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- W2951445820 abstract "Solution structures of hydridorhodium diphosphite dicarbonyl complexes [HRhL⌒L1-9(CO)2] have been studied. Diphosphites L⌒L1 to L⌒L9 are based on C2 symmetric (2R,3R)-butane-2,3-diol, (2R,3R)-diethyl tartrate, (2R,4R)-pentane-2,4-diol, and (2S,5S)-hexane-2,5-diol backbones substituted with 1,1‘-biphenyl-2,2-diyl- or (S)-(−)-1,1‘-binaphthyl-2,2‘-diylphosphoroxy derivatives. Variable-temperature (293−163 K) 31P and 1H NMR spectroscopy revealed fluxional behavior in the trigonal bipyramidal HRhL⌒L(CO)2 complexes of L⌒L1-9 which could be frozen out at low temperatures. Depending on the length of the bridge between the two phosphorus atoms in the diphosphite ligands, equatorial−axial or bis-equatorial coordination takes place. Enthalpies of activation (ΔH⧧) varying between 36.7 and 62.5 kJ mol-1 have been calculated for the phosphorus exchange observed in these hydridorhodium diphosphite dicarbonyl complexes. The enthalpies of activation increase with larger steric bulkiness of the coordinated diphosphite ligands." @default.
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- W2951445820 date "1997-12-01" @default.
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- W2951445820 title "Fluxional Processes in Asymmetric Hydroformylation Catalysts [HRhL⌒L(CO)<sub>2</sub>] Containing <i>C</i><sub>2</sub>-Symmetric Diphosphite Ligands" @default.
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- W2951445820 doi "https://doi.org/10.1021/om970599k" @default.
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