Accessing different binding sites of a multifunctional molecule: IR spectroscopy of propargyl alcohol⋯water complexes in helium droplets

2019 ◽  
Vol 21 (37) ◽  
pp. 20582-20587 ◽  
Author(s):  
Devendra Mani ◽  
Nitish Pal ◽  
Mathias Smialkowski ◽  
Claudio Beakovic ◽  
Gerhard Schwaab ◽  
...  
Keyword(s):  
Ir Spectroscopy ◽  
Binding Sites ◽  
Local Minimum ◽  
Propargyl Alcohol ◽  
Helium Droplets ◽  
Water Complex ◽  
Alcohol Water

Helium droplets facilitate the formation of two distinct local minimum structures for 1 : 1 propargyl alcohol⋯water complex.

From the propargyl alcohol–water complex to the propargyl alcohol dimer: where does the propargyl alcohol–methanol complex fit in?

2019 ◽  
Vol 43 (9) ◽  
pp. 3969-3980 ◽  
Author(s):  
Jyoti Saini ◽  
K. S. Viswanathan
Keyword(s):  
Propargyl Alcohol ◽  
Water Complex ◽  
Alcohol Water

A correlation was recognized between the structures of PA–H2O, PA–MeOH and PA dimer complexes that could help predict the structures of larger systems in a systematic way.

IR Spectroscopy of the Cesium Iodide–Water Complex

2020 ◽  
Vol 124 (32) ◽  
pp. 6528-6535 ◽  
Author(s):  
Julia A. Davies ◽  
Martin Mugglestone ◽  
Shengfu Yang ◽  
Andrew M. Ellis
Keyword(s):  
Ir Spectroscopy ◽  
Cesium Iodide ◽  
Water Complex

scholarly journals IR spectroscopy of protonated leu-enkephalin and its 18-crown-6 complex embedded in helium droplets

2015 ◽  
Vol 17 (34) ◽  
pp. 21902-21911 ◽  
Author(s):  
Ana Isabel González Flórez ◽  
Doo-Sik Ahn ◽  
Sandy Gewinner ◽  
Wieland Schöllkopf ◽  
Gert von Helden
Keyword(s):  
Ir Spectroscopy ◽  
Ir Spectra ◽  
Superfluid Helium ◽  
Free Electron ◽  
Free Electron Laser ◽  
Radiation Source ◽  
Helium Droplets

Ultracold IR spectra of protonated leu-enkephalin and its 18-crown-6 complex embedded in superfluid helium droplets have been recorded using a free-electron laser as radiation source.

Laser desorption single-conformation UV and IR spectroscopy of the sulfonamide drug sulfanilamide, the sulfanilamide–water complex, and the sulfanilamide dimer

2017 ◽  
Vol 19 (22) ◽  
pp. 14625-14640 ◽  
Author(s):  
Thomas Uhlemann ◽  
Sebastian Seidel ◽  
Christian W. Müller
Keyword(s):  
Ir Spectroscopy ◽  
Noncovalent Interactions ◽  
Laser Desorption ◽  
Conformational Preference ◽  
Water Complex ◽  
Sulfonamide Drug ◽  
Sulfonamide Group

We elucidate sulfanilamide's conformational preference and the noncovalent interactions of the sulfonamide group with single-conformation IR spectroscopy.

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