Gas-phase organic reactions of the atomic oxygen radical cation

2013 ◽  
Vol 353 ◽  
pp. 1-6 ◽  
Author(s):  
Charles M. Nichols ◽  
Zhibo Yang ◽  
Veronica M. Bierbaum
2002 ◽  
Vol 106 (23) ◽  
pp. 5697-5702 ◽  
Author(s):  
Silvia Simon ◽  
Mariona Sodupe ◽  
Juan Bertran
Keyword(s):  

Tetrahedron ◽  
1986 ◽  
Vol 42 (22) ◽  
pp. 6235-6244 ◽  
Author(s):  
R.W. Holman ◽  
M.D. Rozeboom ◽  
M.L. Gross ◽  
C.D. Warner

2015 ◽  
Vol 17 (39) ◽  
pp. 25809-25821 ◽  
Author(s):  
Aude Bouchet ◽  
Johanna Klyne ◽  
Giovanni Piani ◽  
Otto Dopfer ◽  
Anne Zehnacker

The effects of ionisation and protonation on the geometric and electronic structure of a prototypical aromatic amino-alcohol with two chiral centres are revealed by IR and UV spectroscopy.


1995 ◽  
Vol 99 (42) ◽  
pp. 15444-15447 ◽  
Author(s):  
Sam P. de Visser ◽  
Leo J. de Koning ◽  
Nico M. M. Nibbering

Author(s):  
Donald T. Sawyer ◽  
R. J. P. Williams

Oxygen radicals are defined as those molecules that contain an oxygen atom with an unpaired, nonbonding electron (e.g., HO·). Although triplet dioxygen (·O2·) and superoxide ion (O2 - ·) come under this definition, their nonradical chemistry dominates their reactivity, which is discussed in Chapters 6 (·O2·) and 7 (O2-·). The hydroxyl radical (HO·) is the most reactive member of the family of oxygen radicals [HO·, RO·, ·O·, HOO·, ROO·, and RC(O)O·], and is the focus of most oxygen radical research. In the gas phase the dramatic example of oxygen radical reactivity with hydrocarbon substrates is combustion, which is initiated by HO· (or RO· or MO·) and propagated by ·O2· and ·O·.


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