In connection with our investigations on the photoelectron (PE) spectra of olefin-transition metal tricarbonyls and bisbutadiene-iron-carbonyls we became interested in the PE spectrum of tricarbonyl-cyclooctatetraene-iron (1) and its electronic structure. The He(I) PE spectrum of 1 has been reported recently [5] and a qualitative interpretation was given, based on a correlation with the PE spec...

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The racemic (6-cyclo-heptadienyl)Fe(CO)(3)(+) cation ((±)-7), prepared from cyclooctatetraene, was treated with a variety of carbon and heteroatom nucleophiles. Attack took place at the less hindered C(1) dienyl carbon and decomplexation of the (cycloheptadiene)Fe(CO)(3) complexes gave products rich in functionality for further synthetic manipulation. In particular, a seven-step route was devel...

The mechanisms of the thermolytic decomposition of a series of unsaturated cyclic C8 hydrocarbons adsorbed on a platinum(111) single crystal surface are described. This study both confirms and extends the results reported by Frei and Campbell which corrected errors in an earlier report from our laboratory on the mechanisms of thermal decomposition seen in this adsorbate system. We find that the...

Acetylene cyclotrimerization catalyzed by palladium has been shown to proceed via the initial rapid formation of a C 4 H 4 species. This can either react with adsorbed acetylene to form benzene or alternatively, as has been recently suggested, it can dimerize forming cyclooctatetraene which decomposes to yield benzene. Trimerization is sufficiently fast that reaction is desorption rather than s...

The synthesis of the cyclooctatetraene dianion (COT(2-)) fused at the [e]-position of trans-10b,10c-dimethyl-10b,10c-dihydropyrene (DHP) is described, and by comparison of (1)H NMR properties and NICSAv to the analogous benzene fused DHP, the relative aromaticity of the dianion is found to be at least as great as that of benzene, and substantially larger than that of the cyclopentadienide anion.

We report the synthesis of TiO2 nanoparticles that uses the low-temperature reaction of low-valent organometallic precursors. Bis(cyclooctatetraene)titanium reacts with dimethyl sulfoxide in organic solution at temperatures as low as room temperature to produce TiO2. In the absence of any supporting ligand, the reaction gives precipitation of amorphous TiO2 powder; however, in the presence of b...

Abstract Tridecacyclene tetraimide, TCTI , an electron‐deficient non‐benzenoid nanocarbon with a C 56 N 4 polycyclic framework was obtained in concise synthesis. has non‐planar structure and forms π‐stacked dimers the solid state. In solution, it undergoes eight single‐electron reductions, yielding range of negatively charged states up to octaanion. Except for latter species, which remarkably l...