Carbazoquinocin Analogues as Small Molecule Biomimetic Organocatalysts in Dehydrogenative Coupling of Amines.

A new series of carbazole-cored biomimetic ortho-quinone catalysts structurally resembling carbazoquinocin alkaloids have been introduced to promote tunable, metal cocatalyst-free, organocatalytic, dehydrogenative amine oxidation under aerobic conditions. Differently substituted benzyl amines were tolerated under optimized conditions to provide imines in excellent yields. Further efficacy of the catalyst was demonstrated by synthesizing cross-coupled imines efficiently. Control experiments and in-depth DFT studies disclosed a covalent transamination pathway as a plausible mechanism for this newly developed catalytic system.

Physical and mechanical properties of Albizia procera glulam beam.

This research was done to evaluate the feasibility of using Albizia procera for manufacturing glulam beams. The physical and mechanical properties of the A. procera glulam beam were evaluated, and these properties were compared to those of the solid A. procera solid timber. The A. procera glulam beam's physical and mechanical properties were all superior to solid A. procera timber. In comparison to A. procera solid timber, A. procera glulam's density, water absorption (WA), linear expansion (LE), and thickness swelling (TS) all improved by 11.1, 48.4, 44.6, and 37.0%, respectively. Again, compared to A. procera solid timber, the modulus of rupture (MOR) and modulus of elasticity (MOE) of the A. procera glulam beam increased by 27.6 and 29.2%, respectively. Additionally, the ASTM specifications were met by the A. procera glulam beam. As a result, based on the properties, it is possible to make A. procera glulam beams as structural timber products.