UV photoelectron spectroscopic investigation of some polycyclic group 5A compounds and related acyclic species. 1. Free and coordinated aminophosphines and related compounds

1982 ◽  
Vol 21 (2) ◽  
pp. 543-549 ◽  
Author(s):  
A. H. Cowley ◽  
M. Lattman ◽  
P. M. Stricklen ◽  
J. G. Verkade
1976 ◽  
Vol 31 (5) ◽  
pp. 558-564 ◽  
Author(s):  
Marianne Baudler ◽  
Burkhard Carlsohn ◽  
Wolfgang Böhm ◽  
Goswin Reuschenbach

The weak resonances at + 22 and + 49 ppm appearing in the 31P NMR spectrum of melts or solutions of (PPh)5 that have been attributed previously in the literature to “dimeric” and “monomeric phenylphosphorus” are caused by (PPh)6 and (PPh)4, respectively. This was proved by comparison with the 31P NMR parameters of related compounds and by 31P NMR spectroscopic investigation of authentic samples of (PPh)6 and (PPh)4, the latter of which was prepared in high yield from (Me3Si)PhP–PPh–PPh(SiMe3) and PhPCl2. (PEt)4 and mixed-substituted phenyl-ethyl-cyclotetraphosphanes exhibit similar chemical shifts as (PPh)4, corresponding mixed-substituted cyclohexaphosphanes have similar chemical shifts as (PPh)6. Generally, cyclophosphanes establish an equilibrium between (PR)n-species of different ring-size. Probably, the ring-interconversion proceeds via a multi-center mechanism. No 31P NMR spectroscopic evidence for the existence of free PPh or P2Ph2 under the conditions described could be detected. On thermolysis of (PEt)4 the existence of (PEt)3 was proved for the first time.


1978 ◽  
Vol 56 (20) ◽  
pp. 2681-2685 ◽  
Author(s):  
Mark A. Ragan

Renewed interest in naturally occurring phenol sulfate ester salts has necessitated modem spectroscopic investigation of these compounds. Synthetic methods, plus spectroscopic (uv, ir, 1H nmr, 13C nmr), chromatographic, and electrophoretic properties are given for the potassium salts of phenyl sulfate (1), pyrocatechol disulfate (2), resorcinol disulfate (3), hydroquinone disulfate (4), phloroglucinol mono- (5), di- (6), and tri- (7) sulfates, and for the 2-sulfate (8) and 2,5-disulfate (9) of 1,2,3,5-tetrahydroxybenzene (10). 13C nmr chemical shift effects resulting from the replacement of phenolic —OH with —OSO3K are reported. Spectroscopic properties of the related compounds 1,2,3-tribenzyloxybenzene (11), 2,6-dibenzyloxy-1,4-benzoquinone (12), 2,6-dimethoxy-1,4-benzoquinone (13), 1,3-dibenzyloxy-2,5-dihydroxybenzene (14), and of a tentatively identified 1,3-dibenzyloxy-2,5-dihydroxybenzene monoethyl ether (15) are available as supplementary material.


1965 ◽  
Vol 5 ◽  
pp. 120-130
Author(s):  
T. S. Galkina

It is necessary to have quantitative estimates of the intensity of lines (both absorption and emission) to obtain the physical parameters of the atmosphere of components.Some years ago at the Crimean observatory we began the spectroscopic investigation of close binary systems of the early spectral type with components WR, Of, O, B to try and obtain more quantitative information from the study of the spectra of the components.


2013 ◽  
Author(s):  
A. V. Kalueff ◽  
A. M. Stewart ◽  
V. Gjeloshi ◽  
D. Kondaveeti ◽  
N. Neelkantan ◽  
...  
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