Physicochemical properties of 1,2-epoxycyclopentane

Temperature dependences of density, viscosity, and saturated vapor pressure of 1,2-epoxycyclopentane were studied and approximated by interpolation equations. Its refraction index and chromato-mass-spectroscopy data are given.

     

Correlation of the physicochemical properties of symmetric 1,3-dialkoylamidopropane-based cationic lipids containing single primary and tertiary amine polar head groups with in vitro transfection activity

The physicochemical properties of a novel series of symmetric 1,3-dialkylamidopropane-based cationic amphiphiles [M. Sheikh, J. Feig, B. Gee, S. Li, M. Savva, In vitro lipofection with novel series of symmetric 1,3-dialkoylamidopropane-based cationic surfactants containing single primary and tertiary amine polar head groups, Chem. Phys. Lipids 124 (2003) 49-61] were studied by several techniques, in an effort to correlate cationic lipid structure with transfection efficacy. It was found that only the unsubstituted amine and tertiary amine dioleoyl derivatives 1,3lmp5 and 1,3lmt5, respectively, mediated in vitro transfection activity in the absence of helper lipids. This activity pattern was consistent with ethidium bromide fluorescence quenching studies, which indicated that only these two derivatives bound to and efficiently condense plasmid DNA at physiological pH. Dynamic light scattering indicated that lipoplexes made by these two cationic lipids were relatively small particles below 1 microm, in sharp contrast to lipoplexes bigger than 3 microm composed of saturated cationic derivatives. Transmission electron microscopy studies clearly indicated that cationic lipid dispersions made by saturated derivatives form multilamellar tubules at physiological pH. Calorimetric studies showed that cationic amphiphiles with saturated acyl chains longer than 12 carbons exhibit solid-to-liquid crystalline phase transitions above 37 degrees C. In agreement with the microscopy and calorimetry studies, Langmuir film balance experiments indicated that saturated derivatives with hydrophobic chains longer that 12 carbons are not well hydrated and exist at a chain-ordered state at ambient temperature. Calculation of compressibility moduli from monolayer compression isotherms at 23 degrees C suggested that monolayers made by cationic lipids bearing saturated acyl chains are less compressible relative to those of the dioleoyl derivatives 1,3lmp5 and 1,3lmt5. In conclusion, high hydration, increased fluidity and high elasticity of cationic lipid assemblies in isolation, all correlate with high in vitro transfection activity.     

Synthesis of new cationic lipids from an unsaturated glycoside scaffold

[see structure]. We report the synthesis of new cationic lipids. These amphiphiles present a hydrophobic domain connected to a guanidinium entity by an unsaturated glycoside scaffold. The synthetic strategy using amide or acetal linkage led to various mono- and bicatenar derivatives. Investigation of their physicochemical properties indicated that these new compounds compact DNA.     

Physicochemical properties of new cellulosic Artisdita hystrix leaf fiber

The characterization of new natural fiber is increasing due to its excellent properties. This drives investigators to create high performance composites. The present investigation was designed to study the physicochemical properties of fibers obtained from the leaf of the Artistida hystrix. The Artistida hystrix fibers (AHFs) had crystallinity index (44.85%), cellulose (59.54 wt%), hemicellulose (11.35 wt%), lignin (8.42 wt%), and density (540 kg m^?3). The tensile strength of AHFs was 440 ± 13.4 MPa with an average strain rate of 1.57 ± 0.04%. The calculated microfibril angle of AHFs was 12.64 ± 0.45°, which influenced the mechanical properties.     

Synthesis and photoluminescent properties of new cationic carbazole-containing luminophores

The synthesis of a series of new π-conjugated amphiphilic derivatives of carbazole of the "stilbene" type, substituted with N-alkylpyridinium groups at positions 2 and 7, is described. Due to the presence of polar cationic groups and nonpolar alkyl substituents, the obtained compounds are potentially capable of acting as agents for the transportation of genetic material inside a cell, and the extended and effective conjugation chain leads to the appearance of intense photoluminescence both in solutions and in biological media, making it possible to use them as cell probes. The absorption maxima of the compounds are in the region of 422-450 nm, while the luminescence maxima are in the yellow-green region at 575-617 nm.     

