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Phenylacetylene as a gas phase sliding balance for solvating alcohols

Karir, Ginny and Luettschwager, Nils O B and Suhm, Martin A (2019) Phenylacetylene as a gas phase sliding balance for solvating alcohols. In: PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 21 (15). pp. 7831-7840.

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Official URL: https://doi.org/10.1039/c9cp00435a

Abstract

Phenylacetylene offers two similarly attractive binding sites to OH containing solvent molecules, the phenyl ring and the acetylenic triple bond. By systematically varying the solvent molecule and by methylating aromatic or acetylenic CH groups, the docking preference can be controlled. It ranges from almost exclusive acetylene docking to predominant phenyl docking, depending on how electron density is deposited into the conjugated system and how large the London dispersion interaction is. FTIR spectroscopy of supersonic jet expansions is used to observe the competitive docking preferences in phenylacetylene and some of its methylated derivatives. A new data evaluation procedure that estimates band strength uncertainties based on a Monte Carlo approach is introduced. We test how well two density functionals (B3LYP-D3 and M06-2X) in combination with a def2-TZVP basis set are able to describe the docking switch. B3LYP-D3 is slightly biased towards acetylenic hydrogen bond docking and M06-2X is strongly biased towards phenyl hydrogen bond docking. More accurate theoretical predictions are invited and some previous experimental assignments are questioned.

Item Type: Journal Article
Additional Information: Copyright of this article belongs to ROYAL SOC CHEMISTRY.
Keywords: CENTER-DOT-PI; INTERNAL-ROTATION; BONDED COMPLEXES; HYDROGEN-BONDS; WATER COMPLEX; MODEL SYSTEM; AB-INITIO; METHANOL; SPECTROSCOPY; DOCKING
Department/Centre: Division of Chemical Sciences > Inorganic & Physical Chemistry
Depositing User: LIS Interns
Date Deposited: 24 May 2019 12:16
Last Modified: 24 May 2019 12:16
URI: http://eprints.iisc.ac.in/id/eprint/62696

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