Fermi resonance at the P=O group frequency in the IR spectrum of ethyl ethylphosphonite

1989 ◽  
Vol 51 (1) ◽  
pp. 690-692 ◽  
Author(s):  
L. Kh. Ashrafullina ◽  
N. I. Monakhova ◽  
R. R. Shagidullin
2020 ◽  
Vol 22 (34) ◽  
pp. 19223-19229
Author(s):  
Jun Young Park ◽  
Hyeok-Jun Kwon ◽  
Saptarsi Mondal ◽  
Hogyu Han ◽  
Kyungwon Kwak ◽  
...  

The 2D-IR spectrum of Ala-N3 shows cross-peak, but cannot be identified clearly. The 1D slice spectra obtained from 2D-IR spectrum reveals the presence of hidden Fermi resonance peak.


Author(s):  
D. F. Fazliev ◽  
R. R. Shagidullin ◽  
L. Kh. Ashrafullina

Author(s):  
Manuel Goubet ◽  
Robert Georges ◽  
P. Roy ◽  
Atef Jabri ◽  
Pascale Soulard ◽  
...  

2017 ◽  
Author(s):  
Curt Wentrup ◽  
Horst Briehl

Flash vacuum pyrolysis (FVP) of 5-azido-1-aryltetrazoles results in triple N<sub>2</sub> elimination and formation of aryl isocyanides RNC, which rearrange in part to aroylnitriles RCN under the reaction conditions. Similar FVP of 5-azido-1-arenesulfonyltetrazoles generates a compound absorbing in the IR spectrum (77 K) at 2090 cm<sup>-1 </sup>and assigned the structure of arenesulfonyl isocyanide, ArSO<sub>2</sub>NC <b>11</b>. FVP at temperatures above 600 <sup>o</sup>C results in progressively more nitrile ArSO<sub>2</sub>CN <b>12</b>. Compound <b>11</b> also disappears on warming above -80 <sup>o</sup>C


2017 ◽  
Author(s):  
Curt Wentrup ◽  
Horst Briehl

Flash vacuum pyrolysis (FVP) of 5-azido-1-aryltetrazoles results in triple N<sub>2</sub> elimination and formation of aryl isocyanides RNC, which rearrange in part to aroylnitriles RCN under the reaction conditions. Similar FVP of 5-azido-1-arenesulfonyltetrazoles generates a compound absorbing in the IR spectrum (77 K) at 2090 cm<sup>-1 </sup>and assigned the structure of arenesulfonyl isocyanide, ArSO<sub>2</sub>NC <b>11</b>. FVP at temperatures above 600 <sup>o</sup>C results in progressively more nitrile ArSO<sub>2</sub>CN <b>12</b>. Compound <b>11</b> also disappears on warming above -80 <sup>o</sup>C


1985 ◽  
Vol 50 (5) ◽  
pp. 1078-1088 ◽  
Author(s):  
Zdeněk Polívka ◽  
Jiří Holubek ◽  
Emil Svátek ◽  
Jan Metyš ◽  
Miroslav Protiva

Reaction of dibenzo[b,e]thiepin-11(6H)-one with 2-(dimethylaminomethyl)cyclohexylmagnesium chloride gave a mixture of stereoisomeric amino alcohols IX from which four homogeneous bases (IXa to IXd) were separated by chromatography. Dehydration of these compounds with boiling dilute hydrochloric acid afforded mixtures of racemic geometric isomers of the title compound VII, which were separated by crystallization. To the prevailing less polar base VIIa (E)-configuration was assigned on the basis of the IR spectrum. Using a similar procedure, thieno[2,3-c]-2-benzothiepin-4(9H)-one gave mixture of amino alcohols X from which three homogeneous stereoisomers X-A to X-C were isolated. Their dehydration resulted in both expected racemic geometric isomers VIII-A and VIII-B. Pharmacological testing proved the character of an antidepressant for the semi-rigid analogue of dithiadene VIII.


2021 ◽  
Vol 125 (9) ◽  
pp. 1910-1918
Author(s):  
Chih-Kai Lin ◽  
Qian-Rui Huang ◽  
Ying-Cheng Li ◽  
Ha-Quyen Nguyen ◽  
Jer-Lai Kuo ◽  
...  

2021 ◽  
Vol 1883 (1) ◽  
pp. 012121
Author(s):  
Jing Li ◽  
Hongxiang Tian ◽  
Tingfeng Ming ◽  
Yunling Sun ◽  
Shuai Zhang

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