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From our work and that of others (references 9–30) it is known that the boronate ester is rapidly and reversibly formed under basic conditions. Noncovalent interactions are described using such terms as “recognition”, “complex” and “binding constants”. These terms will be used to describe the equilibrium between covalent boronate ester and free boronic acid at high pH.
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The reason is not well understood
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A solution containing cholesteryl nanoate
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(1.2XIO-5 mol), cholesteryl chloride (0.8 XIO-5mol) and the 2:1 boronic acid saccharide complex (5.2 X10-7mol) in chloroform was prepared, An aliquot (200 mL) was spread on a quartz plate and mixed with minute glass beads having a uniform diameter (10±0.2mM). The sample was dried and then sandwitched between another quartz plate. The thickness of the sample prepared is then regulated by the glass beads. The wavelength of maximum reflection (XR = nP, where n is the mean index of reflection and P is the helical pitch of the cholesteric mesophase) was measured spectrophotometrically at 27°C. For details of the measurement method see
-
A solution containing cholesteryl nanoate (1.2XIO-5 mol), cholesteryl chloride (0.8 XIO-5mol) and the 2:1 boronic acid saccharide complex (5.2 X10-7mol) in chloroform was prepared. An aliquot (200 mL) was spread on a quartz plate and mixed with minute glass beads having a uniform diameter (10±0.2mM). The sample was dried and then sandwitched between another quartz plate. The thickness of the sample prepared is then regulated by the glass beads. The wavelength of maximum reflection (XR = nP, where n is the mean index of reflection and P is the helical pitch of the cholesteric mesophase) was measured spectrophotometrically at 27°C. For details of the measurement method see: Shannon, P. J. Macromolecules 1984, 17, 1873.
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84954754003
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Energy minimizations of the 1/saccharide complexes was conducted using a semiempirical molecular orbital calculation method with full-geometry optimization (MOPAC ver. 6.0, AMI Hamiltonian).65
-
These calculations were preformed on the engineering workstation system (SUN 4/2 and IRIS 4D/35G). The illustrations in Figure 2 were made by the ORTEPC66 for the optimized structures
-
Energy minimizations of the 1/saccharide complexes was conducted using a semiempirical molecular orbital calculation method with full-geometry optimization (MOPAC ver. 6.0, AMI Hamiltonian).65 The imput structures for the complexes were established using the molecular modeling system (MOL-GRAPH ver3.0, Daikin Ind. Ltd.) These calculations were preformed on the engineering workstation system (SUN 4/2 and IRIS 4D/35G). The illustrations in Figure 2 were made by the ORTEPC66 for the optimized structures.
-
The imput structures for the complexes were established using the molecular modeling system (MOL-GRAPH ver3.0, Daikin Ind. Ltd.)
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