Influence of Adjustable Grafted Side Chains on the Non-Isothermal Crystallisation of a Ternary-Monomer Solid Phase Graft Copolymer of Polypropylene

2008 ◽  
Vol 16 (2) ◽  
pp. 131-138
Author(s):  
Hong Haoqun ◽  
He Hui ◽  
Jia Demin ◽  
Hua Ben ◽  
Lin Gengdong
Keyword(s):  
Graft Copolymer ◽  
Solid Phase ◽  
Side Chains ◽  
Isothermal Crystallisation

A Strategy for Thioamide Incorporation During Fmoc Solid-Phase Peptide Synthesis with Robust Stereochemical Integrity

2019 ◽  
Author(s):  
luis camacho III ◽  
Bryan J. Lampkin ◽  
Brett VanVeller
Keyword(s):  
Amino Acid ◽  
Functional Groups ◽  
Peptide Synthesis ◽  
Solid Phase ◽  
Solid Phase Peptide Synthesis ◽  
Side Chains ◽  
Amino Acid Side Chains ◽  
Peptide Elongation

We describe a method to protect the sensitive stereochemistry of the thioamide—in analogy to the protection of the functional groups of amino acid side chains—in order to preserve the thioamide moiety during peptide elongation.<br>

Synthesis and characterization of amphiphilic graft copolymers with hydrophobic poly(α-methylstyrene) backbone and hydrophilic poly(n-vinylpyrrolidone) side chains

e-Polymers ◽  
2012 ◽  
Vol 12 (1) ◽  
Author(s):  
Fatima Zohra Sebba ◽  
Seghier Ould Kada ◽  
Mohamed Benaicha ◽  
Nerjesse Nemiche
Keyword(s):  
Graft Copolymer ◽  
Graft Copolymers ◽  
Radical Copolymerization ◽  
Side Chains ◽  
Free Radical Copolymerization ◽  
Good Efficiency ◽  
Molecular Weights ◽  
Grafting Reaction ◽  
Viscosity Variation ◽  
End Capping

AbstractIn this study, 2-oxopropylmethacrylate-terminated poly(N-vinyl-2- pyrrolidone) is produced by cationic polymerization using HClO4 as an initiator. Termination (end capping) step is accomplished using 2- hydroxypropylmethacrylate (2HPMA) and the polymer product has different chain lengths of molecular weight averages ranging from 672 to 3049 g/mol. The study also synthesised amphipathic graft copolymers having hydrophobic poly(α- methylstyrene) as a backbone chain and hydrophilic poly(N-vinyl-2-pyrrolidone) (PVP) as side chains of various lengths. The copolymer synthesis was accomplished by free radical copolymerization of ω-oxopropylmethacrylate PVP in the presence of α-methyl styrene initiated with benzoyl peroxide. Measurements of the dynamic viscosity of the polymer solution (20% weight of macromonomers in ethanol) show that the viscosity is proportional to the average molecular weights M̅n . However, a reverse behaviour of the viscosity variation with regard to M̅n is observed for graft copolymer samples. The viscosity variation with respect to the graft copolymer mass must be due to steric effects, which are strongly pronounced in grafted copolymer chains. Appearance of the number of side chains attached to poly(α-methylstyrene) backbone reveals that the grafting reaction has occurred with good efficiency.

Solid-phase synthesis of amino amides and peptide amides with unnatural side chains

2001 ◽  
Vol 42 (11) ◽  
pp. 2073-2076 ◽  
Author(s):  
William L Scott ◽  
Francisca Delgado ◽  
Karen Lobb ◽  
Richard S Pottorf ◽  
Martin J O'Donnell
Keyword(s):  
Solid Phase Synthesis ◽  
Solid Phase ◽  
Side Chains ◽  
Phase Synthesis ◽  
Amino Amides

Spinning of Fibers from Graft Copolymers of Polyacrylonitrile and Poly(Methyl Acrylate)

1976 ◽  
Vol 46 (2) ◽  
pp. 77-81 ◽  
Author(s):  
Samy Abdel Monem El-Garf
Keyword(s):  
Graft Copolymer ◽  
Methyl Acrylate ◽  
Graft Copolymers ◽  
Coagulation Bath ◽  
Side Chains ◽  
Initial Value

