta(calcd) degrees=28.1 kJ mol(-1)) suggests that the carbene adducts SiArCl(Im-Me(4)) may be valuable transfer reagents of the arylsilicon(II) chlorides SiArCl.
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