78 research outputs found
Synthesis of three stereoisomers of p-tert-butylthiacalix[4]arene substituted with (ethoxycarbonyl)methoxy and fluorescent 1-amidoanthraquinone fragments
Β© ISUCT Publishing.New tetrasubstituted at the lower rim thiacalix[4]arenes containing both (ethoxycarbonyl)methoxy and 1-amidoanthraquinone fragments in three conformations: cone, partial cone and 1,3-alternate were synthesized. It was shown that depending on the alkali metal cation (sodium, potassium or cesium) in the alkylation of the diester based on p-tert-butylthiacalix[4]arene by 2-bromo-N-(9',10'-dioxo-9',10'-dihydroanthracene-1'-yl)acetamide template effect of metal cation was observed. The fluorescent properties of the obtained compounds were studied
About the Genesis of Pumice Deposits in the Region of Tarbagania and Pemzovaya Mountains in Kamchatka
Π ΡΠ°Π±ΠΎΡΠ΅ ΠΎΠ±ΡΡΠΆΠ΄Π°ΡΡΡΡ ΡΠ΅Π·ΡΠ»ΡΡΠ°ΡΡ ΠΈΠ·ΡΡΠ΅Π½ΠΈΡ ΠΏΠ΅ΠΌΠ·ΠΎΠ²ΡΡ
ΠΎΡΠ»ΠΎΠΆΠ΅Π½ΠΈΠΉ, ΡΠ°ΡΠΏΠΎΠ»ΠΎΠΆΠ΅Π½Π½ΡΡ
Π² ΠΏΡΠΎΠΌΠ΅ΠΆΡΡΠΊΠ΅ ΠΌΠ΅ΠΆΠ΄Ρ Π²ΡΠ»ΠΊΠ°Π½Π°ΠΌΠΈ ΠΠΎΡΠ΅Π»ΡΠΉ ΠΈ ΠΡΡΠ½ΠΎΠ²ΡΠΊΠΈΠΉ Π½Π° ΠΠ°ΠΌΡΠ°ΡΠΊΠ΅. ΠΡΠΈΠ²Π΅Π΄Π΅Π½Ρ ΡΡ
Π΅ΠΌΠ° ΡΠ°ΡΠΏΡΠΎΡΡΡΠ°Π½Π΅Π½ΠΈΡ ΠΏΠ΅ΠΌΠ·ΠΎΠ²ΡΡ
ΠΏΠΎΠΊΡΠΎΠ²ΠΎΠ² ΠΈ ΡΠ΅Π·ΡΠ»ΡΡΠ°ΡΡ ΠΏΠ΅ΡΡΠΎΡ
ΠΈΠΌΠΈΡΠ΅ΡΠΊΠΈΡ
ΠΈ Π³Π΅ΠΎΡ
ΠΈΠΌΠΈΡΠ΅ΡΠΊΠΈΡ
ΠΈΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π½ΠΈΠΉ ΠΏΠ΅ΠΌΠ· ΠΈ ΠΊΠΈΡΠ»ΡΡ
Π»Π°Π². ΠΡΡΠ²Π»Π΅Π½ ΡΡΠ΄ ΠΏΠ΅ΡΡΠΎΠ³Π΅ΠΎΡ
ΠΈΠΌΠΈΡΠ΅ΡΠΊΠΈΡ
ΠΎΡΠΎΠ±Π΅Π½Π½ΠΎΡΡΠ΅ΠΉ ΠΏΠ΅ΠΌΠ·, ΡΠΊΠ°Π·ΡΠ²Π°ΡΡΠΈΡ
Π½Π° ΠΈΡ
Π²Π΅ΡΠΎΡΡΠ½ΡΡ Π³Π΅Π½Π΅ΡΠΈΡΠ΅ΡΠΊΡΡ ΠΎΠ±ΠΎΡΠΎΠ±Π»Π΅Π½Π½ΠΎΡΡΡ.This paper discusses the results of study of pumice deposits between volcanoes Gorely and Mutnovskiy on Kamchatka. A scheme of the pumice sheets is presented. The results of petrochemical and geochemical studies of pumice and acidic lavas of Mutnovsky and Gorely are discussed. A number of petrogeochemical pumice features indicating their possible genetic isolation is revealed
