2015
DOI: 10.1016/j.eurpolymj.2014.12.041
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Crystallization in segregated supramolecular pseudoblock copolymers

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Cited by 7 publications
(14 citation statements)
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“…They were thymine‐2,4‐diaminotriazine (Thy‐Tr) or 2‐ureido‐4[1 H ]‐pyrimidinone‐2‐ureido‐4[1 H ]‐pyrimidinone (UPy‐UPy) interactions for the reports discussed here. These hydrogen bonding interactions were confirmed by FTIR . Studies have shown that these hydrogen bonding interactions are dominant at low molecular weights of at least one of the blocks and that the hydrogen bonding has a confining effect.…”
Section: Unique Block Copolymers and Their Assembliesmentioning
confidence: 66%
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“…They were thymine‐2,4‐diaminotriazine (Thy‐Tr) or 2‐ureido‐4[1 H ]‐pyrimidinone‐2‐ureido‐4[1 H ]‐pyrimidinone (UPy‐UPy) interactions for the reports discussed here. These hydrogen bonding interactions were confirmed by FTIR . Studies have shown that these hydrogen bonding interactions are dominant at low molecular weights of at least one of the blocks and that the hydrogen bonding has a confining effect.…”
Section: Unique Block Copolymers and Their Assembliesmentioning
confidence: 66%
“…Other unique chemistries of interest include biopolymer conjugates and supramolecular pseudoblock copolymers (SPBCPs) . Biopolymer conjugates include traditional synthetic polymers with a biopolymer block or polypeptoids, which are comb‐like, glycine‐backbone polymers with substituents on the nitrogen of the glycine monomer .…”
Section: Unique Block Copolymers and Their Assembliesmentioning
confidence: 99%
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“…47,48 Cu(I)Br was stirred for 2 days in acetic acid/anhydride, washed with dry diethyl ether several times, and dried in vacuo under an argon atmosphere. N,N-Diisopropylethylamine (DIPEA), N,N-dicyclohexylcarbodiimide (DCC), N,N-dimethylamino-4-pyridine (DMAP) and 2,2 0 -bipyridine were used without further puri-cation.…”
Section: Methodsmentioning
confidence: 99%