TiCl4 promoted menthyl ester chiral auxiliary mediated synthesis of chiral syn-β-amino esters and applications of a representative syn-β-amino ester

β-Amino esters were obtained in up to 78% yield with 72:28–96:4 diastereomeric ratios by the reaction of the chiral titanium enolate of menthyl esters, prepared using the TiCl₄/Et₃N reagent system with prochiral imines. A representative syn-β-amino ester derivative has been used for the resolution of racemic mandelic acid to obtain a sample with >99% ee in a single step. A representative syn-β-amino ester was converted to the corresponding N-deprotected amino ester using the Pd–C/HCOOH reagent system, and then to the corresponding β-amino acid using the glacial CH₃COOH/HCl reagent system, and to the corresponding β-lactam derivative with partial epimerization by the reaction using C₂H₅MgBr.     

Diastereoselective reductive N-alkylation of (R,R)-trans-1,2-diaminocyclohexane with prochiral ketones using the Ti(OiPr)4/NaBH4 system

A simple and convenient one-pot method for the reductive N-alkylation of (R,R)-trans-1,2-diaminocyclohexane by prochiral ketones using a Ti(OⁱPr)₄/NaBH₄ system to obtain the corresponding alkyl amine derivatives in 76–95% yields with good diastereoselectivity (dr = up to 23:1:1) is reported.     

Characterisation of different polymorphs of tris(8-hydroxyquinolinato)aluminium(III) using solid-state NMR and DFT calculations

Background  

Organic light emitting devices (OLED) are becoming important and characterisation of them, in terms of structure, charge distribution, and intermolecular interactions, is important. Tris(8-hydroxyquinolinato)-aluminium(III), known as Alq₃, an organomettalic complex has become a reference material of great importance in OLED. It is important to elucidate the structural details of Alq₃ in its various isomeric and solvated forms. Solid-state nuclear magnetic resonance (NMR) is a useful tool for this which can also complement the information obtained with X-ray diffraction studies.     

Singlet molecular oxygen quantum yield measurements of some porphyrins and metalloporphyrins

Hematoporphyrin IX dimethyl ester (HPDME), tetraphenylporphyrin (TPP), tetra(4-methoxyphenyl)porphyrin (TMPP), tetra(3,4-dimethoxyphenyl)porphyrin (TDMPP), tetra(3,4,5-trimethoxyphenyl)porphyrin (TTMPP), tetraanthrylporphyrin (TAP) and tetraacridylporphyrin (TACP), and their Zn²⁺, SnX ₂ ²⁺ , Pd²⁺ and Pt²⁺ complexes have been prepared and characterized. The singlet molecular oxygen quantum yield (ϕ_Δ) values of the above porphyrins and their metal derivatives in N,N-dimethyl formamide (DMF) have been measured in the presence of 1,3-diphenylisobenzofuran (DPBF) as¹O₂ acceptor using steady state technique after correcting for the intensity of light absorbed by the photosensitizers. The ϕ_Δ values for the free base porphyrins are usually around 0.60. Hematoporphyrin IX dimethyl ester and its metal derivatives follow the order: HPDME (ϕ_Δ = 0.60) > Zn HPDME (0.40) > PdHPDME (0.34) > Sn(OH)₂ HPDME (0.28) > PtHPDME (0.24). Zinc(II) complexes of tetraarylporphyrins show about 65% efficiency in ϕ_Δ values are compared to the ϕ_Δ values of their corresponding free base porphyrins. These results can be explained on the basis of catalyzed intersystem crossing to the ground state. The ϕ_λ values of the above free base porphyrins and their metal complexes in DMF in presence of DPBF using single-pulsed laser excitation technique follow similar trends.     

Laser amplification in an optical fiber by evanescent field coupling

A laser signal propagating in an optical fiber is amplified by the evanescent field interacting with the excited Rhodamine 6 G solution surrounding the fiber. A small signal gain of 430 at 600 nm has been measured in a long fiber with a 2 cm long fiber optic amplifier.     

Esterification of sterically hindered pyrrole carboxylic acids using dimethyl and diethyl sulfate under mild basic conditions

A simple and efficient method for the esterification of sterically hindered pyrrole carboxylic acids using dialkylsulfate and anhydrous potassium carbonate is described.     

Phenanthrene-imidazole-based fluorescent sensor for selective detection of Ag+ and F− ions: real sample application and live cell imaging

Research on Chemical Intermediates - 4-Methyl-2,6-bis(1H-phenanthro[9,10-d]imidazol-2-yl)phenol (probe-MPIP) conjugate has been designed as a selective fluorescent probe for silver (Ag+) ions. The...     

The T3 (π, π) State of acridine

The 00 band maximum of the transition T₃(π, π^*) ← T₁ (π, π^*) of acridine occurs at ≈ 10200 ± 20 cm^?1 in inert (n-hexane, benzene, CCl₄), at 10220 ± 20 cm^?1 in polar (acetonitrile) and at 10170 ± 50 cm^?1 in hydrogen-bonding (methanol, 2-propanol and alkaline water) solvents. Based on the solvent-independent energy of T₁ (π, π^*), the T₃(π, π^*) state of acridine is estimated at 26050 ± 50 cm^?1 in all the solvents.