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Tytuł:
Kataliza procesów hydrosililowania z udziałem cieczy jonowych
Catalysis of hydrosilylation processes with the participation of ionic liquids
Autorzy:
Bartlewicz, Olga
Szymańska, Anna
Jankowska-Wajda, Magdalena
Dąbek, Izabela
Maciejewski, Hieronim
Powiązania:
https://bibliotekanauki.pl/articles/1413312.pdf
Data publikacji:
2021
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
hydrosililowanie
kompleksy Rh
kompleksy Pt
ciecze jonowe
SILPC
kataliza heterogeniczna
hydrosilylation
Rh complexes
Pt complexes
ionic liquids
heterogeneous catalysis
Opis:
Hydrosilylation is a fundamental and elegant method for the laboratory and industrial synthesis of organosilicon compounds. The hydrosilylation reaction is usually performed in a single-phase homogeneous system. A major problem, particularly in homogeneous catalysis, is the separation of catalyst from the reaction mixture. The presence of metals in the reaction products, even in trace quantities, is unacceptable for many applications, therefore efforts have been made at applying heterogeneous catalysts or immobilised metal complexes in order to obtain high catalytic activity and easy product isolation at the same time. One of the methods for producing such catalysts is the employment of ionic liquids as agents for the immobilization of metal complexes. Biphasic catalysis in a liquid-liquid system is an ideal approach through which to combine the advantages of both homogeneous and heterogeneous catalysis. The ionic liquids (ILs) generally form the phase in which the catalyst is dissolved and immobilized. In our research we have obtained a number of catalytic systems of such a type which were based on rhodium and platinum complexes dissolved in phosphonium, imidazolium, pyridinium and ammonium liquids. Currently, there has a common trend to obtain heterogenized systems that combine advantages of homogeneous and heterogeneous catalysis, which makes the hydrosilylation process more cost- effective. Such integration of homo- and heterogeneous catalysts is realized in several variants, as supported IL phase catalysts (SILPC) and solid catalysts with ILs layer (SCILL). Although all the above systems show high catalytic activities, their structure is unknown. This is why we have made attempts to modify selected ionic liquids (corresponding to our most effective systems) and we have applied them as ligands in the synthesis of platinum and rhodium complexes. Another group of catalysts comprises anionic complexes of rhodium and platinum which were obtained by reactions between halide complexes of metals and a respective ionic liquid. Most of the obtained complexes are solids insoluble in hydrosilylation reagents and are characterized by a high catalytic activity. A considerable development of heterogeneous catalysts of this type and their application in many hydrosilylation processes can be expected in the future. This mini-review briefly describes the recent progress in the design and development of catalysts based on the presence of ionic liquids and their applications for hydrosilylation processes.
Źródło:
Wiadomości Chemiczne; 2021, 75, 1-2; 5-29
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Kompleksy metali dużych makrocykli iminowych i aminowych
Metal complexes of large imine and amine macrocycles
Autorzy:
Lisowski, Jerzy
Powiązania:
https://bibliotekanauki.pl/articles/1410886.pdf
Data publikacji:
2021
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
makrocykle
chiralność
kompleksy wielordzeniowe
lantanowce
macrocycles
chirality
polynuclar complexes
lanthanides
Opis:
Macrocyclic complexes continue to attract considerable attention due to their significance in biological systems, catalysis, medical diagnostics and other fields. While the most intensively studied macrocycles containing donor nitrogen atoms are tetraazamacrocycles such as porphyrins or cyclen derivatives, larger macrocyclic ligands containing up to 18 (or even more) donor atoms are also known. Due to their enlarged size, these macrocycles can bind large metal ions such as lanthanide(III) ions or bind multiple metal ions. In this review a subclass of large macrocycles will be discussed i.e. macrocyclic amines and imines that can be generated in the condensation of diamines with dicarbonyl compounds, in particular with 2,6-diformylpyridine or 2,6-diformylphenols. These macrocycles of various sizes lead to a rich variety of structures of metal complexes, including polynuclear complexes. Moreover, macrocycles derived from enantiopure trans-1,2- diaminocylohexane form chiral metal complexes that exhibit unusual effects such as helicity inversion, enantioselective self-recognition or enantiodiscrimination of organic guest molecules.
