scholarly journals The Effect of Functional Group Position of the Piperidine Derivatives on the CO2Absorption Characteristics in the (H2O-Piperidine-CO2) System

2015 ◽  
Vol 53 (1) ◽  
pp. 57-63 ◽  
Author(s):  
Jeong Ho Choi ◽  
Soung Hee Yun ◽  
Yeong Eun Kim ◽  
Yeo Il Yoon ◽  
Sung Chan Nam
2018 ◽  
Vol 462 ◽  
pp. 517-525 ◽  
Author(s):  
Fei Han ◽  
Zeyi Tu ◽  
Zhongquan Wan ◽  
Junsheng Luo ◽  
Jianxing Xia ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (92) ◽  
pp. 89827-89835 ◽  
Author(s):  
Zhen Wang ◽  
Anyang Li ◽  
Lei Gou ◽  
Jingzheng Ren ◽  
Gaohong Zhai

Effects of functional group position on the calculated redox potential for the single electron-withdrawing group substitution of phenanthraquinone analogues.


2005 ◽  
Vol 483 (2) ◽  
pp. 192-204 ◽  
Author(s):  
Brett A. Johnson ◽  
Haleh Farahbod ◽  
Sepideh Saber ◽  
Michael Leon

Polymers ◽  
2021 ◽  
Vol 13 (16) ◽  
pp. 2698
Author(s):  
Donghyuk Kim ◽  
Gyeongdong Yeom ◽  
Hongil Joo ◽  
Byungkyu Ahn ◽  
Hyunjong Paik ◽  
...  

Recently, research conducted on tread compounds with liquid butadiene rubber (LqBR) have been conducted in the tire industry. In particular, the introduction of functional groups into LqBRs is expected to lower hysteresis loss caused by the free chain ends of LqBR. To study this, LqBRs with functional groups at different positions were synthesized. The occurrences of in-chain and chain-end functionalization of functionalized LqBRs (F-LqBRs) were confirmed, the microstructure and functionalization efficiency of F-LqBRs were calculated through the characterizations. This novel functionalization technology was beneficial not only to immobilizing the free chain ends of LqBRs to the surfaces of silica to decrease the number of free chain ends, but also chemically bonding the LqBR chains on the base polymer through a crosslinking reaction to enhance the filler-rubber interaction. The effects of the functional group position and number of the free chain ends on the physical properties and hysteresis of the compounds were investigated by partially replacing the treated distillate aromatic extract (TDAE) oil with LqBR in silica-filled rubber compounds. The results showed that compounds that had applied DF-LqBR with both end functionalization performed better, including improving the silica dispersion, higher extraction resistance, and lower rolling resistance, than other F-LqBRs compounds.


Crystals ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 1596
Author(s):  
Ali K. Brandt ◽  
Derek J. Boyle ◽  
Jacob P. Butler ◽  
Abigail R. Gillingham ◽  
Scott E. Penner ◽  
...  

Families of quasiracemic materials constructed from 3- and 4-substituted chiral diarylamide molecular frameworks were prepared, where the imposed functional group differences systematically varied from H to CF3–9 unique components for each isomeric framework. Cocrystallization from the melt via hot stage thermomicroscopy using all possible racemic and quasiracemic combinations probed the structural boundaries of quasiracemate formation. The crystal structures and lattice energies (differential scanning calorimetry and lattice energy calculations) for many of these systems showed that quasienantiomeric components organize with near inversion symmetry and lattice energetics closely resembling those found in the racemic counterparts. This study also compared the shape space of pairs of quasienantiomers using an in silico alignment-based method to approximate the differences in molecular shape and provide a diagnostic tool for quasiracemate prediction. Comparing these results to our recent report on related 2-substituted diarylamide quasiracemates shows that functional group position can have a marked effect on quasiracemic behavior and provide critical insight to a more complete shape space, essential for defining molecular recognition processes.


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