Synthesis and Optical Properties of Conjugated Polymers Containing Polyoxometalate Clusters as Side-Chain Pendants
Citations Over TimeTop 10% of 2005 papers
Abstract
Hexamolybdate clusters have been covalently attached, for the first time, to the side chains of conjugated polymers. Two sets of such hybrid conjugated polymers have been prepared, one (Ia and Ib) with the clusters linked to the conjugated backbone through a rigid conjugated bridge, the other (IIa and IIb) through flexible alkyl chains. Within each set, polymers with different cluster loading ratios have been prepared. The covalent attachment of POM clusters has been confirmed by 1H NMR, FTIR, and cyclic voltammetry measurements. These hybrid polymers are thermally stable up to 220 °C. Set I polymers (Ia and Ib) exhibit maximum absorption wavelengths (λmax) around 410 nm, while set II polymers (IIa and IIb) show higher λmax values, around 440 nm. Fluorescence studies show that side-chain POM pendants linked through conjugated bridges exhibit a much higher fluorescence quenching effect than those with flexible alkyl bridges, indicating that the through-bond photoinduced electron transfer may be the dominant mechanism for fluorescence quenching. With efficient fluorescence quenching that results in free charge carriers residing in different structural units (positively charged holes in the PPE backbone and negatively charged electrons in the POM clusters), these hybrid polymers may have great potential for applications in photovoltaic (PV) cells.
Related Papers
- → The Interconnection of Two Positive Charges by Conjugation and Cross‐Conjugation in Bis‐Quinolinium Ethynyls(2019)8 cited
- → Carbon‐13 nuclear magnetic resonance spectroscopy of conjugated polyynes(1979)7 cited
- → Determinants of protein side‐chain packing(1994)60 cited
- Effects of inorganic additives on the cyclic voltammetry curves of lead negative(2003)
- → ChemInform Abstract: Cycloadditions of 1,3,4‐Oxadiazin‐6‐ones (4,5‐Diaza‐α‐pyrones). Part 8. Conjugated and Non‐conjugated Cyclopentenones by a Reaction Cascade from Methyl 6‐Oxo‐5‐phenyl‐1,3,4‐oxadiazine‐2‐carboxylate and 1,3‐Butadienes.(1988)