G.W. Gokel's Advances in Supramolecular Chemistry. Volume 4 PDF

By G.W. Gokel

ISBN-10: 1559381817

ISBN-13: 9781559381819

ISBN-10: 1559383291

ISBN-13: 9781559383295

ISBN-10: 1559385464

ISBN-13: 9781559385466

ISBN-10: 1559387947

ISBN-13: 9781559387941

The objective in quantity four of Advances in Supramolecular Chemistry continues to be kind of like for earlier volumes: to provide a large diversity of supramolecular technological know-how recorded through a world panel of unusual researchers. Contributions during this quantity span the clinical variety from digital equipment improvement to novel artificial receptor molecules to biomimetic ion channels.The precise breadth of the supramolecular chemistry box is typically neglected. by way of their very nature, concentrated monographs can't span the variety of efforts that come with analytical, inorganic, natural, actual, and biochemistry. Even contemplating the big variety of reviews underway, there's a few polarization among the organic part of upramolecular technological know-how and fabrics improvement. it truly is was hoping that the standard of the displays during this quantity will show that there's unique, interesting, and perfect technological know-how on each side and in the course of the box of supramolecular chemistry.

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Extra resources for Advances in Supramolecular Chemistry. Volume 4

Example text

77 So it seems reasonable to conclude that the cases discussed here have only scratched the surface of what is possible with targeted and anchored lumophore-spacer-receptor systems. 11. LU M O PH O RE-R ECEPTOR 1-S PAC ER-R ECEPTO R2 SYSTEMS Almost all the examples discussed so far use covalent bonds to hold the receptor at a reasonable distance from the lumophore. However, alternative strategies are available. For instance, receptor 2 selective for the guest ion of interest may be covalently linked to another receptor~ which is chosen for its ability to selectively bind a lumophore.

Since molecular emulation of electronic devices is an important chemical endeavor, ~086 is a contribution to this field. Figure 1 1 outlines the design of such an off-on-off switchable system for pH. Protons are the prototype guest ion for the design of such hybrid systems since efficient off-on and on-off cases are available. System 86 is a molecular example which uses an aminoalkyl aromatic assembly for the off-on segment of the switching, whereas a pyridylalkyl aromatic can be discerned within 86 as the source of the on-off segment.

On the other hand, the PET-type process from the N-phenyl azacrown receptor to the acridinium lumophore in Ag(I)-free 59 is strongly allowed. The tables are turned upon entry of Ag(I) owing to the strong Ag(I)-N interaction. o o hvt~ ! o o, 02" ". uminescenee ' on' Figure 4. (a) Schematic representation of the orthogonal two-module format of an ionically switchable photoactive dyad. The simple picture presented here in terms of an electron transfer driven by excitation localized in the lumophore is convenient and sufficient for our purposes.

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Advances in Supramolecular Chemistry. Volume 4 by G.W. Gokel


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