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http://dx.doi.org/10.1002/anie.201105809 | DOI Listing |
Angew Chem Int Ed Engl
July 2023
Department of Chemistry, Graduate School of Science, Kyoto University, Kitashirakawa Oiwake-cho, Sakyo-ku, Kyoto, 606-8502, Japan.
Internally-bridged octaphyrin(1.1.1.
View Article and Find Full Text PDFPhys Chem Chem Phys
April 2016
Sorbonne Universités, UPMC Univ. Paris 06, UMR7616, Laboratoire de Chimie Théorique, F-75005, Paris, France. and CNRS, UMR 7616, Laboratoire de Chimie Thérique, F-75005, Paris, France.
In recent years, expanded porphyrins have emerged as a promising class of π-conjugated molecules that display unique electronic, optical and conformational properties. Several expanded porphyrins can switch between planar and twisted conformations, which have different photophysical properties. Such a change of topology involves a Hückel-Möbius aromaticity switch in a single molecule and it can be induced by solvent, pH and metallation.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2011
Department of Chemistry, Graduate School of Science, Kyoto University, Kyoto, Japan.
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