Blue AIE luminogens bearing methyl groups: different linkage position, different number of methyl groups, and different intramolecular conjugation

文献情報

出版日 2015-10-08

DOI 10.1039/C5QO00274E

インパクトファクター 5.281

著者

Jing Huang, Min Yang, Jie Yang, Runli Tang, Shanghui Ye, Qianqian Li, Zhen Li

原文を見る

要旨

In this paper, four AIE-active luminogens (Methyl-BTPE, mMethylTPE-pTPE, oMethyl-BTPE and oMethylTPE-pTPE) exhibiting blue emissions were successfully synthesized, in which methyl groups of different numbers were introduced at different positions, to subtly tune the intramolecular conjugation. Their thermal, optical and electronic properties were fully investigated. The corresponding non-doped OLEDs exhibited high electroluminescence efficiencies with Lmax, ηC, max, and ηP, max values of up to 14 644 cd m−2, 4.06 cd A−1, and 9.7 lm W−1, respectively, showing the feasibility of this facile synthetic approach for the construction of blue AIE fluorophores.

掲載誌

Organic Chemistry Frontiers

CiteScore: 7.8

自己引用率: 8.7%

年間論文数: 724

Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

Blue AIE luminogens bearing methyl groups: different linkage position, different number of methyl groups, and different intramolecular conjugation

文献情報

おすすめジャーナル

関連文献

Synthesis of a multimodal molecular imaging probe based on a hyperbranched polymer architecture

Front cover

Post-polymerization modification of reactive polymers derived from vinylcyclopropane: a poly(vinylcyclopropane) derivative with physical gelation and UCST behaviour in ethanol–water mixtures

Switch on/off microcapsules for controllable photosensitive drug release in a ‘release-cease-recommence’ mode

Synthesis and properties of heterografted toothbrush-like copolymers with alternating PEG and PCL grafts and tunable RAFT-generated segments

Statistical terpolymers with thermo-responsive fluorescence response in an ionic liquid: effects of solvatophilicity on LCST phase separation and reversibility

From glycidyl carbonate to hydroxyurethane side-groups in alternating fluorinated copolymers

A conductive copolymer of graphene oxide/poly(1-(3-aminopropyl)pyrrole) and the adsorption of metal ions

Reactive macromolecular micelle crosslinked highly elastic hydrogel with water-triggered shape-memory behaviour

Synthesis of polyethylene and polystyrene miktoarm star copolymers using an “in–out” strategy

こちらもおすすめ

1-{3-[5-(エチルカルボンイル)-2,4-ジメチル-1H-ピロロール-3-基]プロパニル}ピペリジン-4-カルボン酸について、適用される法規ガイドラインは何ですか？

2,2-二氟-1,3-ベンゾジオキサン-5-カルボキシlic酸とは何ですか？

8-氯-4-色原酮の代替品はありますか？

エチル6,6-ジメチル-4,5,6,7-テトラヒドロ-1H-インドアゼー-3-カルボキシレートとは何ですか？

4-叔丁基-6-氯-嘧啶に適用される法規ガイドラインは何ですか？

維库溴铵杂质Bはどのように合成されますか？

2-(4-氟苄基)-吡咯烷の物理化学的性質は何ですか？

3-喹啉甲醛（2-チロール-8-エチル）は安全ですか？

エチル3-(ヒドロキシメチル)-1H-ピロール-2-カルボキシレートはどのように保存すればよいですか？

哌拉西林杂质Dは安全ですか？

掲載誌

Organic Chemistry Frontiers

おすすめ化合物

Pimecrolimus

N-Benzyl-N,N-dimethyl-1-tetradecanaminium chloride

2-{3-[4-(3-Chlorophenyl)-1-piperazinyl]propyl}[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one hydrochloride (1:1)

3-[(4-Nitrobenzyl)oxy]-3-oxopropanoic Acid

Butylphenyl Methylpropional

おすすめサプライヤー