Structure and magnetic properties of a decanuclear Mn(II)₂Mn(III)₂Dy₆ aggregate

Using glycerol (H?gly) as a primary ligand, the decanuclear aggregate [Mn(II)?Mn(III)?Dy?(μ?-OH)?(Hgly)?(H?gly)?-(PhCO?)??(H?O)?]·10CH?CN (1) has been synthesised; it has a structure built up from two Mn?Dy? heterocubane units linked through a central Dy?(μ-benzoate)? paddle-wheel dimer and shows slow relaxation of its magnetisation.     

Stabilization of a Two‐Coordinate Mononuclear Cobalt(0) Compound

Compound (Me₂‐cAAC:)₂Co⁰ ( 2 ; Me₂‐cAAC:=cyclic (alkyl) amino carbene; :C(CH₂)(CMe₂)₂N‐2,6‐iPr₂C₆H₃) was synthesized by the reduction of the precursor (Me₂‐cAAC:)₂Co^ICl ( 1 ) with KC₈ in THF. The cyclic voltammogram of 1 exhibited one‐electron reduction, which suggests that synthesis of a bent 2‐metallaallene ( 2 ) from 1 should be possible. Compound 2 contains one cobalt atom in the formal oxidation state zero, which is stabilized by two Me₂‐cAAC: ligands. Bond lengths from X‐ray diffraction are 1.871(2) and 1.877(2) Å with a C‐Co‐C bond angle of 170.12(8)°. The EPR spectrum of 2 exhibited a broad resonance attributed to the unique quasi‐linear structure, which favors near degeneracy and gives rise to very rapid relaxation conditions. The cAAC?Co bond in 2 can be considered as a typical Dewar–Chatt–Duncanson type of bonding, which in turn retains 2.5 electron pairs on the Co atom as nonbonding electrons.     

C4 Cumulene and the Corresponding Air‐Stable Radical Cation and Dication

A neutral C₄ cumulene 1 that includes a cyclic alkyl(amino) carbene (cAAC), its air‐stable radical cation 1 ^.+, and dication 1 ²⁺ have been synthesized. The redox property of 1 ^.+ was studied by cyclic voltammetry. EPR and theoretical calculations show that the unpaired electron in 1 ^.+ is mainly delocalized over the central C₄ backbone. The commercially available CBr₄ is utilized as a source of dicarbon in the cumulene synthesis.     

Design,Synthesis, and Characterization of Quinoxaline Derivatives as a Potent Antimicrobial Agent

A series of quinoxalinone derivatives were synthesized by the reaction of o‐phenylenediamine with oxalic acid to yield 1, 4‐dihydro quinoxaline‐2, 3‐dione ( 1 ) and then treated with thionyl chloride to yield 2, 3 dichloro quinoxaline ( 2 ). This was further reacted with hydrazine hydrate to produce 2, 3‐dihydrazinyl quinoxaline ( 3 ). This was finally reacted with substituted aromatic aldehydes to produce 2,3‐bis[2‐(sustituted benzylidine) hydrazinyl] quinoxalines ( 4 ). These quinoxalinone derivatives were characterized by infrared spectroscopy and nuclear magnetic resonance spectroscopy and MASS spectral data. All the synthesized compounds were evaluated for their antimicrobial activity. The results of the antimicrobial study revealed that compounds 4c , 4d , and 4i were active and exhibited better inhibitory activities as compared to standard drug ciprofloxacin. The results were further checked with protein legend interaction by using docking studies, and all the compounds exhibited good docking scores between ?8.72 and ?11.29 kcal/mol against dihydrofolate reductase protein fragment from Staphylococcus aureus (PDB ID‐4XE6). Among all compound, 4c has shown maximum docking score and found in agreement to in vitro studies.     

Visible superfluorescence from optically pumped europium atoms

We have observed superfluorescence (SF) on five atomic transitions at visible wavelengths 633.58, 635.00, 640.09, 640.61 and 736.22 nm in Doppler broadened gas of europium (Eu) atom. The nanosecond SF pulses were observed by longitudinally pumping Eu vapor column with a pulsed dye laser to upper states 4f⁶5d6s², ⁸D_7/2at 346.79 nm and 4f⁷5d6p, ¹⁰F_5/2at 348.73 nm from the ground state 4f⁷6s², ⁸S_7/2. High optical conversion efficiency ≈10% was measured for these SF transitions. Our experiment deals with the large sample multilevel SF in the regime where the length of the excited column L is greater than the maximum value of the Arecchi-Courtens length (L_c). The observed variation of SF peak intensity (I_fl) and time delay for SF evolution (τ_D) with number of atoms in the excited state (N) resemble theoretically predicted SF scaling laws for transverse excitation, namely I_fl∝N and t_D μ 1/?N\tau_D \propto 1/{\sqrt N} although the experimental condition is similar to the swept excitation. This could be due to the Rabi frequency associated with the pump transition which is comparable to the SF delay time precluding the initiation of SF at different times along the sample and results in transverse (instantaneous) excitation. The experimental τ_D values were found to be in agreement with the quantum mechanical calculations describing SF.     

Arithmetic properties of the Shimura–Shintani–Waldspurger correspondence

We prove that the theta correspondence for the dual pair , for B an indefinite quaternion algebra over ℚ, acting on modular forms of odd square-free level, preserves rationality and p-integrality in both directions. As a consequence, we deduce the rationality of certain period ratios of modular forms and even p-integrality of these ratios under the assumption that p does not divide a certain L-value. The rationality is applied to give a direct construction of isogenies between new quotients of Jacobians of Shimura curves, completely independent of Faltings’ isogeny theorem. To my parents.     

Triethanolamine‐catalyzed expeditious and greener synthesis of 2‐amino‐4H‐chromenes

Triethanolamine (TEOA), an inexpensive and eco‐friendly base, was used to efficiently catalyze the three‐component condensation reaction of heterocyclic/aromatic aldehyde, (α/β)‐naphthol, and malononitrile in water to give the corresponding substituted 2‐amino‐4H‐chromene derivatives with excellent yields.     

Magnetic anomalies in nanocrystalline , a geometrically frustrated spin-chain compound

We have investigated the magnetic behavior of nano crystals, synthesized by high-energy ball-milling, for a well-known geometrically frustrated spin-chain system, Ca₃CoRhO₆, and compared its magnetic characteristics with those of the bulk form by measuring ac and dc magnetization. The features attributable to the onset of ‘partially disordered antiferromagnetism’ (characterizing the bulk form) are not seen in the magnetization data of the nano particles; the magnetic moment at high fields in the very low temperature range in the magnetically ordered state gets relatively enhanced in the nano particles. It appears that the ferromagnetic intrachain interaction, judged by the sign of the paramagnetic Curie temperature, is preserved in the nano particles. These trends are opposite to those seen in the nano particles of Ca₃Co₂O₆. However, the complex spin-dynamics as evidenced by large frequency dependence of ac susceptibility is retained in the nano particles as well. Thus, there are some similarities and dissimilarities between the properties of the nano particles and those of the bulk. We believe that these findings will be useful to understand correlation lengths deciding various properties of geometrical frustration and/or spin-chain phenomena.