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含芘发色团的新型聚噻吩的合成与表征:热学、光学和电化学性质

Synthesis and Characterization of Novel Polythiophenes Containing Pyrene Chromophores: Thermal, Optical and Electrochemical Properties.

作者信息

Valderrama-García Bianca X, Rodríguez-Alba Efraín, Morales-Espinoza Eric G, Moineau Chane-Ching Kathleen, Rivera Ernesto

机构信息

Instituto de Investigaciones en Materiales, Universidad Nacional Autónoma de México, Circuito Exterior Ciudad Universitaria, Mexico City 04510, Mexico.

Centre National de la Recherche Scientifique (CNRS), Laboratoire de Chimie de Coordination (LCC), 205, Route de Narbonne, Toulouse F-31077, France.

出版信息

Molecules. 2016 Jan 30;21(2):172. doi: 10.3390/molecules21020172.

DOI:10.3390/molecules21020172
PMID:26840286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6273483/
Abstract

A novel series of pyrene containing thiophene monomers TPM1-5 were synthesized and fully characterized by FTIR, MS, ¹H- and (13)C-NMR spectroscopy; their thermal properties were determined by TGA and DSC. These monomers were chemically polymerized using FeCl3 as oxidizing agent to give the corresponding oligomers TPO1-5) and they were electrochemically polymerized to obtain the corresponding polymer films deposited onto ITO. All oligomers exhibited good thermal stability, with T10 values between 255 and 299 °C, and Tg values varying from 36 to 39 °C. The monomers showed an absorption band at 345 nm due to the S0 → S2 transition of the pyrene group, whereas the fluorescence spectra showed a broad emission band arising from the "monomer" emission at 375-420 nm. The obtained polymers exhibited two absorption bands at 244 and 354 nm, due to the polythiophene and the pyrene moieties, respectively. The fluorescence spectra of polymers showed a broad "monomer" emission at 380-420 nm followed by an intense excimer emission band at 570 nm, due to the presence of intramolecular pyrene-pyrene interactions in these compounds.

摘要

合成了一系列新型含芘噻吩单体TPM1 - 5,并通过傅里叶变换红外光谱(FTIR)、质谱(MS)、¹H - 核磁共振光谱和¹³C - 核磁共振光谱对其进行了全面表征;通过热重分析(TGA)和差示扫描量热法(DSC)测定了它们的热性能。使用FeCl₃作为氧化剂对这些单体进行化学聚合,得到相应的低聚物TPO1 - 5,并通过电化学聚合获得沉积在氧化铟锡(ITO)上的相应聚合物薄膜。所有低聚物均表现出良好的热稳定性,T10值在255至299℃之间,玻璃化转变温度(Tg)值在36至39℃之间变化。由于芘基团的S0→S2跃迁,单体在345nm处显示出吸收带,而荧光光谱显示在375 - 420nm处出现由“单体”发射产生的宽发射带。所获得的聚合物在244和354nm处分别显示出两个吸收带,分别归因于聚噻吩和芘部分。聚合物的荧光光谱在380 - 420nm处显示出宽的“单体”发射,随后在570nm处出现强的准分子发射带,这是由于这些化合物中存在分子内芘 - 芘相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/d6272810f216/molecules-21-00172-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/b81e5c794da3/molecules-21-00172-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/ac319a711445/molecules-21-00172-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/438eff8249bb/molecules-21-00172-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/d0e085d9f740/molecules-21-00172-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/d7971283e7c6/molecules-21-00172-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/008d6c2fa45c/molecules-21-00172-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/c33c1e3d87b2/molecules-21-00172-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/3b482c42aefa/molecules-21-00172-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/58823fef6e16/molecules-21-00172-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/0c7ae5514663/molecules-21-00172-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/ddb1bd37e493/molecules-21-00172-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/f1dd812f72fe/molecules-21-00172-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/65e023e103a1/molecules-21-00172-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/d6272810f216/molecules-21-00172-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/b81e5c794da3/molecules-21-00172-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/ac319a711445/molecules-21-00172-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/438eff8249bb/molecules-21-00172-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/d0e085d9f740/molecules-21-00172-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/d7971283e7c6/molecules-21-00172-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/008d6c2fa45c/molecules-21-00172-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/c33c1e3d87b2/molecules-21-00172-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/3b482c42aefa/molecules-21-00172-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/58823fef6e16/molecules-21-00172-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/0c7ae5514663/molecules-21-00172-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/ddb1bd37e493/molecules-21-00172-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/f1dd812f72fe/molecules-21-00172-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/65e023e103a1/molecules-21-00172-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b0/6273483/d6272810f216/molecules-21-00172-g014.jpg

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