Źródło:
Wiadomości Chemiczne; 2021, 75, 5-6; 603-629
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Antybiotyki peptydowe i ich kompleksy z jonami metali
Peptide antibiotics and their complexes with metal ions
Autorzy:
Stokowa-Sołtys, K.
Powiązania:
https://bibliotekanauki.pl/articles/171960.pdf
Data publikacji:
2018
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
antybiotyki peptydowe
metaloantybiotyki
kompleksy jonów metali
peptide antibiotics
metalloantibiotic
metal ion complexes
Opis:
Metal ions are essential for numerous antibiotics. They play a crucial role in the mechanism of action and may be involved in specific interactions with cell membrane or target molecules, such as: proteins and nucleic acids. Due to the fact that complexes usually poses a higher positive charge than free ligands, they might interact more tightly with DNA and RNA molecules. However, complexes may also form during antimicrobial agents application, because a lot of them possess functional groups which can bind metal ions present in physiological fluids. Many recent studies support a hypothesis that drugs may alter the serum metal ions concentration. Moreover, it has been shown that numerous complexes with antibiotics can cause DNA degradation, e.g. bleomycin which form stable complexes with redox metal ions and split the nucleic acids chain via the free radicals mechanism. Therefore, it is widely used in cancer therapy.
Źródło:
Wiadomości Chemiczne; 2018, 72, 7-8; 497-522
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Betainy jako akceptory protonu
Betaines as proton-acceptors
Autorzy:
Dega-Szafran, Z.
Szafran, M.
Powiązania:
https://bibliotekanauki.pl/articles/172795.pdf
Data publikacji:
2017
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
betainy
kompleksy z wiązaniem wodorowym
struktura
betaines
hydrogen bonded complexes
molecular structure
Opis:
Ammonium alkanoates (ammonioalkanocarboxylates) are zwitterions (or inner salts, or betaines), because they possess formally charged ammonium and carboxylate groups separated by one or more sp3 carbon atoms. The chemistry of betaines has become a subject of particular interest due to their applications in biological research, especially with regard to their important role in aminoacid synthesis as methyl transfer agents. The crystals of many betaine complexes display interesting physical properties, exhibiting phase transitions with ferroelectric, antiferroelctric and ferroelastic behavior. Betaines containing a hydrophobic chain in the range of 8–20 carbon atoms show the unique properties characteristic for amphoteric surfactants and their current industrial application is in toiletries and personal care products. The conformational structure of zwitterionic molecules depends on several factors. The electrostatic attraction between two charged groups depends strongly on arm flexibility (energy differences between rotational trans and gauche isomers), bulkiness and hydration of charged groups preventing their close approach, solvent and arm electrical properties which control electrostatic attraction between two opposite charged groups, and polarization of solvent around the molecule caused by the dielectric discontinuity between solvent and solute interior (image charge effect). Electrostatic interaction is the common determinant and probably the most important element in structure-reactivity correlation in organic and biological systems. On the other hand, organic compounds are thought to be pure even though they may be a mixture of conformational isomers. This is because the isomers covert rapidly with each other at room temperature and their individual reactivates are little known. Occasionally the conformers may be stabilized in the crystallographic matrixes of polymorphic structures. This article describes structures of seven groups of aliphatic, aromatic and alicyclic betaines and numbers of their new hydrogen-bonded complexes with mineral and organic acids.
