Non-homologous end joining (NHEJ) is a major repair pathway for DNA double-strand breaks (DSBs), which is the most toxic DNA damage in cells. Unrepaired DSBs can cause genome instability, ...tumorigenesis or cell death. DNA end synapsis is the first and probably the most important step of the NHEJ pathway, aiming to bring two broken DNA ends close together and provide structural stability for end processing and ligation. This process is mediated through a group of NHEJ proteins forming higher-order complexes, to recognise and bridge two DNA ends. Spatial and temporal understanding of the structural mechanism of DNA-end synapsis has been largely advanced through recent structural and single-molecule studies of NHEJ proteins. This review focuses on core NHEJ proteins that mediate DNA end synapsis through their unique structures and interaction properties, as well as how they play roles as anchor and linker proteins during the process of 'bridge over troubled ends'.
Utilizing pyridine catalysis, we developed a visible‐light‐induced transition‐metal‐free radical borylation reaction of unactivated alkyl bromides that features a broad substrate scope and mild ...reaction conditions. Mechanistic studies revealed a novel nucleophilic substitution/photoinduced radical formation pathway, which could be utilized to trigger a variety of radical processes.
To B or not to Br: A visible‐light‐induced organocatalytic borylation reaction of unactivated alkyl bromides was developed. This reaction exhibits a broad substrate scope, and mechanistic studies revealed a novel nucleophilic substitution/photoinduced radical formation pathway.
Using the National Center for Atmospheric Research Thermosphere Ionosphere Electrodynamics General Circulation Model (TIEGCM), the ionospheric Rayleigh‐Taylor instability growth rate is calculated. ...The seasonal and longitudinal variations of the growth rate from the TIEGCM appear to match that of the spread F observed by various satellite missions. The growth rate is strongly dependent on the angle between the sunset terminator and the geomagnetic field line near the magnetic equator. The TIEGCM simulations with nonmigrating tides show the zonal wave number 4 structure in the Rayleigh‐Taylor instability due to the inclusion of the nonmigrating diurnal eastward zonal wave number 3 and semidiurnal eastward zonal wave number 2 tides.
Key Points
Modeled R‐T growth rate resembles the bubble occurrence
Nonmigrating tide can effect the R‐T growth rate
There are other factors affecting the bubble growth rate
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•The mechanisms of microwave absorption were analyzed in detail.•The preparation methods of carbon/magnetic metal composites were summarized.•Composites with different components, ...morphologies and structures were reviewed.•Challenges and future prospects for carbon/magnetic metal composites were proposed.
At present, developing high-efficiency microwave absorption materials with properties including light-weight, thin thickness, strong absorbing intensity and broad bandwidth is an urgent demand to solve the electromagnetic pollution issues. An ideal microwave absorber should have excellent dielectric and magnetic loss capabilities, thereby inducing attenuation and absorption of incident electromagnetic radiation. Recently, various carbon/magnetic metal composites have been developed and expected to become promising candidates for high-performance microwave absorbers. In this review, we introduce the mechanisms of microwave absorption and summarize the recent advances in carbon/magnetic metal composites. Preparation methods and microwave absorption properties of carbon/magnetic metal composites with different components, morphologies and microstructures are discussed in detail. Finally, the challenges and future prospects of carbon/magnetic metal absorbing materials are also proposed, which will be useful to develop high-performance microwave absorption materials.
Heterostructured metal—organic framework (MOF)‐on‐MOF thin films have the potential to cascade the various properties of different MOF layers in a sequence to produce functions that cannot be ...achieved by single MOF layers. An integration method that relies on van der Waals interactions, and which overcomes the lattice‐matching limits of reported methods, has been developed. The method deposits molecular sieving Cu‐TCPP (TCPP=5,10,15,20‐tetrakis(4‐carboxyphenyl)porphyrin) layers onto semiconductive Cu‐HHTP (HHTP=2,3,6,7,10,11‐hexahydrotriphenylene) layers to obtain highly oriented MOF‐on‐MOF thin films. For the first time, the properties in different MOF layers were cascaded in sequence to synergistically produce an enhanced device function. Cu‐TCPP‐on‐Cu‐HHTP demonstrated excellent selectivity and the highest response to benzene of the reported recoverable chemiresistive sensing materials that are active at room temperature. This method allows integration of MOFs with cascading properties into advanced functional materials.
