The effect of isotopic substitution on the chirality of a self-assembled helix
β Scribed by Cantekin, Seda; Balkenende, Diederik W. R.; Smulders, Maarten M. J.; Palmans, Anja R. A.; Meijer, E. W.
- Book ID
- 109913104
- Publisher
- Nature Publishing Group
- Year
- 2010
- Tongue
- English
- Weight
- 499 KB
- Volume
- 3
- Category
- Article
- ISSN
- 1755-4330
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π SIMILAR VOLUMES
Chirality is an essential aspect in nature. [1] Most biomolecules, such as amino acids, sugars, RNA, DNA, and proteins, are chiral, as are the large entities assembled from these molecules. The ability of enzymes and cell receptors to readily distinguish different stereoisomers (enantiomers) of chir
Coordination-driven assembly based on manganese(II) centers and flexible 1,3-bis(4-pyridyl)propane leads to the solid-state formation of electronically neutral, self-templated homochiral helices, closed ring structures, and racemic mixtures of helices depending upon the presence or absence of guests
## Dedicated to Professor Manfred Regitz on the occasion of his 65th birthday Over the past decade, the principles of recognition-driven, spontaneous self-assembly have become further elucidated. In such processes, the overall structure of the product is [\*] Prof.
## Abstract Two complementary classes of molecules based on a triphenylene core are synthesized. The twoβdimensional (2D) assemblies of these molecules deposited on a highly oriented pyrolytic graphite (HOPG) surface are identified with scanning tunneling microscopy (STM). Structures with large cav