Aerogen Bonding in NgO 2 F 2 (Ng = Xe, Kr): A Computational Study

Aerogen bonding in NgO 2 F 2 (Ng = Xe, Kr) was investigated using quantum chemical calculations with O‐, N‐, and C‐donor nucleophiles. Molecular electrostatic potential analysis reveals two σ‐hole regions along the extensions of the Ng─O bonds, making NgO 2 F 2 closer to XeO 3 , but with two binding sites and no distinct π‐hole regions as in XeOF 2 . All nucleophiles form stable 1:1 and 1:2 adducts, with conventional O‐ and N‐donor lewis bases giving moderate stabilization, while the carbene donors 5‐NHC, cAAC, and aNHC bind much more strongly. Structural, atoms‐in‐molecules (AIM), noncovalent interaction (NCI), natural bond orbital (NBO), and energy decomposition (EDA) analyses show that the stronger carbene adducts arise from shorter Ng…C interactions, larger WBI and BCP values, and enhanced LP(C) → BD*(Ng─O) donation. Minor orientation‐dependent LP(donor) → BD*(Ng─F) contributions are also observed in selected adducts. The interactions remain primarily electrostatic, with significant orbital contribution, especially for the carbene adducts. Secondary C─H…O/F interactions, together with smaller but non‐negligible back‐donation from the lone pairs of Ng, provide additional stabilization to the adducts.

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Journal
ChemPhysChem
Published
2026-09-06
DOI
https://doi.org/10.1002/cphc.70551
Primary Topic
Inorganic Fluorides and Related Compounds
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article
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article

Aerogen Bonding in NgO 2 F 2 (Ng = Xe, Kr): A Computational Study

Kumar Vanka, Soumya Ranjan Dash, Jyoti Sharma, Zeel Yogeshbhai Surati
ChemPhysChem
Inorganic Fluorides and Related Compounds
article

Aerogen Bonding in NgO 2 F 2 (Ng = Xe, Kr): A Computational Study

Kumar Vanka, Soumya Ranjan Dash, Jyoti Sharma, Zeel Yogeshbhai Surati
article en

Abstract

Aerogen bonding in NgO 2 F 2 (Ng = Xe, Kr) was investigated using quantum chemical calculations with O‐, N‐, and C‐donor nucleophiles. Molecular electrostatic potential analysis reveals two σ‐hole regions along the extensions of the Ng─O bonds, making NgO 2 F 2 closer to XeO 3 , but with two binding sites and no distinct π‐hole regions as in XeOF 2 . All nucleophiles form stable 1:1 and 1:2 adducts, with conventional O‐ and N‐donor lewis bases giving moderate stabilization, while the carbene donors 5‐NHC, cAAC, and aNHC bind much more strongly. Structural, atoms‐in‐molecules (AIM), noncovalent interaction (NCI), natural bond orbital (NBO), and energy decomposition (EDA) analyses show that the stronger carbene adducts arise from shorter Ng…C interactions, larger WBI and BCP values, and enhanced LP(C) → BD*(Ng─O) donation. Minor orientation‐dependent LP(donor) → BD*(Ng─F) contributions are also observed in selected adducts. The interactions remain primarily electrostatic, with significant orbital contribution, especially for the carbene adducts. Secondary C─H…O/F interactions, together with smaller but non‐negligible back‐donation from the lone pairs of Ng, provide additional stabilization to the adducts.

ChemPhysChemVol. 27(17)
National Chemical Laboratory (IN), Academy of Scientific and Innovative Research (IN)
Affordable and clean energy
Openalex Percentile: Top 24%
Inorganic Fluorides and Related Compounds
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Aerogen Bonding in NgO 2 F 2 (Ng = Xe, Kr): A Computational Study — Kumar Vanka, Soumya Ranjan Dash, et al. · ChemPhysChem (2026) | TGRS Research Map | TGRS