By Alessandro Scarso, Julius Jr. Rebek (auth.), Mercedes Crego-Calama, David N. Reinhoudt (eds.)
From the reviews:
"If supramolecular chemistry is molecular sociology then supramolecular chirality is the layout of molecular sociological order into those molecular structures. the aim of the seven chapters of this e-book is to supply the reader with the most recent learn insights into the uneven association of molecules in a non-covalent meeting, the place chirality is utilised as a device to manufacture supramolecular constructions with new and intersting purposes and homes which may evolve into new nanofabrication technologies."
from: H. Hügel, Chem. RMIT college, Chemistry in Australia, November 2006, S. 29
"Unlike conventional chemical synthesis the place molecules are stitched jointly atom by means of atom via covalent bonds, supramolecular chemistry bargains with noncovalent interactions that make the most of a mix of susceptible and reversible interacting forces to arrange and gather molecules into well-defined structures. This publication is an outline of the following point of molecular association - i.e., how chemical development blocks, either chiral and achiral, are prepared and assembled into uneven (chiral) supramolecular assemblies - and its software in quite a few technology and engineering fields. not just does it offer a very good review of the sphere, directory key literature stories and a few of the most recent findings, the amount is easily equipped and written by means of specialists who element the rules and purposes of every topic.… . total, the publication is definitely written and gives a accomplished assessment of the sector of supramolecular chemistry, with emphasis on molecular chirality. it's a very worthwhile and informative e-book to have as a reference. I hugely suggest it for somebody who's attracted to molecular association and self-assembly, either amateur and practicioner alike." (Danith H. Ly, magazine of the yankee Chemical Society, Vol. 129 (13), 2007)
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Additional resources for Supramolecular Chirality
2 ratio between the two complexes in favor of the heterochiral combination . This observation may be related to the preference in nature for centrosymmetric crystals or, alternatively stated, the higher melting points of racemates vs. enantiopure compounds where the resolution is driven by the less soluble pair [61, 62]. In the cylindrical capsule a single couple of chiral molecules is extrapolated from the bulk and the interactions between the two is governed by the shape of the cavity and their goodness of ﬁt within the cavity.
Other Helical Polymers and Oligomers . . . . . Chirality Sensing by Helix Inversion . . . . . . Memory and Storage of Helical Chirality . . . . . Chirality Sensing in Gel and Solid . . . . . . . Sensing and Ampliﬁcation of Chirality in Liquid Crystal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61 62 67 71 74 78 79 4 Supramolecular Assembly of Helical Polymers . . . . . . . . 80 5 Conclusion .
Bosa for assistance in the preparation of ﬁgures and graphics, and Dr. M. Schramm for reviewing the manuscript. References 1. Feringa BL, van Delden RA (1999) Angew Chem Int Ed 38:3418 2. Goshe AJ, Steele IM, Ceccarelli C, Rheingold AL, Bosnich B (2002) Proc Natl Acad Sci USA 99:4823 3. For hydrogen bond see Prins L, Reinhoudt DN, Timmerman P (2001) Angew Chem Int Ed 40:2383 and references therein 4. for ionic interactions see Hossain MA, Schneider H-J (1999) Chemistry Eur J 5:1284 5. for dispersive forces see Meyer EA, Castellano RK, Diederich F (2003) Angew Chem Int Ed 42:1210 6.