Phosphorylation of p-tert-butyl(thia)calixarenes by ethylene chlorophosphite
The one-step synthesis of a macrocyclic node was performed by the interaction of thiacalix[4]arene with ethylene chlorophosphite; new cyclic derivatives of calix[n]arenes containing phosphorus fragments at the lower rim in the 1,2- (n=4) and 1,2,3-alternate (n=6) configurations were obtained. Β© 2012 Mendeleev Communications. All rights reserved
Selective transmembrane carriers for hydroxycarboxylic acids: Influence of a macrocyclic calix[4]arene platform
Selective transmembrane carriers for a-hydroxy acids, acyclic a-amino phosphonates and calix[4]arenes containing a-aminophosphonate substituents at the lower rim have been synthesized; analytical HPLC has been used to monitor the selective separation of dicarboxylic, a-hydroxy and a-amino acid mixtures by membrane extraction; the attachment of a-aminophosphonate fragments to the macrocyclic calix[4]arene platform results in receptors with markedly modified efficiency and selectivity relative to those of only aminophosphonates. Β© 2012 Mendeleev Communications. All rights reserved
Kinetics and mechanism of the pudovik reaction in the azomethine series: II.1 Hydrolysis and catalysis in the reaction of dialkyl phosphites with benzalaniline
A 31P NMR study show that diisopropyl phosphite and benzalaniline do not react with each other as individual components. Adduct formation is made possible by partial hydrolysis of the dialkyl phosphite
Phosphorus-bridged calixarene phosphites: Dramatic influence of a tert-butyl group at the upper rim of the macrocycle upon anion binding
New cyclic phosphite derivatives of calix[4]arenes in 1,2-alternate configuration were obtained by the interaction of calix[4]arenes with ethylene chlorophosphite; the influence of a tert-butyl group at the upper rim of the macrocycle upon anion binding was shown. Β© 2010 Mendeleev Communications. All rights reserved
