Chalcogen-bonded donor-acceptor complexes of 5,6-dicyano[1,2,5]selenadiazolo[3,4-b]pyrazine with halide ions

Chalcogen-bonded donor-acceptor complexes of 5,6-dicyano[1,2,5]selenadiazolo[3,4-b]pyrazine with halide ions Научная публикация

Журнал

New Journal of Chemistry
ISSN: 1144-0546

Вых. Данные

Год: 2022, Том: 46, Страницы: 14490-14501 Страниц : 12 DOI: 10.1039/d2nj02345h

Авторы

Radiush Ekaterina A. ¹ , Pritchina Elena A. ^2,3 , Chulanova Elena A. ¹ , Dmitriev Alexey A. ^2,4 , Bagryanskaya Irina Yu. ¹ , Slawin Alexandra M.Z. ⁵ , Woollins J.Derek ^5,6 , Gritsan Nina P. ² , Zibarev Andrey V. ¹ , Semenov Nikolay A. ¹

Организации

1	Новосибирский институт органической химии им. Н.Н. Ворожцова СО РАН
2	Федеральное государственное бюджетное учреждение науки Институт химической кинетики и горения им. В.В. Воеводского Сибирского отделения Российской академии наук
3	Новосибирский национальный исследовательский государственный университет
4	Новосибирский национальный исследовательский государственный университет
5	University of St Andrews
6	Khalifa University of Science and Technology

Информация о финансировании (1)

Российский Научный Фонд

21-73-10291

New complexes of 5,6-dicyano[1,2,5]selenadiazolo[3,4-b]pyrazine 1 with halide anions X− (X = Cl, Br, I) are prepared. With XRD, DFT, QTAIM and NBO, it is found that the complexes are formed via Se–X− chalcogen bonding. Diffuse reflectance spectroscopy of polycrystalline samples and UV/Vis spectroscopy of solutions of [1–X]− reveal significant spectral changes upon complexation. According to time-dependent DFT, these changes are caused by the appearance of charge transfer bands (p-AO(X) → LUMO(1)) in the visible region. The equilibrium constants for complex formation were measured with UV/Vis spectrophotometric titration and found to be significantly lower than those reported for structurally similar complexes of 3,4-dicyano-1,2,5-selena(tellura)diazoles, which indicates relatively weak chalcogen bonding in [1–X]−. Dispersion-corrected DFT reproduces well the Gibbs free energies of complexation. The QTAIM descriptors and NBO analyses using second-order perturbation theory suggest that the Se–X− chalcogen bonding in the studied complexes is predominantly electrostatic and dispersive in nature with a small but significant contribution from donor–acceptor (or orbital) interactions. The strongest contribution to the latter comes from negative hyperconjugation, i.e. donation of the electron density of the lone-pair of X− onto the σ*–MO of the Se–N bond of 1.

Radiush E.A. , Pritchina E.A. , Chulanova E.A. , Dmitriev A.A. , Bagryanskaya I.Y. , Slawin A.M.Z. , Woollins J.D. , Gritsan N.P. , Zibarev A.V. , Semenov N.A.
Chalcogen-bonded donor-acceptor complexes of 5,6-dicyano[1,2,5]selenadiazolo[3,4-b]pyrazine with halide ions
New Journal of Chemistry. 2022. V.46. P.14490-14501. DOI: 10.1039/d2nj02345h WOS

Поступила в редакцию:	12 мая 2022 г.
Принята к публикации:	1 июл. 2022 г.
Опубликована online:	4 июл. 2022 г.

Web of science	WOS:000823756000001
OpenAlex	W4285271265