One-Pot Preparation of 3D Nano- and Microaggregates via In Situ Nanoparticlization of Polyacetylene Diblock Copolymers Produced by ROMP

Zero‐dimensional (0D) nanospheres, 1D nanocaterpillars, and 3D aggregates are produced from simple diblock copolymers containing polyacetylene (PA) via in situ nanoparticlization of conjugated polymers. The diblock copolymers are prepared by ring‐opening metathesis polymerization via one‐pot sequent...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Macromolecular rapid communications. 2015-06, Vol.36 (11), p.1069-1074
Hauptverfasser: Yoon, Ki-Young, Shin, Suyong, Kim, Yong-Jae, Kim, Inhye, Lee, Eunji, Choi, Tae-Lim
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Zero‐dimensional (0D) nanospheres, 1D nanocaterpillars, and 3D aggregates are produced from simple diblock copolymers containing polyacetylene (PA) via in situ nanoparticlization of conjugated polymers. The diblock copolymers are prepared by ring‐opening metathesis polymerization via one‐pot sequential addition of an endo‐tricyclo[4.2.2.0]deca‐3,9‐diene (TD) and cyclooctatetraene. Initially, they spontaneously form nanospheres consisting of a PA core and PTD shell, and increasing the length of the PA block leads to the direct nanoparticlization of the higher‐dimensional structures such as 1D and 3D aggregates because of the decreased effective volume ratio of the rigid PTD shell to the solvophobic PA core. 3D aggregates are prepared from simple diblock copolymers containing poly­acetylene via in situ nanoparticlization of conjugated polymers. Ring‐opening metathesis polymerization (ROMP) via one‐pot sequential addition of an endo‐tricyclo[4.2.2.0]deca‐3,9‐diene and cyclooctatetraene is used to produce the diblock copolymer. The nano‐ and microstructures of all the aggregates are confirmed by various imaging and spectroscopic tools. On the basis of these observations, a plausible mechanism for this in situ nanoparticlization is proposed.
ISSN:1022-1336
1521-3927
DOI:10.1002/marc.201400649