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Journal ArticleDOI

Self-Complementarity Achieved through Quadruple Hydrogen Bonding

TLDR
In this paper, a donor-acceptor-donoracceptor array of four hydrogen-bonding sites is used to pre-organize the molecule for dimerization. But the structure of the compound is unknown.
Abstract
Highly stable dimers are formed in solution and in the solid state by a class of readily synthesized, self-complementary building blocks for supramolecular chemistry, which associate through a donor-acceptor-donor-acceptor array of four hydrogen-bonding sites. An additional intramolecular hydrogen bond in the compound whose crystal structure is shown on the right preorganizes the molecule for dimerization.

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Journal ArticleDOI

The hydrogen bond in the solid state.

TL;DR: The hydrogen bond is the most important of all directional intermolecular interactions, operative in determining molecular conformation, molecular aggregation, and the function of a vast number of chemical systems ranging from inorganic to biological.
Journal ArticleDOI

Self-healing polymeric materials

TL;DR: This review outlines the recent advances in the field of self-healing polymers, and the primary classes are the covalent bonding, supramolecular assemblies, ionic interactions, chemo-mechanical self- healing, and shape memory polymers.
Journal ArticleDOI

Noncovalent synthesis using hydrogen bonding

TL;DR: Noncovalent synthesis based on the reversible formation of multiple hydrogen bonds is described and the development of novel materials (nanotubes, liquid crystals, polymers, etc.) and principles that recently have emanated from this intriguing field of research are summarized.
Journal ArticleDOI

Die Wasserstoffbrücke im Festkörper

TL;DR: Wasserstoffbrucke wird heute als ein sehr breites Phanomen with offenen Grenzen zu anderen Effekten begriffen.
Journal ArticleDOI

Helical self-assembled polymers from cooperative stacking of hydrogen-bonded pairs

TL;DR: This work describes a general strategy for the design of functionalized monomer units and their association in either water or alkanes into non-covalently linked polymeric structures with controlled helicity and chain length.
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