Źródło:
Wiadomości Chemiczne; 2017, 71, 7-8; 609-628
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Mimetyki katalazy manganowej w roli syntetycznych antyoksydantów
Mimetics of manganese catalase as synthetic antioxidants
Autorzy:
Zienkiewicz-Machnik, Małgorzata
Barszcz, Barbara
Nosek, Milena
Powiązania:
https://bibliotekanauki.pl/articles/1411167.pdf
Data publikacji:
2021
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
katalaza manganowa
kompleksy manganu
mimetyki katalazy
manganese catalase
manganese complexes
mimics of catalase
Opis:
The coordination chemistry of manganese complexes with heteroaromatic ligands have received considerable attention in modern inorganic chemistry due to its wide range of applications. One of them is related with its potential biological role associated with prevention of oxidative stress injuries. Manganese complexes are one of the most versatile and interesting synthetic systems that can act as artificial mimics of manganese-containing metalloenzymes such as manganese catalase (Mn-CAT). Due to the potential use as catalytic scavengers of H2O2, numerous and diverse, very structurally interesting Mn compounds exhibiting CAT-like activity have been reported so far. In this short review, the relevant features of both, structural, as well as, functional mimics of manganese catalase and their CAT-like activity are presented and some insights into the role of the bridging ligands, endogenous bases, and first- and second-sphere effects on the catalysis are discussed.
Źródło:
Wiadomości Chemiczne; 2021, 75, 3-4; 319-341
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Peptydy jako potencjalne ligandy wiążące jony metali przejściowych
Peptides as potential ligands binding transition metal ions
Autorzy:
Krupa, K.
Lesiów, M. K.
Kowalik-Jankowska, T.
Powiązania:
https://bibliotekanauki.pl/articles/171519.pdf
Data publikacji:
2018
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
peptydy
reszta histydylowa
kompleksy metali
model koordynacyjny
peptides
histidine residue
metal complexes
coordination mode
Opis:
Peptides are crucial ligands for transition metal ions and form complexes with them, that can have important biological activity. Many factors impact on the creation of complexes such as: protection of amine group from N-terminal or carboxylate group from C-terminals of the protein, the presence of noncoordinating and coordinating side chains in the peptide sequence, the number of histidyl residues and their location in the peptide chain. In complexes the metal ion can be bound bound by various donor atoms from amino acids residues (e.g. nitrogen, oxygen or sulphur). In general, the protection of N- or C-terminal groups influences the less stable formation of complexes. Stable complexes are created, if the free amine group from the N-terminal is involved in the coordination process. Peptides with noncoordinating side chains include alanine or glycine. Glycine complexes are more stable than these with alanine. Histidyl residue is the most effective amino acid residue in binding metal ions. The amine group of the lysyl residue, thiol from cysteine or carboxylate from aspartyl or glutamyl residues are also functional groups that coordinate metal ions. The coordination process is initiated by a group that anchors metal ion. A free amine group from N-terminus or imidazole nitrogen are the best examples of anchor groups. The metal ions can also be bound through amide nitrogens, after their forced deprotonation by the anchor group and formation of chelate rings. Peptides containing two or more histidyl residues exhibit high structural diversity in the complexes formation. In addition, these peptides can also form macrochelates and polynuclear complexes. The location of amino acid residues in the peptide chain (especially histydyl residue) also results in the thermodynamically stable formation of complexes.
