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Synthesis of π-Conjugated Organometallic Polymer Networks

✍ Scribed by Akshay Kokil; Christian Huber; Walter R. Caseri; Christoph Weder


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
150 KB
Volume
204
Category
Article
ISSN
1022-1352

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✦ Synopsis


Abstract

The present paper reports the synthesis of π‐conjugated organometallic polymer networks based on poly[2,5‐dioctyloxy‐1,4‐diethynyl‐phenylene‐alt‐2,5,‐bis(2′‐ethylhexyloxy)‐1,4‐phenylene] (EHO‐OPPE), a soluble poly(p‐phenylene ethynylene) (PPE) derivative. The ethynylene moieties of the polymer coordinate to Pt^0^ centers, which act as conjugated cross‐links. These materials are readily accessible through ligand‐exchange reactions between the linear PPE and Pt(styrene)~3~. The in‐situ NMR investigation of model reactions of Pt(styrene)~3~ with diphenylacetylene (DPA) has shown that the ethynylene moieties comprised in the PPE readily coordinate to Pt^0^ centers under release of the relatively weakly‐bound styrene ligands. Spin‐coating has resulted in cross‐linked films of good optical quality. We also have been able to produce PPE‐Pt‐gels with high solvent content (> 95 wt.‐%). As expected, the coordination of Pt markedly influences the photophysical characteristics of the PPE. The photoluminescence is efficiently quenched, and the absorption maximum in the visible regime experiences a hypsochromic shift.

Ligand‐exchange reaction between EHO‐OPPE and [Pt(PhCHCH~2~)~3~] leading to the target EHO‐OPPE‐Pt^0^ networks.

magnified imageLigand‐exchange reaction between EHO‐OPPE and [Pt(PhCHCH~2~)~3~] leading to the target EHO‐OPPE‐Pt^0^ networks.


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