Tryst with a molecular and supramolecular oddity: an anti-Furst-Plattner epoxide opening product as a designer additive for accessing an elusive polymorph

Mehta, Goverdhan ; Sen, Saikat (2009) Tryst with a molecular and supramolecular oddity: an anti-Furst-Plattner epoxide opening product as a designer additive for accessing an elusive polymorph Tetrahedron, 65 (47). pp. 9713-9718. ISSN 0040-4020

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Official URL: http://dx.doi.org/10.1016/j.tet.2009.09.092

Related URL: http://dx.doi.org/10.1016/j.tet.2009.09.092

Abstract

Additive induced polymorphism of a conformationally locked tetraacetate 3 in presence of its diastereomer 4 is described. The ester 3 was specially crafted on a trans-decalin backbone to relegate the O-H···O H-bond donors to the molecular interior and have the peripheral H-bond acceptors in 1,3-syndiaxial relationship. The supramolecular assembly of 3 was destined to evolve along two mutually exclusive pathways, namely one, which employs intermolecular O-H···O H-bonds (pathway 1) and the other that sacrifices these for intramolecular O-H···O H-bonds and settles for a crystal packing dictated by weak intermolecular interactions alone (pathway 2). Exploiting the similarity between the self-assemblies of 4 and the two recently reported dimorphs of 3, the ester 3 has been stimulated to follow the elusive non-hierarchical pathway 2 through preferential inhibition of pathway 1. Interestingly, the inhibitor 4 was obtained serendipitously en route 3 via an apparent breakdown of Furst-Plattner rule.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Crystal Engineering; Hydrolysis; Hydrogen Bonds; Polycyclitols; Polymorphism
ID Code:29308
Deposited On:17 Dec 2010 08:14
Last Modified:01 Mar 2011 08:11

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