Solution properties and photonuclease activity of cationic bis-porphyrins linked with a series of aliphatic diamines.

The development of efficient photo-induced DNA cleavage agents has been of particular interest for biomedical applications such as cancer photodynamic therapy (PDT). Toward this objective, we synthesized a series of cationic bis-porphyrins with various lengths of diamino alkyl linkage, N,N'-bis[4-[10,15,20-tris(1-methylpyridinium-4-yl)porphyrin-5-yl]benzoyl]oligomethylenediamine hexaiodide. They were expected to show more efficient photocleavage of DNA than unichromophore meso-tetrakis(4-N-methylpyridiniumyl)porphine (TMPyP), which is well known to cleave DNA effectively on illumination. The cationic bis-porphyrins were found to self-aggregate in aqueous solution, and the aggregation property was accounted for by the formation of an intermolecular dimer. Because conservative-type circular dichroism spectra of the bis-porphyrins were induced in the Soret region on binding to calf thymus DNA, we assigned their binding mode to outside self-stacking on the DNA surface. Their photonuclease activity using plasmid DNA decreased as the number of their linker hydrocarbons increased, and was well correlated with their tendency for dimerization. The inhibitory effect of azide anion, N3-, and the enhancement effect of D2O suggest that singlet oxygen was probably involved in the photocleavage of DNA.     

Physicochemical properties and structures of room-temperature ionic liquids. 3. Variation of cationic structures

A series of room-temperature ionic liquids (RTILs) were prepared with different cationic structures, 1-butyl-3-methylimidazolium ([bmim]), 1-butylpyridinium ([bpy]), N-butyl-N-methylpyrrolidinium, ([bmpro]), and N-butyl-N,N,N-trimethylammonium ([(n-C(4)H(9))(CH(3))(3)N]) combined with an anion, bis(trifluoromethane sulfonyl)imide ([(CF(3)SO(2))(2)N]), and the thermal property, density, self-diffusion coefficients of the cation and anion, viscosity, and ionic conductivity were measured over a wide temperature range. The self-diffusion coefficient, viscosity, ionic conductivity, and molar conductivity follow the Vogel-Fulcher-Tamman equation for temperature dependencies, and the best-fit parameters have been estimated, together with the linear fitting parameters for the density. The relative cationic and anionic self-diffusion coefficients for the RTILs, independently determined by the pulsed-field-gradient spin-echo NMR method, appear to be influenced by the shape of the cationic structure. A definite order of the summation of the cationic and anionic diffusion coefficients for the RTILs: [bmim][(CF(3)SO(2))(2)N] > [bpy][(CF(3)SO(2))(2)N] > [bmpro][(CF(3)SO(2))(2)N] > [(n-C(4)H(9))(CH(3))(3)N][(CF(3)SO(2))(2)N], has been observed, which coincides with the reverse order to the viscosity data. The ratio of molar conductivity obtained from the impedance measurements to that calculated by the ionic diffusivity using the Nernst-Einstein equation quantifies the active ions contributing to ionic conduction in the diffusion components and follows the order: [bmpro][(CF(3)SO(2))(2)N] > [(n-C(4)H(9))(CH(3))(3)N][(CF(3)SO(2))(2)N] > [bpy][(CF(3)SO(2))(2)N] > [bmim][(CF(3)SO(2))(2)N] at 30 degrees C.     