Aminophosphonates: Synthesis and practical application
There is an increasing interest in amine derivatives of phosphonic acids. The Ξ±- aminophosphonates, organophosphorus analogs of natural amino acids are most studied and attracted for the specialists in various branches of chemistry - biochemists, pharmacologists and synthetic chemists. Phosphonates containing the amine group in the Ξ²-position are less studied but recent studies suggest they may be useful as bioactive species and receptor compounds. Phosphonic acid derivatives are not only biologically active compounds but also effective extractants and membrane carriers for various substrates (metal ions, organic and inorganic acids, etc.). Many of these advantages are due to the combination of several different binding sites, namely, proton donating (NH) and two proton accepting groups (P=O and a lone electron pair of the nitrogen atom), as well as the possibility of varying the lipophilicity and sterical loading of the binding site. The acceptor phosphoryl group of the Ξ²-aminophosphonates is farther away from the nitrogen than that of the Ξ±-aminophosphonates. Hence the increased basicity of the nitrogen atom leads to the peculiar transport properties of these compounds. This chapter discusses the main methods for synthesizing Ξ±- and Ξ²-amine derivatives of phosphonic acids, their biological activity and the application of these compounds as extractants and membrane carriers. Β© 2012 by Nova Science Publishers, Inc. All rights reserved
Β«ΠΠ΅Π»Π΅Π½ΡΠΉΒ» ΠΊΡΠ΅Π΄ΠΈΡ ΠΊΠ°ΠΊ ΠΈΠ½ΡΡΡΡΠΌΠ΅Π½Ρ Β«Π·Π΅Π»Π΅Π½ΠΎΠ³ΠΎΒ» ΡΠΈΠ½Π°Π½ΡΠΈΡΠΎΠ²Π°Π½ΠΈΡ
