Azinyl derivatives of ferrocene and cymantrene. Synthesis and properties

In the present review comparative data concerning various synthetic approaches and methodologies used in the series of ferrocene and cymantrene derivatives to create various materials, namely, catalytic systems, sensory and other molecular devices, polymers as well as physiologically active substances, for the period from 2000 till 2016 are given. Aspects of practical application of the above compounds are also considered.     

Classical and knudsen thermogravimetry to check states and displacements of water in food systems

Water states and displacements can be investigated with thermogravimetry (TG) either in its classical or in the Knudsen version (where standard pans are replaced with Knudsen cells). The case of wheat flour dough is considered in various steps of bread making, namely, mixing, proofing, baking, staling. The split of DTG signals into various components (gaussian functions) support the assumption that the overall dough water is partitioned into various fractions. Few comments are devoted to water displacements during freezing.This revised version was published online in November 2005 with corrections to the Cover Date.     

Capillary electrophoresis and electrochromatography of pesticides and metabolites

Synthetic pesticides are important chemicals since they are widely used to control many types of weeds, insects and other pests in a wide variety of agricultural and nonagricultural settings. This review article is aimed at describing the recent progress made in capillary electrophoresis (CE) and capillary electrochromatography (CEC) of pesticides and their metabolites. The various electrophoretic systems and detection schemes that have been introduced so far for the CE and CEC of pesticides are discussed. Also included in this review article are the various approaches for trace enrichment that are involved in the analysis of dilute pesticide samples.     

Capillary electrophoresis and electrochromatography of pesticides and metabolites

Synthetic pesticides are important chemicals since they are widely used to control many types of weeds, insects, and other pests in a wide variety of agricultural and nonagricultural settings. This review article is aimed at describing the recent progress made in capillary electrophoresis (CE) and capillary electrochromatography (CEC) of pesticides and metabolites. The various electrophoretic systems and detection schemes that were introduced during the period extending from the second half of 1999 to the first half of 2001 for the CE and CEC of pesticides are discussed. Also included in this review article are the various approaches for trace enrichment that are involved in the analysis of dilute pesticide samples.     

Pure and modified TiO2 photocatalysts and their environmental applications

Semiconductor photocatalysis is a process that harnesses light energy in chemical conversions. In particular, its applications to environmental remediation have been intensively investigated. The characteristics of TiO₂, the most popular photocatalyst, is briefly described and selected studies on the degradation/conversion of various recalcitrant pollutants using pure and modified TiO₂ photocatalysts, which were carried out in this group, are reviewed. Photocatalytic reactions are multi-phasic and take place at interfaces of not only water/TiO₂ and air/TiO₂ but also solid/TiO₂. Examples of photocatalytic reactions of various organic and inorganic substrates that are converted through the photocatalytic oxidation or reduction are introduced. TiO₂ has been modified in various ways to improve its photocatalytic activity. Surface modifications of TiO₂ that include surface platinization, surface fluorination, and surface charge alteration are discussed and their applications to pollutants degradation are also described in detail.     

海洋珊瑚中抗肿瘤活性物质及其提取、分离方法

珊瑚主要生长在热带、亚热带海洋中，资源非常丰富且具有显著的生物多样性。研究表明，海洋珊瑚中含有许多结构多样、生理活性独特的次生代谢产物。本文概要地介绍了从珊瑚中发现的具有抗肿瘤活性的各种萜类和甾类化合物的来源、结构、抗肿瘤活性和提取、分离方法，同时展望了海洋药物的研究与开发前景。     

Adhesion and detachment of biological cellsin vitro

Adhesion between biological cells and various surfaces is explained in terms of various models, including coagulation at primary or secondary minima of free energy, macromolecular bridges or matrices, and specialized structures at the surfaces of some cells. These models are used to predict the magnitudes of force necessary to detach a cell in the limiting cases of peeling and simultaneous separation over finite areas of contact. Diverse experimental assays of cellular adhesiveness are reviewed and the forces applied to individual cells are estimated. A very wide range of the forces applied to cells in different assays suggests that different mechanisms of bonding are dominant for different types of cells and surfaces under various conditions of growth and chemical environment. The peeling mode of separation is most consistent with the magnitudes of applied force used experimentally in the detachment of cells.     