Thermal decomposition of a series of 1,2-diazetines

A homologous series of tricyclic diazetines (6a-c), differing by the number of methylene groups in the saturated bridges of the fused carbon bicycles, was synthesized. The DeltaH++ of decomposition for each of the diazetines to afford N2 and the corresponding alkene was determined experimentally: 6a, 31.7; 6b, 39.3; 6c, 38.8 kcal/mol. The ground-state strain energy of each diazetine was estimated utilizing computationally obtained DeltaHf's for each of the experimentally investigated diazetines as well as several other diazetines whose DeltaH++'s had been previously reported in the literature. The sum of the ground-state strain energies and DeltaH++'s of decomposition for all of the diazetines was nearly constant, with an average value of 59 kcal/mol, suggesting that all of the diazetines decompose via the same mechanism. Generally, the higher the ground-state strain energy of the diazetine, the less the DeltaH++ for decomposition. The decomposition transition states for 6a-c and 7 were modeled computationally at the RB3LYP/6-311+G(3df,2p)//UB3LYP/6-31+G(d,p) level. The agreement of the experimentally determined DeltaH++ values with transition-state energies obtained computationally supports the reaction mechanism originally proposed by Yamabe that the elimination process occurs by an unsymmetrical, yet concerted, transition state with strong biradical character.     

Synthesis and ionophore properties of a series of new tetrapyrazolic macrocycles

The synthesis of several macrocycles containing two bipyrazolic subunits, with different cavity sizes and with donor-group-bearing side arms attached, is reported. Their alkali cation binding ability has been studied from two aspects : extraction and transport through an artificial liquid membrane. Macrocycles described here show a high selectivity towards Li⁺ and Na⁺ cations; furthermore one of them is remarkably well adapted to extract selectively and to transport efficiently the lithium cation in competitive conditions.     

Physicochemical properties of alkali-treated new cellulosic fiber from cotton shell

The aim of this present investigation was to identify a new natural fiber from one of the cotton plant’s byproducts, which is chemically modified by alkaline treatment. Its characteristics were examined for the preparation of natural fiber–reinforced polymer composites. The cotton shell fibers (CSFs) were extracted from the cotton shell and its degree of crystallinity, crystallite size, chemical constituents group, and thermal stability were determined by X-ray diffraction, Fourier transform infrared (FTIR) spectroscopy and thermogravimetric analysis. The alkali treatment of CSFs is optimized at 5% (w/v) NaOH aqueous solution with 45 min soaking time.     

Physicochemical properties of a new group of regulatory proteins isolated from various mammal tissues

Russian Chemical Bulletin - The found similarity of the set of physicochemical characteristics of regulatory proteins active in microdoses isolated from various mammal tissues allows them to be...     

Surface-active properties of new cationic gemini surfactants with cyclic spacer

Three cationic gemini surface active compounds of the type (1r,4r)-1,4-dialkyl-1,4-dimethy-l-piperazine-1,4-diium bromide (Ia, Ib, and Ic), were synthesized. They were characterized using elemental analysis and ¹H-NMR spectra. Their surface-active properties were measured in aqueous solutions with different concentrations at different temperatures (25, 40, and 55°C). Various surface measurements of these gemini surfactants, (compared to the conventional one, 1-Dodecyl-1-methylpiperidinium bromide (a)) were estimated, specifically critical micelle concentration (CMC), effectiveness (π_CMC), efficiency (P_C20) as well as maximum surface excess (Γ_max) and minimum surface area (A_min). The measurements of the gemini compounds gave low CMC, high efficiency in reducing the surface tension, and intense adsorption at air/water interface. These surfactants have lower Krafft points and thus better solubility. Thermodynamic data, free energy, entropy, and enthalpy changes (ΔG°, ΔS°, and ΔH°) for micellization at the air/water interface and also for adsorption in the bulk of surface-active solutions were calculated.     

