Microwave spectrum of hydrogen bonded Hexafluoroisopropanol•••water complex

Shahi, Abhishek

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https://hdl.handle.net/2142/51047 Copy

Description

Title

Microwave spectrum of hydrogen bonded Hexafluoroisopropanol•••water complex

Author(s)

Shahi, Abhishek

Contributor(s)

Arunan, Elangannan

Issue Date

2014-06-19

Keyword(s)

Clusters/Complexes

Abstract

Stabilizing $\alpha$-helical structure of protein and dissolving a hard to dissolve polymer, polythene terphthalete, are some of the unique properties of the organic solvent Hexafluoroisopropanol (HFIP). After determining the complete microwave spectrum of HFIP monomer\footnote{A. Shahi and E. Arunan, Talk number RK16, 68th International Symposium on Molecular Spectroscopy 2013, Ohio, USA.}, we have recorded the spectrum of HFIP•••\chem{H_2O} complex. Ab initio calculations were used to optimize three different possible structures. The global minimum, structure 1, had HFIP as proton donor. Another promising structure, Structure 2, has been obtained from a molecular dynamic study\footnote{ Yamaguchi, T.; Imura, S.; Kai, T.; Yoshida, K. Zeitschrift für Naturforsch. A 2013, 68a, 145.}. A total of 46 observed lines have been fitted well for obtaining the rotational and distortion constants within experimental uncertainty. The observed rotational constants are A = 1134.53898(77) MHz, B = 989.67594(44) MHz and C = 705.26602(20) MHz. Interestingly, the rotational constants of structure 1, structure 2 and experiments were very close. Experimentally observed distortion constants were close to structure 1. $\it{b-type}$ transitions were stronger than $\it{c-type}$ which is also consistent with the calculated dipole moment components of structure 1. Calculations predict a non-zero a-dipole moment but experimentally $\it{a-type}$ transitions were absent. Microwave spectra of two of the deuterium isotopologues of this complex i.e. HFIP•••\chem{D_2O} (30 transitions) and HFIP•••HOD (33 transitions) have been also observed. Search for other isotopologues are in progress. To characterize the nature of hydrogen bonding, Atoms in Molecules and Natural Bond Orbital theoretical analysis have been done. Experimental structure and these theoretical analyses indicate that the hydrogen bonding in HFIP•••\chem{H_2O} complex is stronger than that in water dimer.

Publisher

International Symposium on Molecular Spectroscopy

Type of Resource

text

Language

English

Permalink

http://hdl.handle.net/2142/51047

DOI

https://doi.org/10.15278/isms.2014.RB08

Copyright and License Information

Copyright 2014 by the authors. Licensed under a Creative Commons Attribution 4.0 International License. http://creativecommons.org/licenses/by/4.0/

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