The synthesis, characterization, and reactivity of an iminoborane-N-heterocyclic carbene (NHC) adduct were described. The reaction of DmpNHB(OEt)Br [1; Dmp = 2,6-bis(2,4,6-trimethylphenyl)phenyl] with 2 equiv of 1,3-diimethyl-4,5-dimethylimidazol-2-ylidene (IMe4) resulted in the formation of an iminoborane-NHC complex 2. Both X-ray analysis and density functional theory calculations revealed the double-bond character of the B═N bond in 2. Interestingly, compared with the corresponding Lewis-base-free iminoborane, 2 features a nitrogen atom with increased electron density, which could be attributed to coordination of the NHC. Similar to the isoelectronic species imine, this nitrogen center in 2 can be easily attacked by electrophiles. Indeed, the reaction of 2 with trimethylsilyl triflate (Me3SiOTf) afforded an NHC-stabilized borenium cation 3, representing a facile strategy to prepare cationic tricoordinate boron species.Tricyanidonitridorhenium(V) complexes with 2,2'-bipyridine (bpy) derivatives in which the 4 and 4' positions were substituted by X, [ReN(CN)3(X2bpy)]- (X = NMe2, NH2, OMe, Me, Cl, and Br), were newly synthesized and characterized. The structures of the new complexes were determined by single-crystal X-ray analysis. UV-vis spectra of the complexes in dimethyl sulfoxide (DMSO) showed that the peak maximum wavelengths of rhenium-to-π* bpy-type-ligand charge transfer were in the range of 474-542 nm. Cyclic voltammograms in n-(C4H9)4NPF6-DMSO showed one-electron oxidation and reduction waves corresponding to the Re(VI/V) and X2bpy0/- processes, respectively. The new complexes and [ReN(CN)3bpy]- showed photoluminescence in the crystalline phase at 295 and 80 K and in DMSO at 295 K. The origin of the emission in DMSO was attributed to the triplet nature of the rhenium-to-π* bpy-type-ligand charge-transfer transition. Density functional theory calculations showed that the highest occupied and lowest unoccupied molecular orbitals were primarily localized on the dxy orbital of the rhenium and π* orbitals of the bpy-type ligand, respectively.E-cigarette aerosol (particle and gas) is a complex mixture of chemicals, of which the profile is highly dependent on device operating parameters and e-liquid flavor formulation. The thermal degradation of the e-liquid solvents propylene glycol and glycerol often generate multifunctional carbonyls that are challenging to quantify due to unavailability of standards. We developed a theoretical method to calculate the relative electrospray ionization sensitivities of hydrazones of organic acids and carbonyls with 2,4-dinitrophenylhydrazine (DNPH) based on their gas phase basicities (ΔGdeprotonation). This method enabled quantification by liquid chromatography high-resolution mass spectrometry (HPLC-HRMS) in the absence of chemical standards. Accurate mass and tandem multistage mass spectrometry (MSn) were used for structure identification of vaping products. We quantified five simple carbonyls, six hydroxycarbonyls, four dicarbonyls, three acids, and one phenolic carbonyl in the e-cigarette aerosol with Classic Tobacco flavor. Our results suggest that hydroxycarbonyls, such as hydroxyacetone, lactaldehyde, and dihydroxyacetone can be significant components in e-cigarette aerosol, but have received less attention in the literature and have poorly-understood health effects. The data support the radical-mediated e-liquid thermal degradation scheme that has been previously proposed and emphasize the need for more research on the chemistry and toxicology of complex product formation in e-cigarette aerosol.Steric properties of crystallographically and computationally determined structures of linear palladium(0) and square planar palladium(II) complexes of di(tert-butyl)neopentylphosphine (P(t-Bu)2Np), tert-butyldineopentylphosphine (P(t-Bu)Np2), and trineopentylphosphine (PNp3) have been determined. Structures of linear palladium(0) complexes show that steric demand increases as tert-butyl groups are replaced with neopentyl groups (P(t-Bu)2Np less then P(t-Bu)Np2 less then PNp3). In square planar palladium(II) complexes, PNp3 gives the smallest steric parameters, whereas P(t-Bu)Np2 has the largest steric demand. The change in the steric demand of PNp3 compared to P(t-Bu)2Np and P(t-Bu)Np2 results from a significant conformational change in PNp3 depending on the coordination number of the metal. The steric properties of these ligands were also probed by measuring the equilibrium constant for coordination of free phosphine to dimeric [(R3P)Pd(μ-Cl)Cl]2 complexes. Binding equilibria follow the same trend as the steric parameters for square planar complexes with PNp3 having the highest binding constant.  https://www.selleckchem.com/products/Dapagliflozin.html  In contrast to the normal trend, the neopentylphosphines show increased pyramidalization at phosphorus with increasing steric demand. We hypothesize that this unusual dependence reflects the low back side strain of the neopentyl group, which allows the ligand to be more pyramidalized while still exerting a significant front side steric demand.The United States and Canada called for a 40% load reduction of total phosphorus from 2008 levels entering the western and central basins of Lake Erie to achieve a 6000 MTA target and help reduce its central basin hypoxia. The Detroit River is a significant source of total phosphorus to Lake Erie; it in turn has been reported to receive up to 58% of its load from Lake Huron when accounting for resuspended sediment loads previously unmonitored at the lake outlet. Key open questions are where does this additional load originate, what drives its variability, and how often does it occur. We used a hydrodynamic model, satellite images of resuspension events and ice cover, wave hindcasts, and continuous turbidity measurements at the outlet of Lake Huron to determine where in Lake Huron the undetected load originates and what drives its variability. We show that the additional sediment load, and likely phosphorus, is from wave-induced Lake Huron sediment resuspension, primarily within 30 km of the southeastern shore. When the flow is from southwest or down the center of the lake, the resuspended sediment is not detected at Canada's sampling station at the head of the St. Clair River.