Literature DB >> 27992878

Aromatic and antiaromatic ring currents in a molecular nanoring.

Martin D Peeks1, Timothy D W Claridge1, Harry L Anderson1.   

Abstract

Aromatic and antiaromatic molecules-which have delocalized circuits of [4n + 2] or [4n] electrons, respectively-exhibit ring currents around their perimeters. The direction of the ring current in an aromatic molecule is such as to generate a magnetic field that opposes the external field inside the ring (a 'diatropic' current), while the ring current in an antiaromatic molecule flows in the reverse direction ('paratropic'). Similar persistent currents occur in metal or semiconductor rings, when the phase coherence of the electronic wavefunction is preserved around the ring. Persistent currents in non-molecular rings switch direction as a function of the magnetic flux passing through the ring, so that they can be changed from diatropic ('aromatic') to paratropic ('antiaromatic') simply by changing the external magnetic field. As in molecular systems, the direction of the persistent current also depends on the number of electrons. The relationship between ring currents in molecular and non-molecular rings is poorly understood, partly because they are studied in different size regimes: the largest aromatic molecules have diameters of about one nanometre, whereas persistent currents are observed in microfabricated rings with diameters of 20-1,000 nanometres. Understanding the connection between aromaticity and quantum-coherence effects in mesoscopic rings provides a motivation for investigating ring currents in molecules of an intermediate size. Here we show, using nuclear magnetic resonance spectroscopy and density functional theory, that a six-porphyrin nanoring template complex, with a diameter of 2.4 nanometres, is antiaromatic in its 4+ oxidation state (80 π electrons) and aromatic in its 6+ oxidation state (78 π electrons). The antiaromatic state has a huge paramagnetic susceptibility, despite having no unpaired electrons. This work demonstrates that a global ring current can be promoted in a macrocycle by adjusting its oxidation state to suppress the local ring currents of its components.The discovery of ring currents around a molecule with a circumference of 7.5 nanometres, at room temperature, shows that quantum coherence can persist in surprisingly large molecular frameworks.

Entities:  

Year:  2016        PMID: 27992878     DOI: 10.1038/nature20798

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  24 in total

1.  Belt-shaped π-systems: relating geometry to electronic structure in a six-porphyrin nanoring.

Authors:  Johannes K Sprafke; Dmitry V Kondratuk; Michael Wykes; Amber L Thompson; Markus Hoffmann; Rokas Drevinskas; Wei-Hsin Chen; Chaw Keong Yong; Joakim Kärnbratt; Joseph E Bullock; Marc Malfois; Michael R Wasielewski; Bo Albinsson; Laura M Herz; Donatas Zigmantas; David Beljonne; Harry L Anderson
Journal:  J Am Chem Soc       Date:  2011-10-12       Impact factor: 15.419

2.  How aromatic are large (4n + 2)pi annulenes?

Authors:  Chaitanya S Wannere; Paul von Ragué Schleyer
Journal:  Org Lett       Date:  2003-03-20       Impact factor: 6.005

3.  Anisotropy of the induced current density (ACID), a general method to quantify and visualize electronic delocalization.

Authors:  Daniel Geuenich; Kirsten Hess; Felix Köhler; Rainer Herges
Journal:  Chem Rev       Date:  2005-10       Impact factor: 60.622

4.  Persistent currents in normal metal rings.

Authors:  A C Bleszynski-Jayich; W E Shanks; B Peaudecerf; E Ginossar; F von Oppen; L Glazman; J G E Harris
Journal:  Science       Date:  2009-10-09       Impact factor: 47.728

5.  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

6.  A consistent and accurate ab initio parametrization of density functional dispersion correction (DFT-D) for the 94 elements H-Pu.

Authors:  Stefan Grimme; Jens Antony; Stephan Ehrlich; Helge Krieg
Journal:  J Chem Phys       Date:  2010-04-21       Impact factor: 3.488

7.  In-plane aromaticity in cycloparaphenylene dications: a magnetic circular dichroism and theoretical study.

Authors:  Naoyuki Toriumi; Atsuya Muranaka; Eiichi Kayahara; Shigeru Yamago; Masanobu Uchiyama
Journal:  J Am Chem Soc       Date:  2014-12-24       Impact factor: 15.419

8.  Experimental and computational evaluation of the barrier to torsional rotation in a butadiyne-linked porphyrin dimer.

