
Understanding and control of nucleation, growth, habit, dissolution and structure of two‐ and three‐dimensional crystals using `tailor‐made' auxiliaries
Author(s) -
Weissbuch I.,
PopovitzBiro R.,
Lahav M.,
Leiserowitz L.
Publication year - 1995
Publication title -
acta crystallographica section b
Language(s) - English
Resource type - Journals
eISSN - 1600-5740
pISSN - 0108-7681
DOI - 10.1107/s0108768194012061
Subject(s) - nucleation , monolayer , crystallization , dissolution , crystal growth , crystallography , materials science , crystal habit , molecule , crystal (programming language) , amphiphile , solvent , crystal engineering , aqueous solution , chemical engineering , crystal structure , chemistry , chemical physics , nanotechnology , supramolecular chemistry , organic chemistry , polymer , copolymer , engineering , programming language , computer science
Tailor-made auxiliaries for the control of nucleation and growth of molecular crystals may be classified into two broad categories: inhibitors and promoters. Tailor-made inhibitors of crystal growth can be used for a variety of purposes, which include morphological engineering and etching, reduction of crystal symmetry, assignment of absolute structure of chiral molecules and polar crystals, elucidation of the effect of solvent on crystal growth, and crystallization of a desired polymorph. As for crystal growth promoters, monolayers of amphiphilic molecules on water have been used to induce the growth of a variety of three-dimensional crystals at the monolayer-solution interface by means of structural match, molecular complementarity or electrostatic interaction. A particular focus is made on the induced nucleation of ice by monolayers of water-insoluble aliphatic alcohols. The two-dimensional crystalline structures of such monolayers have been studied by grazing incidence X-ray diffraction. It has become possible to monitor, by this method, the growth, dissolution and structure of self-aggregated crystalline nonolayers, and indeed multilayers, affected by the interaction of solvent molecules in the aqueous. suphase with the amphiphilic headgroups, and by the use of tailor-made amphiphilic additives.