Źródło:
Wiadomości Chemiczne; 2018, 72, 7-8; 597-608
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
C,N-cyklometalowane kompleksy irydu(III) : wydajne emitery fosforescencyjne dla organicznych diod elektroluminescencyjnych (OLED). Cz. 1 i 2
C,N-cyclometalated iridium(III) complexes : efficient phosphorescent emitters for organic electroluminescent diodes (OLED). Part 1 and 2
Autorzy:
Orwat, Bartosz
Kownacki, Ireneusz
Powiązania:
https://bibliotekanauki.pl/articles/1413294.pdf
Data publikacji:
2021
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
emitery fosforescencyjne
diody elektroluminescencyjne
kompleksy irydu(III)
phosphorescent emitters
light-emitting diodes
iridium(III) complexes
Opis:
Organic electroluminescent panels have been widely available on the commercial market for several years, in the form of screens used in mobile phones, tablets, and TV sets. The display panels are produced in RGB technology, in which iridium(III) coordination compounds act as phosphorescent emitters of red and green light. Because of their high emission quantum efficiency and stability, the emitters containing 2-phenylpyridinato ligands and their derivatives have proved to be particularly useful. An interesting issue was the contrast between an extensive state of knowledge on the abovementioned compounds and a poor state of knowledge on analogous iridium(III) complexes equipped with benzo[h]quinolinato ligands. Application of the latter seemed interesting because of the similar size of benzo[h]quinoline and 2-phenylpyridine coordination pockets, but much more rigid structure and a greater degree of conjugation of the former, which could have a significant impact on the properties of complexes equipped with this type of ligand. Regarding to the above, this dissertation concerns the subject of the design and synthesis of new iridium(III) coordination compounds equipped with a benzo[h]quinoline motif, as well as the analysis of the structural changes impact on the photophysical, electroluminescent, thermal, electrochemical and spectroscopic properties of selected classes of compounds targeted for the application in OLED technology. Accordingly, the article presents the results of studies on two classes of heteroleptic of C,N-cyclometalated iridium(III) complexes, namely, of the salt type with the general formula [Ir(bzq)2(N^N)]+A-, stabilized by structurally different N,N-donating ligands, as well as neutral coordination compounds of the type [Ir(bzq)2(N^O)], bearing N,O-donating ß-ketoiminato ligands in the structure equipped with aryl moieties of various structure. The work included research on the determination of the correlation between the structure of ancillary ligand introduced into the coordination sphere of the metal and the above-mentioned properties. Additionally, based on the results of quantum-chemical calculations, work was undertaken to develop synthetic pathways enabling the incorporation to the C,N-cyclometalating benzo[h]quinoline ligand of substituents characterized by different stereo-electronic properties, enabling the modification of the emission parameters of the target complexes. In the next phase of research, the functionalized precursors of the bzq ligand were successfully used in the synthesis of binuclear complexes, key reagents in the preparation of corresponding mononuclear iridium coordination derivatives with electroluminescent properties.
Źródło:
Wiadomości Chemiczne; 2021, 75, 1-2; 163-231
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Kompleksy jonów metali d- i f-elektronowych z N-tlenkiem pirydyny i związkami pochodnymi : badania spektroskopowe
Complexes of d- and f-metal ions with pyridine N-oxide and its derivatives: spectroscopic studies
Autorzy:
Hnatejko, Z.
Powiązania:
https://bibliotekanauki.pl/articles/171812.pdf
Data publikacji:
2011
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
kompleksy jonów metali
jony metali
N-tlenki pirydyny
spektroskopia
complexes
metal ions
pyridine N-oxides
spectroscopy
Opis:
This article reviews results of studies, collected in the literature, related to complexation abilities of pyridine N-oxides, including forms and properties of dand f-metal ion complexes with this group of ligands. In this paper the synthetic pathways of the ligands, based on an oxidation of the corresponding heterocyclic compounds are presented (Scheme 3) [2, 4, 5]. Substituted pyridine N-oxides form an interesting group of compounds, which have found numerous applications [296-299, 314-318]. They have been used in catalysis, crystal engineering, synthesis of coordination polymers, as well as drugs and components in pharmaceutical chemistry [300-309]. Some of them are useful in destroying of microorganisms and the HIV virus [277, 278, 303-307]. Moreover, they are important compounds in the thermal and photochemical oxidation processes [296-299]. The complexes of metal ions with the N-oxide ligands can be formed by binding an oxygen atom of the N›O group, and/or by binding the substituents present in the aromatic ring, e.g. oxygen atoms of carboxylic groups. The complexes can be obtained in monomeric [64, 159], dimeric [58] or polymeric forms [60, 153, 175]. The formation of polymeric forms is more effective when the distance between the positions of COOH and N›O groups in the aromatic ring increases [168]. Complexes of Ln3+ ions and particularly of Eu3+ with pyridine N-oxides are good luminescent materials, better than their heterocyclic counterparts [180, 211]. The emission intensity of europium ions in these systems depends on the efficiency of the LMCT (ligand-metal charge transfer) and LMET (ligand-metal energy transfer) transitions, as well as on electron-donor properties of the substituents present in the pyridine N-oxide ring [37, 132, 155]. A special role in the complexation of Ln3+ ions plays cryptands, which can encapsulate the metal ion. This process protects the metal ion from a penetration of its first coordination sphere by solvent molecules or counterions [245, 246]. The complexes of europium(III) with macromonocyclic, macrobicyclic and acyclic ligands, equipped with photoactive units such as pyridine N-oxide, 2,2'-bipyridine-N,N'-dioxide or 3,3'-biisoquinoline-2,2'-dioxide in solutions, solid states, and incorporated in a silicate matrices by sol-gel method, gained a lot of attention [247-274].
