Abstract

Angewandte Chemie International Edition in EnglishVolume 34, Issue 21 Cover PictureFree Access Cover Picture (Angew. Chem. Int. Ed. Engl. 21/1995) First published: November 17, 1995 https://doi.org/10.1002/anie.199522991Citations: 3AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat Abstract The cover picture shows not skydivers, but molecules of trimethylisocyanurate linked with CHċO hydrogen bonds in the layered hexagonal crystal structure of the 1:1 complex formed by this substance with 1,3,5-trinitrobenzene. But supramolecular patterns in crystals resemble the aerial patterns formed by skydivers in that properties of the group are distinct from those of the individual constituents. In this sense, a crystal of an organic compound is the perfect supermolecule and crystal engineering, which is the deliberate design of crystal structures of organic compounds, is the supramolecular equivalent of organic synthesis. By defining a “supramolecular synthon” as a building block that incorporates both chemical and geometrical features of sets of intermolecular interactions, the conceptual similarity between crystal engineering and classical organic synthesis is uncovered. This striking parallel is discussed by G. R. Desiraju on pp. 2328. Citing Literature Volume34, Issue21November 17, 1995 RelatedInformation

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