Template-induced polymorphic selectivity: the effects of surface chemistry and solute concentration on carbamazepine crystallisation†
Abstract
Cooling crystallisation of carbamazepine solution in glass vials functionalised with different silane molecules resulted in preferential nucleation of metastable form II or stable form III polymorphs within a definite range of supersaturation. In contrast, the two crystal forms nucleated concomitantly on a control substrate under similar solution conditions.