Publications by authors named "Sebastian P Smidt"

[reaction: see text] A template containing two secondary dialkylammonium ion recognition sites for encirclement by olefin-bearing dibenzo[24]crown-8 derivatives has been used to promote olefin cross metatheses with ruthenium-alkylidene catalysts. For monoolefin monomers, the rates of metatheses and yields of the dimers are both amplified in the presence of the template. Likewise, for a diolefin monomer, the yield of the dimer is enhanced in the presence of the template under conditions where higher oligomers are not formed.

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The reaction of a [(PHOX)Ir(COD)](+) complex (COD = 1,5-cyclooctadiene) with dihydrogen was studied by NMR spectroscopy (PHOX = chiral phosphinooxazoline ligand). A single [(PHOX)Ir(H)(2)(COD)](+) isomer was formed as the primary product at -40 degrees C in THF. Subsequent reaction with H(2) at -40 to 0 degrees C led to a mixture of two diastereomeric [(PHOX)Ir(H)(2)(solvent)(2)](+) complexes with concomitant loss of cyclooctane.

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In the asymmetric hydrogenation of unfunctionalized olefins with cationic iridium-PHOX catalysts, the reaction kinetics and, as a consequence, catalyst activity and productivity depend heavily on the counterion. A strong decrease in the reaction rate is observed in the series [Al[OC(CF3)3]4]- >BArF- >[B(C6F5)4]- >PF6- >>BF4- >CF3SO3-. With the first two anions, high rates, turnover frequencies (TOF >5000 h(-1) at 4 degrees C), and turnover numbers (TONs) of 2000-5000 are routinely achieved.

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[reaction: see text] New Ir-SimplePHOX complexes Ir-6-Ir-9 catalyze the quantitative, highly enantioselective hydrogenation of a range of unfunctionalized and functionalized olefins. Synthesis, catalytic results, and X-ray crystal structures are presented here.

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