| Literature DB >> 28783347 |
Gonzalo Anguera1, James T Brewster1, Matthew D Moore1, Juhoon Lee1, Gabriela I Vargas-Zúñiga1, Hadiqa Zafar1, Vincent M Lynch1, Jonathan L Sessler1.
Abstract
Using naphthobipyrrole as a functional building block, a new expanded porphyrin, naphthoisoamethyrin, was prepared in 85% yield under acid-catalyzed [4 + 2] MacDonald coupling conditions. Treatment of naphthoisoamethyrin with the nonaqueous uranyl silylamide salt [UO2[N(SiMe3)2]2·2THF] yielded the corresponding uranyl complex. Upon metalation, naphthoisoamethyrin undergoes a two-electron oxidation to yield a formal 22 π-electron aromatic species, as inferred from 1H NMR and UV-vis spectroscopy, as well as cyclic voltammetry.Entities:
Year: 2017 PMID: 28783347 DOI: 10.1021/acs.inorgchem.7b01668
Source DB: PubMed Journal: Inorg Chem ISSN: 0020-1669 Impact factor: 5.165