Evidence for Termination of Intermediate Radical Species in RAFT-Mediated Polymerization

2003 ◽  
Vol 36 (26) ◽  
pp. 9687-9690 ◽  
Author(s):  
F. M. Calitz ◽  
J. B. McLeary ◽  
J. M. McKenzie ◽  
M. P. Tonge ◽  
B. Klumperman ◽  
...  
1989 ◽  
pp. 424-425
Author(s):  
E. Fridell ◽  
B. Hellsing ◽  
S. Ljungström ◽  
T. Wahnström ◽  
A. Rosé ◽  
...  

1974 ◽  
Vol 52 (1) ◽  
pp. 102-110 ◽  
Author(s):  
Allen John Elliot ◽  
Frank Cuthbert Adam

Dilute solutions of aliphatic thiols have been prepared and photolyzed at 253.7 nm in 3-methylpentane glasses at 77°K. The major products formed initially are thiyl radicals RS• and hydrogen atoms. Both of these are hot and yield solvent radicals by abstraction reactions, and relatively small amounts of RS2•, RS•, and possibly R1R2C=S. Thermal annealing of the matrices is accompanied by loss of hydrocarbon radicals through cage reactions and concommitant increase in the RS• concentration. An intermediate radical of the type R1R2ĊSH may also be produced in the annealing process. The photometric and spin resonance characteristics of RS•, RS2•and R1ĊH—SH are discussed and related to other systems in which these intermediates are observed. RS• is characterized in the amorphous phase by an absorption at 405 nm and a broad asymmetrical e.p.r. resonance near [Formula: see text] RS2• has a non-axial g-tensor with principal values of about 2.06, 2.02, and 2.00 and has no detectable absorptions between 350 and 1200 nm.The photolytic behavior of these metastable radical species is also investigated.


2011 ◽  
Vol 30 (15) ◽  
pp. 4115-4122 ◽  
Author(s):  
Adriano Boni ◽  
Tiziana Funaioli ◽  
Fabio Marchetti ◽  
Guido Pampaloni ◽  
Calogero Pinzino ◽  
...  

Synlett ◽  
2021 ◽  
Author(s):  
Evgeny B Ulyankin ◽  
Yulia Petrovna Bogza ◽  
Anastasia S. Kostyuchenko ◽  
Sergey A. Chernenko ◽  
Vyacheslav L. Yurpalov ◽  
...  

4 - [(2-Iodalyloxy) methyl] thiophene-2-carbaldehyde and 5-iodo-4- (aryloxymethyl)thiophene-2-carbaldehydes were obtained by interaction of phenols with 4-chloromethylthiophene-2-carbaldehyde and its 5-iodosubstituted derivative. These compounds underwent ring closure upon irradiation with UV light (254 nm) to form 4H-thieno[3,2-c]chromene-2-carbaldehyde in high yield. The formation of intermediate radical species was detected by EPR method. Comparative analysis of the ring closure methods showed that the photochemical cyclization of 5-iodo-4-(aryloxymethyl) thiophene-2-carbaldehyde is more rational than the Pd-catalyzed intramolecular arylation. A series of substituted 4H-thieno[3,2-c]chromene-2-carbaldehydes was synthesized by the photochemical cyclization of the corresponding precursors. The photophysical properties of the synthesized compounds were studied. The obtained 4H-thieno[3,2-c]chromene-2-carbaldehydes can be used as covert marking pigments.


2009 ◽  
Vol 59 (12) ◽  
Author(s):  
Mihai Contineanu ◽  
iulia Contineanu ◽  
Ana Neacsu ◽  
Stefan Perisanu

The radiolysis of the isomers L-, D- and DL- of the aspartic acid, in solid polycrystalline state, was investigated at room temperature. The analysis of their ESR spectra indicated the formation of at least two radicalic entities. The radical, identified as R3, resulting from the deamination of the acid, exhibits the highest concentration and thermal resistance. Possible mechanisms of formation of three radical species are suggested, based also on literature data. The kinetics of the disappearance of radical R3 indicated a complex mechanism. Three possible variants were suggested for this mechanism.


2021 ◽  
Vol 23 (11) ◽  
pp. 6462-6471
Author(s):  
Piyush Mishra ◽  
Sean M. Fritz ◽  
Sven Herbers ◽  
Alexander M. Mebel ◽  
Timothy S. Zwier

The flash pyrolysis of trans 3-pentenenitrile was studied by mass-correlated broadband microwave spectroscopy, where both molecular and radical species were observed within our jet-cooled molecular beam, including 2,4-pentadienenitrile.


Processes ◽  
2021 ◽  
Vol 9 (2) ◽  
pp. 293
Author(s):  
Jeu-Ming P. Yuann ◽  
Shwu-Yuan Lee ◽  
Meei-Ju Yang ◽  
Shiuh-Tsuen Huang ◽  
Chien-Wei Cheng ◽  
...  

Catechin exhibits numerous physiological characteristics. In this study, we determined the photosensitivity of catechin to various lights under alkaline conditions, and the mechanisms by which catechin generates free radical species and polymerizes via a photoreaction. In addition to this, the application of catechin photolysis was investigated. A solution of catechin is transparent, but turns yellowish under blue light illumination (BLI) in neutral or weak alkaline solutions. When catechin is subjected to BLI, a dimeric catechin (proanthocyanidin) and a superoxide anion radical (O2•−) are generated in a photolytic reaction. When ascorbic acid or gallic acid is added to catechin and the mixture is subjected to BLI at alkaline pH, fewer catechin dimers and less O2•− are produced, because both acids inhibit the photosensitive oxidation of catechin. When AlCl3 is added to catechin and the mixture is subjected to BLI at pH 8, a photolytic reaction is suppressed by AlCl3, and AlCl3 acts as a catalyst for the disconnection of proanthocyanidin during photolysis. Under alkaline conditions, catechin generates O2•− via photosensitive oxidation, which suppresses the growth of Acinetobacter baumannii (A. baumannii) by at least 4 logs, and deactivates its multi-drug-resistant strain. This study shows that catechin photolysis is a process of oxidation, and that it can be safely applied as a tool for environmental applications.


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