Studies of Hydrogen‐Bonded Systems. I. The Electronic Structure and the Double Well Potential of the N–H···N Hydrogen Bond of the Guanine—Cytosine Base Pair

1964 ◽  
Vol 41 (11) ◽  
pp. 3393-3401 ◽  
Author(s):  
Robert Rein ◽  
Frank E. Harris
RSC Advances ◽  
2015 ◽  
Vol 5 (46) ◽  
pp. 36279-36287 ◽  
Author(s):  
Jun-Sheng Chen ◽  
Feng-Jiao Zhao ◽  
Yang Yang ◽  
Tian-Shu Chu

Two different hydrogen bond effects on the photophysical properties of UPy systems in different solutions have been studied.


Evidence is presented that proton transfer occurs in certain special types of hydrogen bond and that as a direct result the association energy is increased. It is probable that this effect is also responsible for a t least a part of the broadening of the v XH absorption band. In support of this, a number of com pounds are described in which the hydrogen bonds are weakened by isotopic substitution. The implications of these findings are discussed.


1986 ◽  
Vol 41 (1-2) ◽  
pp. 225-229 ◽  
Author(s):  
Mariusz Maćkowiak ◽  
Piotr Kozioł ◽  
Jan Stankowski

35Cl NQR measurements were carried out on complexes of pentachlorophenol with nitrogen bases as a function of pressure (up to 300 MPa) and of temperature. It is shown that the sign and magnitude of the pressure coefficient of the 35Cl NQR frequency is related to the degree of proton transfer. An anomaly in the pressure coefficient of ν (35Cl) has been observed near 50% of the proton transfer in the hydrogen bond. This anomaly is discussed assuming that the proton transfer equilibrium is pressure dependent. The fact that the transition from the double-well potential of the hydrogen bond to the single-well potential occurs in the critical manner is also taken into account.


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