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TD-DFT investigation on anion recognition mechanism of anthraldehyde-based fluorescent thiosemicarbazone derivatives.
Basheer, Sabeel M; Gandhaveeti, Rohini.
Afiliación
  • Basheer SM; Department of Chemistry, School of Advanced Sciences, VIT-AP University, Andhra Pradesh, Amaravati, India, 522 237. sabeel.basheer@vitap.ac.in.
  • Gandhaveeti R; Department of Chemistry, National Institute of Technology-Tiruchirappalli, Tiruchirappalli-620015, Tamil Nadu, India.
J Mol Model ; 28(8): 234, 2022 Jul 27.
Article en En | MEDLINE | ID: mdl-35895241
The mechanism of host-guest interaction of receptors towards fluoride ion has been investigated using computational methods. To distinguish the effect of aromaticity in host-guest interaction, we investigated unsubstituted (ATSC) and phenyl-substituted (APTSC) anthracene thiosemicarbazones towards different ions. In the ground state of receptor-fluoride complex, the added fluoride ion made hydrogen bond through N - H…F…H - N, whereas the intramolecular hydrogen bonding was through F - H…N in the excited state of receptor-fluoride complex. Experimental absorption and emission spectra were well reproduced by the calculated vertical excitation energies. The transition state (TS) calculations were performed to understand the thermodynamic features and mechanism of host-guest interaction. The natural bond orbital analyses show that the second perturbation energy for donor-acceptor interaction of F- with hydrogen is more than 300 kcal/mol-1 at the excited state of receptor-fluoride complex, which indicates the strong single bond between fluoride and hydrogen atom. The PES scan confirms that deprotonation took place at the excited state of receptor-fluoride complex. The results indicate the excited-state proton transfer (ESPT) process from N-H group nearby the anthracene moiety. The APTSC is a better chemosensor than ATSC. This infers that the aromaticity will increase the efficiency of fluorescence receptor towards fluoride ion. A schematic representation of sensing mode of anthracene-based thiosemicarbazones toward fluoride ion. The fluoride ion first makes a hydrogen bond with NH proton nearby anthracene moiety. The excited state proton transfer mechanism was confirmed by PES and NBO studies.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Protones / Tiosemicarbazonas Idioma: En Revista: J Mol Model Asunto de la revista: BIOLOGIA MOLECULAR Año: 2022 Tipo del documento: Article Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Protones / Tiosemicarbazonas Idioma: En Revista: J Mol Model Asunto de la revista: BIOLOGIA MOLECULAR Año: 2022 Tipo del documento: Article Pais de publicación: Alemania