Konstantin Bryliakov
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Konstantin Bryliakov
Konstantin P. Bryliakov (born 1 June 1977; ) is a Russian chemist and author of monographs and over 170 research papers, textbooks, and patents. He is a professor at Russian Academy of Sciences and Novosibirsk State University. Biography Bryliakov was born in Yoshkar-Ola, USSR. He studied chemistry at Novosibirsk State University from 1994 to 1999, after which he joined the Boreskov Institute of Catalysis as a PhD student and Novosibirsk State University as a teaching assistant. Academic career Bryliakov received a Cand. Chem. Sci. (PhD) degree in chemical physics from the Voevodsky Institute of Chemical Kinetics and Combustion, Novosibirsk, in 2001, and a Doctor of Chemical Sciences degree (Habilitation) in catalysis from the Boreskov Institute of Catalysis, Novosibirsk, in 2008. He is currently a head of Department of Mechanisms of Catslytic Reactions at the Boreskov Institute of Catalysis (since 2021) and a full professor at Novosibirsk State University (since 2018). In ...
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Yoshkar-Ola
Yoshkar-Ola ( Mari and russian: Йошкар-Ола) is the capital city of the Mari El Republic, Russia. Yoshkar-Ola means “red city” in Mari and was formerly known as Tsaryovokokshaysk () before 1919, as Krasnokokshaysk () between 1919 and 1927 both after the Malaya Kokshaga River and Charla (), by the Mari people. Yoshkar-Ola was established as a military fortress in 1584, following the Russian conquest of the Mari-inhabited regions of the Volga and its tributaries. It is one of the centers of the Mari people (especially of the Meadow Mari subgroup) and the administrative center of the Yoshkar-Ola city district. Demographics Population: History Yoshkar-Ola was established as a military fortress in 1584, following the Russian conquest of the Mari region. Yoshkar-Ola means “red city” in Mari and before 1919 was known as Tsaryovokokshaysk (), between 1919 and 1927 also as Krasnokokshaysk () both after the Malaya Kokshaga River and is known as Charla () amongst t ...
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Habilitation
Habilitation is the highest university degree, or the procedure by which it is achieved, in many European countries. The candidate fulfills a university's set criteria of excellence in research, teaching and further education, usually including a dissertation. The degree, abbreviated "Dr. habil." (Doctor habilitatus) or "PD" (for "Privatdozent"), is a qualification for professorship in those countries. The conferral is usually accompanied by a lecture to a colloquium as well as a public inaugural lecture. History and etymology The term ''habilitation'' is derived from the Medieval Latin , meaning "to make suitable, to fit", from Classical Latin "fit, proper, skillful". The degree developed in Germany in the seventeenth century (). Initially, habilitation was synonymous with "doctoral qualification". The term became synonymous with "post-doctoral qualification" in Germany in the 19th century "when holding a doctorate seemed no longer sufficient to guarantee a proficient transfer o ...
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Homochirality
Homochirality is a uniformity of chirality, or handedness. Objects are chiral when they cannot be superposed on their mirror images. For example, the left and right hands of a human are approximately mirror images of each other but are not their own mirror images, so they are chiral. In biology, 19 of the 20 natural amino acids are homochiral, being L-chiral (left-handed), while sugars are D-chiral (right-handed). Homochirality can also refer to enantiopure substances in which all the constituents are the same enantiomer (a right-handed or left-handed version of an atom or molecule), but some sources discourage this use of the term. It is unclear whether homochirality has a purpose; however, it appears to be a form of information storage. One suggestion is that it reduces entropy barriers in the formation of large organized molecules. It has been experimentally verified that amino acids form large aggregates in larger abundance from an enantiopure samples of the amino acid than fr ...
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Reaction Mechanism
In chemistry, a reaction mechanism is the step by step sequence of elementary reactions by which overall chemical change occurs. A chemical mechanism is a theoretical conjecture that tries to describe in detail what takes place at each stage of an overall chemical reaction. The detailed steps of a reaction are not observable in most cases. The conjectured mechanism is chosen because it is thermodynamically feasible, and has experimental support in isolated intermediates (see next section) or other quantitative and qualitative characteristics of the reaction. It also describes each reactive intermediate, activated complex, and transition state, and which bonds are broken (and in what order), and which bonds are formed (and in what order). A complete mechanism must also explain the reason for the reactants and catalyst used, the stereochemistry observed in reactants and products, all products formed and the amount of each. The electron or arrow pushing method is often used in i ...
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Coordination Polymerization
Coordination polymerisation is a form of polymerization that is catalyzed by transition metal salts and complexes. Types of coordination polymerization of alkenes Heterogeneous Ziegler–Natta polymerization Coordination polymerization started in the 1950s with heterogeneous Ziegler–Natta catalysts based on titanium tetrachloride and organoaluminium co-catalysts. The mixing of TiCl4 with trialkylaluminium complexes produces Ti(III)-containing solids that catalyze the polymerization of ethene and propene. The nature of the catalytic center has been of intense interest but remains uncertain. Many additives and variations have been reported for the original recipes. Homogeneous Ziegler–Natta polymerization In some applications heterogeneous Ziegler–Natta polymerization has been superseded by homogeneous catalysts such as the Kaminsky catalyst discovered in the 1970s. The 1990s brought forward a new range of post-metallocene catalysts. Typical monomers are nonpolar ethene and pro ...
