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Intermolecular Complexes and Molecular Conformations Directed by Hydrogen Bonds: Matrix Isolation and Ab Initio Studies

Saini, Jyoti and Dubey, Jyoti and Verma, Kanupriya and Karir, Ginny and Viswanathan, K S (2019) Intermolecular Complexes and Molecular Conformations Directed by Hydrogen Bonds: Matrix Isolation and Ab Initio Studies. In: JOURNAL OF THE INDIAN INSTITUTE OF SCIENCE .

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Official URL: https://dx.doi.org/10.1007/s41745-019-00152-6

Abstract

Studies on hydrogen bonding interaction in various systems, involving phenylacetylene (PhAc), propargyl alcohol (PA), borazine (BNH), propargyl amine (PAm) were performed using matrix isolation infrared spectroscopy and supported by ab initio computations. Weak intermolecular interactions of the above mentioned precursors with water, methanol, ether, acetylene and benzene were studied. These systems manifested O-H center dot center dot center dot pi n-sigma* interactions, such as C-H center dot center dot center dot O, N-H center dot center dot center dot O, O-H center dot center dot center dot O and O-H center dot center dot center dot N. In several cases the complexes were multiply tethered involving two or more of the above mentioned contacts. Many of the weak complexes exhibited a number of isomers, and the relative importance of the multiple non-covalent contacts resulted in a competition between the various isomers for the global minimum. It was found that subtle changes in the structures of the precursors tilted the balance towards one isomer or the other. Our studies also threw up a systematic method of building possible structures for complex systems starting from the known structures of related simple systems. We also studied the homodimers of PA and BNH. The BNH dimer was particularly interesting as one of its isomers was characterized by a bis-dihydrogen bond. We also studied the influence of hydrogen bonding interactions in determining the conformational landscape and preference in amino acids. Here again we were able to draw some generalizations regarding the conformational stability of amino acids. The combination of matrix isolation and ab initio computation is a powerful tool for studies on weak intermolecular interactions and conformations.

Item Type: Journal Article
Publication: JOURNAL OF THE INDIAN INSTITUTE OF SCIENCE
Publisher: SPRINGER
Additional Information: Copyright of this article belongs to SPRINGER
Keywords: Matrix isolation; Ab initio; Phenylacetylene; Propargyl alcohol; Borazine; Amino acids; Hydrogen bonding; Conformations
Department/Centre: Division of Chemical Sciences > Inorganic & Physical Chemistry
Date Deposited: 22 Jan 2020 06:32
Last Modified: 22 Jan 2020 06:32
URI: http://eprints.iisc.ac.in/id/eprint/64320

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