Źródło:
Wiadomości Chemiczne; 2011, 65, 5-6; 461-501
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Katalizowane cynkiem asymetryczne hydrosililowanie ketonów i imin
Zinc-catalyzed asymmetric hydrosilylation of ketones and imines
Autorzy:
Gajewy, J.
Powiązania:
https://bibliotekanauki.pl/articles/172235.pdf
Data publikacji:
2013
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
kataliza asymetryczna
hydrosililowanie
kompleksy cynku
enancjoselektywność
aktywacja asymetryczna
asymmetric catalysis
hydrosilylation
zinc complexes
enantioselectivity
asymmetric activation
Opis:
One of the fundamental research goals in modern chemistry is the development of efficient and selective procedures to access organic compounds. Among all of the methodologies developed so far, catalysis offers an efficient and economical approach to enantiomericaly pure substances. In particular, transition metal catalysts modified by ligands, usually phosphines, are one of most successful examples of practical catalysis. Unfortunately, most of the applied metals (e.g., Pd, Rh, Ru, Ir) are low abundant, toxic and expensive. For this reason, recent research is focusing on their replacement by cheaper and low toxic metals. For example, the use of zinc can be of great interest, due to its abundance (0.0076% in the earth crust), biological relevance and distinct abilities. In the last two decades many scientific group have been working on finding new, high efficient and inexpensive catalytic system based on zinc for enantioselective transformations. It has been found that many of important organic reactions (for example aldol, Diels-Alder, Friedel-Crafts, Henry reactions) in their asymmetric version can be catalyzed by zinc complexes. One of them is also asymmetric reduction of double carbon-heteroatom bonds through addition of hydride (from silane). Hydrosilylation reduction is a promising alternative for the catalytic transformation of organic molecules to other reduction methods such as: hydrogenation and transfer hydrogenation owing to its operational simplicity and mild conditions. This review will give a general overview of the possible applications of zinc-catalyzed hydrosilylation of carbonyl compounds and imines. Since the understanding of mechanism of reaction is crucial for rational planning of new and more efficient ligands, some part of this article was devoted for mechanical considerations.
Źródło:
Wiadomości Chemiczne; 2013, 67, 5-6; 521-562
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Zastosowanie metod elektrochemicznych w bioanalityce : wybrane zagadnienia
Electrochemical methods in bioanalytics : selected aspects
Autorzy:
Ufnalska, I.
Wiloch, M. Z.
Wesoły, M.
Ćwik, P.
Zabadaj, M.
Ciosek, P.
Wawrzyniak, U. E.
Wróblewski, W.