The article describes one of the main tools of green financing β the green loan. This is a loan designed for environmental projects related to agriculture, renewable energy sources, environmentally friendly industry, etc. The tasks are to analyze the current research on this topic, to study the regulatory aspects of green lending, its main types, impact on the bank economic indicators, advantages and disadvantages. The analysis of the current research has shown insufficient development of the idea of the green loan. It is only the theoretical aspect of its influence on the bank activities that has been defined, not its practical effect. The authors studied the green loan impact on the results of the bank activities on the example of overdue loans. For the analysis, they used the panel data of 10 out of 24 largest banks in China in 2012β2017. The evaluation is based on a random effects model. The calculations have been done by means of the generalized least-squares method in MSEXCEL. It has been revealed that green loans in the loan portfolio of the bank contribute to the overdue loans decrease. It has been determined that the main factors influencing the decision making by the borrower and the lender are reputation, public, equity and regulatory pressure, alternative capital pools, credit profiles, availability, capital requirements. However, there is no standard credit documentation for the green loan today. To make this financial tool efficient and sound, it is necessary to further develop regulations, to change approaches to disclosing information on sustainability issues in the non-financial part of annual reporting. The authors have made a conclusion about the rapid development and expansion of the green loan due to the flexible conditions for its provision and availability.Π ΡΡΠ°ΡΡΠ΅ ΡΠ°ΡΡΠΌΠΎΡΡΠ΅Π½ ΠΎΠ΄ΠΈΠ½ ΠΈΠ· Π³Π»Π°Π²Π½ΡΡ
ΠΈΠ½ΡΡΡΡΠΌΠ΅Π½ΡΠΎΠ² Β«Π·Π΅Π»Π΅Π½ΠΎΠ³ΠΎΒ» ΡΠΈΠ½Π°Π½ΡΠΈΡΠΎΠ²Π°Π½ΠΈΡ β Β«Π·Π΅Π»Π΅Π½ΡΠΉΒ» ΠΊΡΠ΅Π΄ΠΈΡ. ΠΡΠΎ ΠΊΡΠ΅Π΄ΠΈΡ, ΠΏΡΠ΅Π΄Π½Π°Π·Π½Π°ΡΠ΅Π½Π½ΡΠΉ Π΄Π»Ρ ΡΠΊΠΎΠ»ΠΎΠ³ΠΈΡΠ΅ΡΠΊΠΈΡ
ΠΏΡΠΎΠ΅ΠΊΡΠΎΠ², ΡΠ²ΡΠ·Π°Π½Π½ΡΡ
Ρ ΡΠ΅Π»ΡΡΠΊΠΈΠΌ Ρ
