Computing handedness: quantized and superposed switch and dynamic memory of helical polysilylene.

Abstract

Two new conjugating helical polymers comprising a rodlike silicon backbone and enantiopure chiral pendants, poly[(R)-3,7-dimethyloctyl-(S)-3-methylpentylsilylene] (PS-1) and its diastereomeric poly[(S)-3,7-dimethyloctyl-(S)-3-methylpentylsilylene] (PS-2), were prepared. Molecular mechanics calculations of PS-1 and PS-2 model oligomers indicated a double well potential energy curve corresponding to almost enantiomeric helices with dihedral angles of 150-160 degrees (P-motif, global minimum) and 200-210 degrees (M-motif), regardless of their tacticity. Experimentally, it was found that PS-1 in dilute isooctane revealed switchable ambidextrous helicity on application of a thermal energy bias. Although PS-1 featured three distinct switching regions, viz. "region 1, between -80 and -10 degrees C", "region 2, between -10 and +10 degrees C", and "region 3, between +10 degrees C and +80 degrees C", the switching properties were interpreted as the result of superposed P- and M-helicities, undergoing dynamic pseudo-racemization or oscillation. Oscillating helicity in region 2 was roughly estimated to be about 13 cm(-)(1). The superposed helicity in region 2 was critical since it afforded molecular recognition ability with a dynamic memory function that was highly susceptible to solvent molecular topology and volume fraction. This could lead to potential as a molecular information processor to serve as a gauge of chemical properties. On the other hand, PS-2 could not switch its preferential screw-sense in the range of -80 to +80 degrees C. This may be related to greater differences the potential energy curve between P- and M-motifs.