Gayathri Parthasarathy, Nantheeswaran Periyappan, Mariappan Mariappan, Karthikeyan Subramanian, Pannipara Mehboobali, Al-Sehemi Abdullah G, Moon Dohyun, Anthony Savarimuthu Philip
School of Chemical & Biotechnology, SASTRA Deemed University, Thanjavur 613401, Tamil Nadu, India.
Department of Chemistry, SRM IST, Kattankulathur, Chennai 603203, Tamil Nadu, India.
Spectrochim Acta A Mol Biomol Spectrosc. 2023 Feb 5;286:121989. doi: 10.1016/j.saa.2022.121989. Epub 2022 Oct 23.
Introducing methoxy substituent into triphenylamine-acetophenone based donor-π-acceptor fluorophore, 3-(4-(diphenylamino)phenyl)-1-phenylprop-2-en-1-one (1), produced strong solvatofluorochromism including white light emission, fluorescent polymorphs and mechano-responsive fluorescence switching. The unsubstituted and methoxy substituted compounds displayed strong solvent polarity mediated tunable emission in the solution. Interestingly, 3-(4-(diphenylamino)phenyl)-1-(4-methoxyphenyl)prop-2-en-1-one (2) and 3-(4-(diphenylamino)-2-methoxyphenyl)-1-(4-methoxyphenyl)prop-2-en-1-one (3) showed single molecule white light emission in DMSO and ethanol, respectively. 1-3 exhibited strong green/yellow fluorescence in the solid-state (Quantum yield (Φ) = 10 to 23%). 2 produced fluorescent polymorphs (green (2-G) and yellow (2-Y). Single crystal structural analysis revealed that donor and acceptor phenyl units adopted coplanar conformation in 2-G and 3 whereas twisted molecular conformation in 1 and 2-Y. Further, 2-G exhibited π…π interactions facilitated isolated dimers whereas 2-Y showed well separated molecules in the crystal lattice. Aggregation induced emission (AIE) studies showed morphological transformation induced fluorescence tuning for 2. The intramolecular charge transfer (ICT) from TPA to acetophenone was confirmed by computational studies. Mechanofluorochromic (MFC) studies of 1 showed only slight reduction of intensity without modulating fluorescence wavelength significantly but 2 and 3 exhibited visible emissive colour change from yellow to green and vice versa by crushing and heating. Both 2 and 3 also exhibited self-reversible fluorescence switching that was confirmed by PXRD pattern. Thus, methoxy group introduction resulted in obtaining white light emitting fluorescence molecules in the solution state and self-reversible fluorescence switching materials.
将甲氧基取代基引入基于三苯胺 - 苯乙酮的供体 - π - 受体荧光团3-(4-(二苯胺基)phenyl)-1-phenylprop-2-en-1-one (1)中,产生了强烈的溶剂化荧光变色现象,包括白光发射、荧光多晶型物和机械响应荧光开关。未取代和甲氧基取代的化合物在溶液中表现出强烈的溶剂极性介导的可调发射。有趣的是,3-(4-(二苯胺基)phenyl)-1-(4-甲氧基苯基)prop-2-en-1-one (2)和3-(4-(二苯胺基)-2-甲氧基苯基)-1-(4-甲氧基苯基)prop-2-en-1-one (3)分别在二甲基亚砜和乙醇中表现出单分子白光发射。1 - 3在固态下表现出强烈的绿色/黄色荧光(量子产率(Φ)= 10%至23%)。2产生了荧光多晶型物(绿色(2 - G)和黄色(2 - Y))。单晶结构分析表明,供体和受体苯基单元在2 - G和3中呈共平面构象,而在1和2 - Y中呈扭曲的分子构象。此外,2 - G表现出π…π相互作用促进了孤立二聚体的形成,而2 - Y在晶格中显示出分子间分离良好。聚集诱导发光(AIE)研究表明,2会发生形态转变诱导的荧光调谐。通过计算研究证实了从三苯胺(TPA)到苯乙酮的分子内电荷转移(ICT)。1的机械荧光变色(MFC)研究表明,强度仅略有降低,而荧光波长没有明显调制,但2和3通过研磨和加热表现出从黄色到绿色以及反之亦然的可见发射颜色变化。2和3还表现出自可逆荧光开关,这通过粉末X射线衍射(PXRD)图谱得到证实。因此,甲氧基的引入导致在溶液状态下获得白光发射荧光分子和自可逆荧光开关材料。