Piano

F. Cattaneo, C. De Michelis - CISE. R. Cnideli, G.M. Piano - ENEL. Italy. 

Violin Treble Guitar Modern harp Piano... 

The structure of these complexes is not regular and has been described as 4 3 (C ) piano stool , which is obtained by slight distortion of a capped trigonal prism (C2d). 

Fliigel, m. wing flap, lobe, vane, branch casement (of a window) blade (as of a screw propeller) grand piano. 

BMIM]C1/A1C13 have been used for the synthesis of the piano stool complexes [Mn(CO)3(r -arene)] (Scheme 6.1-7) [12]. 

Scheme 6.1-7 The synthesis of [Mn(CO)3(ri -arene)]-F piano stool complexes in [BMIMJCI/AICIj.

It would be desirable to make sample prototype tooling and analyze the flow effects on a product that is likely to present a flow problem. In addition to the usual physical testing of the product, the use of photo-stress analysis techniques plus the exposure to selected solvents to check for stress crack characteristics would lead to changes in the product to minimize the effects of the molding on the product performance. As an example there have been cases in the past where piano keys with frozen-in stresses have been released from perspiration, leaving open flow lines (Chapter 5, STRESS ANALYSIS). 

Institute of Chemistry of Organometallic Compounds, Polo Scientifico Area Via Madonna del Piano 10 1-50019 Sesto Fiorentino Italy... 

Of course, commercially available transition metal complexes are stable at room temperature because they have achieved an 18-electron noble gas-like electronic configuration. Thus, molecules like iron pentacarbonyl [Fe(CO)s], ferrocene [Fe(C5H5)2], as well as piano-stool complexes such as C5H5Co(CO)2 are chemically quite inert. In order to study bimolecular reactions, it is necessary to first prepare unsaturated complexes. For studies using molecular beams, one approach is through photolysis of a stable volatile precursor in a supersonic nozzle. 

The synthesis of (80) from [Ircp Cl2]2 and 2,2 -biimidazole has been detailed.119 The X-ray structure of (80) shows the expected three-legged piano-stool arrangement round the Ir center. 

The synthesis of [Ircp Cl(bpy-cd)]Cl, where bpy-cd is a /3-cyclo-dextrin attached at the 6 position to a bpy ligand, is detailed.138 The complexes [Ircp (diimine)X]+, X = C1, H, diimine = bpy, phen, are active catalysts for the light-driven water-gas-shift reaction.139 The hydride complexes luminesce at 77 K and room temperature, whereas the chloride complexes do not.140 The three-legged piano-stool arrangement of the ligands in [Ircp (bpy)Cl]+ and [Ircp (4,4 -COOFl-bpy)Cl]+ is confirmed by X-ray crystallography.141,142 Further mechanistic studies on the catalytic cycle shown in reaction Scheme 11 indicate that Cl- is substituted by CO and the rate-determining step involves loss of C02 and H+ to leave the Ir1 species, which readily binds Fl+ to yield the lrIH hydride species.143... 

The complex [(cp )IrCl(2,2 -bpy-4,4 -COO(CH2)3-pyrrole)]C104 has a typical three-legged piano-stool structure, with short Ir-cp distances due to the strong 7r-acceptor properties of the bpy ligands.540... 

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