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Cationic Dihydrogen/Dihydride Complexes of Osmium: Structure and Dynamics
Ist Teil von
Organometallics, 2007-04, Vol.26 (9), p.2291-2295
Ort / Verlag
United States: American Chemical Society
Erscheinungsjahr
2007
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
Reaction of Cp*Os(CO)2Cl with [Et3Si][BArF 4] under hydrogen gas affords the cationic hydrogen complex [Cp*Os(CO)2(H2)][BArF 4] (1) (Cp* = C5Me5; ArF = C6F5). When this reaction is carried out with HD gas, complex 1-d 1 results, with J HD = 24.5 Hz. When solutions of complex 1 are monitored by 1H NMR spectroscopy over several days, the gradual formation of a trans dihydride species is observed. Similarly, reaction of CpOs(dppm)Br with Na[BArF*4] (ArF* = 3,5-(CF3)2C6H3) under hydrogen affords the cationic dihydride complex [CpOs(dppm)H2][BArF*4] (2). At 295 K, complex 2 exists as a 10:1 mixture of cis and trans isomers. The 1H NMR spectrum of the cis form in the hydride region exhibits a triplet with J HP = 6.5 Hz, due to rapid exchange of the hydrogen atoms. At low temperature, static spectra of the HH‘PP‘ spin system can be obtained, revealing quantum mechanical exchange coupling between the two hydride ligands. The observed J HH ‘ is temperature dependent, varying from 133 Hz at 141 K to 176 Hz at 198 K. This is the first report of detectable exchange coupling between pairs of chemically equivalent hydrogen atoms.