Issue 27, 2015

From drug to adhesive: a new application of poly(dihydropyrimidin-2(1H)-one)s via the Biginelli polycondensation

Abstract

The reactions for polymer synthesis should be simple and efficient using easily available raw materials. A new difunctional monomer containing benzaldehyde and beta-keto ester groups (monomer AB) has been successfully prepared on a medium scale, and the corresponding poly(dihydropyrimidin-2(1H)-one)s (DP ∼84) can be synthesized via the Biginelli polycondensation in a short time (∼1 h). The in situ generated polycondensates could glue two metal sheets, demonstrating an interesting metal bonding property which cannot be observed in small molecules. The optimized multifunctional monomers (AB2, A2B2 monomers) were subsequently used for the in situ polycondensation between metal sheets, and metal bonding strength could be improved to the similar level of commercial cyanoacrylate glue. Since the monomers could be easily prepared on a large scale and the polymerization could be simply performed, the Biginelli polycondensation might have potential as a new strategy to synthesize new functional polymers.

Graphical abstract: From drug to adhesive: a new application of poly(dihydropyrimidin-2(1H)-one)s via the Biginelli polycondensation

Supplementary files

Article information

Article type
Paper
Submitted
09 May 2015
Accepted
08 Jun 2015
First published
08 Jun 2015

Polym. Chem., 2015,6, 4940-4945

Author version available

From drug to adhesive: a new application of poly(dihydropyrimidin-2(1H)-one)s via the Biginelli polycondensation

Y. Zhao, Y. Yu, Y. Zhang, X. Wang, B. Yang, Y. Zhang, Q. Zhang, C. Fu, Y. Wei and L. Tao, Polym. Chem., 2015, 6, 4940 DOI: 10.1039/C5PY00684H

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements