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供体-受体-供体 1-苯并[]咪唑衍生物作为光波导。

Donor-Acceptor-Donor 1-Benzo[]imidazole Derivatives as Optical Waveguides.

机构信息

Department of Inorganic, Organic Chemistry and Biochemistry, Faculty of Chemical Science and Technologies, University of Castilla-La Mancha-IRICA, 13071 Ciudad Real, Spain.

Madrid Institute for Advanced Studies, IMDEA Nanociencia, Calle Faraday 9, Ciudad Universitaria de Cantoblanco, 28049 Madrid, Spain.

出版信息

Molecules. 2023 Jun 8;28(12):4631. doi: 10.3390/molecules28124631.

DOI:10.3390/molecules28124631
PMID:37375189
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10304989/
Abstract

A new series of donor-acceptor-donor (D-A-D) structures derived from arylethynyl 1-benzo[]imidazole was synthesized and processed into single crystals with the goal of testing such crystals' ability to act as optical waveguides. Some crystals displayed luminescence in the 550-600 nm range and optical waveguiding behavior with optical loss coefficients around 10 dB/μm, which indicated a notable light transport. The crystalline structure, confirmed by X-ray diffraction, contains internal channels that are important for light propagation, as we previously reported. The combination of a 1D assembly, a single crystal structure, and notable light emission properties with low losses from self-absorption made 1-benzo[]imidazole derivatives appealing compounds for optical waveguide applications.

摘要

合成了一系列新型的基于芳基乙炔基 1-苯并[]咪唑的给体-受体-给体(D-A-D)结构,并将其加工成单晶,以测试这些晶体作为光波导的能力。一些晶体在 550-600nm 范围内显示出发光,并具有约 10dB/μm 的光导行为,这表明有明显的光传输。晶体结构通过 X 射线衍射得到证实,其中包含内部通道,这对于光传播很重要,正如我们之前报道的那样。1-苯并[]咪唑衍生物具有一维组装、单晶结构和显著的发光性能,同时自吸收损耗低,因此成为光学波导应用的有吸引力的化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/d5648bbd005f/molecules-28-04631-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/659ddaf08a30/molecules-28-04631-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/62ac0842b530/molecules-28-04631-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/7a2de158cbbb/molecules-28-04631-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/f69fbfe352b6/molecules-28-04631-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/ebfd6091eb75/molecules-28-04631-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/025e6406d0c8/molecules-28-04631-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/a78a54f488b6/molecules-28-04631-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/d225bceee223/molecules-28-04631-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/c4344c9dd0f7/molecules-28-04631-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/55b038563571/molecules-28-04631-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/d5648bbd005f/molecules-28-04631-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/659ddaf08a30/molecules-28-04631-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/62ac0842b530/molecules-28-04631-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/7a2de158cbbb/molecules-28-04631-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/f69fbfe352b6/molecules-28-04631-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/ebfd6091eb75/molecules-28-04631-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/025e6406d0c8/molecules-28-04631-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/a78a54f488b6/molecules-28-04631-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/d225bceee223/molecules-28-04631-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/c4344c9dd0f7/molecules-28-04631-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/55b038563571/molecules-28-04631-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4819/10304989/d5648bbd005f/molecules-28-04631-g010.jpg

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