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Biomimetic Synthesis
Biomimetic synthesis is an area of organic chemical synthesis that is specifically biologically inspired. The term encompasses both the testing of a "biogenetic hypothesis" (''conjectured'' course of a biosynthesis in nature) through execution of a series of reactions designed to parallel the proposed biosynthesis, as well as programs of study where a synthetic reaction or reactions aimed at a desired synthetic goal are designed to mimic one or more ''known'' enzymic transformations of an established biosynthetic pathway. The earliest generally cited example of a biomimetic synthesis is Sir Robert Robinson's organic synthesis of the alkaloid tropinone. A more recent example is E.J. Corey's carbenium-mediated cyclization of an engineered linear polyene to provide a tetracyclic steroid ring system, which built upon studies of cationic cyclizations of linear polyenes by the Albert Eschenmoser and Gilbert Stork, and the extensive studies of the W.S. Johnson to define the requireme ...
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Redox
Redox (reduction–oxidation, , ) is a type of chemical reaction in which the oxidation states of substrate (chemistry), substrate change. Oxidation is the loss of Electron, electrons or an increase in the oxidation state, while reduction is the gain of electrons or a decrease in the oxidation state. There are two classes of redox reactions: * ''Electron-transfer'' – Only one (usually) electron flows from the reducing agent to the oxidant. This type of redox reaction is often discussed in terms of redox couples and electrode potentials. * ''Atom transfer'' – An atom transfers from one substrate to another. For example, in the rusting of iron, the oxidation state of iron atoms increases as the iron converts to an oxide, and simultaneously the oxidation state of oxygen decreases as it accepts electrons released by the iron. Although oxidation reactions are commonly associated with the formation of oxides, other chemical species can serve the same function. In hydrogen ...
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Enantioselective Synthesis
Enantioselective synthesis, also called asymmetric synthesis, is a form of chemical synthesis. It is defined by IUPAC as "a chemical reaction (or reaction sequence) in which one or more new elements of chirality are formed in a substrate molecule and which produces the stereoisomeric (enantiomeric or diastereomeric) products in unequal amounts." Put more simply: it is the synthesis of a compound by a method that favors the formation of a specific enantiomer or diastereomer. Enantiomers are stereoisomers that have opposite configurations at every chiral center. Diastereomers are stereoisomers that differ at one or more chiral centers. Enantioselective synthesis is a key process in modern chemistry and is particularly important in the field of pharmaceuticals, as the different enantiomers or diastereomers of a molecule often have different biological activity. Overview Many of the building blocks of biological systems such as sugars and amino acids are produced exclusively as ...
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Green Chemistry
Green chemistry, also called sustainable chemistry, is an area of chemistry and chemical engineering focused on the design of products and processes that minimize or eliminate the use and generation of hazardous substances. While environmental chemistry focuses on the effects of polluting chemicals on nature, green chemistry focuses on the environmental impact of chemistry, including lowering consumption of nonrenewable resources and technological approaches for preventing pollution. The overarching goals of green chemistry—namely, more resource-efficient and inherently safer design of molecules, materials, products, and processes—can be pursued in a wide range of contexts. History Green chemistry emerged from a variety of existing ideas and research efforts (such as atom economy and catalysis) in the period leading up to the 1990s, in the context of increasing attention to problems of chemical pollution and resource depletion. The development of green chemistry in Europe a ...
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ChemCatChem
''ChemCatChem'' is a biweekly peer-reviewed scientific journal covering heterogeneous, homogeneous, and biocatalysis. It is published by Wiley-VCH on behalf of Chemistry Europe. According to the ''Journal Citation Reports'', the journal has a 2021 impact factor The impact factor (IF) or journal impact factor (JIF) of an academic journal is a scientometric index calculated by Clarivate that reflects the yearly mean number of citations of articles published in the last two years in a given journal, as i ... of 5.497. References External links * {{Official website, https://chemistry-europe.onlinelibrary.wiley.com/journal/18673899 Chemistry Europe academic journals Chemistry journals English-language journals Wiley-VCH academic journals Biweekly journals ...
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Arkivoc
''Arkivoc'' (''Archive for Organic Chemistry'') is a peer-reviewed open access scientific journal covering all aspects of organic chemistry. It is published by the non-profit organization Arkat USA, which was established in 2000 through a personal donation from Alan R. Katritzky and Linde Katritzky. ''Arkivoc'' is the primary publication of Arkat USA. According to the ''Journal Citation Reports'', the journal has a 2014 impact factor The impact factor (IF) or journal impact factor (JIF) of an academic journal is a scientometric index calculated by Clarivate that reflects the yearly mean number of citations of articles published in the last two years in a given journal, as i ... of 1.165, ranking it 37th out of 57 journals in the category "Chemistry, Organic". Abstracting and Indexing According to the Journal Citation Reports, the journal has a 2018 impact factor of 1.253. The journal is indexed in Web of Science: Science Citation Index Expanded. References External link ...
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ScienceDirect
ScienceDirect is a website which provides access to a large bibliographic database of scientific and medical publications of the Dutch publisher Elsevier. It hosts over 18 million pieces of content from more than 4,000 academic journals and 30,000 e-books of this publisher. The access to the full-text requires subscription, while the bibliographic metadata is free to read. ScienceDirect is operated by Elsevier. It was launched in March 1997. Usage The journals are grouped into four main sections: ''Physical Sciences and Engineering'', ''Life Sciences'', ''Health Sciences'', and ''Social Sciences and Humanities''. Article abstracts are freely available, and access to their full texts (in PDF and, for newer publications, also HTML) generally requires a subscription or pay-per-view purchase unless the content is freely available in open access. Subscriptions to the overall offering hosted on ScienceDirect, rather than to specific titles it carries, are usually acquired through a ...
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