ΠΎΠ·ΡΠΉΡΡΠ²ΠΎΠΌ, Π²ΠΎΠ·ΠΎΠ±Π½ΠΎΠ²Π»ΡΠ΅ΠΌΡΠΌΠΈ ΠΈΡΡΠΎΡΠ½ΠΈΠΊΠ°ΠΌΠΈ ΡΠ½Π΅ΡΠ³ΠΈΠΈ, ΡΠΊΠΎΠ»ΠΎΠ³ΠΈΡΠ΅ΡΠΊΠΈ ΡΠΈΡΡΠΎΠΉ ΠΏΡΠΎΠΌΡΡΠ»Π΅Π½Π½ΠΎΡΡΡΡ ΠΈ Π΄Ρ. ΠΠΎΡΡΠ°Π²Π»Π΅Π½Ρ Π·Π°Π΄Π°ΡΠΈ: ΠΏΡΠΎΠ°Π½Π°Π»ΠΈΠ·ΠΈΡΠΎΠ²Π°ΡΡ ΡΡΡΠ΅ΡΡΠ²ΡΡΡΠΈΠ΅ ΠΈΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π½ΠΈΡ ΠΏΠΎ Π΄Π°Π½Π½ΠΎΠΉ ΡΠ΅ΠΌΠ΅, ΠΈΡΡΠ»Π΅Π΄ΠΎΠ²Π°ΡΡ ΡΠ΅Π³ΡΠ»ΠΈΡΡΡΡΠΈΠ΅ Π°ΡΠΏΠ΅ΠΊΡΡ Β«Π·Π΅Π»Π΅Π½ΠΎΠ³ΠΎΒ» ΠΊΡΠ΅Π΄ΠΈΡΠΎΠ²Π°Π½ΠΈΡ, Π΅Π³ΠΎ ΠΎΡΠ½ΠΎΠ²Π½ΡΠ΅ Π²ΠΈΠ΄Ρ, Π²Π»ΠΈΡΠ½ΠΈΠ΅ Π½Π° ΡΠΊΠΎΠ½ΠΎΠΌΠΈΡΠ΅ΡΠΊΠΈΠ΅ ΠΏΠΎΠΊΠ°Π·Π°ΡΠ΅Π»ΠΈ Π±Π°Π½ΠΊΠ°, ΠΏΡΠ΅ΠΈΠΌΡΡΠ΅ΡΡΠ²Π° ΠΈ Π½Π΅Π΄ΠΎΡΡΠ°ΡΠΊΠΈ. ΠΠ½Π°Π»ΠΈΠ· ΡΡΡΠ΅ΡΡΠ²ΡΡΡΠΈΡ
ΠΈΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π½ΠΈΠΉ ΠΏΠΎΠΊΠ°Π·Π°Π» Π½Π΅Π΄ΠΎΡΡΠ°ΡΠΎΡΠ½ΡΡ ΠΏΡΠΎΡΠ°Π±ΠΎΡΠΊΡ ΡΡΡΠ½ΠΎΡΡΠΈ Β«Π·Π΅Π»Π΅Π½ΠΎΠ³ΠΎΒ» ΠΊΡΠ΅Π΄ΠΈΡΠ°. ΠΠΏΡΠ΅Π΄Π΅Π»Π΅Π½ ΡΠΎΠ»ΡΠΊΠΎ ΡΠ΅ΠΎΡΠ΅ΡΠΈΡΠ΅ΡΠΊΠΈΠΉ Π°ΡΠΏΠ΅ΠΊΡ Π΅Π³ΠΎ Π²Π»ΠΈΡΠ½ΠΈΡ Π½Π° Π΄Π΅ΡΡΠ΅Π»ΡΠ½ΠΎΡΡΡ Π±Π°Π½ΠΊΠ° Π±Π΅Π· ΠΎΡΠ΅Π½ΠΊΠΈ ΠΏΡΠ°ΠΊΡΠΈΡΠ΅ΡΠΊΠΎΠ³ΠΎ ΡΡΡΠ΅ΠΊΡΠ°. ΠΠ²ΡΠΎΡΡ ΠΈΠ·ΡΡΠΈΠ»ΠΈ Π²Π»ΠΈΡΠ½ΠΈΠ΅ Β«Π·Π΅Π»Π΅Π½ΠΎΠ³ΠΎΒ» ΠΊΡΠ΅Π΄ΠΈΡΠ° Π½Π° ΡΠ΅Π·ΡΠ»ΡΡΠ°ΡΡ ΡΠ°Π±ΠΎΡΡ Π±Π°Π½ΠΊΠ° Π½Π° ΠΏΡΠΈΠΌΠ΅ΡΠ΅ ΠΏΠΎΠΊΠ°Π·Π°ΡΠ΅Π»Ρ ΠΏΡΠΎΡΡΠΎΡΠ΅Π½Π½ΡΡ
ΠΊΡΠ΅Π΄ΠΈΡΠΎΠ². ΠΠ»Ρ Π°Π½Π°Π»ΠΈΠ·Π° ΠΈΡΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π½Ρ ΠΏΠ°Π½Π΅Π»ΡΠ½ΡΠ΅ Π΄Π°Π½Π½ΡΠ΅ Π΄Π΅ΡΡΡΠΈ ΠΈΠ· 24 ΠΊΡΡΠΏΠ½Π΅ΠΉΡΠΈΡ
Π±Π°Π½ΠΊΠΎΠ² ΠΠΈΡΠ°Ρ Ρ 2012 ΠΏΠΎ 2017 Π³. ΠΡΠ΅Π½ΠΊΠ° ΠΎΡΡΡΠ΅ΡΡΠ²Π»Π΅Π½Π° Π½Π° ΠΎΡΠ½ΠΎΠ²Π΅ ΠΌΠΎΠ΄Π΅Π»ΠΈ ΡΠΎ ΡΠ»ΡΡΠ°ΠΉΠ½ΡΠΌΠΈ ΡΡΡΠ΅ΠΊΡΠ°ΠΌΠΈ. Π Π°ΡΡΠ΅ΡΡ ΠΏΡΠΎΠ²Π΅Π΄Π΅Π½Ρ Ρ ΠΈΡΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π½ΠΈΠ΅ΠΌ ΠΎΠ±ΠΎΠ±ΡΠ΅Π½Π½ΠΎΠ³ΠΎ ΠΌΠ΅ΡΠΎΠ΄Π° Π½Π°ΠΈΠΌΠ΅Π½ΡΡΠΈΡ
ΠΊΠ²Π°Π΄ΡΠ°ΡΠΎΠ² Π² MSEXCEL. ΠΡΡΠ²Π»Π΅Π½ΠΎ, ΡΡΠΎ ΠΏΡΠΈΡΡΡΡΡΠ²ΠΈΠ΅ Β«Π·Π΅Π»Π΅Π½ΡΡ
Β» ΠΊΡΠ΅Π΄ΠΈΡΠΎΠ² Π² ΠΊΡΠ΅Π΄ΠΈΡΠ½ΠΎΠΌ ΠΏΠΎΡΡΡΠ΅Π»Π΅ Π±Π°Π½ΠΊΠ° ΡΠΏΠΎΡΠΎΠ±ΡΡΠ²ΡΠ΅Ρ ΡΠ½ΠΈΠΆΠ΅Π½ΠΈΡ ΠΏΠΎΠΊΠ°Π·Π°ΡΠ΅Π»Ρ ΠΏΡΠΎΡΡΠΎΡΠ΅Π½Π½ΡΡ