Authors:  Martin D Peeks; Patrik Neuhaus; Harry L Anderson
Journal:  Phys Chem Chem Phys       Date:  2016-02-21       Impact factor: 3.676

9.  Non-perturbative magnetic phenomena in closed-shell paramagnetic molecules.

Authors:  Erik I Tellgren; Trygve Helgaker; Alessandro Soncini
Journal:  Phys Chem Chem Phys       Date:  2009-04-16       Impact factor: 3.676

10.  Transient EPR Reveals Triplet State Delocalization in a Series of Cyclic and Linear π-Conjugated Porphyrin Oligomers.

Authors:  Claudia E Tait; Patrik Neuhaus; Martin D Peeks; Harry L Anderson; Christiane R Timmel
Journal:  J Am Chem Soc       Date:  2015-06-19       Impact factor: 15.419

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  20 in total

Review 1.  Aromatic hydrocarbon belts.

Authors:  Qing-Hui Guo; Yunyan Qiu; Mei-Xiang Wang; J Fraser Stoddart
Journal:  Nat Chem       Date:  2021-04-15       Impact factor: 24.427

2.  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

3.  Ring currents modulate optoelectronic properties of aromatic chromophores at 25 T.

Authors:  Bryan Kudisch; Margherita Maiuri; Luca Moretti; Maria B Oviedo; Leon Wang; Daniel G Oblinsky; Robert K Prud'homme; Bryan M Wong; Stephen A McGill; Gregory D Scholes
Journal:  Proc Natl Acad Sci U S A       Date:  2020-05-08       Impact factor: 11.205

4.  3D global aromaticity in a fully conjugated diradicaloid cage at different oxidation states.

Authors:  Yong Ni; Tullimilli Y Gopalakrishna; Hoa Phan; Taeyeon Kim; Tun Seng Herng; Yi Han; Tao Tao; Jun Ding; Dongho Kim; Jishan Wu
Journal:  Nat Chem       Date:  2020-01-20       Impact factor: 24.427

5.  Single-Acetylene Linked Porphyrin Nanorings.

Authors:  Michel Rickhaus; Andreas Vargas Jentzsch; Lara Tejerina; Isabell Grübner; Michael Jirasek; Timothy D W Claridge; Harry L Anderson
Journal:  J Am Chem Soc       Date:  2017-11-09       Impact factor: 15.419

6.  Unexpected Interactions between Alkyl Straps and Pyridine Ligands in Sulfur-Strapped Porphyrin Nanorings.

Authors:  Cécile Roche; Qianfu Luo; Guzmán Gil-Ramírez; Hua-Wei Jiang; Daniel R Kohn; Yaoyao Xiong; Amber L Thompson; Harry L Anderson
Journal:  J Org Chem       Date:  2017-07-07       Impact factor: 4.354

7.  Fluorescence-Lifetime Imaging and Super-Resolution Microscopies Shed Light on the Directed- and Self-Assembly of Functional Porphyrins onto Carbon Nanotubes and Flat Surfaces.

Authors:  Boyang Mao; David G Calatayud; Vincenzo Mirabello; Navaratnarajah Kuganathan; Haobo Ge; Robert M J Jacobs; Ashley M Shepherd; José A Ribeiro Martins; Jorge Bernardino De La Serna; Benjamin J Hodges; Stanley W Botchway; Sofia I Pascu
Journal:  Chemistry       Date:  2017-05-19       Impact factor: 5.236

8.  Studying an antiaromatic polycyclic hydrocarbon adsorbed on different surfaces.

Authors:  Zsolt Majzik; Niko Pavliček; Manuel Vilas-Varela; Dolores Pérez; Nikolaj Moll; Enrique Guitián; Gerhard Meyer; Diego Peña; Leo Gross
Journal:  Nat Commun       Date:  2018-03-22       Impact factor: 14.919

9.  A reversible single-molecule switch based on activated antiaromaticity.

Authors:  Xiaodong Yin; Yaping Zang; Liangliang Zhu; Jonathan Z Low; Zhen-Fei Liu; Jing Cui; Jeffrey B Neaton; Latha Venkataraman; Luis M Campos
Journal:  Sci Adv       Date:  2017-10-27       Impact factor: 14.136

10.  Electronic Delocalization in the Radical Cations of Porphyrin Oligomer Molecular Wires.

Authors:  Martin D Peeks; Claudia E Tait; Patrik Neuhaus; Georg M Fischer; Markus Hoffmann; Renée Haver; Arjen Cnossen; Jeffrey R Harmer; Christiane R Timmel; Harry L Anderson
Journal:  J Am Chem Soc       Date:  2017-07-24       Impact factor: 15.419

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