INFRARED STUDY OF THE PHOTOCHEMISTRY OF TETRAMETHYLCYCLOBUTAN-1,3-DIONE

1965 ◽  
Vol 43 (12) ◽  
pp. 3165-3172 ◽  
Author(s):  
Ivan Haller ◽  
R. Srinivasan
Keyword(s):  
Carbon Monoxide ◽  
Infrared Spectra ◽  
Room Temperature ◽  
Infrared Study ◽  
Intense Absorption ◽  
Effect Of Light ◽  
Do So

The photolysis of tetramethylcyclobutan-1,3-dione was investigated in a nitrogen matrix at 4°K and in solution in cyclohexane at room temperature. Infrared spectra of the reactant after irradiation showed the formation of carbon monoxide, dimethylketene, tetramethylethylene, and a compound with an intense absorption at 1 840 cm−1 which has been identified as tetramethylcyclopropanone. Since the dimethylketene that was formed was also capable of undergoing secondary photolysis, the effect of light (mainly 2 537 Å) on dimethylketene in solution or in a nitrogen matrix, was also studied. It has been found that in solution 0.2 of the molecules of tetramethylcyclobutandione which decompose, do so to give two molecules of dimethylketene, while approximately the same number of molecules decompose to tetramethylcyclopropanone and carbon monoxide. The remainder of the molecules seem to give tetramethylethylene and carbon monoxide in a concerted process.

Transmission infrared study of acid-catalyzed sol-gel silica coatings during room ambient drying

1992 ◽  
Vol 7 (8) ◽  
pp. 2230-2239 ◽  
Author(s):  
T.M. Parrill
Keyword(s):  
Thin Films ◽  
Fourier Transform ◽  
Infrared Spectra ◽  
Spin Coating ◽  
Room Temperature ◽  
Sol Gel ◽  
Infrared Study ◽  
Silica Coatings ◽  
Acidic Conditions ◽  
Acid Catalyzed

Sol-gel solutions prepared from tetraethylorthosilicate (TEOS) hydrolyzed in acidic conditions were used to make thin films on Si wafers via spin coating. Solutions with H2O/TEOS ratios of 2, 5, and 10 were prepared and aged at room temperature in sealed containers for times ranging from <2.5 h to 1 month. Transmission Fourier transform infrared spectra acquired around 1 min after spinning showed peaks characteristic of both SiO2 and SiOH. Additional features at ≍580, 1093, and 1130 cm−1 were observed and possible origins are discussed. Peaks at ≍580 and 1130 cm−1, which increased in intensity with solution age time, are attributed to cyclic Si–O, e.g., 4-member rings. When films were exposed to room air, ring concentration decreased significantly within 30 min. Rings were stable for hours, however, when films were kept in N2. The feature at 1093 cm−1, most sensitive to H2O/TEOS, is attributed to residual Si–O–C.

INFRARED SPECTRA OF CARBON MONOXIDE AND CARBON DIOXIDE ADSORBED ON CHROMIA–ALUMINA AND ON ALUMINA

1962 ◽  
Vol 40 (10) ◽  
pp. 1997-2006 ◽  
Author(s):  
L. H. Little ◽  
C. H. Amberg
Keyword(s):  
Carbon Dioxide ◽  
Carbon Monoxide ◽  
Infrared Spectra ◽  
Room Temperature ◽  
Ion Formation ◽  
Carbonate Ion

Infrared spectra of CO and CO2 adsorbed on chromia–alumina and on alumina surfaces have been determined. A band near 2200 cm−1 formed by CO on both surfaces at room temperature was due to a weak, non-activated sorption, but also contained a contribution from a more strongly sorbed, activated species on the chromia–alumina. The assignment of this band was discussed in some detail. Bands in the region 1200–1800 cm−1 were considered in terms of surface CO2− species, although in certain instances the appearance of bands at 1750 and 1430 cm−1 may have indicated carbonate ion formation.

