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Acridine Orange as a Highly Sensitive Probe to Study the Stability of Onium Salts. / Сысоева, Александра Александровна; Путнин, Иван Олегович; Коваленко, Алексей Валерьевич; Ильин, Михаил Вячеславович; Болотин, Дмитрий Сергеевич.

в: New Journal of Chemistry, Том 49, № 22, 2025, стр. 9408-9415.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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@article{9f34810afbbd4479ae9d81ea192b95a1,
title = "Acridine Orange as a Highly Sensitive Probe to Study the Stability of Onium Salts",
abstract = "Halogen and chalcogen bond donors can undergo decomposition in solution, leading to the formation of Lewis acids. When these compounds act as catalysts, an important inquiry emerges: are the observed catalytic effects attributable solely to the parent salts, or do they involve contributions from the resulting decomposition products? Addressing this query necessitates a thorough evaluation of the degree of salt degradation. Conventional analytical methods such as NMR and HPLC, while widely employed for reaction monitoring, often lack sensitivity to detect trace levels of acidic species. In our study, we utilized UV-vis spectrophotometric titrations to assess the stability of halogen and chalcogen bond donor molecules. The findings revealed no discernible relationship between their stability profiles and their catalytic performance. Our data unequivocally support the conclusion that σ-hole carrier-mediated catalysis cannot be categorized as concealed Br{\o}nsted-type catalysis.",
author = "Сысоева, {Александра Александровна} and Путнин, {Иван Олегович} and Коваленко, {Алексей Валерьевич} and Ильин, {Михаил Вячеславович} and Болотин, {Дмитрий Сергеевич}",
year = "2025",
doi = "10.1039/d5nj01326g",
language = "English",
volume = "49",
pages = "9408--9415",
journal = "New Journal of Chemistry",
issn = "1144-0546",
publisher = "Royal Society of Chemistry",
number = "22",

}

RIS

TY - JOUR

T1 - Acridine Orange as a Highly Sensitive Probe to Study the Stability of Onium Salts

AU - Сысоева, Александра Александровна

AU - Путнин, Иван Олегович

AU - Коваленко, Алексей Валерьевич

AU - Ильин, Михаил Вячеславович

AU - Болотин, Дмитрий Сергеевич

PY - 2025

Y1 - 2025

N2 - Halogen and chalcogen bond donors can undergo decomposition in solution, leading to the formation of Lewis acids. When these compounds act as catalysts, an important inquiry emerges: are the observed catalytic effects attributable solely to the parent salts, or do they involve contributions from the resulting decomposition products? Addressing this query necessitates a thorough evaluation of the degree of salt degradation. Conventional analytical methods such as NMR and HPLC, while widely employed for reaction monitoring, often lack sensitivity to detect trace levels of acidic species. In our study, we utilized UV-vis spectrophotometric titrations to assess the stability of halogen and chalcogen bond donor molecules. The findings revealed no discernible relationship between their stability profiles and their catalytic performance. Our data unequivocally support the conclusion that σ-hole carrier-mediated catalysis cannot be categorized as concealed Brønsted-type catalysis.

AB - Halogen and chalcogen bond donors can undergo decomposition in solution, leading to the formation of Lewis acids. When these compounds act as catalysts, an important inquiry emerges: are the observed catalytic effects attributable solely to the parent salts, or do they involve contributions from the resulting decomposition products? Addressing this query necessitates a thorough evaluation of the degree of salt degradation. Conventional analytical methods such as NMR and HPLC, while widely employed for reaction monitoring, often lack sensitivity to detect trace levels of acidic species. In our study, we utilized UV-vis spectrophotometric titrations to assess the stability of halogen and chalcogen bond donor molecules. The findings revealed no discernible relationship between their stability profiles and their catalytic performance. Our data unequivocally support the conclusion that σ-hole carrier-mediated catalysis cannot be categorized as concealed Brønsted-type catalysis.

UR - https://www.mendeley.com/catalogue/580b6c4e-9da5-3e58-bbf0-b5dd4b49f83a/

U2 - 10.1039/d5nj01326g

DO - 10.1039/d5nj01326g

M3 - Article

VL - 49

SP - 9408

EP - 9415

JO - New Journal of Chemistry

JF - New Journal of Chemistry

SN - 1144-0546

IS - 22

ER -

ID: 135155162