Fluorescence and stimuli-responsive performance of polymer composites filled with tetraphenylethene derivatives
文献信息
In this study, a series of tetraphenylethene (TPE) derivatives with 3-butenloxy moieties were synthesized. The developed TPE with different numbers of substituent groups showed controlled aggregation-induced emission performance and variable fluorescence properties, and theoretical calculations were carried out to explain these phenomena. TPE and its derivatives were further employed to construct composites through physical blending or a hydrosilylation reaction between the TPE derivative and polydimethylsiloxane. It was found that chemical bonding could improve the solubility of TPE derivatives in the polymer matrix without obvious phase separation. The fluorescence intensity of composites filled with TPE derivatives decreased with increasing temperature or mechanical force, thus giving the material a stimuli-responsive fluorescence property.
期刊推荐

New Journal of Chemistry

Journal of Saudi Chemical Society

Current Opinion in Colloid & Interface Science

Russian Chemical Bulletin

Acta Materialia

Saudi Pharmaceutical Journal

Organic Process Research & Development

Journal of Peptide Science

Russian Journal of Organic Chemistry

Russian Journal of Bioorganic Chemistry
相关文献
Topological behaviour of ternary non-symmorphic crystals KZnX (X = P, As, Sb) under pressure and strain: a first principles study
Atahar Parveen, E. Narsimha Rao, B. Adivaiah, P. Anees, G. Vaitheeswaran
DOI: 10.1039/C7CP08121A
High-pressure and temperature dependence of the spontaneous resolution of 1,1′-binaphthyl enantiomers
Kinga Roszak, Andrzej Katrusiak
DOI: 10.1039/C7CP07234A
Disorder in the hydrogen-atoms uninvolved in hydrogen bonds in a metal–organic framework
DOI: 10.1039/C8CP03709D
Direct visualization of diffuse unoccupied molecular orbitals at a rubrene/graphite interface
Takashi Yamada, Mariko Kinoshita, Kento Araragi, Yu Watanabe, Takahiro Ueba, Hiroyuki S. Kato, Toshiaki Munakata
DOI: 10.1039/C8CP01796D
Preventing iron(ii) precipitation in aqueous systems using polyacrylic acid: some molecular insights
Pierre-Arnaud Artola, Bernard Rousseau, Carine Clavaguéra, Marion Roy, Dominique You, Gabriel Plancque
DOI: 10.1039/C7CP02743E
Optical properties of quadrupolar and bi-quadrupolar dyes: intra and inter chromophoric interactions
Manon Catherin, Elena Zaborova, Anthony D’Aléo, Frédéric Fages, Frédéric Castet, David Casanova
DOI: 10.1039/C8CP05048A
Superconductivity and phase stability of potassium-doped biphenyl
Guo-Hua Zhong, Dong-Yu Yang, Kai Zhang, Ren-Shu Wang, Chao Zhang, Hai-Qing Lin, Xiao-Jia Chen
DOI: 10.1039/C8CP05184D
Solvation dynamics in polar solvents and imidazolium ionic liquids: failure of linear response approximations
Esther Heid, Christian Schröder
DOI: 10.1039/C7CP07052G
Influence of a silver salt on the nanostructure of a Au(111)/ionic liquid interface: an atomic force microscopy study and theoretical concepts
Viktor Hoffmann, Giridhar Pulletikurthi, Timo Carstens, Abhishek Lahiri, Andriy Borodin, Frank Endres
DOI: 10.1039/C7CP08243F
您可能还喜欢
3 - (二氟甲基)-1 -氟苯(CAS号:26029-52-7)适用哪些法规指南?
3 - (二氟甲基)-1 -氟苯需遵循联合国全球化学品统一分类和标签制度(GHS),包括急性毒性、皮肤腐蚀/刺激、严重眼损伤/眼刺激等分类。同时,该化合物还需符...
3,5-二甲基苯胺(CAS号:108-69-0)通常如何合成?
3,5-二甲基苯胺通常通过乙苯的氨解反应合成。反应中使用硫酸作为催化剂,反应温度为120-130°C。乙苯在硫酸存在下与氨反应,生成3,5-二甲基苯胺和苯胺副产...
3-甲基异噻唑-5-胺(CAS号:24340-76-9)安全吗?
3-甲基异噻唑-5-胺在适当使用和储存条件下是相对安全的,但在操作时应注意防护措施。应避免吸入粉尘,避免与皮肤和眼睛直接接触。在操作过程中,应穿戴适当的防护装备...
3-(1,3-Thiazol-2-yl)-1H-indole(CAS号:135531-86-1)通常如何合成?
3-(1,3-噻唑-2-基)-1H-吲哚通常通过多步合成方法制备。首先,由噻唑-2-基溴化物和吲哚进行偶联反应,得到中间体。然后,通过还原反应将中间体转化为所需...
4-溴-2-氟苯甲基氯(CAS号:85510-82-3)的主要用途是什么?
4-溴-2-氟苯甲基氯主要用于有机合成中间体,特别是在医药、农药和染料等领域。作为一种具有特定结构的化合物,它在合成复杂有机分子时扮演重要角色。
处理Fmoc-β-(3-噻吩基)-D-Ala-OH(CAS号:220497-90-5)时应注意哪些实验室安全事项?
处理Fmoc-β-(3-噻吩基)-D-Ala-OH时,应佩戴防护手套、护目镜和实验服。操作应在通风橱内进行。如发生泄露,应立即用大量水冲洗,并通知实验室管理人员...
氮化硅(CAS号:12033-89-5)通常如何合成?
氮化硅通常通过氮化硅的直接反应合成,即在高温下将四氯化硅与氨气反应。具体步骤是将四氯化硅和氨气混合并加热至1300-1700℃,在该条件下,四氯化硅与氨气反应生...
Cetirizine EP Impurity B DiHCl(CAS号:1000690-91-4)通常如何合成?
Cetirizine EP Impurity B DiHCl通常通过一锅法合成,首先将4-氯苯基-苯甲基氯甲酸酯与1-哌嗪乙酸反应,生成相应的酸,然后与盐酸反应...
如何储存1-哌啶-4-基丁-1-酮(CAS号:3509-15-7)?
1-哌啶-4-基丁-1-酮应储存在阴凉、干燥的地方,避免阳光直射。存储容器应密封,并确保通风良好。建议储存温度不超过25℃,湿度保持在相对较低的水平。
如何处理含有VORUCICLIB(CAS号:1000023-04-0)的废料?
含有VORUCICLIB的废料应进行专业的收集和处理,包括使用适当的容器进行隔离,避免与其他化学品接触。处理方法通常包括化学中和、沉淀反应或吸附过程,随后进行焚...
来源期刊
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.

![2,6-Di(thiophen-2-yl)dithieno[3,2-b:2',3'-d]thiophene structure 2,6-Di(thiophen-2-yl)dithieno[3,2-b:2',3'-d]thiophene structure](https://cnstatic.chemtradehub.com/structs/910/910788-24-8-5b70.webp)


