Manipulating Stereoselectivity of Parahydrogen Addition to Acetylene to Unravel Interconversion of Ethylene Nuclear Spin Isomers | Sciact - CRIS-система Института катализа

Manipulating Stereoselectivity of Parahydrogen Addition to Acetylene to Unravel Interconversion of Ethylene Nuclear Spin Isomers Научная публикация

Журнал

PCCP: Physical Chemistry Chemical Physics
ISSN: 1463-9076 , E-ISSN: 1463-9084

Вых. Данные

Год: 2024, Том: 26, Номер: 9, Страницы: 7821-7829 Страниц : 9 DOI: 10.1039/d3cp04983c

Ключевые слова

Acetylene; Catalysts; Iridium compounds; Isomers; Lighting; Nuclear magnetic resonance spectroscopy; Stereoselectivity

Авторы

Sviyazov Sergey V. ^1,2 , Babenko Simon V. ^1,3 , Skovpin Ivan V. ¹ , Kovtunova Larisa M. ^1,4 , Chukanov Nikita V. ^1,2 , Stakheev Alexander Yu. ⁵ , Burueva Dudari B. ¹ , Koptyug Igor V. ¹

Организации

1	Laboratory of Magnetic Resonance Microimaging, International Tomography Center, SB RAS, Novosibirsk 630090, Russia
2	Novosibirsk State University, Novosibirsk 630090, Russia
3	V.V. Voevodsky Institute of Chemical Kinetics and Combustion, SB RAS, Novosibirsk 630090, Russia
4	Boreskov Institute of Catalysis, SB RAS, Novosibirsk 630090, Russia
5	N.D. Zelinsky Institute of Organic Chemistry, RAS, Moscow 119991, Russia

Информация о финансировании (1)

Российский научный фонд

23-23-00394

Symmetric molecules exist as distinct nuclear spin isomers (NSIMs). A deeper understanding of their properties, including interconversion of different NSIMs, requires efficient techniques for NSIM enrichment. In this work, selective hydrogenation of acetylene with parahydrogen (p-H2) was used to achieve the enrichment of ethylene NSIMs and to study their equilibration processes. The effect of the stereoselectivity of H2 addition to acetylene on the imbalance of ethylene NSIMs was experimentally demonstrated by using three different heterogeneous catalysts (an immobilized Ir complex and two supported Pd catalysts). The interconversion of NSIMs with time during ethylene storage was studied using NMR spectroscopy by reacting ethylene with bromine water, which rendered the p-H2-derived protons in the produced 2-bromoethan(2H)ol (BrEtOD) magnetically inequivalent, thereby revealing the non-equilibrium nuclear spin order of ethylene. A thorough analysis of the shape and transformation of the 1H NMR spectra of hyperpolarized BrEtOD allowed us to reveal the initial distribution of produced ethylene NSIMs and their equilibration processes. Comparison of the results obtained with three different catalysts was key to properly attributing the derived characteristic time constants to different ethylene NSIM interconversion processes: ∼3–6 s for interconversion between NSIMs with the same inversion symmetry (i.e., within g or u manifolds) and ∼1700–2200 s between NSIMs with different inversion symmetries (i.e., between g and u manifolds).

Sviyazov S.V. , Babenko S.V. , Skovpin I.V. , Kovtunova L.M. , Chukanov N.V. , Stakheev A.Y. , Burueva D.B. , Koptyug I.V.
Manipulating Stereoselectivity of Parahydrogen Addition to Acetylene to Unravel Interconversion of Ethylene Nuclear Spin Isomers
PCCP: Physical Chemistry Chemical Physics. 2024. V.26. N9. P.7821-7829. DOI: 10.1039/d3cp04983c WOS Scopus РИНЦ CAPlusCA PMID OpenAlex

Поступила в редакцию:	13 окт. 2023 г.
Принята к публикации:	5 февр. 2024 г.
Опубликована online:	6 февр. 2024 г.
Опубликована в печати:	7 мар. 2024 г.

Web of science:	WOS:001166405800001
Scopus:	2-s2.0-85186148360
РИНЦ:	66246033
Chemical Abstracts:	2024:391527
Chemical Abstracts (print):	186:56497
PMID (PubMed):	38375632
OpenAlex:	W4391581719

БД	Цитирований
OpenAlex	1
Scopus	1
Web of science	2