Synthesis and properties of the cationic fluorocarbon emulsifier-free latex in a new micellar system

Cationic fluorocarbon emulsifier-free latex (CFEL) based on hexafluorobutyl methacrylate (FA), styrene, butyl acrylate, and methacrylatoethyl trimethyl ammonium chloride is successfully prepared in a new micellar system in which the fluorinated surface active monomer (FSM) based on isophorone diisocyanate, dodecafluoroheptanol, and allyl polyethylene glycol is used. The chemical structure of FSM is characterized by Fourier transform infrared spectroscopy, ¹H-NMR, and its surface-active properties have been investigated by surface tension determinator. Besides, effect of FSM, FA, and also the curing temperature on the latex and film properties has been investigated by the coagulation ratio (W _c ), precipitation ratio (W _p ), Nano-ZS particle sizer, contact angle, and water absorption ratio, respectively. The results show that the FSM is successfully prepared. The CMC of FSM is 2.37 g L^?1 and the γ _CMC is 26.31mN m^?1 accordingly. The more FSM content makes more stable emulsion and have only little adverse effect on its film properties. When the FSM content increases from 1.05 to 13.11 %, the W _c and W _p decrease by 83.5 and 32.1 %, respectively, and the surface free energy (γ) of CFEL film only increases by 8.3 %. The more FA content makes less stable emulsion but have favorable effect on its film properties. When the FA content increases from 0 to 25.11 %, the γ is decreased by 55.1 %. The curing temperature has much impact on film property. For example, the γ from 27.47 to 20.36 mJ?·?m^?2 when the curing temperature rises from 30 to 110 °C.     

Synthesis, structures and properties of a new series of platinum-diimine-dithiolate complexes

The new square-planar platinum-diimine-dithiolate compounds [Pt(mesBIAN)SS] have been synthesised {mesBIAN = bis(mesityl)biazanaphthenequinone; SS = 1,2-dithiooxalate (dto) , maleonitriledithiolate (mnt) , 1,2-benzenedithiolate (bdt) , 3,4-toluenedithiolate (tdt) and 1,3-dithia-2-thione-4,5-dithiolate (dmit) }, and the X-ray crystal structures of and determined. Cyclic voltammetry reveals that all the compounds form stable anions, and ESR spectroscopy of these anions shows that the SOMO is based upon the mesBIAN ligand; compounds also show a reversible oxidation wave in their CV. Computational studies reveal that charge-transfer processes from orbitals that are combinations of metal and dithiolate ligand to a mesBIAN pi-based LUMO are responsible for the low energy absorptions seen in the UV/visible spectra of these compounds, and that the reverse process is responsible for the observed room-temperature solution luminescence of [Pt(mesBIAN)Cl(2)] and , and . Compounds and , containing aromatic thiolates, were not found to luminesce under the same conditions. Resonance Raman experiments have shown the origin of band-broadening of the lowest-energy absorption band in the absorption spectra of to be due to vibronic structure within one electronic transition.     

Asymmetric synthesis of dialkyloxy-3-alkylammonium cationic lipids

The cationic diether-linked cytofectin DOTMA (available commercially as a mixture, Lipofectin comprised of DOTMA:DOPE, 1:1) and analogues including DIMRIE and DORIE are frequently used for in vitro and in vivo transfections. Despite this wide usage direct synthetic routes to the optical isomers have received little attention to date. Here we describe strategies to synthesize enantiomers of DOTMA and analogues, including an extremely concise procedure to the trimethylammonium salts. One strategy utilized N-protection, as the imine, with concomitant ether formation and deprotection during the workup. Methylation of the 1-amino-2,3-dialkyloxypropane then generated the trimethylammonium cationic lipids directly. This methodology was extended to synthesize a novel headgroup functionalized lipid. A second route was also developed using an alternative chiral synthon.     

