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Exploring the reactivity of β-cyclodextrin-encapsulated anthraquinone-2,6-disulfonate. / Babenko, Simon V.; Melnikov, Anatoly R.; Tsentalovich, Yuri P. et al.

In: Journal of Inclusion Phenomena and Macrocyclic Chemistry, Vol. 97, No. 1-2, 01.06.2020, p. 121-127.

Research output: Contribution to journalArticlepeer-review

Harvard

Babenko, SV, Melnikov, AR, Tsentalovich, YP & Kruppa, AI 2020, 'Exploring the reactivity of β-cyclodextrin-encapsulated anthraquinone-2,6-disulfonate', Journal of Inclusion Phenomena and Macrocyclic Chemistry, vol. 97, no. 1-2, pp. 121-127. https://doi.org/10.1007/s10847-020-00991-2

APA

Babenko, S. V., Melnikov, A. R., Tsentalovich, Y. P., & Kruppa, A. I. (2020). Exploring the reactivity of β-cyclodextrin-encapsulated anthraquinone-2,6-disulfonate. Journal of Inclusion Phenomena and Macrocyclic Chemistry, 97(1-2), 121-127. https://doi.org/10.1007/s10847-020-00991-2

Vancouver

Babenko SV, Melnikov AR, Tsentalovich YP, Kruppa AI. Exploring the reactivity of β-cyclodextrin-encapsulated anthraquinone-2,6-disulfonate. Journal of Inclusion Phenomena and Macrocyclic Chemistry. 2020 Jun 1;97(1-2):121-127. doi: 10.1007/s10847-020-00991-2

Author

Babenko, Simon V. ; Melnikov, Anatoly R. ; Tsentalovich, Yuri P. et al. / Exploring the reactivity of β-cyclodextrin-encapsulated anthraquinone-2,6-disulfonate. In: Journal of Inclusion Phenomena and Macrocyclic Chemistry. 2020 ; Vol. 97, No. 1-2. pp. 121-127.

BibTeX

@article{3d9e9daed5fa443da103d31e14656ca4,
title = "Exploring the reactivity of β-cyclodextrin-encapsulated anthraquinone-2,6-disulfonate",
abstract = "The intracomplex reaction of anthraquinone-2,6-disulfonate (AQDS) in triplet excited state (3AQDS) with beta-cyclodextrin (CD) and the reaction of 3AQDS:CD complex with external quencher, N-Acetyl-l-Tyrosine (TyrO−), have been studied using laser flash photolysis, 1H NMR and 1H CIDNP. The two reactions were found to be competing with each other. The intracomplex hydrogen abstraction previously proposed for 3AQDS:CD complex may represent a two-step process, where at first stage an electron is transferred from the –OH group of CD to 3AQDS followed by a proton transfer and recombination of AQDS and CD radicals resulting in a stable AQDS-CD product. The rate constant of the intracomplex electron transfer from CD to 3AQDS was found to be 6 ± 1 × 106 s−1 and the rate of subsequent proton transfer is 1 ± 0.1 × 106 s−1. The rate constant of electron transfer between TyrO− and 3AQDS:CD complex (0.4 ± 0.1 × 109 M−1 s−1) drops approx. by half compared to that in the reaction between TyrO− and free 3AQDS (0.8 ± 0.1 × 109 M−1 s−1).",
keywords = "Anthraquinone, CIDNP, Hydrogen abstraction, Inclusion complex, β-Cyclodextrin, INCLUSION COMPLEXATION, DYNAMICS, PHOTOCHEMISTRY, CONSTANT, beta-Cyclodextrin",
author = "Babenko, {Simon V.} and Melnikov, {Anatoly R.} and Tsentalovich, {Yuri P.} and Kruppa, {Alexander I.}",
year = "2020",
month = jun,
day = "1",
doi = "10.1007/s10847-020-00991-2",
language = "English",
volume = "97",
pages = "121--127",
journal = "Journal of Inclusion Phenomena and Macrocyclic Chemistry",
issn = "0923-0750",
publisher = "Springer Netherlands",
number = "1-2",

}

RIS

TY - JOUR

T1 - Exploring the reactivity of β-cyclodextrin-encapsulated anthraquinone-2,6-disulfonate

AU - Babenko, Simon V.

AU - Melnikov, Anatoly R.

AU - Tsentalovich, Yuri P.

AU - Kruppa, Alexander I.

PY - 2020/6/1

Y1 - 2020/6/1

N2 - The intracomplex reaction of anthraquinone-2,6-disulfonate (AQDS) in triplet excited state (3AQDS) with beta-cyclodextrin (CD) and the reaction of 3AQDS:CD complex with external quencher, N-Acetyl-l-Tyrosine (TyrO−), have been studied using laser flash photolysis, 1H NMR and 1H CIDNP. The two reactions were found to be competing with each other. The intracomplex hydrogen abstraction previously proposed for 3AQDS:CD complex may represent a two-step process, where at first stage an electron is transferred from the –OH group of CD to 3AQDS followed by a proton transfer and recombination of AQDS and CD radicals resulting in a stable AQDS-CD product. The rate constant of the intracomplex electron transfer from CD to 3AQDS was found to be 6 ± 1 × 106 s−1 and the rate of subsequent proton transfer is 1 ± 0.1 × 106 s−1. The rate constant of electron transfer between TyrO− and 3AQDS:CD complex (0.4 ± 0.1 × 109 M−1 s−1) drops approx. by half compared to that in the reaction between TyrO− and free 3AQDS (0.8 ± 0.1 × 109 M−1 s−1).

AB - The intracomplex reaction of anthraquinone-2,6-disulfonate (AQDS) in triplet excited state (3AQDS) with beta-cyclodextrin (CD) and the reaction of 3AQDS:CD complex with external quencher, N-Acetyl-l-Tyrosine (TyrO−), have been studied using laser flash photolysis, 1H NMR and 1H CIDNP. The two reactions were found to be competing with each other. The intracomplex hydrogen abstraction previously proposed for 3AQDS:CD complex may represent a two-step process, where at first stage an electron is transferred from the –OH group of CD to 3AQDS followed by a proton transfer and recombination of AQDS and CD radicals resulting in a stable AQDS-CD product. The rate constant of the intracomplex electron transfer from CD to 3AQDS was found to be 6 ± 1 × 106 s−1 and the rate of subsequent proton transfer is 1 ± 0.1 × 106 s−1. The rate constant of electron transfer between TyrO− and 3AQDS:CD complex (0.4 ± 0.1 × 109 M−1 s−1) drops approx. by half compared to that in the reaction between TyrO− and free 3AQDS (0.8 ± 0.1 × 109 M−1 s−1).

KW - Anthraquinone

KW - CIDNP

KW - Hydrogen abstraction

KW - Inclusion complex

KW - β-Cyclodextrin

KW - INCLUSION COMPLEXATION

KW - DYNAMICS

KW - PHOTOCHEMISTRY

KW - CONSTANT

KW - beta-Cyclodextrin

UR - http://www.scopus.com/inward/record.url?scp=85084006898&partnerID=8YFLogxK

U2 - 10.1007/s10847-020-00991-2

DO - 10.1007/s10847-020-00991-2

M3 - Article

AN - SCOPUS:85084006898

VL - 97

SP - 121

EP - 127

JO - Journal of Inclusion Phenomena and Macrocyclic Chemistry

JF - Journal of Inclusion Phenomena and Macrocyclic Chemistry

SN - 0923-0750

IS - 1-2

ER -

ID: 24092750