Two homochiral organocatalytic metal organic materials with nanoscopic channels.

Two homochiral organocatalytic MOMs were prepared using tetra- and octa-carboxylate ligands, respectively. The nanoscopic channels in these MOMs are lined by organonocatalytic chiral phosphoric acid derivatives of binol and ocMOM-1 exhibited improved enantioselectivity over the parent ligand in the context of transfer hydrogenation of a series of benzoxazines.

Reinterpretation of the Brønsted alpha for redox reactions based on the effect of substituents on hydride transfer reaction rates between NAD+ analogues.

Rate and equilibrium constants have been determined spectrophotometrically for two sets of hydride transfer redox reactions between acridine and benzothiazoline derivatives and between pyridine and benzimidazoline derivatives that can be regarded as NAD+/NADH analogues. According to generally accepted ideas of the relation between equilibrium constants, K, and rate constants, k, these reactions would all have Brønsted alpha values close to 0.5 since the equilibrium constants, K, for these reactions range from 10(-1) to 10(2). However, when the structural variation is in the hydride acceptor, the Brønsted alpha is less than 0.5 (0.38 and 0.42, respectively), and when the structural variation is in the hydride donor, the Brønsted alpha is greater than 0.5 (0.63 and 0.61, respectively) for the present systems. The Marcus theory of atom and group transfer can explain the difference of alpha values in terms of the tightness factor in the critical configuration. When the transition state is loose and symmetrical, the deviation of the Brønsted alpha from 0.5 can be obtained by adding or subtracting a tightness factor that depends on the location of the substituents.