scholarly journals Carbon–Hydrogen Bond Breaking and Making in the Open-Shell Singlet Molecule Cp*2Yb(4,7-Me2phen)

2014 ◽  
Vol 33 (23) ◽  
pp. 6819-6829 ◽  
Author(s):  
Grégory Nocton ◽  
Corwin H. Booth ◽  
Laurent Maron ◽  
Louis Ricard ◽  
Richard A. Andersen
1974 ◽  
Vol 52 (21) ◽  
pp. 3612-3622 ◽  
Author(s):  
Thérèse Di Paolo ◽  
C. Sandorfy

Infrared measurements show that fluorocarbons containing higher halogens are able to open O—H---O, N—H---N, S—H---S, N—H---O=C, type hydrogen bonds. This is probably due to a competitive mechanism of association consisting in the formation of donor–acceptor complexes. It is suggested that the breaking or perturbation of hydrogen bonds by this mechanism is of importance for the explanation of the anesthetic activity of these compounds.


1983 ◽  
Vol 87 (22) ◽  
pp. 4355-4357 ◽  
Author(s):  
T. L. Mathers ◽  
G. Schoffler ◽  
S. P. McGlynn
Keyword(s):  

1985 ◽  
Vol 63 (7) ◽  
pp. 1864-1869
Author(s):  
T. L. Mathers ◽  
G. Schoeffler ◽  
S. P. McGlynn

The temperature dependency of the phosphorescence properties of aromatic hydrocarbons in alcoholic glasses exhibits a number of phenomena that have not been described previously. Chief among these are the effects of added gases (O2, N2, C2H6, Ar), some of which produce major changes in the luminescence characteristics. These are discussed, and rationalized in terms of a model which presumes that O2 and N2 can disrupt the normal hydrogen bonding process between alcohol molecules.


2010 ◽  
Vol 122 (23) ◽  
pp. 3988-3992 ◽  
Author(s):  
Anouk M. Rijs ◽  
Nadja Sändig ◽  
Martine N. Blom ◽  
Jos Oomens ◽  
Jeffrey S. Hannam ◽  
...  
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document