Unraveling the spectroscopy of coupled intramolecular tunneling modes: A study of double proton transfer in the formic-acetic acid complex

2011 ◽  
Vol 134 (5) ◽  
pp. 054316 ◽  
Author(s):  
Michael C. D. Tayler ◽  
Bin Ouyang ◽  
Brian J. Howard
2018 ◽  
Vol 35 (9) ◽  
pp. 098201 ◽  
Author(s):  
Qing-Chi Meng ◽  
Song-Qiu Yang ◽  
Guang-Hua Ren ◽  
Tian-Shu Chu

2003 ◽  
Vol 107 (18) ◽  
pp. 3244-3253 ◽  
Author(s):  
Fa-Tsai Hung ◽  
Wei-Ping Hu ◽  
Tsung-Hui Li ◽  
Chung-Chih Cheng ◽  
Pi-Tai Chou

2001 ◽  
Vol 114 (4) ◽  
pp. 1567-1574 ◽  
Author(s):  
Antonio Fernández-Ramos ◽  
Zorka Smedarchina ◽  
Jesús Rodrı́guez-Otero

1981 ◽  
Vol 46 (4) ◽  
pp. 957-962 ◽  
Author(s):  
Milan Remko

Complexes containing two hydrogen bonds of the systems 1-methylthymine-acetamide and 1-methylthymine-acetic acid have been studied by the quantum-chemical PCILO method. In accordance with experiment our PCILO calculations have shown that acetic acid forms stronger hydrogen bonds than acetamide with 1-methylthymine. Further the PCILO method has been used to study of double proton transfer in O-H...O and N-H...O bonds of the complexes 1-methylthymine-acetamide and 1-methylthymine-acetic acid. Using equilibrium O...O and N...O distances, the PCILO calculations have given one-minimum proton potential functions. The proton transfer has not been observed. At somewhat longer N...O and O...O distances (0.30 nm) the PCILO calculations indicate a second minimum as a shoulder.


2015 ◽  
Vol 17 (2) ◽  
pp. 1142-1150 ◽  
Author(s):  
Jinfeng Zhao ◽  
Junsheng Chen ◽  
Yanling Cui ◽  
Jing Wang ◽  
Lixin Xia ◽  
...  

Two excited state proton transfer mechanisms of 3-hydroxyisoquinoline (3HIQ) in cyclohexane and acetic acid (ACID) were investigated.


2005 ◽  
Vol 109 (51) ◽  
pp. 11707-11714 ◽  
Author(s):  
Ewa Sikorska ◽  
Igor Khmelinskii ◽  
Marcin Hoffmann ◽  
Isabel F. Machado ◽  
Luis F. V. Ferreira ◽  
...  

2018 ◽  
Vol 10 (1) ◽  
pp. 11
Author(s):  
Abdalla Mustafa Walwil

The aim of this educational work is targeting chemistry students and interested instructors. The presented work will analyze the mass spectrum of butyl butyrate (butyl butanoate). The analysis will concentrate on the mechanisms showing how the characteristic fragments are formed. The mechanisms discussed in this paper include α-cleavage, β-cleavage, McLafferty Rearrangements, first and second proton transfer, a double proton transfer. 


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