Share Email Print

Proceedings Paper

Porphodimethenes/porphyrins: redox-switchable tetrapyrrolic macrocycles
Author(s): Hubert S. Gill; Michael Harmjanz; Michael J. Scott
Format Member Price Non-Member Price
PDF $14.40 $18.00
cover GOOD NEWS! Your organization subscribes to the SPIE Digital Library. You may be able to download this paper for free. Check Access

Paper Abstract

Utilizing a general two-step procedure, a new class of porphodimethene macrocycles has been prepared, which can be easily converted to porphyrins bearing two 8-functionalized naphthalene spacers. Through straightforward modifications in the precursor molecules, macrocycles with a wide range of steric and electronic attributes can be isolated. With these simple ligands, metal-porphyrin complexes exhibiting interesting properties can be produced. For example, when two reactive groups are poised above the porphyrin, a reversible ring closure can take place under mild conditions, allowing for potential recognition sites close to a metal center to be electrochemically and chemically activated and deactivated. This intramolecular porphodimethene-porphyrin interconversion offers many exciting possibilities for the development of catalysis adept at specific transformations and for the design of novel sensors or photosensitizers.

Paper Details

Date Published: 23 October 2001
PDF: 7 pages
Proc. SPIE 4512, Complex Adaptive Structures, (23 October 2001); doi: 10.1117/12.446774
Show Author Affiliations
Hubert S. Gill, Univ. of Florida (United States)
Michael Harmjanz, Univ. of Florida (United States)
Michael J. Scott, Univ. of Florida (United States)

Published in SPIE Proceedings Vol. 4512:
Complex Adaptive Structures
William B. Spillman, Editor(s)

© SPIE. Terms of Use
Back to Top