Polymerization reactions of acrylonitrile on zeolite surfaces

1980 ◽  
Vol 33 (3) ◽  
pp. 653 ◽  
Author(s):  
AT Petfield ◽  
RP Cooney

Infrared and mass spectral analyses are reported of the surface species generated when the adsorption complexes zeolite+acrylonitrile are heated. The evidence presented indicates that H2O competes favourably for zeolitic adsorption sites with acrylonitrile. Infrared spectra suggest that a C2 π-bonding interaction may be important in the adsorption of acrylonitrile. Heating adsorbed acrylonitrile appears to generate polyacrylonitrile products which may include a cyclic dimer. Extended heating results in the possible formation of conjugated nitrile species, polyenes and even more extensively carbonized products.

2019 ◽  
Vol 16 (6) ◽  
pp. 511-516
Author(s):  
Adnan Cetin

Efficient steps towards the synthesis of novel (phenyl)(1'-aryl-1,5,5'-triphenyl[3,3'-bi-1Hpyrazol]- 4-yl)methanones 4a-e were developed. The procedure starts from 1-(4-benzoyl-1,5-diphenyl- 1H-3-pyrazolyl)-3-phenyl-2-propyn-1-one (2) which was synthesized by a palladium catalyzed crosscoupling reaction. Compound 2 reacted with various hydrazines to give (E)-(phenyl)[1,5-diphenyl-3- [3-phenyl-1-(2-arylhydrazono)-2-propyn-1-yl]-1H-4-pyrazolyl]methanones E-3a-e. The bis-pyrazole derivatives 4a-e were synthesized from electrophilic cyclization reaction of α,β-acetylenic hydrazones E-3a-e and copper(I) iodide. All synthesized compounds were characterized by FT-IR, 1H, 13C NMR and Mass spectral analyses.


2016 ◽  
Vol 259 ◽  
pp. 19-26 ◽  
Author(s):  
Alan J. McCue ◽  
Greg A. Mutch ◽  
Andrew I. McNab ◽  
Steven Campbell ◽  
James A. Anderson

2015 ◽  
Vol 17 (11) ◽  
pp. 7477-7488 ◽  
Author(s):  
Manuel Goubet ◽  
Pascale Soulard ◽  
Olivier Pirali ◽  
Pierre Asselin ◽  
Florent Réal ◽  
...  

The dimerization equilibrium of acetic acid in the gas phase at 298 K has been characterized from the analysis of jet-cooled and static cell infrared spectra supported by calculations.


1967 ◽  
Vol 15 (4) ◽  
pp. 713-717 ◽  
Author(s):  
Masahide. Nonaka ◽  
Dale Robert. Black ◽  
Eldon L. Pippen

2010 ◽  
Vol 58 (24) ◽  
pp. 12642-12649 ◽  
Author(s):  
Richard F. Helm ◽  
Judith Jervis ◽  
W. Keith Ray ◽  
Nicholas Willoughby ◽  
Benjamin Irvin ◽  
...  

1984 ◽  
Vol 62 (9) ◽  
pp. 1845-1849 ◽  
Author(s):  
Shanker Ram

The infrared spectra (200–4000 cm−1) of 2-thiopyrrole-1,2-dicarboximide (TPH) in solid and solution forms have been measured as a function of temperature, and a direct correlation has been obtained between the two phases and the type and extent of hydrogen bonding. It is suggested that TPH exists as cyclic dimer in the solid state (below 310 K) and in dilute solutions by the formation of two equivalent hydrogen bonds. At the transition temperature, ~310 K, the cyclic dimer undergoes to the open-cyclic dimer and persists in this structure till 410 K. In addition, the thermodynamical functions ΔH0, and ΔS0 have been estimated using the spectral data in solution.


Author(s):  
Adolfo Borges ◽  
Carmen C. García ◽  
Elizabeth Lugo ◽  
Marcelo J. Alfonzo ◽  
Michael J. Jowers ◽  
...  

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