Circularly polarized luminescence (CPL) is attractive in understanding the excited‐state chirality and developing advanced materials. Herein, we propose a chiral reticular self‐assembly strategy to unite achiral AIEgens, chirality donors, and metal ions to fabricate optically pure AIEgen metal–organic frameworks (MOFs) as efficient CPL materials. We have found that CPL activity of the single‐crystal AIEgen MOF was generated by the framework‐enabled strong emission from AIEgens and through‐space chirality transfer from chirality donors to achiral AIEgens via metal‐ion bridges. For the first time, a dual mechano‐switched blue and red‐shifted CPL activity was achieved via ultrasonication and grinding, which enabled the rotation or stacking change of AIEgen rotors with the intact homochiral framework. This work provided not only an insightful view of the aggregation induced emission (AIE) mechanism, but also an efficient and versatile strategy for the preparation of stimuli‐responsive CPL materials.
The North China craton (NCC) is one of oldest cratons in the world, with crust up to c. 3.8 Ga old, and has a complicated evolution. The main Early Precambrian geological events and key tectonic issues are as follows. (1) Old continental nuclei have been recognized in the NCC, and the oldest remnants of granitic gneiss and supracrustal rocks are 3.8 Ga old. The main crustal growth in the NCC took place at 2.9–2.7 Ga. The NCC can be divided into several microblocks, which are separated by Archaean greenstone belts that represent continental accretion surrounding the old continental nuclei. (2) By 2.5 Ga, the microblocks amalgamated to form a coherent craton by continent–continent, arc–continent or arc–arc collisions. The tectonic processes in Neoarchaean and modern times appear to differ more in degree than in principle. Extensive intrusion of K-granite sills and mafic dykes and regional upper amphibolite- to granulite-facies metamorphism occurred, and marked the beginning of cratonization in the NCC. Coeval ultramafic–mafic and syenitic dykes of c. 2500 Ma in Eastern Hebei indicate that the NCC became a stable, thick and huge continent at the end of the Archaean, and probably was a part of the Neoarchaean supercontinent that has been suggested by previous studies. (3) In the period between 2500 and 2350 Ma, the NCC was tectonically inactive, but the development of a Palaeoproterozoic volcanic and granitic rocks occurred between 2300 and 1950 Ma. The volcanic–sedimentary rocks are termed Palaeoproterozoic mobile belts; these have a linear distribution, and were affected by strong folding and metamorphism at 1900–1850 Ma, and intruded by granites and pegmatites at 1850–1800 Ma. The Palaeoproterozoic mobile belts formed and evolved within the craton or continental margin (epicontinental geosyncline). Some 2.30–1.95 Ga rift-margin, passive continental margin deposits, analogous arc or back-arc assemblages, as well as HP and HT–UHT metamorphic complexes seem to be comparable with many in the late Phanerozoic orogenic belts. Regarding Palaeoproterozoic orogeny in other cratons, it is possible that a global Palaeoproterozoic orogenic event occurred, existed and resulted in the formation of a pre-Rodinian supercontinent at c. 2.0–1.85 Ga. (4) In contrast, the c. 1800 Ma event is an extension–migmatization event, which includes uplift of the lower crust of the NCC as a whole, the emplacement of mafic dyke swarms, continental rifting, and intrusion of an orogenic magmatic association. This event has been considered to be related to the break-up of the pre-Rodinian supercontinent at 1.8 Ga, attributed to a Palaeoproterozoic plume. (5) As HP and HT–UHT metamorphic rocks occur widely in the NCC, their high pressure of 10–14 kbar has attracted attention from researchers, and several continental collisional models have been proposed. However, it is argued that these rocks have much higher geothermal gradient and much slower uplift rate than those in Phanerozoic orogenic belts. Moreover, HP and HT–UHT rocks commonly occur together and are not distributed in linear zones, suggesting that the geological and tectonic implications of these data should be reassessed.
A novel "tunnel-like" cyclopalladated arylimine was prepared and immobilized on graphene oxide nano-sheet to form a hybrid catalytic material (denoted as F-GO-Pd) by self-assembly. The F-GO-Pd catalyst was characterized by XRD, FTIR, Raman, XPS, SEM, and TEM. This novel hybrid catalytic material was proven to be an efficient catalyst for the Suzuki-Miyaura coupling reaction of aryl halides (I, Br, Cl) with arylboronic acids in aqueous media under mild conditions with a very low amount of catalyst (0.01 mol%) and a high turnover frequency (TOF) (>20 000 h). In particular, high yields also could be obtained at room temperature with prolonged time. F-GO-Pd also showed good stability and recyclability seven times with a superior catalytic activity. The heterogeneous catalytic mechanism was investigated with kinetic studies, hot filtration tests, catalyst poisoning tests, and in situ FTIR spectroscopy with a ReactIR and the deactivation mechanism of the catalysts was proposed through analysis of its chemical stability by TEM, SEM, Raman, and XRD, indicating that a heterogeneous catalytic process occurred on the surface and the changes of the catalytic activity during the recycling were related to the micro-environment of the catalyst surface.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.