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源自苯并噻吩和苯并呋喃的新型方酸菁染料的合成与光电特性研究

Synthesis and Optoelectrical Characterization of Novel Squaraine Dyes Derived from Benzothiophene and Benzofuran.

作者信息

Rao G Hanumantha, Pandey Manish, Narayanaswamy Kamatham, Srinivasa Rao Ravulakollu, Pandey Shyam S, Hayase Shuzi, Singh Surya Prakash

机构信息

Polymers and Functional Materials Division, CSIR-Indian Institute of Chemical Technology, Uppal Road, Tarnaka, Hyderabad 500007, India.

Academy of Scientific and Innovative Research (AcSIR), CSIR-Human Resource Development Centre, (CSIR-HRDC) Campus, Kamla Nehru Nagar, Ghaziabad, Uttar Pradesh 201002, India.

出版信息

ACS Omega. 2018 Oct 23;3(10):13919-13927. doi: 10.1021/acsomega.8b01240. eCollection 2018 Oct 31.

DOI:10.1021/acsomega.8b01240
PMID:31458088
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6645072/
Abstract

Synthesis and photophysical characterizations of two novel small molecules and with D-A-D molecular structure consisting of squaraine as central unit and benzothiophene and benzofuran as end groups are being reported. Apart from very sharp and intense light absorption by these molecular sensitizers in near-infrared (NIR) wavelength region, their possibility as small molecular organic semiconductor was also explored after fabricating organic field-effect transistors (OFETs). Results obtained from photophysical, electrochemical, and quantum chemical studies were combined to elucidate the structural and optoelectronic properties. Electrical characterization pertaining to the charge-transport properties carried after OFET fabrication exhibited field-effect mobilities of 4.0 × 10 and 5.4 × 10 cm/(V s) for and , respectively. After thermal annealing at 130 °C, the field-effect mobility was found to increase for both squaraine dyes. Relatively facile carrier transport in compared to that of could be attributed to relatively higher backbone planarity as indicated from optimized molecular structure obtained after density functional theory calculations. This work may guide for further molecular design and synthesis of novel squaraine dyes for high-performance OFET applications.

摘要

本文报道了两种新型小分子的合成及其光物理特性,这两种小分子具有由方酸菁作为中心单元、苯并噻吩和苯并呋喃作为端基的D-A-D分子结构。除了这些分子敏化剂在近红外(NIR)波长区域具有非常尖锐且强烈的光吸收外,在制备有机场效应晶体管(OFET)后,还探索了它们作为小分子有机半导体的可能性。结合光物理、电化学和量子化学研究获得的结果,以阐明其结构和光电性质。与OFET制备后所承载的电荷传输性质相关的电学表征显示,对于[具体分子1]和[具体分子2],场效应迁移率分别为4.0×10[具体数值1]和5.4×10[具体数值2] cm²/(V·s)。在130℃进行热退火后,发现两种方酸菁染料的场效应迁移率均有所增加。与[具体分子2]相比,[具体分子1]中相对容易的载流子传输可归因于密度泛函理论计算得到的优化分子结构所表明的相对较高的主链平面度。这项工作可为高性能OFET应用的新型方酸菁染料的进一步分子设计和合成提供指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c5/6645072/b837d888579e/ao-2018-01240e_0007.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c5/6645072/b837d888579e/ao-2018-01240e_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c5/6645072/8d015d33a1dc/ao-2018-01240e_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c5/6645072/3b62bcd18423/ao-2018-01240e_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c5/6645072/f72e91f38d75/ao-2018-01240e_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c5/6645072/aac06a448307/ao-2018-01240e_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c5/6645072/6362d7da957c/ao-2018-01240e_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c5/6645072/75682e8c8c3b/ao-2018-01240e_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c5/6645072/8bd86e91506d/ao-2018-01240e_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c5/6645072/b837d888579e/ao-2018-01240e_0007.jpg

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