Evaluation of Meldola Blue‐Carbon Nanotube‐Sol‐Gel Composite for Electrochemical NADH Sensors and Their Application for Lactate Dehydrogenase‐Based Biosensors

A novel MB‐SWNT‐sol‐gel nanocomposite material was prepared by the sol‐gel process incorporating a redox mediator and carbon nanotubes. The electrocatalytic properties of the nanomaterial based sensor toward NADH oxidation were studied by electrochemical measurements. Significant enhancement of oxidation current is obtained at electrodes modified by MB‐SWNT‐sol‐gel in comparison with the analogous carbon black and/or graphite composite modified electrode. The usefulness of the nanocomposite material as a matrix for immobilizing enzymes is also demonstrated. Analytical parameters of D ‐lactate biosensors with and without SWNT in the hybrid film were compared demonstrating that performance of the biosensor was significantly improved when introducing SWNT.     

Integral Equations on Function Spaces and Dichotomy on the Real Line

The purpose of this paper is to give new and general characterizations for uniform dichotomy and uniform exponential dichotomy of evolution families on the real line. We consider two general classes denoted and and we prove that if V,W are Banach function spaces with and , then the admissibility of the pair for an evolution family implies the uniform dichotomy of . In addition, we consider a subclass and we prove that if , then the admissibility of the pair implies the uniform exponential dichotomy of the family . This condition becomes necessary if . Finally, we present some applications of the main results.     

Diorganotin(IV) compounds containing 2-(Et2NCH2)C6H4 moieties: Configurational stability in solution and solid state structures

Hypercoordinated diorganotin(IV) dichloride, [2-(Et₂NCH₂)C₆H₄]₂SnCl₂ (1), was prepared by reacting [2-(Et₂NCH₂)C₆H₄]Li with SnCl₄. Halide-exchange reactions between 1 and the appropriate potassium halides gave [2-(Et₂NCH₂)C₆H₄]₂SnX₂ [X = F (2), Br (3), I (4)]. Reaction of 1 with excess of Na₂S gave the cyclo-[{2-(Et₂NCH₂)C₆H₄}₂SnS]₂ (5). The solution behavior of the title compounds in solution was investigated by multinuclear (¹H, ¹³C, ¹⁹F and ¹¹⁹Sn) NMR spectroscopy, including variable temperature studies. Single-crystal X-ray diffraction analysis revealed for all compounds intramolecular N → Sn coordination thus resulting in distorted octahedral (C,N)₂SnX₂ configurations. Planar chirality is observed as result of the non-planarity of the SnC₃N rings; all compounds, however, crystallizing as racemates. The isomers are linked by extensive hydrogen bonds to give different supramolecular architectures in the crystals of compounds 1, 3 and 4.     

Improving the Photoinduced Charge Separation Parameters in Corrole–Perylene Carboximide Dyads by Tuning the Redox and Spectroscopic Properties of the Components

A couple of corrole–perylene carboximide dyads ( C2‐PIa and C2‐PIx ) have been synthesized and their photoreactivity has been evaluated. We aimed at obtaining better performances for photoinduced charge separation, both in terms of efficiency and in terms of lifetime, with respect to formerly studied systems. The energy level of the charge‐separated state was tuned by selecting perylene and corrole components with diverse redox and spectroscopic properties. High spectroscopic energy levels of the perylene carboximide derivatives (PIs) allow a fast charge separation to be maintained in competition with an energy‐transfer process from the PI to the corrole unit. Yields and lifetimes of charge separation in toluene are, respectively, 75 % and 2.5 μs for C2‐PIa and 65 % and 24 ns for C2‐PIx . The results and the effect of solvent polarity are discussed in the framework of current energy‐ and electron‐transfer theories.     

