Photochemical reactions of Ru3(CO)12 involving metalmetal bond fission

Photolysis of Ru₃(CO)₁₂ in the presence of donor ligands rapidly produces monomeric ruthenium species.     

New colorimetric and fluorimetric methods for the determination of 1,4-cyclohexanedione

1,4-Cyclohexanedione has been determined by reaction with o-phthalaldehyde in sulfuric acid. The determinations depend on the formation of a dicationic salt of pentacenequinone. A sensitive and highly selective fluorimetric method is recommended, but the reaction can also be used spectrophotometrically. Many organic compounds, as well as the isomers of 1,4-cyclohexanedione, give negative results. A spot test is described which can be used for quick preliminary investigations of complex mixtures for I,4-cyclohexanedione.     

A comparison of SCF-Xα and extended Hückel methods for metal clusters

A comparison of some results from Xα-scattered wave (Xα-SW) and extended Hückel (EH) calculations for metal clusters is given. It is found that small clusters of atoms (≈ 13 atoms) using the Xα-SW method reproduce many of the features of the electronic structure of the bulk metals, whereas this is not the case for the same clusters using the EH method. A more systematic approach to EH parametrizations is suggested in order to make this method a more viable approach to treating metal clusters.     

Mössbauer studies on the series La1-xSrxFeO3

Mössbauer spectra have been recorded at 4.2 and 300 K on the series La_1–x Sr _x FeO₃, wherex varies from 0 to 1.0 in steps of 0.1. Neutron diffraction experiments have shown that the crystal structure is orthorhombic for 0x<0.3, rhombohedral for 0.4x0.7, and cubic for 0.8<x1.0. Mössbauer spectra at 4.2 K are composed of magnetic sextet components arising from different charge states of iron ions. In the orthorhombic and rhombohedral phases, the charge states Fe³⁺ and Fe⁵⁺ coexist. In the cubic phase, iron is present as Fe³⁺ and Fe⁴⁺ states. At 300 K, the samples are magnetically ordered in the range 0 x0.3 and the coexistence of Fe³⁺ and Fe⁵⁺ remains. For samples 0.4x1.0, the samples are paramagnetic. Fits to these spectra require two components, one corresponding to an Fe⁴⁺ state, the other being best described as an Fe³⁺ ion forx0.7 but forx>0.7 having a mean charge state which increases to 3.5 forx=1.0.     

Direct product and decomposition of certain physically important algebras

I consider the direct product algebra formed from two isomorphic Clifford algebras. More specifically, for an element x in each of the two component algebras I consider elements in the direct product space with the form x x. I show how this construction can be used to model the algebraic structure of particular vector spaces with metric, to describe the relationship between wavefunction and observable in examples from quantum mechanics, and to express the relationship between the electromagnetic field tensor and the stress-energy tensor in electromagnetism. To enable this analysis I introduce a particular decomposition of the direct product algebra.