Relaxationszeiten des Elektronenspins von Radikalen in einigen bestrahlten Aminosäuren bei 4,2 °K

1966 ◽  
Vol 21 (3) ◽  
pp. 296-300 ◽  
Author(s):  
G. Bürk ◽  
G. Schoffa

Electron spin relaxation times of the irradiated amino acids acetyl valine, sarcosine, betaine, and glycine have been measured at 4.2 °K with two different methods. From the exponential decrease of signals due to saturation after rapid adjustment of the ESR spectrometer on resonance, the following spin-lattice relaxation times have been measured: acetyl valine T1= 0.2 sec, sarcosine T1=0.14 sec, betaine T1=0.07 sec, glycine T1 ∼ 0.3 sec. By the PORTIS saturation method the product T1 T2 was measured, and, T1 being known, the following spin-spin relaxation times T2 have been obtained: acetyl valine 2.1.10-9sec, sarcosine 1.10-9sec, betaine 9.10-10sec. All measured amino acids show the saturation behaviour of substances with “inhomogeneous” line broadening.

1975 ◽  
Vol 30 (6-7) ◽  
pp. 883-890 ◽  
Author(s):  
F. Köksal ◽  
G. J. Krüger

Abstract The electron relaxation times T1 and T2 have been measured by ESR pulse techniques in solutions of normal and perdeuterated (diphenyl)- in dimethoxyethane at various radical concentrations and temperatures. The results are discussed in terms of different relaxation mechanisms. The most important contribution to spin-lattice relaxation at high concentration is dipolar interaction with other radical electrons modulated by translational diffusion. Spin-spin relaxation has in addition contributions from electron exchange and ion pairing.


Biochemistry ◽  
1982 ◽  
Vol 21 (20) ◽  
pp. 4916-4920 ◽  
Author(s):  
Keiko Kanamori ◽  
Timothy L. Legerton ◽  
Richard L. Weiss ◽  
John D. Roberts

1996 ◽  
Vol 51 (1-2) ◽  
pp. 83-86
Author(s):  
Hiroyuki Ishida ◽  
Yoshihiro Furukawa

Abstract Spin-lattice relaxation times (T1) and spin-spin relaxation times (T2) of 1H NMR and the electrical conductivity (σ) of trimethylammonium perchlorate were measured in the ionic plastic phase obtainable above 480 K. In this phase, both the cation and anion were revealed to perform self-diffusion. The activation energy (Ea ) of the cationic diffusion was evaluated to be 55 ± 4 and 50 ± 4 kJ mol-1 from 1H T1 and 1H T2 respectively, while Ea of the anionic diffusion was 64 ±3 kJ mol-1 from the electrical conductivity.


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