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ROMPI-CDSA: ring-opening metathesis polymerization-induced crystallization-driven self-assembly of metallo-block copolymers
Polymerization-induced self-assembly (PISA) and crystallization-driven self-assembly (CDSA) are among the most prevailing methods for block copolymer self-assembly. Taking the merits of scalability of PISA and dimension control of CDSA, we report one-pot synchronous PISA and CDSA via ring-opening me...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6993615/ https://www.ncbi.nlm.nih.gov/pubmed/32055347 http://dx.doi.org/10.1039/c9sc03056e |
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author | Sha, Ye Rahman, Md Anisur Zhu, Tianyu Cha, Yujin McAlister, C. Wayne Tang, Chuanbing |
author_facet | Sha, Ye Rahman, Md Anisur Zhu, Tianyu Cha, Yujin McAlister, C. Wayne Tang, Chuanbing |
author_sort | Sha, Ye |
collection | PubMed |
description | Polymerization-induced self-assembly (PISA) and crystallization-driven self-assembly (CDSA) are among the most prevailing methods for block copolymer self-assembly. Taking the merits of scalability of PISA and dimension control of CDSA, we report one-pot synchronous PISA and CDSA via ring-opening metathesis polymerization (ROMP) to prepare nano-objects based on a crystalline poly(ruthenocene) motif. We denote this self-assembly methodology as ROMPI-CDSA to enable a simple, yet robust approach for the preparation of functional nanomaterials. |
format | Online Article Text |
id | pubmed-6993615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-69936152020-02-13 ROMPI-CDSA: ring-opening metathesis polymerization-induced crystallization-driven self-assembly of metallo-block copolymers Sha, Ye Rahman, Md Anisur Zhu, Tianyu Cha, Yujin McAlister, C. Wayne Tang, Chuanbing Chem Sci Chemistry Polymerization-induced self-assembly (PISA) and crystallization-driven self-assembly (CDSA) are among the most prevailing methods for block copolymer self-assembly. Taking the merits of scalability of PISA and dimension control of CDSA, we report one-pot synchronous PISA and CDSA via ring-opening metathesis polymerization (ROMP) to prepare nano-objects based on a crystalline poly(ruthenocene) motif. We denote this self-assembly methodology as ROMPI-CDSA to enable a simple, yet robust approach for the preparation of functional nanomaterials. Royal Society of Chemistry 2019-09-04 /pmc/articles/PMC6993615/ /pubmed/32055347 http://dx.doi.org/10.1039/c9sc03056e Text en This journal is © The Royal Society of Chemistry 2019 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0) |
spellingShingle | Chemistry Sha, Ye Rahman, Md Anisur Zhu, Tianyu Cha, Yujin McAlister, C. Wayne Tang, Chuanbing ROMPI-CDSA: ring-opening metathesis polymerization-induced crystallization-driven self-assembly of metallo-block copolymers |
title | ROMPI-CDSA: ring-opening metathesis polymerization-induced crystallization-driven self-assembly of metallo-block copolymers
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title_full | ROMPI-CDSA: ring-opening metathesis polymerization-induced crystallization-driven self-assembly of metallo-block copolymers
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title_fullStr | ROMPI-CDSA: ring-opening metathesis polymerization-induced crystallization-driven self-assembly of metallo-block copolymers
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title_full_unstemmed | ROMPI-CDSA: ring-opening metathesis polymerization-induced crystallization-driven self-assembly of metallo-block copolymers
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title_short | ROMPI-CDSA: ring-opening metathesis polymerization-induced crystallization-driven self-assembly of metallo-block copolymers
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title_sort | rompi-cdsa: ring-opening metathesis polymerization-induced crystallization-driven self-assembly of metallo-block copolymers |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6993615/ https://www.ncbi.nlm.nih.gov/pubmed/32055347 http://dx.doi.org/10.1039/c9sc03056e |
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