Quantifying the exchange coupling in linear copper porphyrin oligomers
Quantifying the exchange coupling in linear copper porphyrin oligomers
Linear π-conjugated porphyrin oligomers are of significant current interest due to their potential applications as molecular wires. In this study we investigate electronic communication in linear butadiyne-linked copper porphyrin oligomers by electron paramagnetic resonance (EPR) spectroscopy via measurement of the exchange interaction, J, between the copper(II) centers. The contributions of dipolar and exchange interactions to the frozen solution continuous wave (cw) EPR spectra of the compounds with two or more copper porphyrin units were explicitly accounted for in numerical simulations using a spin Hamiltonian approach. It is demonstrated that a complete numerical simulation of the powder spectrum of a large spin system with a Hamiltonian dimension of 26[thin space (1/6-em)]244 and beyond can be made feasible by simulating the spectra in the time domain. The exchange coupling in the Cu2 dimer (Cu⋯Cu distance 1.35 nm) is of the order of tens of MHz (Ĥ = −2JS1·S2) and is strongly modulated by low-energy molecular motions such as twisting of the molecule.
Richert, Sabine
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Kuprov, Ilya
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Peeks, Martin D.
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Suturina, Elizaveta
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Cremers, Jonathan
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Anderson, Harry L.
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Timmel, Christiane R.
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Richert, Sabine
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Kuprov, Ilya
bb07f28a-5038-4524-8146-e3fc8344c065
Peeks, Martin D.
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Suturina, Elizaveta
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Cremers, Jonathan
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Anderson, Harry L.
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Timmel, Christiane R.
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Richert, Sabine, Kuprov, Ilya, Peeks, Martin D., Suturina, Elizaveta, Cremers, Jonathan, Anderson, Harry L. and Timmel, Christiane R.
(2017)
Quantifying the exchange coupling in linear copper porphyrin oligomers.
Physical Chemistry Chemical Physics.
(doi:10.1039/c7cp01787a).
Abstract
Linear π-conjugated porphyrin oligomers are of significant current interest due to their potential applications as molecular wires. In this study we investigate electronic communication in linear butadiyne-linked copper porphyrin oligomers by electron paramagnetic resonance (EPR) spectroscopy via measurement of the exchange interaction, J, between the copper(II) centers. The contributions of dipolar and exchange interactions to the frozen solution continuous wave (cw) EPR spectra of the compounds with two or more copper porphyrin units were explicitly accounted for in numerical simulations using a spin Hamiltonian approach. It is demonstrated that a complete numerical simulation of the powder spectrum of a large spin system with a Hamiltonian dimension of 26[thin space (1/6-em)]244 and beyond can be made feasible by simulating the spectra in the time domain. The exchange coupling in the Cu2 dimer (Cu⋯Cu distance 1.35 nm) is of the order of tens of MHz (Ĥ = −2JS1·S2) and is strongly modulated by low-energy molecular motions such as twisting of the molecule.
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Accepted/In Press date: 29 May 2017
e-pub ahead of print date: 9 June 2017
Organisations:
Computational Systems Chemistry, Magnetic Resonance
Identifiers
Local EPrints ID: 411620
URI: http://eprints.soton.ac.uk/id/eprint/411620
ISSN: 1463-9076
PURE UUID: 1fc5389a-83a8-40a6-9215-a7bd41632984
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Date deposited: 21 Jun 2017 16:31
Last modified: 16 Mar 2024 05:27
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Contributors
Author:
Sabine Richert
Author:
Martin D. Peeks
Author:
Elizaveta Suturina
Author:
Jonathan Cremers
Author:
Harry L. Anderson
Author:
Christiane R. Timmel
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