Formation of stable ionized complexes between coinage metal containing superhalogens and moderately reactive molecules: a DFT approach View Full Text


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Article Info

DATE

2019-01-12

AUTHORS

Subhendu Sarkar, Tamalika Ash, Tanay Debnath, Abhijit K. Das

ABSTRACT

The possibility of ionization of six moderately reactive molecules (Y), namely silicon dioxide (SiO2), ammonia (NH3), water (H2O), carbon dioxide (CO2), chloroform (CHCl3) and dichlorodifluoromethane (CCl2F2) by two properly chosen superhalogens (SHs), gold tetrafluoride (AuF4), and gold hexafluoride (AuF6) denoted as AuXn (n = 4 and 6) has been explored at density functional theory (DFT) level. With increasing electron affinity (EA) of superhalogen, its capability to oxidize molecules with higher ionization potential also increases. We have demonstrated that this competition between the electron-binding energy of the superhalogen system and the ionization potential (IP) of the molecule with which the superhalogen combines is a key factor to predict the stability and nature of the formed complex. Binding energies have been evaluated to predict the stability of the formed complexes. The charge flow between Y and AuXn and localization of spin density distribution on the Y molecules have been estimated to verify the nature of interaction between the two. Atom in molecule (AIM) analysis has been performed to predict the nature of the bonds formed between the two interacting species. Overall, our study gives a comprehensive idea about the nature and stability of the complexes formed when moderately reactive (or inert) molecules interact with superhalogens containing coinage metal. More... »

PAGES

1-11

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11224-019-1278-6

DOI

http://dx.doi.org/10.1007/s11224-019-1278-6

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https://app.dimensions.ai/details/publication/pub.1111390075


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