Reaction Pathway and Free Energy Profile for Conversion of π-Conjugation Modes in Porphyrin Isomer-Reference-Cited by-同舟云学术

Reaction Pathway and Free Energy Profile for Conversion of π-Conjugation Modes in Porphyrin Isomer

Published:2012-10-11 Issue:20 Volume:77 Page:8946-8955
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Matsuo Takashi¹,Tohi Yuji²,Hayashi Takashi²

Affiliation:

1. Graduate School of Materials Science, Nara Institute of Science and Technology (NAIST), Ikoma, Nara 630-0192, Japan

2. Department of Applied Chemistry, Graduate School of Engineering, Osaka University, Suita, Osaka 565-0871, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo3013379

Reference49 articles.

1. Stępień, M.; Latos-Grażyński, L.InTopics in Hetercyclic Chemsitry 19. Aromaticity in Heterocyclic Compounds;Gupta, R. R., Ed.Springer-Verlag Berlin Heidelberg:Heidelberg, Germany, 2009, p83–153.

2. Sessler, J. L.; Gebauer, A.; Vogel, E.InThe Porphyrin Handbook;Kadish, K. M., Smith, K. M., Guilard, E., Eds.Academic Press:San Diego, 2000; Vol.1, p1.

3. Antiaromaticity in Monocyclic Conjugated Carbon Rings

4. Paolesse, R.InPorphyrin Handbook;Kadish, K. M.; Smith, K. M.; Guilard, R., Eds.Academic Press:San Diego, 2000; Vol.2, pp201–232.

5. Nonlinear Optical Properties and Excited-State Dynamics of Highly Symmetric Expanded Porphyrins

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