Powiązania:
https://bibliotekanauki.pl/articles/171732.pdf
Data publikacji:
2015
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
elektrochemia
elektroniczny język
chemometria
kompleksy peptydjony miedzi(II)
warstwy boroorganiczne
electrochemistry
electronic tongue
chemometrics
peptide-copper(II) complexes
boroorganic layers
Opis:
The cooperation of scientists specializing in different fields has given rise to the integration of previously distinct thematic areas and creation of new multidimensional disciplines as a result. Biochemistry, which has derived from the borderline of chemistry and biology, can be set as a good example. In this short review an insight into electrochemical studies, which are currently carried out in the Department of Microbioanalytics at the Faculty of Chemistry (Warsaw University of Technology), was presented. Three independent scientific pathways introducing electrochemical methods for biochemical and bioanalytical purposes can be distinguished among the ongoing researches. The first one embraces the design of the so-called electronic tongue – a system used for the qualitative and quantitative analysis of liquid samples of complex composition. In this work, potentiometric sensor arrays were applied to develop an electronic tongue system enabling the evaluation of the effectiveness of bitter taste masking of pharmaceuticals. The second scientific pathway involves voltammetric studies of the interactions of biologically active peptides with copper(II) ions. The interest was drawn to clarify and describe the role of β-amyloid and NSFRY copper(II) complexes, relevant to Alzheimer’s disease occurrence and cardiovascular system disorder respectively. Finally, boronic acids and their derivatives, exhibiting the affinity for molecules possessing 1,2 or 1,3-diol group in their structure, were used as selective molecular receptors in the third research project. The studies include the selection of the optimal method and conditions of the immobilization process, providing the most favorable receptor layer structure, and the determination of the performances of constructed electrochemical sensor towards particular bioanalytes.
Źródło:
Wiadomości Chemiczne; 2015, 69, 9-10; 931-946
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Luminescencyjne sensory tlenu, ciśnienia i temperatury
Oxygen, pressure and temperature luminescent sensors
Autorzy:
Tsvirko, M.
Kalota, B.
Powiązania:
https://bibliotekanauki.pl/articles/171947.pdf
Data publikacji:
2011
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
luminescencja
metaloporfiryny
kompleksy europu
sensory tlenu
sensory ciśnienia
sensory temperatury
luminescence
metalloporphyrins
europium complexes
oxygen sensors
pressure sensors
temperature sensors
Opis:
Optical chemical sensors enlarge the definition of a classical chemical sensor; they present results in two-dimensional (2D) or three-dimensional (3D) aspect. They can determine parameters of micro and macro scale objects without using a lot of electronic equipment. This article is focused on sensors based on porphyrin derivatives and europium complexes, being the most frequently used substances sensitive to oxygen concentration, pressure and temperature changes. Along with the presentation of characteristics of substances employed to sensors’ construction, also the general principle of luminescent sensors operation, composition and operation range of selected mono- and bifunctional luminescent sensors are described; moreover the selected achievements, such as the “traffic light” sensor are shown.
Źródło:
Wiadomości Chemiczne; 2011, 65, 11-12; 1069-1097
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Kompleksy platyny typu Markó zawierające n-heterocykliczne ligandy karbenowe O właściwościach supersterycznych
Markó-type platinum complexes containing bulky n-heterocyclic carbene ligands
Autorzy:
Bolt, Małgorzata
Żak, Patrycja
Powiązania:
https://bibliotekanauki.pl/articles/1413313.pdf
Data publikacji:
2021
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
N-heterocykliczne ligandy karbenowe
kompleksy platyny
kataliza homogeniczna
hydrosililowanie
dimeryzacja
N-heterocyclic carbene ligands
platinum complexes
homogeneous catalysis
hydrosilylation
dimerization
Opis:
Progress in technology implying increasing demand for advanced materials dedicated for specific application has become a driving force stimulating research in different branches of science. It has been estimated that over 90% highly processed compounds have been obtained by the methods whose pivotal processes take place in the presence of catalysts based on transition metal complexes. Although these processes permit obtaining desired products, they are often charged with numerous drawbacks that prevent their implementation in industry. That is why the search for new catalytic systems ensuring high efficiency of final products and a possibility of reaction control is still an important direction of studies. Markó complexes are a group of platinum(0) coordination compounds of type [(NHC)Pt(dvtms)]. Although much attention has been recently attracted to these class of compounds, their number reported in hitherto literature is still limited. Owing to the possibility of wide modification of NHC carbene ligand attached to metal, the structures, and thus also properties, of the final complexes can be relatively easily matched to the requirements of individual catalytic reactions. It is particularly interesting in view of permanent development of new technologies and still increasing demand for new synthetic methods of more sophisticated materials dedicated to specific applications. In this paper, the synthesis and characterization of Markó type platinum(0) complexes containing bulky N-heterocyclic carbene ligands is described and their applications in the synthesis of new and unknown organic and organosilicon compounds are discussed. The main advantages of these complexes are highlighted providing an overview of this fascinating area of research.
