Temperature-dependent hyperfine coupling constant of the dianion radical of Fremy's salt, a convenient internal thermometer for EPR spectroscopy

被引:16
作者
Bales, BL [1 ]
Wainberg, E [1 ]
Nascimento, OR [1 ]
机构
[1] CTR BRASILEIRO PESQUISAS FIS,BR-22290 RIO JANEIRO,BRAZIL
基金
巴西圣保罗研究基金会;
关键词
D O I
10.1006/jmra.1996.0031
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
The hyperfine coupling constant, A(0), of peroxylamine disulfonate in aqueous solutions depends upon the temperature and the concentration of added K2CO3 buffer. Near room temperature, Ao varies from 13.036 to 13.201 G for K2CO3 concentrations varying from zero to near saturation. For samples prepared in 50.0 mM K2CO3, the results are independent of Fremy's salt concentration in the range 0.005-2.8 mM as follows: A(0)(T) = 12.978 + 0.00311 T, where the hyperfine coupling constant at temperature T, A(0)(T), is given in gauss when the temperature is given in degrees C. This temperature dependence is an order of magnitude larger and of opposite sign than that found for doxylstearic acid esters and is proposed as the basis of an internal thermometer for EPR spectroscopy. The variation of Ao with solvent polarity is found to be a factor of about 27-30 less than for the neutral radicals di-tert-butyl nitroxide and doxylstearic acid esters. It is shown that microwave heating of aqueous samples at high microwave powers can be monitored by measuring Ao while conventional thermometry can lead to significant errors even for a thermocouple immersed within the sample just above the microwave cavity. The value of A(0)(25 degrees C) = 13.056 +/- 0.002 G is significantly different than previously used standards; therefore, some previous data may require recalibration. Correction procedures for nonlinearities in the held sweep are presented. (C) 1996 Academic Press, Inc.
引用
收藏
页码:227 / 233
页数:7
相关论文
共 15 条
[1]   Dielectric constants of some organic solvent-water mixtures at various temperatures [J].
Akerlof, G .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1932, 54 :4125-4139
[2]  
Bevington R., 1969, DATA REDUCTION ERROR
[4]   ESR-STUDIES OF HEISENBERG SPIN EXCHANGE .2. EFFECTS OF RADICAL CHARGE AND SIZE [J].
EASTMAN, MP ;
BRUNO, GV ;
FREED, JH .
JOURNAL OF CHEMICAL PHYSICS, 1970, 52 (05) :2511-&
[5]   DYNAMIC FREQUENCY SHIFTS AND EFFECTS OF MOLECULAR MOTIONS IN ELECTRON SPIN RESONANCE SPECTRA OF DINITROBENZENE ANION RADICALS [J].
FABER, RJ ;
FRAENKEL, GK .
JOURNAL OF CHEMICAL PHYSICS, 1967, 47 (07) :2462-&
[6]   STATIC AND DYNAMIC FREQUENCY SHIFTS IN ELECTRON SPIN RESONANCE SPECTRA [J].
FRAENKEL, G .
JOURNAL OF CHEMICAL PHYSICS, 1965, 42 (12) :4275-&
[7]   ESR STUDIES OF ANISOTROPIC ROTATIONAL REORIENTATION AND SLOW TUMBLING IN LIQUID AND FROZEN MEDIA .2. SATURATION AND NONSECULAR EFFECTS [J].
GOLDMAN, SA ;
BRUNO, GV ;
FREED, JH .
JOURNAL OF CHEMICAL PHYSICS, 1973, 59 (06) :3071-3091
[8]   ESR STUDY OF ANISOTROPIC ROTATIONAL REORIENTATION AND SLOW TUMBLING IN LIQUID AND FROZEN MEDIA [J].
GOLDMAN, SA ;
FREED, JH ;
BRUNO, GV ;
POLNASZEK, CF .
JOURNAL OF CHEMICAL PHYSICS, 1972, 56 (02) :716-+
[9]   RAPID QUANTITATION OF PARAMETERS FROM INHOMOGENEOUSLY BROADENED EPR-SPECTRA [J].
HALPERN, HJ ;
PERIC, M ;
YU, C ;
BALES, BL .
JOURNAL OF MAGNETIC RESONANCE SERIES A, 1993, 103 (01) :13-22
[10]   ELECTRON SPIN EXCHANGE IN AQUEOUS SOLUTIONS OF K2(SO3)2NO [J].
JONES, MT .
JOURNAL OF CHEMICAL PHYSICS, 1963, 38 (12) :2892-&