Zg. Ding et al., SYNTHESIS OF FERRIC COORDINATION COMPOUND OF BIS (6-O-M-CARBONYL BENZENESULFONYL)-BETA-CYLODEXTRIN WITH CATALYSIS OF OXIDOREDUCTASE, Huaxue xuebao, 53(6), 1995, pp. 578-582
As beta-cyclodextrin reacted with m-carbonyl benzenesulfonyl chloride
in solution of pyridine at 80 degrees C, bis(6-O-m-carbonyl benzenesul
fonyl)-beta-cyclodextrin, which was characterized by H-1-C-13 NMR, IR
spectra and elemental analysis, was obtained. The ferric coordination
compound of this new product could effectively catalyse benzal alcohol
oxidized into benzaldehyde and benzoic acid. The catalytic rate was 1
.4x 10(4) times as much as that FeCl3 catalysing the same reaction.