Theoretical and experimental vibrational spectroscopy study on rotational isomer of 4-phenylbutylamine

Author(s):  
A. Ünal ◽  
M. Okur
2005 ◽  
Vol 405 (1-3) ◽  
pp. 108-113 ◽  
Author(s):  
Francesco Toffolo ◽  
Matteo Tommasini ◽  
Mirella Del Zoppo ◽  
Giuseppe Zerbi

2007 ◽  
Vol 353 (18-21) ◽  
pp. 1875-1881 ◽  
Author(s):  
L.F. Santos ◽  
L. Wondraczek ◽  
J. Deubener ◽  
R.M. Almeida

2019 ◽  
Vol 1175 ◽  
pp. 663-676 ◽  
Author(s):  
Jonas Kausteklis ◽  
Valdemaras Aleksa ◽  
Maximiliano A. Iramain ◽  
Silvia Antonia Brandán

1973 ◽  
Vol 27 (1) ◽  
pp. 27-30 ◽  
Author(s):  
T. S. Wang ◽  
J. J. Mannion

The chloromethyl group (—CH2Cl) attached to a normal hydrocarbon chain gives rise to two characteristic Raman bands near 660 and 730 cm−1. The band at 660 cm−1, which is very intense, is assigned to a stretching mode of the C-Cl linkage when the chlorine atom is trans to a hydrogen atom. The less intense peak at 730 cm−1 is assigned to the same mode of the rotational isomer with the chlorine atom trans to a carbon atom. These assignments are consistent with those reported in infrared studies. In contrast to almost equal intensities for both bands in the infrared, the band at 660 cm−1 proved to be the strongest by far in Raman spectra.


1998 ◽  
Vol 31 (8) ◽  
pp. 1771-1782 ◽  
Author(s):  
Kreshnik Angoni ◽  
Jurgen Popp ◽  
Wolfgang Kiefe

2011 ◽  
Vol 115 (19) ◽  
pp. 5999-6010 ◽  
Author(s):  
Jernej Stare ◽  
Janez Mavri ◽  
Jože Grdadolnik ◽  
Jernej Zidar ◽  
Zvonimir B. Maksić ◽  
...  

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