Standard

Excitation of singlet-triplet coherences in pairs of nearly-equivalent spins. / Sheberstov, Kirill F.; Kiryutin, Alexey S.; Bengs, Christian et al.

In: Physical Chemistry Chemical Physics, Vol. 21, No. 11, 13.03.2019, p. 6087-6100.

Research output: Contribution to journalArticlepeer-review

Harvard

Sheberstov, KF, Kiryutin, AS, Bengs, C, Hill-Cousins, JT, Brown, LJ, Brown, RCD, Pileio, G, Levitt, MH, Yurkovskaya, AV & Ivanov, KL 2019, 'Excitation of singlet-triplet coherences in pairs of nearly-equivalent spins', Physical Chemistry Chemical Physics, vol. 21, no. 11, pp. 6087-6100. https://doi.org/10.1039/c9cp00451c

APA

Sheberstov, K. F., Kiryutin, A. S., Bengs, C., Hill-Cousins, J. T., Brown, L. J., Brown, R. C. D., Pileio, G., Levitt, M. H., Yurkovskaya, A. V., & Ivanov, K. L. (2019). Excitation of singlet-triplet coherences in pairs of nearly-equivalent spins. Physical Chemistry Chemical Physics, 21(11), 6087-6100. https://doi.org/10.1039/c9cp00451c

Vancouver

Sheberstov KF, Kiryutin AS, Bengs C, Hill-Cousins JT, Brown LJ, Brown RCD et al. Excitation of singlet-triplet coherences in pairs of nearly-equivalent spins. Physical Chemistry Chemical Physics. 2019 Mar 13;21(11):6087-6100. doi: 10.1039/c9cp00451c

Author

Sheberstov, Kirill F. ; Kiryutin, Alexey S. ; Bengs, Christian et al. / Excitation of singlet-triplet coherences in pairs of nearly-equivalent spins. In: Physical Chemistry Chemical Physics. 2019 ; Vol. 21, No. 11. pp. 6087-6100.

BibTeX

@article{e1e99b73bfe441a0946d5c09e7758697,
title = "Excitation of singlet-triplet coherences in pairs of nearly-equivalent spins",
abstract = " We present approaches for an efficient excitation of singlet-triplet coherences in pairs of nearly-equivalent spins. Standard Nuclear Magnetic Resonance (NMR) pulse sequences do not excite these coherences at all or with very low efficiency. The single quantum singlet-triplet coherences, here termed the outer singlet-triplet coherences, correspond to lines of low intensity in the NMR spectrum of a strongly-coupled spin pair (they are sometimes referred to as {"}forbidden transitions{"}), whereas the zero-quantum coherences, here termed the inner singlet-triplet coherences, do not have a direct spectral manifestation. In the present study, we investigated singlet-triplet coherences in a pair of nearly-equivalent carbon spins of the 13 C-isotopomer of a specially designed naphthalene derivative with optimized relaxation properties. We propose and compare several techniques to drive the singlet-triplet coherence in strongly coupled spin pairs. First, we study different methods for efficient excitation of the outer singlet-triplet coherences. The achieved conversion efficiency of magnetization to the coherences of interest is close to the theoretically allowed maximum. Second, we propose methods to convert the outer coherences into the inner singlet-triplet coherence. The inner singlet-triplet coherence is insensitive to field inhomogeneity and can be long-lived. By probing this coherence, we perform a very precise measurement of the spin-spin J-couplings. A remarkable property of this coherence is that it can be preserved even in absence of a spin-locking radiofrequency field. Consequently, it is possible to shuttle the sample between different magnetic fields preserving the coherence. This allows one to study the field dependence of the relaxation time, T IST , of the inner singlet-triplet coherence by performing field-cycling experiments. We observed dramatic changes of the ratio T IST /T 1 from about 1 (in strong fields) up to 2.4 (in weak fields), which is the evidence of a significant influence of the chemical shift anisotropy on relaxation. We have detected a remarkably long lifetime of the inner singlet-triplet coherence of about 200 s at the magnetic field of 5 mT. ",
keywords = "LONG-LIVED STATES, NMR-SPECTROSCOPY, ORDER",
author = "Sheberstov, {Kirill F.} and Kiryutin, {Alexey S.} and Christian Bengs and Hill-Cousins, {Joseph T.} and Brown, {Lynda J.} and Brown, {Richard C.D.} and Giuseppe Pileio and Levitt, {Malcolm H.} and Yurkovskaya, {Alexandra V.} and Ivanov, {Konstantin L.}",
year = "2019",
month = mar,
day = "13",
doi = "10.1039/c9cp00451c",
language = "English",
volume = "21",
pages = "6087--6100",
journal = "Physical Chemistry Chemical Physics",
issn = "1463-9076",
publisher = "Royal Society of Chemistry",
number = "11",

}

RIS

TY - JOUR

T1 - Excitation of singlet-triplet coherences in pairs of nearly-equivalent spins

AU - Sheberstov, Kirill F.

