Self-assembly is now being intensively studied in chemistry, physics, biology, and materials engineering and has become an important "bottom-up" approach to create intriguing structures for different applications. Self-assembly is not only a practical approach for creating a variety of nanostructures, but also shows great superiority in building hierarchical structures with orders on different length scales. The early work in self-assembly focused on molecular self-assembly in bulk solution, including the resultant dye aggregates, liposomes, vesicles, liquid crystals, gels and so on. Interfacial self-assembly has been a great concern over the last two decades, largely because of the unique and ingenious roles of this method for constructing materials at interfaces, such as self-assembled monolayers, Langmuir-Blodgett films, and capsules. Nanocrystal superlattices, honeycomb films and coffee rings are intriguing structural materials with more complex features and can be prepared by interfacial self-assembly on different length scales. In this critical review, we outline the recent development in the preparation and application of colloidal nanocrystal superlattices, honeycomb-patterned macroporous structures by the breath figure method, and coffee-ring-like patterns (247 references).
The successful use of electrochemiluminescence (ECL) in immunoassay for clinical diagnosis requires development of novel ECL signal probes. Herein, we report lanthanide (Ln) metal−organic frameworks (LMOFs) as ECL signal emitters in the ECL immunoassay. The LMOFs were prepared from precursors containing Eu (III) ions and 5-boronoisophthalic acid (5-bop), which could be utilized to adjust optical properties. Investigations of ECL emission mechanisms revealed that 5-bop was excited with ultraviolet photons to generate a triplet-state, which then triggered Eu (III) ions for red emission. The electron-deficient boric acid decreased the energy-transfer efficiency from the triplet-state of 5-bop to Eu (III) ions; consequently, both were excited with highefficiency at single excitation. In addition, by progressively tailoring the atomic ratios of Ni/Fe, NiFe composites (Ni/Fe 1:1) were synthesized with more available active sites, enhanced stability, and excellent conductivity. As a result, the self-luminescent europium LMOFs displayed excellent performance characteristics in an ECL immunoassay with a minimum detectable limit of 0.126 pg mL −1 , using Cytokeratins21-1 (cyfra21-1) as the target detection model. The probability of false positive/false negative was reduced dramatically by using LMOFs as signal probes. This proposed strategy provides more possibilities for the application of lanthanide metals in analytical chemistry, especially in the detection of other disease markers.
An
intriguing aggregation-induced electrochemiluminescence (AIECL)
bioconjugate was fabricated by encapsulating fac-tris(2-phenylpyridine)iridium(III)
complexes [Ir(ppy)3] in the apoferritin (apoFt) cavity
for biosensing application. Based on the unique pH-dependent disassembly/reassembly
characteristic of apoFt, approximately 44.3 molecules of Ir(ppy)3 aggregated in the single cavity through both intermolecular
π–π-stacking interactions and hydrogen bonds that
efficiently restricted the intramolecular motions to trigger the AIECL
effect. Compared to monomers, Ir(ppy)3 aggregates performed
5.3-fold-enhanced ECL emission using tri-n-propylamine
(TPrA) as a coreactant. The fabricated Ir(ppy)3@apoFt bioconjugate
was flexibly labeled with a detection antibody to act as a transducer
for the immunosensor construction. To further catalyze the ECL reaction
between the reductive TPrA• and the oxidative Ir(ppy)3
+• radicals, a conductive and electroactive
substrate of Fe2N and gold nanoparticle-codecorated reduced
graphene oxide (Fe2N/rGO/Au) was established to incubate
the capture antibody. Therefore, a “signal on” immunosensor
was developed for sensitive assay of cytokeratin 19 fragment 21–1
(CYFRA 21–1), in which good linearity ranging from 1 pg/mL
to 50 ng/mL with a low detection limit of 0.43 pg/mL (S/N = 3) was
obtained. This study shares with an inspiration of using apoFt to
design iridium(III)-based AIECL emitters, which will expand more possibilities
of organic iridium(III) complexes in establishing innovative ECL immunoassays.
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