Exploring the structure–aromaticity relationship in Hückel and Möbius N-fused pentaphyrins using DFT-Reference-Cited by-同舟云学术

Exploring the structure–aromaticity relationship in Hückel and Möbius N-fused pentaphyrins using DFT

Published:2014 Issue:28 Volume:16 Page:14396-14407
ISSN:1463-9076
Container-title:Phys. Chem. Chem. Phys.
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Alonso M.¹²³,Geerlings P.¹²³,. De Proft F¹²³

Affiliation:

1. Eenheid Algemene Chemie (ALGC)

2. Vrije Universiteit Brussel (VUB)

3. 1050 Brussels, Belgium

Abstract

Fine-tuning of the molecular topology and macrocyclic aromaticity of N-fused pentaphyrins by changing the number of π electrons and meso-substituents.

Funder

European Commission

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2014/CP/C3CP55509G

Reference57 articles.

1. Expanded Porphyrins: Intriguing Structures, Electronic Properties, and Reactivities

2. Figure Eights, Möbius Bands, and More: Conformation and Aromaticity of Porphyrinoids

3. Oligopyrrole Macrocycles: Receptors and Chemosensors for Potentially Hazardous Materials

4. Water-soluble doubly N-confused hexaphyrin: a near-IR fluorescent Zn(ii) ion sensor in water

5. Fused porphyrinoids as promising near-infrared absorbing dyes

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