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Hydrogen product quenching

Photochemical hydrogen production via oxidative quenching of [Ru(bipy)3]2+ by... [Pg.487]

Hydrogen production via oxidative quenching of ruthenium(H) complexes containing chemically... [Pg.487]

Photochemical hydrogen production via reductive quenching of lR u(bipy)3]2+ ... [Pg.508]

All the teabags were put into a resin kettle under nitrogen. Fifteen equivalents of boric acid and 15 equiv. of trimethylborate were added followed by the slow addition of 45 equiv. of borane (1 M in THF). After hydrogen production ceased, the reaction was heated at 65° for 72 h. The reaction solution was decanted and quenched by the slow addition of methanol. The resin was washed with methanol, THF, and piperidine. The polyamine-borane complex was disproportionated by overnight treatment (16 h) with piperidine at 65° followed by washes with DMF, DCM, and methanol. [Pg.515]

Thus, the data on photochemical hydrogen production indicate that macrobicyclic complexes can be effective ETAs only in a narrow redox potential range (-400 mVexperiments demonstrated that cage complexes with such potentials are efficient for quenching of [Ru(bpy)3]2+ and [Ru(4,4 -Me2bpy)3] + cations (Table 63). [Pg.365]

Photochemical properties of [Ru(bipy)j] and its excited states Photochemical hydrogen production via oxidative quenching of[Ru(bipy)j] by methylviologen (l,l -dimethyl-4,4 -bipyridinium dication)... [Pg.487]


See other pages where Hydrogen product quenching is mentioned: [Pg.109]    [Pg.109]    [Pg.115]    [Pg.155]    [Pg.20]    [Pg.487]    [Pg.502]    [Pg.505]    [Pg.506]    [Pg.506]    [Pg.508]    [Pg.510]    [Pg.511]    [Pg.512]    [Pg.522]    [Pg.99]    [Pg.326]    [Pg.190]    [Pg.163]    [Pg.93]    [Pg.618]    [Pg.239]    [Pg.366]    [Pg.502]    [Pg.506]    [Pg.506]    [Pg.508]    [Pg.510]    [Pg.511]    [Pg.512]    [Pg.522]   
See also in sourсe #XX -- [ Pg.326 ]




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Hydrogen quenching

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