Synthesis and Structural Insight into poly(dimethylsiloxane)-b-poly(2-vinylpyridine) Copolymers

Author:

Manesi Gkreti-Maria1ORCID,Moutsios Ioannis12ORCID,Moschovas Dimitrios1,Papadopoulos Georgios1,Ntaras Christos1,Rosenthal Martin3ORCID,Vidal Loic2,Ageev Georgiy G.4ORCID,Ivanov Dimitri A.2456ORCID,Avgeropoulos Apostolos15ORCID

Affiliation:

1. Department of Materials Science & Engineering, University of Ioannina, University Campus-Dourouti, 45110 Ioannina, Greece

2. Institut de Sciences des Matériaux de Mulhouse—IS2M, CNRS UMR7361, 15 Jean Starcky, 68057 Mulhouse, France

3. Department of Chemistry, KU Leuven, Celestijnenlaan 200F, P.O. Box 2404, B-3001 Leuven, Belgium

4. Scientific Center for Genetics and Life Sciences, Sirius University of Science and Technology, 1 Olympic Ave., 354340 Sochi, Russia

5. Faculty of Chemistry, Lomonosov Moscow State University (MSU), GSP-1, 1-3 Leninskiye Gory, 119991 Moscow, Russia

6. Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry RAS, Russian Academy of Sciences, Chernogolovka, 142432 Moscow, Russia

Abstract

In this study, the use of anionic polymerization for the synthesis of living poly(dimethylsiloxane) or PDMS-Li+, as well as poly(2-vinylpyridine) or P2VP-Li+ homopolymers, and the subsequent use of chlorosilane chemistry in order for the two blocks to be covalently joined leading to PDMS-b-P2VP copolymers is proposed. High vacuum manipulations enabled the synthesis of well-defined materials with different molecular weights (Μ¯n, from 9.8 to 36.0 kg/mol) and volume fraction ratios (φ, from 0.15 to 0.67). The Μ¯n values, dispersity indices, and composition were determined through membrane/vapor pressure osmometry (MO/VPO), size exclusion chromatography (SEC), and proton nuclear magnetic resonance spectroscopy (1H NMR), respectively, while the thermal transitions were determined via differential scanning calorimetry (DSC). The morphological characterization results suggested that for common composition ratios, lamellar, cylindrical, and spherical phases with domain periodicities ranging from approximately 15 to 39 nm are formed. A post-polymerization chemical modification reaction to quaternize the nitrogen atom in some of the P2VP monomeric units in the copolymer with the highest P2VP content, and the additional characterizations through 1H NMR, infrared spectroscopy, DSC, and contact angle are reported. The synthesis, characterization, and quaternization of the copolymer structure are important findings toward the preparation of functional materials with enhanced properties suitable for various nanotechnology applications.

Funder

Ministry of Science and Higher Education of the Russian Federation

Hellenic Foundation for Research and Innovation

Publisher

MDPI AG

Subject

Polymers and Plastics,General Chemistry

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