Structures of the solvated organic-based ferromagnet decamethylferrocenium tetracyanoethenide, [FeCp*2](*+)[TCNE]*- x yRCN (R = Me, Et, n-Pr).

The ferromagnet [FeCp*(2)][TCNE] (T(c) = 4.80 K) has two structural phase transitions at 249 and 282 K that has thwarted the determination of its structure by single crystal X-ray diffraction; however, its structure at 100 K is reported [P2(1)/c, a = 9.710(1) A, b = 14.

Disorder and intermolecular interactions in a family of tetranuclear Ni(II) complexes probed by high-frequency electron paramagnetic resonance.

High-frequency electron paramagnetic resonance (HFEPR) data are presented for four closely related tetranuclear Ni(II) complexes, [Ni(hmp)(MeOH)Cl]4.H2O (1a), [Ni(hmp)(MeOH)Br]4.H2O (1b), [Ni(hmp)(EtOH)Cl]4.

Hydrocarbation chemistry proceeding from nickel carbenes.

Nickel carbene complex 2 [Ni(triphos)C(H)N(H)xylyl]2+(BF4-)2 reacts with alkenes quantitatively and regiospecifically to give the anti-Markovnikov hydrocarbation products. X-ray crystallography shows significant iminium alkyl character of the hydrocarbation products, similar to that observed in parent carbene 2. Mechanistic studies suggest the importance of a "hydride" pathway over "alkene" (metallocycle formation or carbocation) pathways.

Sesquiterpenes from Omphalotus illudens.

Three sesquiterpenes, illudosone hemiacetal (1a), isoomphadione (2) and illudiolone (3) were isolated from the liquid culture extract of Omphalotus illudens. Their structures were elucidated by spectroscopic techniques as well as by X-ray crystallographic analysis.

Effects of Sterics and Electronic Delocalization on the Photophysical, Structural, and Electrochemical Properties of 2,9-Disubstituted 1,10-Phenanthroline Copper(I) Complexes.

The syntheses, crystal structures, electronic absorption spectra, electrochemical properties, and photophysical properties of a series of copper(I) bis(phenanthroline) complexes are reported. The phenanthroline ligands that have been prepared and investigated are the following: dop (2,9-di-(2-methylphenyl)-1,10-phenanthroline), xop (2-(2-methylphenyl)-9-(2,6-dimethylphenyl)-1,10-phenanthroline), dpep (2,9-diphenylethynyl-1,10-phenanthroline), and dmesp (2,9-dimesityl-1,10-phenanthroline). The complex [Cu(dop)(2)](PF(6)).

Structures of the Copper(I) and Copper(II) Complexes of 2,9-Diphenyl-1,10-phenanthroline: Implications for Excited-State Structural Distortion.

The syntheses, crystal structures, and electronic absorption spectra of the copper(I) and copper(II) complexes of 2,9-diphenyl-1,10-phenanthroline (dpp) are reported. The complex [Cu(dpp)(2)](PF(6)) (1) crystallizes in space group P2(1)/c with a = 11.081(4) Å, b = 25.

Electron Transfer in Mixed-Valence [Fe(III)(2)Fe(II)O(O(2)CCH(3))(6)(3-Cl-py)(3)].3-Cl-py: Effects of a Crystallographic Phase Transition and Conversion of Solvate and Ligand Molecules from Statically Disordered to Dynamically Disordered on the Valence Detrapping.

A crystallographic phase transition involving changes in the solvate molecule has been found for mixed-valence [Fe(3)O(O(2)CCH(3))(6)(3-Cl-py)(3)].3-Cl-py (1), where 3-Cl-py is 3-chloropyridine. Single-crystal X-ray structures were determined at 300, 228, 200, 169, and 122 K for complex 1.

A Photoluminescent Copper(I) Complex with an Exceptionally High Cu /Cu Redox Potential: [Cu(bfp) ] (bfp=2,9-bis(trifluoromethyl)-1,10-phenanthroline).

Unprecedented stabilization of the copper(I) oxidation state is demonstrated for the complex cation [Cu(bfp) ] (1) due to the steric and electronic effects of the CF groups (E (Cu /Cu )=+1.55 V vs. SCE).