Singh Neetika, Singh Sumit, Kumar Prabhat, Riaz Ufana
Materials Research Laboratory Department of Chemistry, Jamia Millia Islamia New Delhi-110025 India
Advance Instrumentation Research Facility, Jawaharlal Nehru University New Delhi-110067 India.
RSC Adv. 2020 Oct 9;10(61):37456-37462. doi: 10.1039/d0ra07714c. eCollection 2020 Oct 7.
The present manuscript reports the synthesis of benzoquinone (BQ) modified polythiophene (PTh) by chemical and microwave-assisted polymerization techniques. The synthesized oligomers were investigated for their spectral, morphological and thermal properties FTIR, UV-visible, scanning electron microscopy (SEM) and thermogravimetric (TGA) analyses. Theoretical calculations were performed by using Gaussian 09 software the DFT/B3LYP method with the 6-311G basis set. FTIR confirmed the formation of hydroquinone modified PTh when the polymerization was carried out by magnetic stirring and ultrasonication, while the formation of BQ modified PTh was obtained by microwave irradiation. The electronic transitions obtained experimental UV-visible studies were also found to be in close agreement with the theoretical spectra. SEM revealed a well-formed morphology comprising needle shaped rods for the oligomer synthesized under microwave irradiation. The TGA-DTA studies revealed low char content for the above oligomer, while the florescence studies revealed intense emission around 450 nm. The highest quantum yield was found to be 0.024, which also showed high singlet oxygen generation tendency as well as a high single oxygen quantum yield of 0.30 and could be utilized to design imaging probes applicable in photodynamic therapy.
本手稿报道了通过化学和微波辅助聚合技术合成苯醌(BQ)修饰的聚噻吩(PTh)。对合成的低聚物进行了光谱、形态和热性能研究,包括傅里叶变换红外光谱(FTIR)、紫外可见光谱、扫描电子显微镜(SEM)和热重分析(TGA)。使用高斯09软件,采用密度泛函理论(DFT)/B3LYP方法和6-311G基组进行理论计算。FTIR证实,当通过磁力搅拌和超声进行聚合时,形成了对苯二酚修饰的PTh,而通过微波辐射则得到了BQ修饰的PTh。实验紫外可见研究获得的电子跃迁也与理论光谱密切吻合。SEM显示,在微波辐射下合成的低聚物具有由针状棒组成的良好形态。TGA-DTA研究表明上述低聚物的炭含量较低,而荧光研究表明在450nm左右有强烈发射。发现最高量子产率为0.024,其单线态氧生成倾向以及单氧量子产率也很高,为0.30,可用于设计适用于光动力疗法的成像探针。