Strong covalent chemical bonds that can also be reversed, cleaved or exchanged are the subject of so-called dynamic covalent chemistry (DCC). Applications range from classical protective groups in organic chemistry and cleavable linkers for solid phase synthesis, to more modern applications in dynamic compound libraries and adaptive materials. Interest in dynamic, reversible or responsive chemistries has risen in particular in the last few decades for the design and synthesis of new DCC-based polymer materials. Implementation of DCC in polymers yields materials with unique combinations of properties and in some cases even unprecedented properties for covalent materials, such as self-healing materials, covalent adaptable networks (CANs) and vitrimers. In particular, the incorporation of DCC in polymer materials aims to find a balance between a swift and triggerable reactivity, combined with a high degree of intrinsic robustness and stability.  https://www.selleckchem.com/products/deg-35.html  Applying harsh conditions, highly active catalysts or highly reactive bonding groups, as is done in classical DCC, is often not feasible or desirable, as it can damage the polymer's integrity, leading to loss of function and properties. In this context, so-called internally catalysed DCC platforms have started to receive more interest in this area. This approach relies on the relative proximity and orientation of common functional groups, which can influence a chemical exchange reaction in a subtle but significant way. This approach mimicks the strategies found in enzymic reactions, and is known in classical organic chemistry as neighbouring group participation (NGP). The use of internal catalysis or NGP within polymer material science has proven to be a highly attractive strategy. This tutorial review will outline examples showing the scope, advantages and pitfalls of using internal catalysis within different DCC applications, ranging from small molecules to dynamic polymer materials.Catering to the general trend of artificial intelligence development, simulating humans' learning and thinking behavior has become the research focus. Second-order memristors, which are more analogous to biological synapses, are the most promising devices currently used in neuromorphic/brain-like computing. However, few second-order memristors based on two-dimensional (2D) materials have been reported, and the inherent bionic physics needs to be explored. In this work, a second-order memristor based on 2D SnSe films was fabricated by the pulsed laser deposition technique. The continuously adjustable conductance of Au/SnSe/NSTO structures was achieved by gradually switching the polarization of a ferroelectric SnSe layer. The experimental results show that the bio-synaptic functions, including spike-timing-dependent plasticity, short-term plasticity and long-term plasticity, can be simulated using this two-terminal devices. Moreover, stimulus pulses with nanosecond pulse duration were applied to the device to emulate rapid learning and long-term memory in the human brain. The observed memristive behavior is mainly attributed to the modulation of the width of the depletion layer and barrier height is affected, at the SnSe/NSTO interface, by the reversal of ferroelectric polarization of SnSe materials. The device energy consumption is as low as 66 fJ, being expected to be applied to miniaturized, high-density, low-power neuromorphic computing.A highly sensitive AIE fluorescent chemosensor, N'-((4'-(6,6-dimethyl-4,5,6,7-tetrahydro-1H-5,7-methanoindazol-3-yl)-[1,1'-biphenyl]-4-yl)methylene)picolinohydrazide (PBPHS), for the detection of Hg2+ and Cu2+ ions in near 100% aqueous solution was developed based on the renewable β-pinene derivative nopinone. The probe PBPHS was designed and synthesized via a four reaction steps, including condensation, cyclization, Suzuki coupling reaction, and Schiff-base reaction. PBPHS could recognize Hg2+ and Cu2+ over other competitive metal ions via specific complexation ability towards them. The detection limits of PBPHS for Hg2+ and Cu2+ were 15 nM and 17 nM, respectively. The fluorescent probe PBPHS could also be utilized to detect S2- and Hg2+/Cu2+ reversibly for five cycle. Moreover, the different binding mechanisms of PBPHS with Hg2+ and Cu2+ were confirmed by HRMS analysis, 1H NMR titration, DFT calculation, and molecular logic gate. Furthermore, the probe PBPHS was applied for the analysis of real water and soil samples and living HeLa cells and zebrafish bioimaging.Correction for 'FRET-based intracellular investigation of nanoprodrugs toward highly efficient anticancer drug delivery' by Farsai Taemaitree et al., Nanoscale, 2020, 12, 16710-16715, DOI 10.1039/D0NR04910G.Organic ionic compounds, especially those with organic cations, are commonly applied in ionic liquids (ILs), organocatalysts, (a)NHC ligands, ion recognition, and optoelectronic materials. The direct C-H functionalization of organic cations offers valuable opportunities for the rapid assembly of diverse functionalized cations and for their further exploitation in material science applications. This review summarizes the substantial progress that has been made in the C-H functionalization of organic cations from the 1960s to May 2020, including transition metal-mediated/catalyzed C-H alkylation, arylation, and annulation, and photo-induced C-H functionalization. Substrate scopes, limitations, regio-/chemoselectivity, and reaction mechanisms are discussed. In addition, the applications of some new organic functional materials are briefly exemplified. This review also aims to serve as a reminder that much care should be taken when using organic ionic compounds as solvents, because they can behave as reactants that can break up desired coupling reactions.Bismuth(iii) oxidation of 3,5-di-substituted-1,2,4-triazolato anions afforded a paddlewheel 1,2,4-triazolato dibismuth complex [L2(Bi-Bi)L2] (L = η1,η1-3,5-R2tz, R = Ph (3), iPr (4)) with very short Bi(ii)-Bi(ii) bonds (2.8650(4)-2.8721(3) Å). The reaction involved the intermediates of the organobismuth radical [Bi(R2tz)2]˙ and neutral N-1,2,4-triazolyl radical [3,5-R2tz]˙. The dimerization of the former produced the corresponding dibismuth complex while the latter was trapped by using spin trap 5,5-dimethyl-1-pyrroline-N-oxide (DMPO) to give the radical adduct of (3,5-R2tz)(DMPO)˙ which was unambiguously evidenced by EPR analysis.