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液晶磁光活性全烷基化氮杂蒄。

Liquid Crystalline Magneto-Optically Active Peralkylated Azacoronene.

作者信息

Delage-Laurin Léo, Swager Timothy M

机构信息

Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States.

Institute for Soldier Nanotechnologies, Cambridge, Massachusetts 02139, United States.

出版信息

JACS Au. 2023 Jul 8;3(7):1965-1974. doi: 10.1021/jacsau.3c00212. eCollection 2023 Jul 24.

DOI:10.1021/jacsau.3c00212
PMID:37502152
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10369420/
Abstract

Organic Faraday rotators have gained significant attention in recent years as a promising alternative to traditional inorganic magneto-optical (MO) materials as a result of their lower cost, superior mechanical properties, and potential for large-scale deployment. This interest is peaked by the fact that a number of high symmetry, rigid, strongly optically absorbing organic chromophores display Verdet constants an order of magnitude higher than commercial inorganic Faraday rotators. Critical to the development of new generations of organic materials is the ability to organize them in optimal structures for optical coupling/measurements. We report herein the synthesis of a dodecyl-substituted hexapyrrolohexaazacoronene () displaying discotic liquid crystalline (LC) properties and large Faraday rotation. Thin films with a redox mixed / composition display a discotic columnar LC phase, are stable to air and moisture in the solid and solution states, and achieve a maximum Verdet constant of 3.36 × 10 deg T m at 700 nm. This result is consistent with Serber's model of magnetic circular birefringence and displays one of the largest reported Verdet constants for organic materials in the UV-Vis range. The LC phase aligns the molecules and leads to gains in Verdet constants of up to 105% through the favorable orientation of the molecules' magnetic and electric transition dipole moments with respect to the applied magnetic field.

摘要

近年来,有机法拉第旋转器作为传统无机磁光(MO)材料的一种有前景的替代物,因其成本较低、机械性能优越以及具有大规模部署的潜力而备受关注。一些高对称性、刚性、强光学吸收的有机发色团的Verdet常数比商用无机法拉第旋转器高一个数量级,这一事实进一步激发了人们的兴趣。开发新一代有机材料的关键在于能够将它们组织成用于光耦合/测量的最佳结构。我们在此报告了一种具有盘状液晶(LC)性质和大法拉第旋转的十二烷基取代的六吡咯并六氮杂蒄()的合成。具有氧化还原混合/组成的薄膜呈现盘状柱状LC相,在固态和溶液状态下对空气和水分稳定,并且在700nm处实现了3.36×10 deg T m的最大Verdet常数。该结果与Serber的磁圆双折射模型一致,并且在紫外-可见范围内显示出有机材料中报道的最大Verdet常数之一。LC相对分子进行排列,并通过分子的磁偶极矩和电偶极矩相对于外加磁场的有利取向,使Verdet常数提高了高达105%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/503b/10369420/bb3a6e77bd5a/au3c00212_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/503b/10369420/e7fe47fb4bc4/au3c00212_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/503b/10369420/057ed4138b1b/au3c00212_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/503b/10369420/0e96f20b6ff6/au3c00212_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/503b/10369420/dfac536b8d36/au3c00212_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/503b/10369420/8d0b1cb90ba5/au3c00212_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/503b/10369420/bb3a6e77bd5a/au3c00212_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/503b/10369420/e7fe47fb4bc4/au3c00212_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/503b/10369420/057ed4138b1b/au3c00212_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/503b/10369420/0e96f20b6ff6/au3c00212_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/503b/10369420/dfac536b8d36/au3c00212_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/503b/10369420/8d0b1cb90ba5/au3c00212_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/503b/10369420/bb3a6e77bd5a/au3c00212_0007.jpg

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