Thermal behaviour and spectroscopic studies of complexes of some divalent transitional metals with 2-benzoil-pyridil-izonicotinoylhydrazone

New complexes of 2-benzoyl-pyridil-isonicotinoylhydrazone (L) with Cu(II), Co(II), Ni(II) and Mn(II), having formula of type [ML₂] SO₄·xH₂O (M = Cu²⁺, Co²⁺, Ni²⁺, x = 2 and M = Mn²⁺, x = 3), have been synthesised and characterised. All complexes were characterised on the basis of elemental analyses, IR spectroscopy, UV–VIS–NIR, EPR, as well as thermal analysis and determination of molar conductivity and magnetic moments. The thermal behaviour of complexes was studied using thermogravimetry (TG), differential thermal analysis (DTA) and differential scanning calorimetry (DSC). The structure of L hydrazone was established by X-ray study on single crystal. The ligand works as tridentate NNO, being coordinated through the azomethine nitrogen, the pyridine nitrogen and carbonylic oxygen. Heats of decomposition, ΔH, associated with the exothermal effects were also determined.     

Synthesis, spectral and thermal studies of new copper (II) complexes with 1,2-di(imino-2-aminomethylpyridil)ethane

New copper (II) complexes of Schiff bases with 1,2-di(imino-2-aminomethylpyridil)ethane with the general composition CuLX _m (H₂O) _x , [L = Schiff base, X = Cl^?, Br^?, NO₃ ^?, ClO₄ ^?, CH₃COO^?, m = 2; X = SO₄ ^2?, m = 1] were prepared by template synthesis. The complexes were characterized by elemental analysis, conductivity measurements, magnetic moments, IR, UV–VIS and EPR spectra. The thermal behavior of complexes was studied using thermogravimetry (TG), differential thermal analysis (DTA) and differential scanning calorimetry (DSC). Infrared spectra of all complexes are in good agreement with the coordination of a neutral tetradentate N₄ ligand to the cooper (II) through azomethinic and pyridinic nitrogen. Magnetic, EPR and electronic spectral studies show a monomeric distorted octahedral geometry for all Cu(II) complexes. Conductance measurements suggest the non-electrolytic nature of the compounds, except for copper (II) nitrate and perchlorate complexes which are 1:2 electrolytes. Heats of decomposition, ΔH, associated with the exothermal effects were also determined.     

Parametrized riccati equations associated to input-output operators for discrete-time systems with state-dependent noise

An input-output linear time-varying discrete system with statedependent noise and mean square exponential stable evolution is considered. It is proved that if the norm of the input-output operator is less than γ then a corresponding parametrized by γ Riccati equation has a unique global bounded and stabilizing solution. An application to the estimate of a stability radius is given     

Helical aquatubes of calix[4]arene di-methoxycarboxylic acid

Two trimeric units of calix[4]arene di-methoxycarboxylic acid form a six-pointed star architecture that, in turn, generates triple helical aquatubes which intermesh between themselves by aromatic-aromatic interdigitation of the macrocycle.     

Observation of the formation of supported bilayers by amphiphilic peptidyl-RNA

Amphiphilic peptidyl-RNA conjugates, molecules that mimic natural peptidyl-transfer RNA, are capable of self-assembling on glass substrates as vesicles and supported bilayers.     

Exponential trichotomy and p-admissibility for evolution families on the real line

The aim of this paper is to obtain necessary and sufficient conditions for uniform exponential trichotomy of evolution families on the real line. We prove that if p ∈ (1,∞) and the pair (C_b(R,X),C_c(R,X)) is uniformly p-admissible for an evolution family ={U(t,s)}_t≥_s then is uniformly exponentially trichotomic. After that we analyze when the uniform p-admissibility of the pair (C_b(R, X), C_c(R, X)) becomes a necessary condition for uniform exponential trichotomy. As applications of these results we study the uniform exponential dichotomy of evolution families. We obtain that in certain conditions, the admissibility of the pair (C_b(R,X),L^p(R,X)) for an evolution family ={U(t,s)}_t≥_s is equivalent with its uniform exponential dichotomy.