Źródło:
Wiadomości Chemiczne; 2021, 75, 1-2; 31-53
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Białka błony zewnętrznej fusobacterium nucleatum jako potencjalny czynnik promocji nowotworu jelita grubego
Outer membrane proteins of fusobacterium nucleatum as a potential factor of colorectal cancer promotion
Autorzy:
Lesiów, M. K.
Krupa, K.
Komarnicka, U. K.
Walencik, P. K.
Powiązania:
https://bibliotekanauki.pl/articles/171956.pdf
Data publikacji:
2018
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
Fusobacterium nucleatum
białka błony zewnętrznej
kompleksy miedzi(II)
reaktywne formy tlenu
Fusobacteriumnucleatum
outer membrane proteins
copper(II) complexes
reactive oxygen species
Opis:
Fusobacterium nucleatum is a Gram-negative, anaerobic bacterium located in an oral cavity. This bacterium can migrate with blood to the different part of the human body e.g colon. The studies suggest participation of Fn in a colorectal cancer promotion, but a particular mechanism of this disease is still unclear. Colorectal cancer leads to million of new death cases each year. It is third in the worldwide in terms of mortality. The predictions for the coming years are not optimistic. The statistics encourage researchers to know the details of the mechanism of colorectal cancer. It is suggest, that outer membrane proteins of Fn are responsible for development of this disease. Transition metal ions such as Cu(I), Cu(II), Fe(II) can coordinate to proteins and generate free radicals by Fenton reaction. Reactive oxygen species (ROS) destroy important biological macromolecules such as DNA, proteins or lipids and cause different diseases. The paper presents characteristics of Fn and its outer membrane proteins, description of copper(II) complexes and their ability to ROS generation.
Źródło:
Wiadomości Chemiczne; 2018, 72, 7-8; 585-596
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Rozdzielenie mieszanin racemicznych za pomocą krystalizacji. Część 1, Optymalizacja warunków rozdziału
Separation of the racemic mixtures by crystallization. Part 1, Optymlization of resolution conditions
Autorzy:
Kołodziejska, R.
Kopkowska, E.
Studzińska, R.
Karczmarska-Wódzka, A.
Augustyńska, B.
Powiązania:
https://bibliotekanauki.pl/articles/172764.pdf
Data publikacji:
2015
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
krystalizacja
mieszanina racemiczna
rozdzielenie mieszaniny racemicznej
diastereoizomeryczne sole
diastereoizomeryczne kompleksy
crystallization
racemic mixture
resolution of racemic mixture
diastereoisomeric salts
diastereoisomeric complexes
Opis:
Methods for obtaining optically active compounds in enantiopure form are commonly classified into three categories: utilization of chiral pool starting materials (stereoselective multistep synthesis), creation of chirality from achiral precursors (asymmetric synthesis) and separation of racemates into their enantiomer constituents (crystallization, chromatography on chiral phases, kinetic resolution). The most important method for the separation of enantiomers is the crystallization. The crystallization can be carried out in the variants: direct crystallization of enantiomer mixtures (homo- and heterochiral aggregates – Scheme 2, 3) and separation of diastereoisomer mixtures (classical resolution) (Scheme 1) [1–5]. The most widely used method for the separation of enantiomers rests on the crystallization of diastereoisomers formed from a racemate and an enantiopure reagent – resolving agent (resolution via salt-formation and complex-formation). The pair of diastereoisomers exhibit different physicochemical properties (e.g., solubility, melting point, boiling point, adsorbtion, phase distribution). For this reason, the crystalline material can be separated from the residue by filtration (Scheme 22) [4, 27], distillation (Scheme 23, 24) [28, 29], sublimation (Scheme 25) [4, 30], or extraction (Scheme 26) [2, 31]. The composition of crystalline diastereoisomers is influenced by resolving agent (structure (Scheme 4) [4] and amount of resolving agent (Scheme 5) [4]), structure of racemates (Scheme 10) [2, 15], the character and amount of supplementary additives (Scheme 6–9) [4, 12–15], nature of the solvent (crystallization with solvent) – Scheme 11–18 [2, 4, 16–23] and time of crystaillzation (Scheme 19–21) [4, 14, 25, 26].
