Literature DB >> 21403958

Expanded porphyrins and aromaticity.

Atsuhiro Osuka1, Shohei Saito.   

Abstract

meso-Aryl-substituted expanded porphyrins that are porphyrin homologues consisting of more than five pyrrolic units are a nice platform to realize diverse aromatic and antiaromatic species as well as stable radical species. They are also an ideal series to realize topologically twisted molecules with distinct Möbius aromaticity and antiaromaticity. © The Royal Society of Chemistry 2011

Entities:  

Year:  2011        PMID: 21403958     DOI: 10.1039/c1cc10534e

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  13 in total

1.  Supramolecular Chemistry of Anionic Dimers, Trimers, Tetramers and Clusters.

Authors:  Qing He; Peiyu Tu; Jonathan L Sessler
Journal:  Chem       Date:  2017-12-14       Impact factor: 22.804

2.  Protonation-coupled redox reactions in planar antiaromatic meso-pentafluorophenyl-substituted o-phenylene-bridged annulated rosarins.

Authors:  Masatoshi Ishida; Soo-Jin Kim; Christian Preihs; Kei Ohkubo; Jong Min Lim; Byung Sun Lee; Jung Su Park; Vincent M Lynch; Vladimir V Roznyatovskiy; Tridib Sarma; Pradeepta K Panda; Chang-Hee Lee; Shunichi Fukuzumi; Dongho Kim; Jonathan L Sessler
Journal:  Nat Chem       Date:  2012-12-09       Impact factor: 24.427

3.  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

4.  Theoretical investigation of the aromaticity and electronic properties of protonated and unprotonated molecules in the series hexaphyrin(1.0.0.1.0.0) to hexaphyrin(1.1.1.1.1.1).

Authors:  Gang Sun; Xi-Xin Duan; Chun-Hui Yu; Chun-Guang Liu
Journal:  J Mol Model       Date:  2015-11-20       Impact factor: 1.810

5.  5,20-Bis(α-oligothienyl)-substituted [26]hexaphyrins possessing electronic circuits strongly perturbed by meso-oligothienyl substituents.

Authors:  Hirotaka Mori; Masaaki Suzuki; Woojae Kim; Jong Min Lim; Dongho Kim; Atsuhiro Osuka
Journal:  Chem Sci       Date:  2014-12-02       Impact factor: 9.825

Review 6.  Porphyrinoids as a platform of stable radicals.

Authors:  Daiki Shimizu; Atsuhiro Osuka
Journal:  Chem Sci       Date:  2018-01-08       Impact factor: 9.825

7.  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

8.  Reversible π-system switching of thiophene-fused thiahexaphyrins by solvent and oxidation/reduction.

Authors:  Tomohiro Higashino; Atsushi Kumagai; Shigeyoshi Sakaki; Hiroshi Imahori
Journal:  Chem Sci       Date:  2018-08-14       Impact factor: 9.825

Review 9.  Transition metal catalyzed borylation of functional π-systems.

Authors:  Hiroshi Shinokubo
Journal:  Proc Jpn Acad Ser B Phys Biol Sci       Date:  2014       Impact factor: 3.493

10.  Aromaticity as a Guiding Concept for Spectroscopic Features and Nonlinear Optical Properties of Porphyrinoids.

Authors:  Tatiana Woller; Paul Geerlings; Frank De Proft; Benoît Champagne; Mercedes Alonso
Journal:  Molecules       Date:  2018-06-01       Impact factor: 4.411

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.