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Full-Text Articles in Chemistry
Synthesis Of Homo- And Heterobimetallic NiIi–MIi (M = Fe, Co, Ni, Zn) Complexes Based On An Unsymmetric Ligand Framework: Structures, Spectroscopic Features, And Redox Properties, Denan Wang, Sergey V. Lindeman, Adam T. Fiedler
Synthesis Of Homo- And Heterobimetallic NiIi–MIi (M = Fe, Co, Ni, Zn) Complexes Based On An Unsymmetric Ligand Framework: Structures, Spectroscopic Features, And Redox Properties, Denan Wang, Sergey V. Lindeman, Adam T. Fiedler
Chemistry Faculty Research and Publications
Several homo- and heterobimetallic NiII–MII complexes (MII = Fe, Co, Ni, Zn) supported by an unsymmetric polydentate ligand (L13−) are reported (L13− is the trianion of 2-[bis(2-hydroxy-3,5-tert-butylphenyl)aminomethyl]-4-methyl-6-[(2-pyridylmethyl)iminomethyl]phenol). The L13− chelate provides two distinct coordination environments: a planar tridentate {N2O} site (A) and a tetradentate {NO3} site (B). Reaction of L13− with equimolar amounts of NiII and MII salts provides bimetallic complexes in which the NiII ion exclusively occupies the tetragonal A-site and the MII ion is found …
Intramolecular Hydrogen Bonding In CuIi Complexes With 2,6-Pyridinedicarboxamide Ligands: Synthesis, Structural Characterization, And Physical Properties, Denan Wang, Sergey V. Lindeman, Adam T. Fiedler
Intramolecular Hydrogen Bonding In CuIi Complexes With 2,6-Pyridinedicarboxamide Ligands: Synthesis, Structural Characterization, And Physical Properties, Denan Wang, Sergey V. Lindeman, Adam T. Fiedler
Chemistry Faculty Research and Publications
The significance of second-sphere interactions in synthetic catalysts and metalloenzyme active sites has encouraged the development of ligand frameworks capable of supporting intramolecular hydrogen-bonding networks. With this approach in mind, we prepared a series of 2,6-pyridinedicarboxamide ligands (H2LX) that feature outer-sphere heterocyclic groups (pyridine, pyrimidine, or quinoline rings). Reaction with CuCl2 yields complexes with the general formula [CuCl2(LX{H}2)] (1X), in which the pincer ligands coordinate to the CuII center in a tridentate fashion through the central pyridine and two amidato nitrogen atoms. The LX …
Tricarbonylrhenium(I) And Manganese(I) Complexes Of 2-(Pyrazolyl)-4-Toluidine, Brendan J Liddle, Sarath Wanniarachchi, Sergey V. Lindeman, James R. Gardinier
Tricarbonylrhenium(I) And Manganese(I) Complexes Of 2-(Pyrazolyl)-4-Toluidine, Brendan J Liddle, Sarath Wanniarachchi, Sergey V. Lindeman, James R. Gardinier
Chemistry Faculty Research and Publications
A series of tricarbonyl rhenium(I) and manganese(I) complexes of the electroactive 2-(pyrazolyl)-4-toluidine ligand, H(pzAnMe), has been prepared and characterized including by single crystal X-ray diffraction studies. The reactions between H(pzAnMe) and M(CO)5Br afford fac-MBr(CO)3[H(pzAnMe)] (M = Mn, 1a; Re, 1b) complexes. The ionic species {fac-M(CH3CN)(CO)3[H(pzAnMe)]}(PF6) (M = Mn, 2a; Re, 2b) were prepared by metathesis of 1a or 1b with TlPF6 in acetonitrile. Complexes 1a and 1b partly ionize to {M(CH3CN)(CO)3[H(pzAnMe)]+ …
Β-Diketonate, Β-Ketoiminate, And Β-Diiminate Complexes Of Difluoroboron, Felipe P. Macedo, Chengeto Gwengo, Sergey Lindeman, Mark D. Smith, James R. Gardinier
Β-Diketonate, Β-Ketoiminate, And Β-Diiminate Complexes Of Difluoroboron, Felipe P. Macedo, Chengeto Gwengo, Sergey Lindeman, Mark D. Smith, James R. Gardinier
Chemistry Faculty Research and Publications
A series of β-diketonate, keto(aryl)iminato, and β-bis(aryl)iminato complexes of difluoroboron, twenty in total, have been prepared to assess the impact of chelate ring and aniline substitution on the structural, electrochemical, and photophysical properties of these ubiquitous chelates. DFT (B3LYP/6-31G*) calculations supplemented the experimental results and both demonstrated that replacing oxygen with the more electron-donating aniline groups serves to only fine-tune the electronic properties because both the HOMO and LUMO energies are affected by such substitution. The electronic properties of all compounds are most greatly influenced by the nature of the substituents bound to the carbon portion of the chelate ring. …
Electrochemistry And Spectroscopy Of Sulfate And Thiosulfate Complexes Of Iron Porphyrins, Philip Walter Crawford, Michael D. Ryan
Electrochemistry And Spectroscopy Of Sulfate And Thiosulfate Complexes Of Iron Porphyrins, Philip Walter Crawford, Michael D. Ryan
Chemistry Faculty Research and Publications
The electrochemical and spectroscopic properties of the complex formed by the addition of thiosulfate to ferric porphyrins were examined. The NMR spectrum of the thiosulfate–ferric porphyrin complex was consistent with a high-spin ferric complex, while the EPR spectrum at liquid nitrogen temperatures indicated that the complex under these conditions was low-spin. Such behavior has been previously observed for other ferric porphyrin complexes. The visible spectra were characterized by a shift in the Soret band to higher energies, with smaller changes in the longer wavelength region. The complex was reasonably stable in DMF, but slowly reduced over several hours to Fe …
Effect Of Sodium Ions On The Electrochemical Reduction Of Diethyl Fumarate In Dimethylsulfoxide And Acetonitrile, Michael D. Ryan, Dennis H. Evans
Effect Of Sodium Ions On The Electrochemical Reduction Of Diethyl Fumarate In Dimethylsulfoxide And Acetonitrile, Michael D. Ryan, Dennis H. Evans
Chemistry Faculty Research and Publications
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