MOF‐on‐MOF thin films were prepared from Cu‐HHTP (HHTP=hexahydrotriphenylene) and Cu‐TCPP (TCPP=tetrakis(4‐carboxyphenyl)porphyrin frameworks). The properties of the MOF layers cascade to produce functionality not achieved by a single layer. The MOF‐on‐MOF films demonstrate excellent selectivity and the highest response to benzene among reported recoverable chemiresistive sensing materials active at room temperature.
The exploration of efficient electrocatalysts is the central issue for boosting the overall efficiency of water splitting. Herein, pertinently creating active sites and improving conductivity for ...metal–organic frameworks (MOFs) is proposed to tailor electrocatalytic properties for overall water splitting. An Ni(II)‐MOF nanosheet array is presented as an ideal material model and a facile alkali‐etched strategy is developed to break its NiO bonds accompanied with the introduction of extra‐framework K cations, which contribute to creating highly active open metal sites and largely improving the electrical conductivity. As a result, the assembled defect‐Ni‐MOF||defect‐Ni‐MOF electrolyte cell delivers a lower and stable voltage of 1.50 V at 10 mA cm−2 in alkaline medium for overall water splitting, comparable to the combination of iridium and platinum as benchmark catalysts.
The introduction of defects into metal–organic framework (MOF) by alkali‐etching treatment to create rich active sites and tailor electrical conductivity is proposed. The resultant defect‐rich Ni(II)‐MOF nanosheet array exhibits excellent electrocatalytic overall water splitting performance, comparable to the noble metal‐based benchmark catalysts.
Single‐ligand‐based electronically conductive porous coordination polymers/metal–organic frameworks (EC‐PCPs/MOFs) fail to meet the requirements of numerous electronic applications owing to their ...limited tunability in terms of both conductivity and topology. In this study, a new 2D π‐conjugated EC‐MOF containing copper units with mixed trigonal ligands was developed: Cu3(HHTP)(THQ) (HHTP=2,3,6,7,10,11‐hexahydrotriphenylene, THQ=tetrahydroxy‐1,4‐quinone). The modulated conductivity (σ≈2.53×10−5 S cm−1 with an activation energy of 0.30 eV) and high porosity (ca. 441.2 m2 g−1) of the Cu3(HHTP)(THQ) semiconductive nanowires provided an appropriate resistance baseline and highly accessible areas for the development of an excellent chemiresistive gas sensor.
Makes sense: As two ligands offer more opportunity than one to tune MOF conductivity and topology, a 2D π‐conjugated copper‐based electronically conductive MOF with two different trigonal organic ligands was developed (see structure). The semiconductivity and high porosity of the resulting nanowires provided a low conductivity baseline and highly accessible surface areas, thus resulting in excellent room‐temperature chemiresistive sensing properties.
Despite numerous inherent merits of metal–organic frameworks (MOFs), structural fragility has imposed great restrictions on their wider involvement in many applications, such as in catalysis. Herein, ...a strategy for enhancing stability and enabling functionality in a labile Zr(IV)‐MOF has been proposed by in situ porphyrin substitution. A size‐ and geometry‐matched robust linear porphyrin ligand 4,4′‐(porphyrin‐5,15‐diyl)dibenzolate (DCPP2−) is selected to replace the 4,4′‐(1,3,6,8‐tetraoxobenzolmn3,8phenanthroline‐2,7(1H,3H,6H,8H)‐diyl)dibenzoate (NDIDB2−) ligand in the synthesis of BUT‐109(Zr), affording BUT‐110 with varied porphyrin contents. Compared to BUT‐109(Zr), the chemical stability of BUT‐110 series is greatly improved. Metalloporphyrin incorporation endows BUT‐110 MOFs with high catalytic activity in the photoreduction of CO2, in the absence of photosensitizers. By tuning the metal species and porphyrin contents in BUT‐110, the resulting BUT‐110‐50%‐Co is demonstrated to be a good photocatalyst for selective CO2‐to‐CO reduction, via balancing the chemical stability, photocatalytic efficiency, and synthetic cost. This work highlights the advantages of in situ ligand substitution for MOF modification, by which uniform distribution and high content of the incoming ligand are accessible in the resulting MOFs. More importantly, it provides a promising approach to convert unstable MOFs, which mainly constitute the vast MOF database but have always been neglected, into robust functional materials.
The in situ porphyrin substitution strategy is developed for modifying labile interpenetrated BUT‐109(Zr), affording BUT‐110 with enhanced chemical stability and photocatalytic activity. By tuning the species and contents of metalloporphyrin in BUT‐110, some of the BUT‐110 MOFs may serve as potential photocatalysts for selective CO2‐to‐CO reduction, in the absence of photosensitizer.
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