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Pyridine, reactions with—continued reduction

Darr and Poliakoff conducted one of the first studies where SC-CO2 was used in a two-stage continuous reaction and purification process to form pure organo-metallic products. The ds-W(CO)4(pyridine)2 or novel c/ -W(CO)4(3,5 lutidine)2 were formed in a continuous flow reactor at 488 K and were then removed from solution via precipitation, with a second flow of CO2 used to remove the excess solvent and reactant for reclamation and recycle. The benefits of this system, aside from the production of novel materials, include reduction of organic solvent consumption, decrease in number of stages and time, and production of 100% purity product. [Pg.1344]


See other pages where Pyridine, reactions with—continued reduction is mentioned: [Pg.185]    [Pg.1234]    [Pg.167]    [Pg.430]    [Pg.207]    [Pg.22]    [Pg.249]    [Pg.122]    [Pg.788]    [Pg.191]    [Pg.690]    [Pg.613]    [Pg.345]    [Pg.14]    [Pg.129]    [Pg.817]    [Pg.129]    [Pg.286]    [Pg.461]    [Pg.357]    [Pg.193]    [Pg.20]    [Pg.25]    [Pg.39]   
See also in sourсe #XX -- [ Pg.281 ]




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Continuous reactions

Pyridination reaction

Pyridine reduction

Pyridine reductions with

Pyridine with

Pyridine, reactions

Pyridine, reactions with—continued

Pyridines reductive

Pyridines—continued

Pyridine—continued reaction

Pyridine—continued reduction

Reactions, with pyridine

Reduction continued)

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