Membrane-forming properties of gemini lipids possessing aromatic backbone between the hydrocarbon chains and the cationic headgroup

Membrane-forming properties of five new gemini cationic lipids possessing an aromatic backbone between the headgroup and hydrocarbon chains have been presented. These gemini lipids differ by the number of polymethylene units [-(CH(2))(n)-] between the cationic ammonium -[N(+)(CH(3))(2)]- headgroups. The membrane-forming properties of these gemini lipids have been studied in detail by transmission electron microscopy (TEM), dynamic light scattering (DLS), X-ray diffraction (XRD), high-sensitivity differential scanning calorimetry (DSC), Paldan fluorescence studies, and UV-vis absorption spectroscopy. The electron micrographs and dynamic light scattering of their aqueous suspensions confirmed the formation of vesicular-type aggregates. The vesicle sizes and morphologies were found to depend strongly on the n-value of the spacer. Information on the thermotropic and hydration properties of the resulting vesicles was obtained from differential scanning calorimetry and temperature-dependent Paldan fluorescence studies, respectively. Examination of the thermotropic phase-transition properties of the lipid aggregates revealed interesting features of these lipids, which were found to depend on the length of the spacer chain. Paldan fluorescence studies indicate that the membranes of the gemini lipids are less hydrated as compared to that of the monomeric counterpart in their solid-gel state. In contrast in their fluid, liquid-crystalline phase, the hydration of gemini lipid aggregates was found to depend strongly on the length of the spacer. UV-vis absorption studies suggest an apparent H-type aggregate formation in the gemini lipid membranes in the gel states. In fluid state of the lipid membranes, H-aggregate formation was found to be enhanced depending on the length of the spacer. Such an understanding of the properties upon membrane formation from this new class of gemini lipids will be useful for further development of related gene delivery systems.     

Electro-optical properties of a new series of fluorinated antiferroelectric orthoconic liquid crystalline esters

The electro-optical properties of orthoconic antiferroelectric liquid crystals of some analogues of (S)?MHPOBC ((S)?4?(1?methylheptyloxy)carbonylphenyl 4'-octyloxy-4-biphenylcarboxylate) have been investigated and discussed in terms of the structure property correlations of liquid crystalline molecules. Polarisation field reversal technique has been used for their characterisation. In this study the occurrence of such a high value of spontaneous polarisation (P_s) for the investigated compound is especially noteworthy as they comprise a bulky chiral unit, zigzag ester linkage and polar fluorinated terminal. Lengthening of oligomethylene spacer in the terminal chain and placement of fluorine atom in the molecular core structure leads to reduction in the value of P_s. The P_s data suggest that the nature of the chiral smectic C (SmC*) to smectic A (SmA) phase transition is of second order and the critical exponent β is in the range 0.19–0.34. The ‘V-shaped’ mode or thresholdless switching in such high-polarisation ferroelectric liquid crystals has also been discussed.     

Synthesis and monolayer film of a series of new twin-tailed gemini cationic surfactants at the air/water interface

A series of new dimeric surfactants, twin-tailed gemini surfactants, 2(12)-s-2(12), were successfully prepared and characterized, and their monolayer films investigated by the measurement of surface pressure-area (π-A) and surface pressure-time (π-t) isotherms at the air/water interface by a Langmuir film balance. Compared to their monomeric counterparts, their collapse pressure (γ_collapse) is smaller, whilst all the molecular area parameters are larger. The limited area (A_limited) and the initial area (A_initial) of these twin-tailed gemini surfactants change with increasing spacer length s, and the surface pressure decreases with increasing time. It was also found that the higher the initial surface pressure, the larger the attenuation.      

Physicochemical properties of new cellulosic fibers from the bark of Acacia arabica

With the growing environmental consciousness toward carbon emissions, natural fibers are the best alternative and act as a substitute for synthetic fibers due to their potential properties. New cellulosic fibers were identified from Acacia arabica bark. This study aimed at understanding the characteristics of Acacia arabica fibers (AAFs) extracted from the bark of the A. arabica, and its physicochemical properties were examined by thermal stability analyses, X-ray diffraction, chemical constitutions, and Fourier transform infrared spectroscopy analysis. Cellulose content (68.1 wt%), density (1028 kg m^?3), and crystallinity index (51.72%) properties were identified.