<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(7)</volume><submitter>Spasojevic M</submitter><pubmed_abstract>The synthesis of poly(&lt;i>N&lt;/i>-isopropylacrylamide)-b-poly(L-lysine) and poly(&lt;i>N&lt;/i>- isopropylacrylamide-co-acrylamide)-b-poly(L-lysine) copolymers was accomplished by combining atom transfer radical polymerization (ATRP) and ring opening polymerization (ROP). For this purpose, a di-functional initiator with protected amino group was successfully synthetized. The ATRP of &lt;i>N&lt;/i>-isopropylacrylamide yielded narrowly dispersed polymers with consistent high yields (~80%). Lower yields (~50%) were observed when narrowly dispersed random copolymers of &lt;i>N&lt;/i>-isopropylacrylamide and acrylamide where synthesized. Amino-terminated poly(&lt;i>N&lt;/i>-isopropylacrylamide) and poly(&lt;i>N&lt;/i>-isopropylacrylamide- co-acrylamide) were successfully used as macroinitiators for ROP of &lt;i>N&lt;/i>₆-carbobenzox</pubmed_abstract><journal>Materials (Basel, Switzerland)</journal><pagination>5305-5326</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5455825</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Synthesis and Phase Behavior of Poly(&lt;i>N&lt;/i>-isopropylacrylamide)-b- Poly(L-Lysine Hydrochloride) and Poly(&lt;i>N&lt;/i>-Isopropylacrylamide- co-Acrylamide)-b-Poly(L-Lysine Hydrochloride).</pubmed_title><pmcid>PMC5455825</pmcid><pubmed_authors>Schouten AJ</pubmed_authors><pubmed_authors>Jansen MRPACS</pubmed_authors><pubmed_authors>Spasojevic M</pubmed_authors><pubmed_authors>de Vos P</pubmed_authors><pubmed_authors>Vorenkamp J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis and Phase Behavior of Poly(&lt;i>N&lt;/i>-isopropylacrylamide)-b- Poly(L-Lysine Hydrochloride) and Poly(&lt;i>N&lt;/i>-Isopropylacrylamide- co-Acrylamide)-b-Poly(L-Lysine Hydrochloride).</name><description>The synthesis of poly(&lt;i>N&lt;/i>-isopropylacrylamide)-b-poly(L-lysine) and poly(&lt;i>N&lt;/i>- isopropylacrylamide-co-acrylamide)-b-poly(L-lysine) copolymers was accomplished by combining atom transfer radical polymerization (ATRP) and ring opening polymerization (ROP). For this purpose, a di-functional initiator with protected amino group was successfully synthetized. The ATRP of &lt;i>N&lt;/i>-isopropylacrylamide yielded narrowly dispersed polymers with consistent high yields (~80%). Lower yields (~50%) were observed when narrowly dispersed random copolymers of &lt;i>N&lt;/i>-isopropylacrylamide and acrylamide where synthesized. Amino-terminated poly(&lt;i>N&lt;/i>-isopropylacrylamide) and poly(&lt;i>N&lt;/i>-isopropylacrylamide- co-acrylamide) were successfully used as macroinitiators for ROP of &lt;i>N&lt;/i>₆-carbobenzox</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Jul</publication><modification>2025-04-22T16:41:17.283Z</modification><creation>2019-03-27T02:46:38Z</creation></dates><accession>S-EPMC5455825</accession><cross_references><pubmed>28788130</pubmed><doi>10.3390/ma7075305</doi></cross_references></HashMap>