The Ultraviolet Absorption Spectra of the Acridone Alkaloids. II. Compounds related to 4-Quinolone

1950 ◽  
Vol 3 (4) ◽  
pp. 615 ◽  
Author(s):  
RD Brown ◽  
FN Lahey

A qualitative discussion, based mainly upon the MO approximation, is presented for the ultraviolet spectra of naphthalene, quinolone, and some degradation products of the acridone alkaloids related to 4-quinolone.

1950 ◽  
Vol 3 (4) ◽  
pp. 593 ◽  
Author(s):  
RD Brown ◽  
FN Lahey

The ultraviolet spectra of the acridone alkaloids and some derivatives have been studied. The various bands in the spectra of these compounds are interpreted by starting with theoretical treatments of the spectrum of anthracene and tracing spectral changes through acridine and phenazine to acridone. An interesting relation between the π-electron density of a given position in the acridone ring and the shift in wavelength of absorption bands due to an alkoxyl derivative is noted and the spectra of the alkaloids are shown to comply with this relationship. Compounds containing a 4-hydroxy-10-methylacridone structure are found to have unusual spectra and a possible explanation of this is proposed.


1968 ◽  
Vol 46 (8) ◽  
pp. 1005-1011 ◽  
Author(s):  
A. Trombetti

The infrared spectrum of N2H2 in the 3.1 μ region and the ultraviolet spectra of N2H2 and N2D2 have been examined. The analysis of the infrared spectrum indicates that N2H2 in the ground state has a planar trans-conformation with with rN−N = 1.238 ± 0.007 Å and [Formula: see text], assuming rN−H to be between 1.05 and 1.08 Å. In the vacuum ultraviolet spectrum near 1700 Å, progressions of bands with spacings of 1180 and 950 cm−1 have been observed for N2H2 and N2D2, respectively. From the intensity alternation in the J structure of the vacuum ultraviolet spectrum it seems to follow that the electronic ground state of N2H2 is not totally symmetric.


1951 ◽  
Vol 29 (2) ◽  
pp. 182-191 ◽  
Author(s):  
Paul E. Gagnon ◽  
Jean L. Boivin ◽  
Paul A. Boivin ◽  
R. Norman Jones

Twenty-five pyrazolones were prepared by reacting mono- or disubstituted cyanoacetic esters with hydrazine, phenylhydrazine and semicarbazide. 4-Benzyl-3-amino-1-phenyl-5-pyrazolone has been synthesized and its properties have been compared with those of the corresponding 2-phenylpyrazolone derivative. The ultraviolet absorption spectra of several pyrazolones have been determined.


1976 ◽  
Vol 54 (19) ◽  
pp. 3026-3030 ◽  
Author(s):  
P. R. Olivato ◽  
H. Viertler ◽  
B. Wladislaw ◽  
K. C. Cole ◽  
C. Sandorfy

Photoelectron spectra show that in CH3SCH2COCH3 the sulfur and carbonyl lone pair orbitals [Formula: see text] are both stabilized with respect to the compounds containing S or CO only. This is in keeping with the observed values of the basicity constants. The ultraviolet absorption spectra contain the expected [Formula: see text] and [Formula: see text] bands and give evidence for a significant amount of mixing between the excited orbitals.


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

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

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