scholarly journals Polar Conjugative Effect of Aryldithia Group on the Dissociation and Ultraviolet Spectra of Substituted Phenols

1968 ◽  
Vol 41 (9) ◽  
pp. 2082-2086 ◽  
Author(s):  
Shigeru Oae ◽  
Masakuni Yoshihara
1976 ◽  
Vol 73 ◽  
pp. 902-904
Author(s):  
G. N. R. Tripathi ◽  
V. M. Pandey
Keyword(s):  

1981 ◽  
Vol 31 (1) ◽  
pp. 279-284 ◽  
Author(s):  
Vishwas V. Wadekar ◽  
Man Mohan Sharma
Keyword(s):  

2008 ◽  
Vol 59 (11) ◽  
Author(s):  
Adrian Beteringhe ◽  
Ana Cristina Radutiu ◽  
Titus Constantinescu ◽  
Luminita Patron ◽  
Alexandru T. Balaban

In a preceding study, the molecular hydrophobicity (RM0) was determined experimentally from reverse-phase thin-layer chromatography data for several substituted phenols and 2-(aryloxy-a-acetyl)-phenoxathiin derivatives, obtained from the corresponding phenoxides and 2-(a-bromoacetyl)-phenoxathiin. QSPR correlations for RM0 were explored using four calculated molecular descriptors: the water solubility parameter (log Sw), log P, the Gibbs energy of formation (DGf), and the aromaticity index (HOMA). Triparametric correlations do not improve substantially the biparametric correlation of RM0 in terms of log Sw and HOMA.


1984 ◽  
Vol 80 ◽  
pp. 281-286
Author(s):  
Y. Kondo ◽  
G. E. McCluskey ◽  
S. B. Parsons

AbstractWe report recent International Ultraviolet Explorer (IUE) observations of two interacting binaries, R Arae and HD 207739. The ultraviolet spectra indicate the presence of optically-thick, variable hot plasma in those binary systems. These two binaries may belong to a class of binaries that are currently undergoing a rarely observed and probably short-lived phase in their evolution. Their properties are compared with those of two other interacting binaries, U Cephei and ß Lyrae.


1995 ◽  
Vol 98 (3/4) ◽  
pp. 149
Author(s):  
K. I. McDavitt ◽  
J. W. Manweiler ◽  
J. P. Davidson

1959 ◽  
Vol 37 (11) ◽  
pp. 1859-1869 ◽  
Author(s):  
R. J. Abraham ◽  
E. Bullock ◽  
S. S. Mitra

The structures of the ions formed by several alkyl pyrroles in hydrochloric acid are deduced from proton resonance spectra. Basicity values for three alkyl pyrroles are determined from ultraviolet spectra of their salts in buffer solutions. An attempt is made to estimate the basicity of other pyrroles from the variation of the—OD stretching frequency of methanol-d in solution in the pyrroles. Variations of the free and bonded NH frequencies of alkyl pyrroles are shown to be a simple function of the positions and number of the substituents.


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