Literature DB >> 25866899

Stable [48]-, [50]-, and [52]dodecaphyrins(1.1.0.1.1.0.1.1.0.1.1.0): the largest Hückel aromatic molecules.

Takanori Soya1, Woojae Kim2, Dongho Kim3, Atsuhiro Osuka4.   

Abstract

[52]Dodecaphyrin(1.1.0.1.1.0.1.1.0.1.1.0) was quantitatively oxidized with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) to the corresponding [50]dodecaphyrin. Further oxidation of [50]dodecaphyrin with MnO2 quantitatively afforded [48]dodecaphyrin. Of the three, [50]dodecaphyrin showed Hückel aromatic character as the largest aromatic molecule reported to date. Protonation of [50]dodecaphyrin with methanesulfonic acid (MSA) led to the formation of a planar tetraprotonated species that displayed a sharp and intense Soret-like band at 906 nm with ε=6.5×10(5) M(-1) cm(-1) and Q-band-like bands at 1346 and 1600 nm.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  aromaticity; dodecaphyrins; expanded porphyrins; planar molecules; protonation

Year:  2015        PMID: 25866899     DOI: 10.1002/chem.201500650

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  4 in total

1.  Aromatic and antiaromatic ring currents in a molecular nanoring.

Authors:  Martin D Peeks; Timothy D W Claridge; Harry L Anderson
Journal:  Nature       Date:  2016-12-19       Impact factor: 49.962

2.  Choice of a spin singlet or triplet: electronic properties of Bis-Co(II), Bis-Ni(II), Bis-Cu(II) and Bis-Zn(II) oxygen doubly N-confused hexaphyrin (1.1.1.1.1.1).

Authors:  Gang Sun; E Lei; Xiang-Shuai Liu; Xi-Xin Duan; Chun-Guang Liu
Journal:  J Mol Model       Date:  2018-06-30       Impact factor: 1.810

3.  Switchable π-electronic network of bis(α-oligothienyl)-substituted hexaphyrins between helical versus rectangular circuit.

Authors:  Juwon Oh; Hirotaka Mori; Young Mo Sung; Woojae Kim; Atsuhiro Osuka; Dongho Kim
Journal:  Chem Sci       Date:  2015-12-08       Impact factor: 9.825

4.  Circular linkage of intramolecular multi-hydrogen bonding frameworks through nucleophilic substitutions of β-dicarbonyls onto cyanuric chloride and subsequent tautomerisation.

Authors:  Ayano Awatani; Masaaki Suzuki
Journal:  RSC Adv       Date:  2020-10-23       Impact factor: 4.036

  4 in total

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