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Diazabutadiene complexes

A large range of different ionic liquids have been screened in the epoxidation of cyclooctene with dioxomolybdenum(VI) complexes and ferf-butyl hydrogenperoxide as oxidant, as shown in Table 5.2.[32] With the diazabutadiene complex, 48, as catalyst, inferior turnover frequencies were observed relative to the reaction in neat substrate or in dichloromethane and the recycling potential of the catalyst turned out to be only limited. Catalyst immobilisation was better with the cationic tris(methylaminomethyl)ethane complex, 49, however at the expense of selectivity. Of the ionic liquids tested, [C4Ciim][Tf2N] gave the best results for both molybdenum complexes. [Pg.93]

Figure 50 Effect of halide on clearing point for diazabutadiene complexes of Re(I). Figure 50 Effect of halide on clearing point for diazabutadiene complexes of Re(I).
Nitrogen Donor Ligands.— Hetal carbonyl-diazabutadiene complexes continue to be studied. The complexes... [Pg.202]


See other pages where Diazabutadiene complexes is mentioned: [Pg.1161]    [Pg.406]    [Pg.442]    [Pg.451]    [Pg.213]    [Pg.620]    [Pg.112]    [Pg.136]    [Pg.142]    [Pg.182]    [Pg.186]    [Pg.1968]    [Pg.5836]    [Pg.154]    [Pg.39]    [Pg.312]    [Pg.290]    [Pg.5835]    [Pg.1266]    [Pg.625]    [Pg.247]    [Pg.300]    [Pg.348]    [Pg.371]   
See also in sourсe #XX -- [ Pg.154 ]

See also in sourсe #XX -- [ Pg.321 , Pg.322 ]




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Diazabutadienes

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