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Highly Fluorescent Self-Coordinated Phthalocyanine Dimers

✍ Scribed by Kazuya Kameyama; Mitsuhiko Morisue; Akiharu Satake; Yoshiaki Kobuke

Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
380 KB
Volume
117
Category
Article
ISSN
0044-8249

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πŸ“œ SIMILAR VOLUMES

A self-assembled phthalocyanine dimer
A self-assembled phthalocyanine dimer
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The synthesis of phthalocyanines 1a and 1b appended with four glycoluril modules is presented. 1 H NMR spectroscopy showed that 1a and 1b self-assemble by means of hydrogen bonding to form discrete dimers. Capsule formation is solvent dependent where the dimeric assembly is most pronounced in aromat

Bis(BF2)-2,2β€²-Bidipyrrins (BisBODIPYs):
Bis(BF2)-2,2β€²-Bidipyrrins (BisBODIPYs): Highly Fluorescent BODIPY Dimers with Large Stokes Shifts
✍ Martin BrΓΆring; Robin KrΓΌger; Stephan Link; Christian Kleeberg; Silke KΓΆhler; Xi πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 443 KB

## Abstract Four new dimeric bis(BF~2~)‐2,2′‐bidipyrrins (bisBODIPYs), and their corresponding BODIPY monomers, have been prepared and studied with respect to their structural and photophysical properties. The solid‐state molecular structure of the dimers and the relative orientation of the subunit