ConspectusDicarbon, the molecule formed from two carbon atoms, is among the most abundant molecules in the universe. Said by some to exhibit a quadruple bond, it is bound by more than 6 eV and supports a large number of valence electronic states. It thus has a rich spectroscopy, with 19 one-photon band systems, four of which were discovered by the author and co-workers. Its spectrum was among the first to be described Wollaston reported the emission spectra from blue flames in 1802.C2 is observed in a variety of astronomical objects, including stars, circumstellar shells, nebulae, comets and the interstellar medium. It is responsible for the green color of cometary comae but is not observed in the comet tail. It can be observed in absorption and emission by optical spectroscopy in the infrared, visible, and ultraviolet regions of the spectrum, and because it has no electric-dipole-allowed vibrational or rotational transitions, its spectral signature is a sensitive probe of the local environment.Before the worl piece of the C2 puzzle would be understanding how long it survives before being broken into carbon atom fragments. Though predicted by Herzberg, predissociation in the e3Πg state had never been observed. To find it would require the complicated ultraviolet spectroscopy of C2 to be disentangled. In so doing, we identified the 43Πg and 33Πg states of C2, thus uncovering two new band systems. The 43Πg state allowed the first accurate determination of the ionization energy of C2. With these new band systems secure, we extracted new levels of the D1Σu+ state (Mulliken bands) and the e3Πg state (Fox-Herzberg bands) from our spectra. Upon climbing the energy ladder in the e3Πg state to v = 12, we finally identified the route to predissociation of C2 via non-adiabatic coupling to the d3Πg state. This observation provided the first laboratory evidence for why C2 is observed in the coma of a comet but not the tail.Continuously enhanced photoresponsivity and suppressed dark/noise current combinatorially lead to the recent development of high-detectivity organic photodetectors with broadband sensing competence. Despite the achievements, reliable photosensing enabled by organic photodetectors (OPDs) still faces challenges. Herein, we call for heed over a universal phenomenon of detrimental sensitivity of dark current to illumination history in high-performance inverted OPDs. The phenomenon, unfavorable to the attainment of high sensitivity and consistent figures-of-merit, is shown to arise from exposure of the commonly used electron transport layer in OPDs to high-energy photons and its consequent loss of charge selectivity via systematic studies. To solve this universal problem, "double" layer tin oxide as an alternative electron transport layer is demonstrated, which not only eliminates the inconsistency between the initial and after-illumination dark current characteristics but also preserves the low magnitude of dark current, good external quantum efficiency, and rapid transient response.The biomedical application of discrete supramolecular metal-based structures, specifically self-assembled metallacages, is still an emergent field of study. Capitalizing on the knowledge gained in recent years on the development of 3-dimensional (3D) metallacages as novel drug delivery systems and theranostic agents, we explore here the possibility to target [Pd2L4]4+ cages (L = 3,5-bis(3-ethynylpyridine)phenyl ligand) to the brain. In detail, a new water-soluble homoleptic cage (CPepH3) tethered to a blood brain barrier (BBB)-translocating peptide was synthesized by a combination of solid-phase peptide synthesis (SPPS) and self-assembly procedures. The cage translocation efficacy was assessed by inductively coupled mass spectrometry (ICP-MS) in a BBB cellular model in vitro. Biodistribution studies of the radiolabeled cage [[99mTcO4]- ⊂ CPepH3] in the CD1 mice model demonstrate its brain penetration properties in vivo. https://www.selleckchem.com/products/zilurgisertib-fumarate.html Further DFT studies were conducted to model the structure of the [[99mTcO4]- ⊂ cage] complex. Moreover, the encapsulation capabilities and stability of the cage were investigated using the [ReO4]- anion, the "cold" analogue of [99mTcO4]-, by 1H NMR spectroscopy. Overall, our study constitutes another proof-of-concept of the unique potential of supramolecular coordination complexes for modifying the physiochemical and biodistribution properties of diagnostic species.The interplay of the isotropic-nematic transition and phase separation in lyotropic solutions of two types of semiflexible macromolecules with pronounced difference in chain stiffness is studied by Density Functional Theory and Molecular Dynamics simulations. While the width of the isotropic-nematic two-phase coexistence region is narrow for solutions with a single type of semiflexible chain, the two-phase coexistence region widens for solutions containing two types of chains with rather disparate stiffness. In the nematic phase, both types of chains contribute to the nematic order, with intermediate values of the order parameter compared to the corresponding single component solutions. As the difference in bending stiffness is increased, the two chain types separate into two coexisting nematic phases. The phase behavior is rationalized by considering the chemical potentials of the two components and the Gibbs excess free energy. The geometric properties of the chain conformations under the various conditions are also discussed.Pseudokinases play important roles in signal transduction and cellular processes similar to those of catalytically competent kinases. However, pseudokinase pharmacological