Literature DB >> 12974651

Core-modified expanded porphyrins: new generation organic materials.

Tavarekere K Chandrashekar1, Sundararaman Venkatraman.   

Abstract

Even though the first expanded porphyrin was reported in the mid-1960s, the advances in its chemistry are more recent. New and powerful synthetic methods have facilitated the availability in affordable quantities of expanded porphyrins in general and core modified systems in particular. This has stimulated interest in studying various properties pertaining to their potential applications in biomedicine and materials chemistry. In this Account, we not only summarize the details of the synthetic methodologies reported, but we also highlight studies that focus on the structural diversity, aromaticity, and anion and cation binding abilities of expanded porphyrins.

Entities:  

Year:  2003        PMID: 12974651     DOI: 10.1021/ar020284n

Source DB:  PubMed          Journal:  Acc Chem Res        ISSN: 0001-4842            Impact factor:   22.384


  10 in total

Review 1.  Transition-metal complexes of expanded porphyrins.

Authors:  Jonathan L Sessler; Elisa Tomat
Journal:  Acc Chem Res       Date:  2007-03-31       Impact factor: 22.384

2.  Core-modified expanded porphyrins with large third-order nonlinear optical response.

Authors:  Harapriya Rath; Jeyaraman Sankar; Viswanathan Prabhuraja; Tavarekere K Chandrashekar; Amit Nag; Debabrata Goswami
Journal:  J Am Chem Soc       Date:  2005-08-24       Impact factor: 15.419

3.  Syntheses of calix[4]pyrroles by amberlyst-15 catalyzed cyclocondensations of pyrrole with selected ketones.

Authors:  Shive Murat Singh Chauhan; Bhaskar Garg; Tanuja Bisht
Journal:  Molecules       Date:  2007-11-09       Impact factor: 4.411

4.  Tripyrrin-armed isosmaragdyrins: synthesis, heterodinuclear coordination, and protonation-triggered helical inversion.

Authors:  Chengjie Li; Kai Zhang; Masatoshi Ishida; Qizhao Li; Keito Shimomura; Glib Baryshnikov; Xin Li; Mathew Savage; Xin-Yan Wu; Sihai Yang; Hiroyuki Furuta; Yongshu Xie
Journal:  Chem Sci       Date:  2020-02-04       Impact factor: 9.825

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

6.  Computational Studies on Optoelectronic and Nonlinear Properties of Octaphyrin Derivatives.

Authors:  Nasarul Islam; Irfan H Lone
Journal:  Front Chem       Date:  2017-03-06       Impact factor: 5.221

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

9.  Fine-Tuning of Nonlinear Optical Contrasts of Hexaphyrin-Based Molecular Switches Using Inverse Design.

Authors:  Eline Desmedt; Tatiana Woller; Jos L Teunissen; Freija De Vleeschouwer; Mercedes Alonso
Journal:  Front Chem       Date:  2021-12-03       Impact factor: 5.221

10.  Oxidation-Induced Detachment of Ruthenoarene Units and Oxygen Insertion in Bis-Pd(II) Hexaphyrin π-Ruthenium Complexes.

Authors:  Akito Nakai; Takayuki Tanaka; Atsuhiro Osuka
Journal:  Molecules       Date:  2020-06-15       Impact factor: 4.411

  10 in total

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