Ralf Reinhardt

发表

Multistep redox sequences of azopyridyl (L) bridged reaction centres in stable radical complex ions {(μ-L)[MCl(η5-C5Me5)]2}˙+, M = Rh or Ir: spectroelectrochemistry and high-frequency EPR spectroscopy

W. Kaim, S. Greulich, J. Fiedler, 2003 .

Coupling of Electron Transfer and Bond Dissociation Processes in Dinuclear Complexes with Rhodium and Iridium Reaction Centres Bridged by 2,2'-Bipyrimidine

W. Kaim, S. Greulich, A. Klein, 2001 .

2,5-Bis(1-phenyliminoethyl)pyrazine (bpip): a conjugated metal–metal bridging acceptor ligand and its homodinuclear complexes with low-valent metal centres

W. Kaim, A. Klein, J. Fiedler, 1999 .

Electron transfer and chloride ligand dissociation in complexes [(C5Me5)ClM(bpy)]+/[(C5Me5)M(bpy)]n (M=Co, Rh, Ir;n = 2+, +, 0, −): A combined electrochemical and spectroscopic investigation

W. Kaim, J. Fiedler, Ralf Reinhardt, 1996 .

Electronic coupling of two [Cp*ClM]+/[Cp*M] reaction centers via π conjugated bridging ligands: similarities and differences between rhodium and iridium analogues☆

W. Kaim, S. Greulich, J. Fiedler, 1999 .

α-Diimin-Komplexe des Pentamethylcyclopentadienylrhodiums in verschiedenen Oxidationsstufen

W. Kaim, Ralf Reinhardt, 1993 .

Chemical and Electrochemical Generation of Hydride-Forming Catalytic Intermediates (bpy)M(CnRn): M = Rh, Ir (n = 5); M = Ru, Os (n = 6). Coordinatively Unsaturated Ground State Models of MLCT Excited States?

W. Kaim, M. Sieger, Ralf Reinhardt, 1994 .

Ultrasensitive detection of unstained proteins in acrylamide gels by native UV fluorescence.

Helmut E Meyer, Martin Blüggel, Petra Lutter, 2003, Analytical chemistry.

Resolving the Two-Electron Process for the Couple [(C5Me5)M(N∧N)Cl]+/[(C5Me5)M(N∧N)] (M = Rh, Ir) into Two One-Electron Steps Using the 2,2‘-Azobis(pyridine) N∧N Ligand, Fast Scan Cyclovoltammetry, and Spectroelectrochemistry: Detection of Radicals instead of MIIIntermediates

W. Kaim, S. Greulich, J. Fiedler, 2003 .

Metal vs ligand reduction in complexes of dipyrido[3,2-a:2',3'-c]phenazine and related ligands with [(C5Me5)ClM]+ (M = Rh or Ir): evidence for potential rather than orbital control in the reductive cleavage of the metal-chloride bond.

W. Kaim, J. Fiedler, S. Berger, 2004, Inorganic chemistry.