Photochromism of dihydroindolizines part X. Photo‐responsive self‐assembling organogelators based on photochromic dihydroindolizines and 11‐aminoundecanoic acid (AUDA)

Multi‐addressable photophysical properties of new synthesized photochromic materials based on photochromic dihydroindolizine system (DHI) covalently linked to N‐acyl‐11 aminoundecanoic acid (AUDA) or to its sodium salt or to its ester, through an amidic or urethane linkage have been studied. The DHI skeleton in these compounds is substituted in both the fluorene part (region A) or in the heterocyclic base (region B) with the gelling moieties. These molecules have been designed to respond to their environment. Interestingly, they are shown to act as efficient gelators for polar organic fluids, water and obviously they exhibit a thermosensitive answer as low molecular mass organogelators. In these fluids, the aggregative properties are totally suppressed upon conversion to neutral carboxylic species. The gels of these carboxylate sodium salts are shown to be markedly affected by light irradiation. Supramolecular gelating assemblies can be disrupted by the photoinduced ring opening of the DHI subunit, so that the macroscopic flowing property is recovered. Upon a further thermal treatment, the system is reversibly converted back to the supramolecular network. Controlled gelation could be achieved using temperature, light, or acidity as external stimuli. These new synthesized photochromic gels with their multi‐addressable properties will find their applications as super photoresponsive materials. Developing and tuning of the photophysical properties of the synthesized compounds by the amide and urethane substituents in the 4‐position of the fluorene and pyridazine regions have been achieved. The absorption maxima (λ_max) and the half‐lives (t_1/2) of the colored betaines were detected in all cases using UV/VIS spectrophotometric measurements. Irradiation of DHI 12‐20 in CH₂Cl₂ or in acetonitrile solutions at ambient temperature with polychromatic light leads to the formation of red to red‐violet colored betaines 12 ′ ‐20 ′. The kinetics of the bleaching process of betaines 12 ′ ‐20 ′ to DHIs 12‐20 were found to take place in the second range (96‐218 s) and fit well the first order thermal back reaction. Some of these DHIs showed a photostability higher than that of the standard one. These interesting photophysical properties will help this family of compounds to find useful applications. Copyright © 2008 John Wiley & Sons, Ltd.     

Group 6 metal carbonyl complexes of 3′H-spiro[indole-3,2′-[1,3]benzothiazole-2(1H)]-one

The spiro-compound 3′H-spiro[indole-3,2′-[1,3]benzothiazole-2(1H)-one (IBTH₂) was synthesized and its structure was determined using spectroscopic techniques (FTIR, ¹H NMR and mass) and X-ray crystallography. This ligand possesses different centers for coordination. Reactions of [M(CO)₆], M = Cr, Mo or W with IBTH₂ in THF under reduced pressure were studied. For chromium a complex with molecular formula [Cr(ITP)₂] was isolated; where ITP is the opened form of the ligand which occurred through C_spiro–S bond, while [Mo(CO)₅(IBTH₂)] and [W(CO)₅(IBTH₂)] were isolated from the reaction of IBTH₂ with molybdenum and tungsten carbonyls, respectively. All complexes were characterized by elemental analysis, IR, mass and ¹H NMR spectroscopy. The biological activity of the ligand and its complexes were studied and compared with the parent compound isatin.     

Entanglement and Sudden Death of a Nonlinear Two-Level-Atom Pair Interacting with a Radiation Field

We study the entanglement between a pair of two-level atoms simultaneously interacting via a singlemode thermal field. The Hamiltonian also describes a two-photon process. The entanglement between a nonlinear atom-field interacting system is also studied using atomic and field entropy changes. We use concurrence to detect the sudden death phenomenon. Furthermore, we discuss the relationship between entropy changes and concurrence entanglement. Our results show that the behavior of the entropy change is in agreement with the behavior of the concurrence when we measure the entanglement between the two-subsystem structure.     

Additional stringy sources for electric dipole moments

We show that string models with low energy supersymmetry which accommodate the fermion mass hierarchy generally give nonuniversal soft trilinear couplings (A terms). In conjunction with the apparently large Cabibbo-Kobayashi-Maskawa (CKM) phase, this results in large fermion electric dipole moments (EDMs) even in the absence of CP violating phases in the supersymmetry breaking auxiliary fields and the micro term. Nonobservation of the EDMs therefore implies that strings select special flavor and/or supersymmetry breaking patterns.     

Determination of Mn and Na in geological samples

Neutron activation technique using a low intensity²⁵²Cf source has been applied for Mn and Na analysis in geological samples. The series of samples tested in the present work were collected from the boreholes Nádudvar-9, Hajdúböszörmény-1 and Nagyecsed-1 in Hungary, from different strata.     

Isometries of certain operator spaces

Let and be Banach spaces, and be the spaces of bounded linear operators from into In this paper we give full characterization of isometric onto operators of for a certain class of Banach spaces, that includes We also characterize the isometric onto operators of and the compact operators on Furthermore, the multiplicative isometric onto operators of , when multiplication on is taken to be the Schur product, are characterized.

     

Non-linear Semigroup of a Class of Abstract Semilinear Functional Differential Equations with a Non-Dense Domain

In this work, we are concerned with a general class of abstract semilinear autonomous functional differential equations with a non-dense domain on a Banach space. Our objective is to study, using the Crandall-Liggett approach, the solutions as a semigroup of non-linear operators.     

Synthesis of zerovalent nanophase metal particles stabilized with poly(ethylene glycol)

Concurrent sonolysis of iron pentacarbonyl and poly(ethylene glycol)-400 (PEG-400) in hexadecane solvent proceeds via zero-order kinetics and results in Fe nanoparticles encapsulated in PEG-400 (Fe-PEG). The transmission electron microscopy images show Fe-PEG consisting of <3 nm Fe particles that are evenly dispersed in the PEG matrix. M?ssbauer and X-ray absorption fine structure/X-ray absorption near-edge structure data reveal an ordered PEG assembly that helps protect the zerovalent Fe core. The Fe nanoparticles in Fe-PEG are superparamagnetic with a magnetization value of 45 emu/g-Fe at 10 KOe. The rheology of the synthesized material shows an unusual increase in viscosity with temperature that is likely due to lower critical saturation temperature phase segregation over 40 degrees C. The low-temperature mobility of the PEG-400 moiety in Fe-PEG would allow facile ligation of the Fe0 core with biologically and chemically active groups.