Spectroscopic Studies of Naphthol Compounds, Part V. Ultraviolet Absorption Spectra of Some H-Mesyloxy-Naphthalene Derivatives

1975 ◽  
Vol 8 (4) ◽  
pp. 209-215 ◽  
Author(s):  
L. Prajer-janczewska ◽  
J. Wróblewski
Keyword(s):  
Absorption Spectra ◽  
Spectroscopic Studies ◽  
Ultraviolet Absorption ◽  
Naphthalene Derivatives

SPECTROSCOPIC STUDIES OF KETO–ENOL EQUILIBRIA: PART 2. ANOMALOUS ULTRAVIOLET ABSORPTION SPECTRA OF SATURATED 1,2-DICYANO ESTERS

1962 ◽  
Vol 40 (12) ◽  
pp. 2272-2277 ◽  
Author(s):  
T. R. Kasturi ◽  
B. N. Mylari ◽  
A. Balasubramanian ◽  
C. N. R. Rao
Keyword(s):  
Absorption Band ◽  
Absorption Spectra ◽  
Spectroscopic Studies ◽  
Anomalous Behavior ◽  
Enol Form ◽  
Ultraviolet Absorption ◽  
Polar Solvents ◽  
Solvent Dependence

1,2-Dicyano esters show an absorption band around 245 mμ in alcoholic solutions which is not found in non-polar and other polar solvents. This anomalous behavior has been found to be due to the unusual solvent dependence of the equilibrium between the keto and enol forms. The intensity of the absorption band in alcoholic solutions decreases with increase in concentration of the 1,2-dicyano ester, indicating association of the enol form. The keto–enol equilibrium is also found to be sensitive to the substituent R of the alcohol ROH.

STERIC INHIBITION OF RESONANCE: IV. FURTHER SPECTROSCOPIC STUDIES OF 9-NITROANTHRACENE AND 9,10-DINITROANTHRACENE

1959 ◽  
Vol 37 (6) ◽  
pp. 1009-1011 ◽  
Author(s):  
James Trotter
Keyword(s):  
Absorption Spectra ◽  
Spectroscopic Studies ◽  
Ultraviolet Absorption ◽  
Stretching Vibrations ◽  
Steric Inhibition Of Resonance

The frequencies of the NO2 symmetrical stretching vibrations, and the ultraviolet absorption spectra, of solutions of 9-nitroanthracene and 9,10-dinitroanthracene have been measured and correlated with the deviations from coplanarity and resultant resonance inhibition.

FAR ULTRAVIOLET ABSORPTION SPECTRA OF N3AND N2+GENERATED BY ELECTRONS IMPACTING GASEOUS N2

2013 ◽  
Vol 779 (1) ◽  
pp. 40 ◽  
Author(s):  
Yu-Jong Wu ◽  
Hui-Fen Chen ◽  
Shiang-Jiun Chuang ◽  
Tzu-Ping Huang
Keyword(s):  
Absorption Spectra ◽  
Ultraviolet Absorption ◽  
Far Ultraviolet

scholarly journals ULTRAVIOLET ABSORPTION SPECTRA AT REDUCED TEMPERATURES

1950 ◽  
Vol 187 (1) ◽  
pp. 299-312
Author(s):  
R.L. Sinsheimer ◽  
J.F. Scott ◽  
J.R. Loofbourow
Keyword(s):  
Absorption Spectra ◽  
Ultraviolet Absorption

ULTRAVIOLET ABSORPTION SPECTRA AND ACIDITIES OF ISOMERIC THIATRIAZOLE AND TETRAZOLE DERIVATIVES

1959 ◽  
Vol 37 (3) ◽  
pp. 563-574 ◽  
Author(s):  
Eugene Lieber ◽  
J. Ramachandran ◽  
C. N. R. Rao ◽  
C. N. Pillai
Keyword(s):  
Absorption Spectra ◽  
Absorption Maximum ◽  
Dipole Moments ◽  
Ring System ◽  
Ultraviolet Absorption ◽  
Characteristic Absorption ◽  
Tetrazole Derivatives

The ultraviolet absorption spectra of 5-(substituted)amino-1,2,3,4-thiatriazoles and the corresponding isomeric 1-substituted-tetrazoline-5-thiones have been studied. The spectra and the dipole moments of the 5-(substituted)amino-1,2,3,4-thiatriazoles eliminate the possibility of meso-ionic structures for these compounds. The dipole moments of 5-amino-, 5-methylamino-, and 5-dimethylamino-1,2,3,4-thiatriazole were all high but approximately of the same value (5.77 to 5.84 D). This suggests that the amino thiatriazoles are best represented by conventional covalent structures with significant ionic resonance contributions. The thiatriazole ring system exhibits a characteristic absorption maximum at 250–255 mμ and an electron-withdrawing effect approximately equal to the tetrazolyl ring system. The tetrazolinethionolyl ring system is similarly electron-withdrawing. The relative acidities of the 1-substituted-tetrazoline-5-thiones and the 5-alkylmercaptotetrazoles have also been studied and the results support the observations made on the basis of their ultraviolet absorption spectra.

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