Updates on synthesis and biological activities of 1,3,4-oxadiazole: A review

The new era of heterocyclic moieties which are developed in the decades plays a very important role in the treatment of various diseases. Among them are 1,3,4-oxadiazoles, a heterocyclic five-membered ring which plays an vital role in the development of newer medicinal compounds for treating various biological activities, such as proliferation of cells, tuberculosis, allergy, viral diseases, etc. The present review will summarize the various synthetic approaches which will be correlated with the biological activities so that the information in future may be used by many researches to give a path breaking lead in the field of medicinal chemistry.     

Natural and Synthetic Agents Targeting Reactive Carbonyl Species against Metabolic Syndrome

Reactive carbonyl species (RCS) may originate from the oxidation of unsaturated fatty acids and sugar in conditions of pathology. They are known to have high reactivity towards DNA as well as nucleophilic sites of proteins, resulting in cellular dysfunction. It has been considered that various pathological conditions are associated with an increased level of RCS and their reaction products. Thus, regulating the levels of RCS may be associated with the mitigation of various metabolic and neurodegenerative disorders. In order to perform a comprehensive review, various literature databases, including MEDLINE, EMBASE, along with Google Scholar, were utilized to obtain relevant articles. The voluminous review concluded that various synthetic and natural agents are available or in pipeline research that hold tremendous potential to be used as a drug of choice in the therapeutic management of metabolic syndrome, including obesity, dyslipidemia, diabetes, and diabetes-associated complications of atherosclerosis, neuropathy, and nephropathy. From the available data, it may be emphasized that various synthetic agents, such as carnosine and simvastatin, and natural agents, such as polyphenols and terpenoids, can become a drug of choice in the therapeutic management for combating metabolic syndromes that involve RCS in their pathophysiology. Since the RCS are known to regulate the biological processes, future research warrants detailed investigations to decipher the precise mechanism.     

A critical comparison of studies of complex formation between copper(II) and fulvic substances of natural waters

The results obtained by various authors in discussing complex formation between copper(II) and fulvic substances in natural waters are compared; particular attention is given to results obtained in the natural pH range (6–9). The influence of the experimental conditions used for the complexation measurements is discussed, as well as the hypotheses used in interpretation of the data. The ligand concentration, and the possible formation of mixed complexes and precipitation of copper hydroxide, are considered. When these factors are taken into account, a better agreement may be found between the results of the various workers. Further, the relative importance of the various possible reactions may be defined from such a comparison. As a result, various recommendations are given about the features of the experimental conditions that must be considered to obtain meaningful data on complex formation.     

糖类的毛细管电泳及芯片毛细管电泳

 糖类化合物在生物体内发挥多方面的作用。糖研究的复杂性在于其结构的复杂多变。高效毛细管电泳作为一种快速、高效的分离分析手段已广泛应用于糖的研究。芯片毛细管电泳是近几年来发展起来的新的分析技术 ,并已经在生命科学的研究中得到较广泛的应用。就各种糖类化合物的毛细管电泳的分析策略、检测条件及糖类化合物的芯片毛细管电泳进行了阐述 ,共 4 8篇。     

Push-pull structures with a pyrazine core and hexatriene chain: synthesis and light-emitting properties

In this paper, we describe the synthesis of various push-pull molecules with a central pyrazine unit connected to a hexatriene chain terminated by various p-substituted phenyl groups. The key steps involve metallation and subsequent transmetallation of 2-chloro and 2,6-dichloropyrazine followed by a Negishi cross-coupling reaction of the intermediate organozinc derivative with (2E,4E)-5-bromopentadienal. The aldehydes are then submitted to a Wittig reaction with the appropriate phosphonium salts readily obtained from various substituted benzyl alcohols. The light-emitting properties of the so obtained molecules are then investigated in terms of absorption and emission spectra and non-linear optics experiments have been carried out in two cases.     

Fluorescent and luminescent probes for detection of reactive oxygen and nitrogen species

Oxidative and nitrosative stress induced by ROS/RNS play crucial roles in a wide range of physiological processes and are also implicated in various diseases, including cancer and neurodegenerative disorders. Sensitive and selective methods for the detection of ROS/RNS based on fluorescent and luminescent probes are of great use in monitoring the in vivo production of these species and elucidating their biological functions. This critical review highlights recent advances that have been made in the development of fluorescent and luminescent probes employed to monitor various ROS/RNS (132 references).     

Synthesis of racemic sugars and their analogs from dihydropyrans (review)

New methods for the synthesis of glycosides of racemic sugars and some of their derivatives from various dihydropyran compounds are discussed. The problems involved in the preparation of 2-alkoxydihydropyrans with multiple bonds in various positions of the ring and problems of the stereospecificity of the epoxidation and hydroxylation of substituted dihydropyrans are examined. The stereospecificity and regiospecificity of opening of the epoxide ring of a large number of epoxytetrahydropyrans were studied in detail. It is shown that dihydropyran compounds are convenient substrates for the preparation of various racemic deoxy sugars, amino deoxy sugars, and their derivatives.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 867–880, July, 1977. 26, 1976.     

