TY - JOUR

T1 - Hydrogen-Bond-Assisted Chalcogen Transfer between Phosphine Selenides and Arsine Oxides

AU - Крутин, Данил Вячеславович

AU - Цыбулин, Семен Валерьевич

AU - Муллоярова, Валерия Вячеславовна

AU - Тупикина, Елена Юрьевна

AU - Толстой, Петр Михайлович

AU - Антонов, Александр Сергеевич

PY - 2025/5/19

Y1 - 2025/5/19

N2 - The Brønsted acid catalysis is widely regarded as one of the most effective methods for activating inert substrates and enabling unique reactivity. In this work, we introduce the first example of H-bond-assisted chalcogen exchange between arsine oxides and phosphine selenides under mild conditions, providing a powerful approach to the synthesis of arsine selenides. The reaction proceeds successfully in both protic and aprotic solvents and is accelerated by the presence of any nonaqueous acid. This newly discovered reaction is tested for various arsine oxides R 3AsO (R = Ph, Et, nBu, iPr) and phosphine selenides R 3PSe (R = Ph, Me, Et, tBu) and overall demonstrates high conversion, although the use of reagents with bulky substituents significantly hinders its efficiency. The reaction mechanism involves the formation of a four-membered cyclic transition state, which requires overcoming steric and electrostatic repulsion, as well as significant distortion of the reagents' tetrahedral geometry. Hydrogen bonding with the As═O fragment helps to reduce electrostatic repulsion between the P═Se and As═O groups, making the formation of the cyclic intermediate more favorable.

AB - The Brønsted acid catalysis is widely regarded as one of the most effective methods for activating inert substrates and enabling unique reactivity. In this work, we introduce the first example of H-bond-assisted chalcogen exchange between arsine oxides and phosphine selenides under mild conditions, providing a powerful approach to the synthesis of arsine selenides. The reaction proceeds successfully in both protic and aprotic solvents and is accelerated by the presence of any nonaqueous acid. This newly discovered reaction is tested for various arsine oxides R 3AsO (R = Ph, Et, nBu, iPr) and phosphine selenides R 3PSe (R = Ph, Me, Et, tBu) and overall demonstrates high conversion, although the use of reagents with bulky substituents significantly hinders its efficiency. The reaction mechanism involves the formation of a four-membered cyclic transition state, which requires overcoming steric and electrostatic repulsion, as well as significant distortion of the reagents' tetrahedral geometry. Hydrogen bonding with the As═O fragment helps to reduce electrostatic repulsion between the P═Se and As═O groups, making the formation of the cyclic intermediate more favorable.

UR - https://www.mendeley.com/catalogue/3d0bbd8f-9c0d-3b7f-95d9-3f41c0367a1d/

U2 - 10.1021/acs.inorgchem.4c05433

DO - 10.1021/acs.inorgchem.4c05433

M3 - Article

C2 - 40325344

VL - 64

SP - 9447

EP - 9456

JO - Inorganic Chemistry

JF - Inorganic Chemistry

SN - 0020-1669

IS - 19

ER -