AU - Kiryutin, Alexey S.

AU - Bengs, Christian

AU - Hill-Cousins, Joseph T.

AU - Brown, Lynda J.

AU - Brown, Richard C.D.

AU - Pileio, Giuseppe

AU - Levitt, Malcolm H.

AU - Yurkovskaya, Alexandra V.

AU - Ivanov, Konstantin L.

PY - 2019/3/13

Y1 - 2019/3/13

N2 - We present approaches for an efficient excitation of singlet-triplet coherences in pairs of nearly-equivalent spins. Standard Nuclear Magnetic Resonance (NMR) pulse sequences do not excite these coherences at all or with very low efficiency. The single quantum singlet-triplet coherences, here termed the outer singlet-triplet coherences, correspond to lines of low intensity in the NMR spectrum of a strongly-coupled spin pair (they are sometimes referred to as "forbidden transitions"), whereas the zero-quantum coherences, here termed the inner singlet-triplet coherences, do not have a direct spectral manifestation. In the present study, we investigated singlet-triplet coherences in a pair of nearly-equivalent carbon spins of the 13 C-isotopomer of a specially designed naphthalene derivative with optimized relaxation properties. We propose and compare several techniques to drive the singlet-triplet coherence in strongly coupled spin pairs. First, we study different methods for efficient excitation of the outer singlet-triplet coherences. The achieved conversion efficiency of magnetization to the coherences of interest is close to the theoretically allowed maximum. Second, we propose methods to convert the outer coherences into the inner singlet-triplet coherence. The inner singlet-triplet coherence is insensitive to field inhomogeneity and can be long-lived. By probing this coherence, we perform a very precise measurement of the spin-spin J-couplings. A remarkable property of this coherence is that it can be preserved even in absence of a spin-locking radiofrequency field. Consequently, it is possible to shuttle the sample between different magnetic fields preserving the coherence. This allows one to study the field dependence of the relaxation time, T IST , of the inner singlet-triplet coherence by performing field-cycling experiments. We observed dramatic changes of the ratio T IST /T 1 from about 1 (in strong fields) up to 2.4 (in weak fields), which is the evidence of a significant influence of the chemical shift anisotropy on relaxation. We have detected a remarkably long lifetime of the inner singlet-triplet coherence of about 200 s at the magnetic field of 5 mT.

AB - We present approaches for an efficient excitation of singlet-triplet coherences in pairs of nearly-equivalent spins. Standard Nuclear Magnetic Resonance (NMR) pulse sequences do not excite these coherences at all or with very low efficiency. The single quantum singlet-triplet coherences, here termed the outer singlet-triplet coherences, correspond to lines of low intensity in the NMR spectrum of a strongly-coupled spin pair (they are sometimes referred to as "forbidden transitions"), whereas the zero-quantum coherences, here termed the inner singlet-triplet coherences, do not have a direct spectral manifestation. In the present study, we investigated singlet-triplet coherences in a pair of nearly-equivalent carbon spins of the 13 C-isotopomer of a specially designed naphthalene derivative with optimized relaxation properties. We propose and compare several techniques to drive the singlet-triplet coherence in strongly coupled spin pairs. First, we study different methods for efficient excitation of the outer singlet-triplet coherences. The achieved conversion efficiency of magnetization to the coherences of interest is close to the theoretically allowed maximum. Second, we propose methods to convert the outer coherences into the inner singlet-triplet coherence. The inner singlet-triplet coherence is insensitive to field inhomogeneity and can be long-lived. By probing this coherence, we perform a very precise measurement of the spin-spin J-couplings. A remarkable property of this coherence is that it can be preserved even in absence of a spin-locking radiofrequency field. Consequently, it is possible to shuttle the sample between different magnetic fields preserving the coherence. This allows one to study the field dependence of the relaxation time, T IST , of the inner singlet-triplet coherence by performing field-cycling experiments. We observed dramatic changes of the ratio T IST /T 1 from about 1 (in strong fields) up to 2.4 (in weak fields), which is the evidence of a significant influence of the chemical shift anisotropy on relaxation. We have detected a remarkably long lifetime of the inner singlet-triplet coherence of about 200 s at the magnetic field of 5 mT.

KW - LONG-LIVED STATES

KW - NMR-SPECTROSCOPY

KW - ORDER

UR - http://www.scopus.com/inward/record.url?scp=85062816315&partnerID=8YFLogxK

U2 - 10.1039/c9cp00451c

DO - 10.1039/c9cp00451c

M3 - Article

C2 - 30810569

AN - SCOPUS:85062816315

VL - 21

SP - 6087

EP - 6100

JO - Physical Chemistry Chemical Physics

JF - Physical Chemistry Chemical Physics

SN - 1463-9076

IS - 11

ER -

ID: 18860633