Fibers were spun from graft copolymers of polyacrylonitrile and poly(methyl acrylate). Increasing poly(methyl acrylate) side chains from 5 to 8% decreased the viscosity of the spinning solution in dimethylformamide. The spinning solutions were unstable. When the graft copolymer contained 5% side chains, the viscosity of these solutions returned to almost its initial value by heating. Fibers were obtained from graft copolymers containing from 5–13% poly(methyl acrylate) side chains. These were formed at the temperature of the coagulation bath (50°C), while at temperatures less than 50°C the fibers were not obtained. Weak fibers were produced from a graft copolymer containing 13% side chains at the temperatures of the coagulation bath (20 and 50°C). No fibers were obtained from graft copolymer containing 25% side chains. The method of dissolution of the graft copolymers does affect the drawing of fibers produced from them. It was observed that the heating of the spinning solution decreases the amount of drawing of the produced fibers. The presence of the flexible side chains of poly(methyl acrylate) in the graft copolymer improves the maximum possible degree of drawing of the fibers relative to that of fibers from the initial linear copolymer and homopolyacrylonitrile.

The Effect of a Method of Dissolution of Graft Copolymer of Polyacrylonitrile and Poly(Methyl Acrylate) on Drawability and Properties of Spun Fibers

1976 ◽  
Vol 46 (10) ◽  
pp. 767-770
Author(s):  
Samy Abdel Monem El-Garf
Keyword(s):  
Graft Copolymer ◽  
Methyl Acrylate ◽  
Modulus Of Elasticity ◽  
Abrasion Resistance ◽  
Side Chains ◽  
Yarn Strength ◽  
Dissolution Temperature ◽  
Initial Modulus ◽  
Spun Fibers

It was found that dissolution of the graft copolymer has an effect on drawability and other properties of fibers spun from this graft copolymer. The resistance to double bending and abrasion resistance are considerably decreased with the increase of the dissolution temperature. The breaking properties were not greatly changed. The maximum loop and knotted yarn strength was reached when the polymer was dissolved by heating. These values are 100% and 99% of the original, respectively—higher than those obtained from PAN and PANM. The presence of 5% PMA in the side chains of the graft copolymer increased the flexibility of these chains. This is evident from the decrease of the initial modulus of elasticity from the values obtained for PANM and PAN.

Construction of semi-fluorinated amphiphilic graft copolymer bearing a poly(2-methyl-1,4-bistrifluorovinyloxybenzene) backbone and poly(ethylene glycol) side chains via the grafting-onto strategy

RSC Advances ◽  
2015 ◽  
Vol 5 (50) ◽  
pp. 39668-39676 ◽  
Author(s):  
Guolin Lu ◽  
Hao Liu ◽  
Haifeng Gao ◽  
Chun Feng ◽  
Yongjun Li ◽  
...  
Keyword(s):  
Ethylene Glycol ◽  
Graft Copolymer ◽  
Graft Copolymers ◽  
Side Chains ◽  
Poly Ethylene Glycol ◽  
Amphiphilic Graft Copolymer ◽  
Amphiphilic Graft Copolymers ◽  
Poly Ethylene ◽  
Williamson Reaction ◽  
Grafting Onto

Amphiphilic graft copolymers bearing a hydrophobic PMBTFVB backbone and hydrophilic PEG side chains were synthesized by Williamson reaction through the grafting-onto strategy.

scholarly journals Ultra-large sheet formation by 1D to 2D hierarchical self-assembly of a “rod–coil” graft copolymer with a polyphenylene backbone

2016 ◽  
Vol 7 (6) ◽  
pp. 1234-1238 ◽  
Author(s):  
Yinjuan Huang ◽  
Rui Yuan ◽  
Fugui Xu ◽  
Yiyong Mai ◽  
Xinliang Feng ◽  
...  
Keyword(s):  
Ethylene Oxide ◽  
Graft Copolymer ◽  
Self Assembly ◽  
Side Chains ◽  
Poly Ethylene Oxide ◽  
Poly Ethylene ◽  
Large Sheet

This study presents a unique ultra-large sheet formation through 1D to 2D hierarchical self-assembly of a rod–coil graft copolymer containing a rigid polyphenylene backbone tethered with flexible poly(ethylene oxide) side chains.

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