Źródło:
Wiadomości Chemiczne; 2015, 69, 1-2; 65-88
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Ditlenek węgla w syntezie organicznej
Carbon dioxide in organic synthesis
Autorzy:
Burczyk, B.
Powiązania:
https://bibliotekanauki.pl/articles/172758.pdf
Data publikacji:
2013
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
wiązanie ditlenku węgla
surowce odnawialne
synteza organiczna
kataliza
kompleksy metali przejściowych
carbon dioxide fixation
renewable resources
organic synthesis
catalysis
transition metal complexes
Opis:
Carbon dioxide is an abundant, cheap, almost nontoxic, thermodynamically stable, inert electrophile. Exploitation of CO 2 as a chemical feedstock, although will almost certainly not reduce its atmospheric concentration significantly, aims to generate high-value products and more-efficient processes. In recent years efficient transition-metal complexes have been used to perform homogeneously catalyzed transformations of CO 2 . This paper presents an overview of available catalytic routes for the synthesis of carboxylic acids, lactones, urea and carbamates, linear and cyclic carbonates as well as polycarbonates. Reduction processes of CO 2 are shortly men - tioned as well. C arboxylic acids have been synthesized via : (i) carboxylation of organolithium, organomagnesium (Scheme 2 [35]), organoboron (Scheme 3 [40 -42]), organozinc (Scheme 4 [43, 44]) and organotin (Scheme 5 [45, 46]) compounds; (ii) oxidative cycloaddition of CO 2 to olefins and alkynes (Scheme 6 -10 [47 -50, 57]) catalyzed by Ni(0)-complexes; (iii) transition-metal catalyzed reductive hydrocarboxylation of unsaturated compounds (Scheme 11, 12 [64 -67]); (iv) carboxylation of C-H bond (Scheme 13 [69 -71]). Telomerization of dienes, for instance 1,3-butadiene, and CO 2 in the presence of Ni(II) and Pd(II) complexes leads to lactones and esters of carboxylic acids (Scheme 14, 15 [73 -79]). Nucleophilic ammonia, primary and secondary amines react with CO 2 to give, respectively, urea and carbamic acid esters - carbamates and isocyanates (Scheme 16 -18 [94, 95]), thus eliminating the use of phosgene in their synthesis. CO 2 reacts with alcohols, diols and epoxides in the presence of transition-metal complexes (Fig. 2) and the reaction products are: linear carbonates (Scheme 20, 21 [110 -118]), cyclic carbonates (Scheme 22 -24 [153 -170]) and polycarbonates (Scheme 25, 26, Fig. 3, Tab. 1 [179 -186]). Finally, hydrogenation of CO 2 , leading to the formation of CO, HCOOH, CH 3 OH, CH 4 , C 2 H 6 and C 2 H 4 (Scheme 27), as well as electrochemical and photochemical reductions in the pre - sence of homogeneous and heterogeneous catalysts have been shortly reviewed.
Źródło:
Wiadomości Chemiczne; 2013, 67, 1-2; 1-53
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł

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