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二茚并稠合二苯并[a,h]蒽和二苯并[c,l]屈:合成、结构分析及性质

Diindeno-Fused Dibenzo[a,h]anthracene and Dibenzo[c,l]chrysene: Syntheses, Structural Analyses, and Properties.

作者信息

Boominathan Siva Senthil Kumar, Chang Kai-Hsin, Liu Yu-Chiao, Wang Chi-Shin, Wu Cheng-Feng, Chiang Ming-Hsi, Chou Pi-Tai, Wu Yao-Ting

机构信息

Department of Chemistry, National Cheng Kung University, 70101, Tainan, Taiwan.

Department of Chemistry, National (Taiwan) University, 10617, Taipei, Taiwan.

出版信息

Chemistry. 2019 May 28;25(30):7280-7284. doi: 10.1002/chem.201901021. Epub 2019 May 2.

Abstract

Diindeno-fused dibenzo[a,h]anthracene 6 and diindeno-fused dibenzo[c,l]chrysene 9 contain the key moieties 1,4-quinodipropene (1,4-QDP) and 2,6-naphthoquinodipropene (2,6-NQDP), respectively, and they both have an open-shell singlet ground state. The latter compound exhibits a strong biradical character and interesting properties, including a low ΔE (2.44 kcal mol ), a small HOMO-LUMO gap (1.06 eV), a wide photoabsorption range (250-1172 nm), and a large two-photon absorption cross-section (σ=1342±56 GM). This work verifies that 6 has a slightly larger HOMO-LUMO gap and ΔE than its helical isomer diindeno[2,1-f:1',2'-j]picene (DIP), but is a much stronger two-photon absorber, verifying the important effect of geometry on the photophysical properties.

摘要

二茚并稠合二苯并[a,h]蒽6和二茚并稠合二苯并[c,l]并四苯9分别含有关键部分1,4-醌二丙烯(1,4-QDP)和2,6-萘醌二丙烯(2,6-NQDP),且二者均具有开壳单重基态。后一种化合物表现出很强的双自由基特性和有趣的性质,包括低ΔE(2.44 千卡·摩尔)、小的HOMO-LUMO能隙(1.06 电子伏特)、宽的光吸收范围(250 - 1172 纳米)以及大的双光子吸收截面(σ = 1342±56 GM)。这项工作证实,6与其螺旋异构体二茚并[2,1-f:1',2'-j]并五苯(DIP)相比,具有稍大的HOMO-LUMO能隙和ΔE,但却是更强的双光子吸收剂,这证实了几何结构对光物理性质的重要影响。

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