Synthesis, Optical Properties, and Electronic Structures of Tetrakis(pentafluorophenyl)tetrathiaisophlorin Dioxide.

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ID: 238221
2016
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Abstract
The synthesis, structure, optical and redox properties, and electronic structure of tetrakis(pentafluorophenyl)tetrathiaisophlorin dioxide (12) are reported. Oxidation of tetrakis(pentafluorophenyl)tetrathiaisophlorin (11) with dimethyldioxirane afforded the oxidized product, which was the tetrathiaisophlorin with two thiophene 1-oxide moieties (12). More significant nonplanarity and greater bond length alternation in 12 than those of 11 were observed by X-ray structural analysis. The absorption spectrum of 12 contains two bands at λ=348 and 276 nm, with a weak tail that extends to λ≈650 nm. Analysis of the magnetic circular dichroism spectrum of 12, based on Michl's 4N-perimeter model and molecular orbital calculations, indicate that the broad band at λ=348 nm appears to contain N2 and P2 bands, and 12 is classified as a 4nπ system, similar to 11. The nuclear-independent chemical shift values and (1) H NMR spectroscopy data indicate that 12 has more antiaromatic character than 11.
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mishra2016synthesischemistry Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Mishra, Vijay Lakshmi;Furuyama, Taniyuki;Kobayashi, Nagao;Goto, Kenta;Miyazaki, Takaaki;Yang, Jye-Shane;Shinmyozu, Teruo;
Journal Chemistry (Weinheim an der Bergstrasse, Germany)
Year 2016
DOI
10.1002/chem.201505079
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