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Solvent vapour induced rare single-crystal-to-single-crystal transformation of stimuli-responsive fluorophore: Solid state fluorescence tuning, switching and role of molecular conformation and substituents

机译:溶剂蒸气诱导稀有的刺激荧光团的单晶单晶转化:固态荧光调谐,切换和分子兼容和取代基的作用

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摘要

Supramolecular interactions and molecular conformations play significant role on producing fluorescent polymorphs with tunable emission in the solid state from single fluorophore. External stimuli-induced structural transformation from one polymorph to another polymorph without losing single crystalline character (single-crystal-to-single-crystal transition (SC-SC)) provides perfect model to understand the structure-property of molecules in the solid state and designing new functional fluorescent materials. Herein we have tailored the substituent groups in the aggregation-induced-emissive (AIE) tetraphenylethylene (TPE) based donor (D)-acceptor (A) fluorophores (TPPA-1-6) and explored fluorescent polymorphs formation and SC-SC transition in the solid state. TPPA-1 showed conformational fluorescent polymorphs via twisted and co-planar conformation between TPE phenyl group and cyanophenyl acceptor phenyl ring. However, single crystal analysis of other derivatives revealed that substituent groups and supramolecular interactions control the molecular conformation and SC-SC transition. Fluorophore with same substituent but positional change also show drastic effect on the fluorescent polymorphs formation and SC-SC transition. Substituents that can form strong intermolecular interactions stabilize the less stable co-planar structure whereas bulky substituents with weak intermolecular interactions produced twisted or both conformers. Photophysical, powder X-ray diffraction (PXRD), differential scanning calorimetry (DSC) and thermogravimteric (TG) analysis were performed to substantiate and get insight on the structural transformation. The formation of fluorescent polymorphs and SC-SC transition exhibited tunable and switchable solid state fluorescence. The non-planar TPE core has been made use to demonstrate high contrast stimuli induced reversible fluorescence switching. Overall, the present studies attempted to gain information on the structural design for developing SC-SC transforming functional organic fluorescent materials that could be of potential interests for optoelectronic and display devices.
机译:超分子相互作用和分子构象在从单一荧光团中产生具有可调谐发射的荧光多晶型物起着显着作用。外部刺激诱导从一种多晶型物到另一个多晶型物的结构转化,而不失去单晶特征(单晶 - 单晶转变(SC-SC))提供了完美的模型,以了解固态中分子的结构性质设计新的功能荧光材料。在此,我们在聚集诱导的发射(AIE)四苯基乙烯(TPE)的供体(D) - 感染者(A)荧光团(TPPA-1-6)中定制了取代基的取代基(TPPA-1-6),并探索了荧光多晶型物形成和SC-SC过渡固态。 TPPA-1通过TPE苯基和氰基苯基受体苯环之间的扭曲和共平面构象显示了构象荧光多晶晶啉。然而,其他衍生物的单晶分析显示取代基和超分子相互作用控制分子构象和SC-SC过渡。具有相同取代基但位置变化的荧光团也对荧光多晶型物形成和SC-SC过渡表现出激烈影响。可以形成强分子间相互作用的取代基稳定稳定的共平面结构,而具有弱分子间相互作用的笨重的取代基产生扭曲的或两个簇。表演,粉末X射线衍射(PXRD),差示扫描量热法(DSC)和热升降钳(TG)分析进行了证实,并对结构转变进行了洞察。荧光多晶型物和SC-SC转变的形成表现出可调和可切换的固态荧光。已经使用非平面TPE核心来证明高对比度刺激诱导的可逆荧光切换。总体而言,本研究试图利用用于开发SC-SC变换功能性有机荧光材料的结构设计的信息,该功能有机荧光材料可能具有潜在的光电和显示装置的潜在利益。

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