Relationship between the molar volume and enthalpy of formation, polarizability, and ionization potential of CHNO-containing organic substances

A new approach to revealing a relationship between various physicochemical properties of organic compounds is suggested. The basic principle of this approach consists in that deviations of experimental values of various molecular parameters from linear dependences for the constituent elements are due to intramolecular forces of the same nature.     

Structures of silylenoids and effects of metallic and haloid atoms on their stability

The structural characteristics of silylenoids, H2SiMX, where M = Li or Na and X = F or Cl, have been studied by ab initio calculations. H2SiMX can be represented as adducts of silylene H2Si with alkali metal halogenides, MX. The associative energies at different calculational levels of various structures of H2SiMX are given. Effects of metallic and haloid atoms on the stability of various structures of H2SiMX are also discussed in this paper.     

Bone Grafts and Substitutes in Dentistry: A Review of Current Trends and Developments

After tooth loss, bone resorption is irreversible, leaving the area without adequate bone volume for successful implant treatment. Bone grafting is the only solution to reverse dental bone loss and is a well-accepted procedure required in one in every four dental implants. Research and development in materials, design and fabrication technologies have expanded over the years to achieve successful and long-lasting dental implants for tooth substitution. This review will critically present the various dental bone graft and substitute materials that have been used to achieve a successful dental implant. The article also reviews the properties of dental bone grafts and various dental bone substitutes that have been studied or are currently available commercially. The various classifications of bone grafts and substitutes, including natural and synthetic materials, are critically presented, and available commercial products in each category are discussed. Different bone substitute materials, including metals, ceramics, polymers, or their combinations, and their chemical, physical, and biocompatibility properties are explored. Limitations of the available materials are presented, and areas which require further research and development are highlighted. Tissue engineering hybrid constructions with enhanced bone regeneration ability, such as cell-based or growth factor-based bone substitutes, are discussed as an emerging area of development.     

The evaluation and use of properties of individual ions in slution

A critical examination is given of extra-thermodynamic methods for evaluation of properties of individual ions in solution. The ways in which such data may be applied, or are required in various problems concerning specific properties of electrolyte solutions and in the fields of kinetics, electrochemistry, colloid and interfacial chemistry, are outlined. Special attention is given to the problem of evaluation of individual ionic thermodynamic functions for the hydration of ions but, in some cases, corresponding data for nonaqueous solutions are available for discussion and are of interest in a comparative way. The reliability of the various methods is assessed and estimates of numerical values for various individual ionic functions are tabulated. The question of scales of individual ionic radii, on which some of the derived data depend, is also examined. The dependence of various properties for anions and for cations on ionic radius is discussed and data are plotted comparatively. It is shown that for most, but not all, properties, the values for anions are more sensitive to increasing ionic radius than are the values for cations. This behavior, as well as the exceptions, is of theoretical interest. The significance of ion-specific behavior at interfaces is considered and the importance of interactions between ions of like sign of charge is indicated.Presented at the Symposium on Electrolytes, University of Reading, September 13, 1977.     

Environmental and pharmaceutical analysis of dithiocarbamates

The current review aims at a comprehensive survey of analytical methods for the determination of dithiocarbamates (DTCs) in environmental and pharmaceutical samples. Besides parent compounds, analytical approaches for various metabolites and degradation products of DTCs are considered. Special emphasis is given to analyte stability as DTCs are considerably reactive interacting with various organic and inorganic compounds; in addition, depending on the chemical nature of the substance, DTCs are prone to oxidation and hydrolysis under alkaline and acidic conditions, respectively. The review mainly focuses on chromatography but also covers applications in electrophoresis, spectrophotometry, and biosensing.     

Strategies for the determination of the volume and composition of the stationary phase in reversed-phase liquid chromatography

The fundamental difficulties currently impeding the elucidation of retention mechanisms in RPLC are reviewed. The various definitions and conventions concerning void volume and excess adsorption in liquid-solid systems are compared and contrasted. The utility and integrity of various chromatographic methods for the measurement of excess adsorption isotherms of HPLC eluents are discussed. Finally, literature methods for obtaining absolute adsorption data from excess quantities are reviewed and evaluated.