| Literature DB >> 27268663 |
Tetsuo Okujima1, Chie Ando1, Saurabh Agrawal2, Hiroki Matsumoto1, Shigeki Mori3, Keishi Ohara1, Ichiro Hisaki4, Takahiro Nakae1, Masayoshi Takase1, Hidemitsu Uno1, Nagao Kobayashi2.
Abstract
An acenaphthylene-fused cyclo[10]pyrrole 1b was selectively synthesized via an oxidative coupling reaction of the corresponding 2,2'-bipyrrole with the appropriate dianion template, croconate anion. The structure of 1b as the isolated largest cyclo[n]pyrrole was elucidated by X-ray crystallographic analysis. The absorption spectrum exhibited a markedly red-shifted, intensified L band at 1982 nm, which was interpreted by application of Michl's perimeter and Gouterman's 4-orbital models, supported by magnetic circular dichroism (MCD) data and theoretical calculations.Entities:
Year: 2016 PMID: 27268663 DOI: 10.1021/jacs.6b04941
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419