New functional chiral P-based ligands and application in ruthenium-catalyzed enantioselective transfer hydrogenation of ketones

Metal-catalyzed asymmetric transfer hydrogenation is a powerful and practical method for the reduction of ketones to produce the corresponding secondary alcohols, which are valuable building blocks in the pharmaceutical, perfume, and agrochemical industries. Hence, a series of novel chiral β-amino alcohols were synthesized by chiral amines with regioselective ring opening of (S)-propylene oxide or reaction with (S)-(+)-2-hydroxypropyl p-toluenesulfonate by a straightforward method. The chiral ruthenium catalytic systems generated from [Ru(arene)(μ-Cl)Cl]₂ complexes and chiral phosphinite ligands based on amino alcohol derivatives were employed in asymmetric transfer hydrogenation of ketones to give the corresponding optically active alcohols; (2S)-1-{[(2S)-2-[(diphenylphosphanyl)oxy]propyl][(1R)-1-phenylethyl]amino}propan-2-yldiphenylphosphinitobis[dichol-oro(η⁶-benzene)ruthenium(II)] acts an excellent catalyst in the reduction of α-naphthyl methyl ketone, giving the corresponding alcohol with up to 99% ee. The substituents on the backbone of the ligands were found to have a remarkable effect on both the conversion and enantioselectivity of the catalysts. Furthermore, this transfer hydrogenation is characterized by low reversibility under these conditions.     

Giant improvement of time-delayed feedback control by spatio-temporal filtering

Control of spatio-temporal chaos by the time-delay autosynchronization method is improved by several orders of magnitude. Unstable time periodic patterns are efficiently stabilized if one employs filters and couplings which originate from the Floquet eigenvalue problem of the unstable orbit. We illustrate our scheme by an application to a globally coupled reaction-diffusion model which describes charge transport in semiconductor devices.     

Formation of Coanda jet from sharp-edged swirl nozzle with base plate

Experiments were conducted using tufts and PIV to determine the conditions for which a swirled gas jet issuing from a sharp-edge nozzle, in flush with a base plate, would form a Coanda jet. The flow field was also simulated. The inception of the Coanda jet was observed to be associated with the formation of a recirculation bubble at the nozzle exit. A threshold value of swirl number, which increased monotonically with Reynolds number, was required for the formation of the Coanda jet. The Coanda jet was associated with hysteresis. The flow features and transition from a diverging jet to a Coanda jet are discussed.     

Viscous dissipation effect on heat transfer characteristics of rectangular microchannels under slip flow regime and H1 boundary conditions

Viscous dissipation effect on heat transfer characteristics of a rectangular microchannel is studied. Flow is governed by the Navier–Stokes equations with the slip flow and temperature jump boundary conditions. Integral transform technique is applied to derive the temperature distribution and Nusselt number. The velocity distribution is taken from literature. The solution method is verified for the case where viscous dissipation is neglected. It is found that, the viscous dissipation is negligible for gas flows in microchannels, since the contribution of this effect on Nu number is about 1%. However, this effect should be taken into account for much more viscous flows, such as liquid flows. Neglecting this effect for a flat microchannel with an aspect ratio of 0.1 for Br=0.04 underestimates the Nu number about 5%.     

Bounded Engel elements in groups satisfying an identity

We prove that a residually finite group G satisfying an identity \(w\equiv 1\) and generated by a commutator closed set X of bounded left Engel elements is locally nilpotent. We also extend such a result to locally graded groups, provided that X is a normal set. As an immediate consequence, we obtain that a locally graded group satisfying an identity, all of whose elements are bounded left Engel, is locally nilpotent.     

On Fully Idempotent Modules

A submodule N of a module M is idempotent if N = Hom(M, N)N. The module M is fully idempotent if every submodule of M is idempotent. We prove that over a commutative ring, cyclic idempotent submodules of any module are direct summands. Counterexamples are given to show that this result is not true in general. It is shown that over commutative Noetherian rings, the fully idempotent modules are precisely the semisimple modules. We also show that the commutative rings over which every module is fully idempotent are exactly the semisimple rings. Idempotent submodules of free modules are characterized.     

Lifting Modules with Indecomposable Decompositions

A module M is called a “lifting module” if, any submodule A of M contains a direct summand B of M such that A/B is small in M/B. This is a generalization of projective modules over perfect rings as well as the dual of extending modules. It is well known that an extending module with ascending chain condition (a.c.c.) on the annihilators of its elements is a direct sum of indecomposable modules. If and when a lifting module has such a decomposition is not known in general. In this article, among other results, we prove that a lifting module M is a direct sum of indecomposable modules if (i) rad(M ^(I)) is small in M ^(I) for every index set I, or, (ii) M has a.c.c. on the annihilators of (certain) elements, and rad(M) is small in M.     

Biological assays and theoretical density functional theory calculations of Rh(I), Ir(III), and Ru(II) complexes of chiral phosphinite ligand

Four metal complexes, IL-OPPh₂-Ru-p-cymene (3) , IL-OPPh₂-Ru-benzene (4) , IL-OPPh₂-Ir-Cp* (5) , IL-OPPh₂-Rh-COD (6) , have been evaluated for in vitro antioxidant activity such as 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging and reducing power activity. Maximum scavenging activity (71.43%) was obtained with IL-OPPh₂-Ru-p-cymene, whereas IL-OPPh₂-Rh-COD showed the highest reducing power ability. The complexes were also studied for their antimicrobial activity against three Gram-positive and three Gram-negative bacteria. In addition, DNA binding of the complexes was evaluated using calf thymus DNA. Both Ru(II) complexes exhibited good DNA-binding activity while the other complexes did not have any activity. Furthermore, ab initio quantum calculations of four complexes were also carried out using density functional theory to better understand their chemical behaviors.