tractability and conformational space accessibility are poorly understood. Pseudokinases have only recently been suggested to adopt "inactive" conformations or interact with conformation-specific kinase inhibitors (e.g., type II compounds). In this work, the heavily substituted pseudokinase STRADα, which possesses a DFG → GLR substitution in the catalytic site that permits nucleotide binding while impairing divalent cation coordination, is used as a test case to demonstrate the potential applicability of conformation-specific, type II compounds to pseudokinase pharmacology. Integrated structural modeling is employed to generate a "GLR-out" conformational ensemble. Likely interacting type II compounds are identified through virtual screening against this ensemble model. Biophysical validation of compound binding is demonstrated through protein thermal stabilization and ATP competition. Localization of a top-performing compound through surface methylation strongly suggests that STRADα can adopt the "GLR-out" conformation and interact with compounds that comply with the standard type II pharmacophore. These results suggest that, despite a loss of catalytic function, some pseudokinases, including STRADα, may retain the conformational switching properties of conventional protein kinases.Corrosion of metallic substrates is a problem for a variety of applications. Corrosion can be mitigated with the use of an electrically insulating coating protecting the substrate. Thick millimetric coatings, such as paints, are generally more corrosion-resistant when compared to nanoscale coatings. However, for thermal systems, thick coatings are undesirable due to the resulting decrease in the overall heat transfer stemming from the added coating thermal resistance. Hence, the development of ultrathin ( less then 10 μm) coatings is of great interest. Ultrathin inorganic silicon dioxide (SiO2) coatings applied by sol-gel chemistries or chemical vapor deposition, as well as organic coatings such as Parylene C, have great anticorrosion performance due to their high dielectric breakdown and low moisture permeability. However, their application to arbitrarily shaped metals is difficult or expensive. Here, we develop a sol-gel solution capable of facile and controllable dip coating on arbitrary metals, resulting sol-gel and Parylene C coatings demonstrated a 95% decrease in corrosion rate during electrochemical tests. Copper tube weight loss was reduced by 75% for the sol-gel SiO2-coated tubes when seawater was used as the corrosive fluid in the test loop. This work not only demonstrates scalable coating methodologies for applying ultrathin anticorrosion coatings but also develops mechanistic understanding of corrosion mechanisms on a variety of functional surfaces and substrates.Efficient charge injection at organic semiconductor/metal interfaces is crucial for the performance of organic field effect transistors. Interfacial hybrid band formation between electronic states of the organic compound and the metal electrode facilitates effective charge injection. Here, we show that a long-range ordered monolayer of a flat-lying N-heteropolycyclic aromatic compound on Au(111) leads to dispersing occupied and unoccupied interfacial hybrid bands. Using angle-resolved two-photon photoemission we determine their energy level alignment and dispersion relations. We suggest that band formation proceeds via hybridization of a localized occupied molecular state with the d-bands of the Au substrate, where the large effective mass of the d-bands is significantly reduced in the hybrid band. link2 Hybridization of an unoccupied molecular state with the Au sp-band leads to a band with an even smaller effective mass.Low-energy nitrogen removal under mainstream conditions is a technology that has received significant attention in recent years as the water industry drives toward long-term sustainability goals. Simultaneous partial nitritation-Anammox (PN/A) is one process that can provide substantial energy reduction and lower sludge yields. Mathematical modeling of the PN/A process offers engineers insights into the operating conditions necessary to maximize its potential. Laureni et al. (Laureni et al. Water Res. 2019, 14) have recently published a simplified mechanistic model of the process operated as a sequencing batch reactor that investigated the effect of three key operating parameters on performance (Anammox biofilm activity, dissolved oxygen concentration and fraction of solids wasted). The analysis of the model was limited, however, to simulation with relatively few discrete parameter sets. Here, we demonstrate through the use of bifurcation theory applied to an impulsive dynamical system that the parameter space can be partitioned into regions in which the system converges to different fixed points that represent different outcomes either the washout of nitrite-oxidizing bacteria or their survival. Mapping process performance data onto these spaces allows engineers to target suitable operating regimes for specific objectives. Here, for example, we note that the nitrogen removal efficiency is maximized close to the curve that separates the regions in parameter space where nitrite-oxidizing bacteria washout from the region in which they survive. Further, control of solids washout and Anammox biofilm activity can also reduce oxygen requirements while maintaining an appropriate hydraulic retention time. The approach taken is significant given the possibility for using such a methodology for models of increasing complexity. link3 This will enable engineers to probe the entire parameter space of systems of higher dimension and realism in a consistent manner.