Molecular Structures, Tautomerism, and Carbon Nucleophilicity of Free-Base Inverted Porphyrins and Carbaporphyrins: A Density Functional Theoretical Study-Reference-Cited by-同舟云学术

Molecular Structures, Tautomerism, and Carbon Nucleophilicity of Free-Base Inverted Porphyrins and Carbaporphyrins: A Density Functional Theoretical Study

Published:1998-11-17 Issue:50 Volume:102 Page:10459-10467
ISSN:1520-6106
Container-title:The Journal of Physical Chemistry B
language:en
Short-container-title:J. Phys. Chem. B

Author:

Ghosh Abhik¹,Wondimagegn Tebikie¹,Nilsen Henning J.¹

Affiliation:

1. Institute of Chemistry, Faculty of Science, University of Tromsø, N-9037 Tromsø, Norway

Publisher

American Chemical Society (ACS)

Subject

Materials Chemistry,Surfaces, Coatings and Films,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jp983010j

Reference33 articles.

1. (a) Sessler, J. L.; Weghorn, S. J.Expanded, Contracted & IsomericPorphyrins; Pergamon/Elsevier: Wiltshire, U.K., 1997.

2. Novel porphyrinoid macrocycles and their metal complexes

3. Tetra-p-tolylporphyrin with an Inverted Pyrrole Ring: A Novel Isomer of Porphyrin

4. "N-Confused Porphyrin": A New Isomer of Tetraphenylporphyrin

5. Reactions of Nickel(II) 2-Aza-5,10,15,20-tetraphenyl-21- carbaporphyrin with Methyl Iodide. The First Structural Characterization of a Paramagnetic Organometallic Nickel(II) Complex

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