2019
DOI: 10.1039/c8nj05159c
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Multifunctional polyurethanes synthesized from different triarylamine units with electrochromic, photogeneration, memory storage and sensing properties

Abstract: Herein, we report three multifunctional polyurethane materials, which exhibit excellent electrochromic, photoelectric, memory and sensing properties, and also have good mechanical properties.

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Cited by 8 publications
(6 citation statements)
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“…[13][14][15] On this firm basis, we advocate the use of bridged triarylamines, known as N-heterotriangulenes (N-HTAs), in the role of chromophoric aromatic lids, in order to achieve redox-active nanosized cavities [16][17][18][19][20] for larger chiral guests, aiming at setting foot on the realm of enantioselective discrimination. [21][22][23] Precedents of sensing examples involving triarylamines range from the detection of metallic cations, [24] to toxic anions [25] or anions present in chemical weapons, [26] nitroaromatic explosives, [27] biological metabolites, [28] toxic gases, [29,30] and pH determination. [31] Regarding the implementation of triarylamines in both macrocyclic and cage structures, few examples can be tracked down in literature, [32][33][34][35][36][37][38][39] and even scarcer examples are found for their bridged analogues, N-HTAs, whose presence in complexing and sensing processes is limited.…”
mentioning
confidence: 99%
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“…[13][14][15] On this firm basis, we advocate the use of bridged triarylamines, known as N-heterotriangulenes (N-HTAs), in the role of chromophoric aromatic lids, in order to achieve redox-active nanosized cavities [16][17][18][19][20] for larger chiral guests, aiming at setting foot on the realm of enantioselective discrimination. [21][22][23] Precedents of sensing examples involving triarylamines range from the detection of metallic cations, [24] to toxic anions [25] or anions present in chemical weapons, [26] nitroaromatic explosives, [27] biological metabolites, [28] toxic gases, [29,30] and pH determination. [31] Regarding the implementation of triarylamines in both macrocyclic and cage structures, few examples can be tracked down in literature, [32][33][34][35][36][37][38][39] and even scarcer examples are found for their bridged analogues, N-HTAs, whose presence in complexing and sensing processes is limited.…”
mentioning
confidence: 99%
“…Precedents of sensing examples involving triarylamines range from the detection of metallic cations, [24] to toxic anions [25] or anions present in chemical weapons, [26] nitroaromatic explosives, [27] biological metabolites, [28] toxic gases,[ 29 , 30 ] and pH determination. [31] Regarding the implementation of triarylamines in both macrocyclic and cage structures, few examples can be tracked down in literature,[ 32 , 33 , 34 , 35 , 36 , 37 , 38 , 39 ] and even scarcer examples are found for their bridged analogues, N ‐HTAs, whose presence in complexing and sensing processes is limited.…”
mentioning
confidence: 99%
“…59 It has been well-explored in the literature that the presence of formyl, as well as multiple fluorine groups, in the small naphthalimide derivative enhances the strong H-bonding driven intermolecular π−π stacking interaction in aqueous media and forms homogeneously dispersed stable spherical nanoparticles. The synthesized molecule was characterized by high-resolution mass spectrometry (HRMS) and multinuclear ( 1 H, 13 C, and 19 F) NMR spectroscopy (Figures S1−S7).…”
Section: Resultsmentioning
confidence: 99%
“…HPLC grade solvents used in this study were purchased from Fisher Scientific Ltd. and RANKEM. NMR ( 1 H, 13 C) spectra were recorded with a Bruker Avance 600 MHz spectrometer. All solutions for 1 H and 13 C spectra were obtained by taking residual solvent signal as an internal reference.…”
Section: Introductionmentioning
confidence: 99%
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