44
Views
1
CrossRef citations to date
0
Altmetric
Original Articles

Synthesis and Characterization of a Novel, Water‐Soluble Polymer with Pendant Groups Carrying cis‐Platinum Complex

&
Pages 859-871 | Received 01 Mar 2003, Accepted 01 Dec 2003, Published online: 23 Aug 2007
 

Abstract

The synthesis and characterization of a polymer with pendant groups carrying a cis‐platinum complex by the chemical modification route is discussed. Diethyloxomalonate functionalized polystyrene (DPS) is synthesized by the Friedel–Crafts acylation of polystyrene with diethyloxomalonate in the presence of SnCl4, by a batch‐wise addition process. The reaction of DPS with cis‐diaquo(trans‐1,2‐diaminocyclohexane)platinum(II) results in the formation of a cis‐platinum chelated polymer (PtDPS). Proton NMR and IR spectroscopies are used to confirm the transformation. The polymer synthesized is further characterized using thermogravimetric analysis (TGA) as well as UV and fluorescence spectroscopic techniques. PtDPS thus synthesized is further modified into a water‐soluble polymer by another polymer modification reaction resulting in the introduction of thiobarbituric acid moieties.

Acknowledgment

We wish to thank the Defense Research and Development Organization (DRDO), India for financial support.

Log in via your institution

Log in to Taylor & Francis Online

PDF download + Online access

  • 48 hours access to article PDF & online version
  • Article PDF can be downloaded
  • Article PDF can be printed
USD 61.00 Add to cart

Issue Purchase

  • 30 days online access to complete issue
  • Article PDFs can be downloaded
  • Article PDFs can be printed
USD 1,060.00 Add to cart

* Local tax will be added as applicable

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.