Infrared spectra of carbon monoxide on platinum, iridium and copper ; comparison of flat and rough surfaces

1981 ◽  
Vol 78 ◽  
pp. 927-932 ◽  
Author(s):  
F.J.C.M. Toolenaar ◽  
G.J. van der Poort ◽  
F. Stoop ◽  
V. Ponec
Keyword(s):  
Carbon Monoxide ◽  
Infrared Spectra ◽  
Rough Surfaces

Asymetrical Dimer - allyl-palladiu Complexes II. Data from Infrared Spectra and Chemical Behaviour

2008 ◽  
Vol 59 (7) ◽  
Author(s):  
Maria Maganu ◽  
Filip Chiraleu ◽  
Constantin Draghici ◽  
Gheorghe Mihai
Keyword(s):  
Carbon Monoxide ◽  
Nmr Spectroscopy ◽  
1H Nmr ◽  
Infrared Spectra ◽  
Analytical Methods ◽  
1H Nmr Spectroscopy ◽  
Chemical Behaviour ◽  
The Asymmetry ◽  
Pd Complexes

The previous data obtained by 1H-NMR spectroscopy established the existence of an asymmetry of the bond between Pd and p-allylic groups, even in the p-allyl-Pd complexes dimers which are considered usually symmetric dimers. The asymmetry of the bond depends by the substitutes of the allylic group. Other analytical methods were investigated for additional proof of the obtained results. Thus, this paper discusses how this asymmetry would be reflected in the infrared spectra and in the reaction of the complexes with carbon monoxide.

Circular dichroism and infrared study of β-turn formation in repeat peptides of elastin

1987 ◽  
Vol 52 (5) ◽  
pp. 1356-1361
Author(s):  
S. Abdel Rahman ◽  
M. Elsafty ◽  
A. Hattaba
Keyword(s):  
Circular Dichroism ◽  
Solid State ◽  
Ir Spectra ◽  
Chain Length ◽  
Room Temperature ◽  
Infrared Study ◽  
Feature Characteristic ◽  
C 50 ◽  
The Stability ◽  
Circular Dichroïsm

The conformation of elastin-like peptides Boc-Ala-Pro-Gly-Val-APEGM, Boc-Ala-Pro-Gly-Val-Gly-Val-APEGM, Boc-Ala-Pro-Gly-Val-Ala-Pro-Gly-Val-Gly-Val-APEGM, Boc-Ala-Pro-Gly-Val-Gly-Val-Ala-Pro-Gly-Val-Gly-Val-APEGM were examined in solution using circular dichroism at 30 °C, 50 °C, and 70 °C and in solid state by IR at room temperature. The studies show that the β-turn is a significant conformational feature for peptides under investigation in solution at 30 °C and 50 °C, but at 70 °C the tetra, hexa, and decapeptides show the CD feature characteristic of the β-structure while the dodecapeptide spectra show the presence of β-turn which indicates the stability of the β-turn at this chain length. The IR spectra show that in the solid state at room temperature all investigated peptides assume essentially a β-turn except the tetrapeptide which present evidence of antiparallel β-structure. The β-turn contribution in the IR spectra increases with the increase of the chain length of the peptide.

Infrared spectra of N-acetyl-L-α-amino-acid N'-methylamides with aliphatic side chains in non-polar solvents

1981 ◽  
Vol 46 (3) ◽  
pp. 772-780 ◽  
Author(s):  
Jorga Smolíková ◽  
Jan Pospíšek ◽  
Karel Bláha
Keyword(s):  
Amino Acid ◽  
Conformational Changes ◽  
Infrared Spectra ◽  
Room Temperature ◽  
Side Chains ◽  
Polar Solvents

Infrared spectra of the L-alanine (I), L-leucine (II), L-valine (III) and L-tert-leucine (IV) N-acetyl N'-methylamides were measured. Amides I-IV are not self associated in tetrachlormethane in the concentration 2 . 10-5 mol l-1 at room temperature and in tetrachloroethylene in the concentration 1.5 . 10-4 mol l-1 at temperatures above 65° C. True conformational changes are observable only with the least flexible amide IV which exists at room temperature in a C5 conformation. This conformational type is also highly populated in the valine derivative III, but is less important in the alanine and leucine derivatives I and II in which the intramolecularly bonded C7 and the distorted hydrogen-nonbonded conformations contribute seriously.

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