Differentiation of Δ-THC and CBD Using Silver-Ligand Ion Complexation and Electrospray Ionization Tandem Mass Spectrometry (ESI-MS/MS).

The 2018 Farm Bill defines marijuana as L. or any derivative thereof that contains greater than 0.3% Δ-tetrahydrocannabinol (Δ-THC) on a dry weight basis.

Structure and Thermodynamic Hydricity in Cobalt(triphosphine)(monophosphine) Hydrides.

The mononuclear cobalt hydride complex [HCo(triphos)(PMe)], in which triphos = PhP(CHCHPPh), was synthesized and characterized by X-ray crystallography and by H and P NMR spectroscopy. The geometry of the compound is a distorted trigonal bipyramid in which the axial positions are occupied by the hydride and the central phosphorus atom of the triphos ligand, while the PMe and terminal triphos donor atoms occupy the equatorial positions. Protonation of [HCo(triphos)(PMe)] generates H and the Co(I) cation, [Co(triphos)(PMe)], and this reaction is reversible under an atmosphere of H when the proton source is weakly acidic.

Computational Study of Triphosphine-Ligated Cu(I) Catalysts for Hydrogenation of CO to Formate.

The catalyzed hydrogenation of CO to formate via a triphosphine-ligated Cu(I) was studied computationally at the density functional theory level in the presence of a self-consistent reaction field. Of the four functionals benchmarked, M06 was generally in the best agreement with the available experimentally estimated values. Two bases, DBU and TBD, were studied in the context of two proposed mechanisms in the MeCN solvent.

Triphosphine-Ligated Copper Hydrides for CO2 Hydrogenation: Structure, Reactivity, and Thermodynamic Studies.

The copper(I) triphosphine complex LCu(MeCN)PF6 (L = 1,1,1-tris(diphenylphosphinomethyl)ethane), which we recently demonstrated is an active catalyst precursor for hydrogenation of CO2 to formate, reacts with H2 in the presence of a base to form a cationic dicopper hydride, [(LCu)2H]PF6. [(LCu)2H](+) is also an active precursor for catalytic CO2 hydrogenation, with equivalent activity to that of LCu(MeCN)(+), and therefore may be a relevant catalytic intermediate. The thermodynamic hydricity of [(LCu)2H](+) was determined to be 41.

Solvent influence on the thermodynamics for hydride transfer from bis(diphosphine) complexes of nickel.

The thermodynamic hydricity of a metal hydride can vary considerably between solvents. This parameter can be used to determine the favourability of a hydride-transfer reaction, such as the reaction between a metal hydride and CO2 to produce formate. Because the hydricities of these species do not vary consistently between solvents, reactions that are thermodynamically unfavourable in one solvent can be favourable in others.

Mixed-valent dicobalt and iron-cobalt complexes with high-spin configurations and short metal-metal bonds.

Cobalt-cobalt and iron-cobalt bonds are investigated in coordination complexes with formally mixed-valent [M2](3+) cores. The trigonal dicobalt tris(diphenylformamidinate) compound, Co2(DPhF)3, which was previously reported by Cotton, Murillo, and co-workers (Inorg. Chim.

A combined spectroscopic and computational study of a high-spin S = 7/2 diiron complex with a short iron-iron bond.

The nature of the iron-iron bond in the mixed-valent diiron tris(diphenylforamidinate) complex Fe(2)(DPhF)(3), which was first reported by Cotton, Murillo et al. (Inorg. Chim.