ΠΊΡΠ΅Π΄ΠΈΡΠΎΠ². ΠΠΏΡΠ΅Π΄Π΅Π»Π΅Π½ΠΎ, ΡΡΠΎ ΠΎΡΠ½ΠΎΠ²Π½ΡΠΌΠΈ ΡΠ°ΠΊΡΠΎΡΠ°ΠΌΠΈ, Π²Π»ΠΈΡΡΡΠΈΠΌΠΈ Π½Π° ΠΏΡΠΈΠ½ΡΡΠΈΠ΅ ΡΠ΅ΡΠ΅Π½ΠΈΡ Π·Π°Π΅ΠΌΡΠΈΠΊΠΎΠΌ ΠΈ ΠΊΡΠ΅Π΄ΠΈΡΠΎΡΠΎΠΌ, ΡΠ²Π»ΡΡΡΡΡ ΡΠ΅ΠΏΡΡΠ°ΡΠΈΡ, ΠΎΠ±ΡΠ΅ΡΡΠ²Π΅Π½Π½ΠΎΠ΅, Π°ΠΊΡΠΈΠΎΠ½Π΅ΡΠ½ΠΎΠ΅ ΠΈ Π½ΠΎΡΠΌΠ°ΡΠΈΠ²Π½ΠΎΠ΅ Π΄Π°Π²Π»Π΅Π½ΠΈΠ΅, Π°Π»ΡΡΠ΅ΡΠ½Π°ΡΠΈΠ²Π½ΡΠ΅ ΠΏΡΠ»Ρ ΠΊΠ°ΠΏΠΈΡΠ°Π»Π°, ΠΊΡΠ΅Π΄ΠΈΡΠ½ΡΠ΅ ΠΏΡΠΎΡΠΈΠ»ΠΈ, Π΄ΠΎΡΡΡΠΏΠ½ΠΎΡΡΡ, ΡΡΠ΅Π±ΠΎΠ²Π°Π½ΠΈΡ ΠΊ ΠΊΠ°ΠΏΠΈΡΠ°Π»Ρ. ΠΠ΄Π½Π°ΠΊΠΎ ΡΠ΅ΠΉΡΠ°Ρ ΠΎΡΡΡΡΡΡΠ²ΡΠ΅Ρ ΡΡΠ°Π½Π΄Π°ΡΡ ΠΊΡΠ΅Π΄ΠΈΡΠ½ΠΎΠΉ Π΄ΠΎΠΊΡΠΌΠ΅Π½ΡΠ°ΡΠΈΠΈ Π΄Π»Ρ Β«Π·Π΅Π»Π΅Π½ΠΎΠ³ΠΎΒ» ΠΊΡΠ΅Π΄ΠΈΡΠ°. ΠΠ»Ρ ΡΡΡΠ΅ΠΊΡΠΈΠ²Π½ΠΎΡΡΠΈ ΠΈ ΡΠ΅Π»Π΅ΡΠΎΠΎΠ±ΡΠ°Π·Π½ΠΎΡΡΠΈ Π΄Π°Π½Π½ΠΎΠ³ΠΎ ΡΠΈΠ½Π°Π½ΡΠΎΠ²ΠΎΠ³ΠΎ ΠΈΠ½ΡΡΡΡΠΌΠ΅Π½ΡΠ° Π½Π΅ΠΎΠ±Ρ
ΠΎΠ΄ΠΈΠΌΠΎ Π΄Π°Π»ΡΠ½Π΅ΠΉΡΠ΅Π΅ ΡΠ°Π·Π²ΠΈΡΠΈΠ΅ Π½ΠΎΡΠΌΠ°ΡΠΈΠ²Π½ΡΡ
ΡΠ΅Π³ΡΠ»ΠΈΡΡΡΡΠΈΡ
ΠΏΠΎΠ»ΠΎΠΆΠ΅Π½ΠΈΠΉ, ΠΈΠ·ΠΌΠ΅Π½Π΅Π½ΠΈΠ΅ ΠΏΠΎΠ΄Ρ
ΠΎΠ΄ΠΎΠ² ΠΊ ΡΠ°ΡΠΊΡΡΡΠΈΡ ΠΈΠ½ΡΠΎΡΠΌΠ°ΡΠΈΠΈ ΠΏΠΎ Π²ΠΎΠΏΡΠΎΡΠ°ΠΌ ΡΡΡΠΎΠΉΡΠΈΠ²ΠΎΡΡΠΈ Π² Π½Π΅ΡΠΈΠ½Π°Π½ΡΠΎΠ²ΠΎΠΉ ΡΠ°ΡΡΠΈ Π² ΡΠ°ΠΌΠΊΠ°Ρ
Π³ΠΎΠ΄ΠΎΠ²ΠΎΠΉ ΠΎΡΡΠ΅ΡΠ½ΠΎΡΡΠΈ. Π‘Π΄Π΅Π»Π°Π½ Π²ΡΠ²ΠΎΠ΄ ΠΎ Π±ΡΡΡΡΠΎΠΌ ΡΠ°Π·Π²ΠΈΡΠΈΠΈ ΠΈ ΡΠ°ΡΡΠΈΡΠ΅Π½ΠΈΠΈ ΠΏΡΠ°ΠΊΡΠΈΠΊΠΈ ΠΈΡΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π½ΠΈΡ Β«Π·Π΅Π»Π΅Π½ΠΎΠ³ΠΎΒ» ΠΊΡΠ΅Π΄ΠΈΡΠ°, ΡΡΠΎ ΠΎΠ±ΡΡΠ»ΠΎΠ²Π»Π΅Π½ΠΎ Π³ΠΈΠ±ΠΊΠΎΡΡΡΡ ΡΡΠ»ΠΎΠ²ΠΈΠΉ Π΅Π³ΠΎ ΠΏΡΠ΅Π΄ΠΎΡΡΠ°Π²Π»Π΅Π½ΠΈΡ ΠΈ Π΄ΠΎΡΡΡΠΏΠ½ΠΎΡΡΡ
Synthesis and spatial structure of novel organosilicon derivatives of p-tert-butylthiacalix[4]arene from two-dimensional NMR data
New organosilicon derivatives of p-tert-butylthiacalix[4]arene with one or two ring fragments at the macrocycle lower rim were synthesized. The spatial structures of the resulting compounds were established by two-dimensional NMR spectroscopy. On going from the methyl substituents at the silicon atom to phenyl substituents, closure of the second silicon-containing ring is hampered because of steric hindrance in the reaction site. Β© 2007 Springer Science+Business Media, Inc
Synthesis and fluorescence properties of lower rim functionalized p-tert-butyl thiacalix[4]arenes containing anthraquinone and n,n-diethylacetamide fragments
It was shown that the chemo- and stereoselective alkylation of the lower rim 1,3-disubstituted p-tert-butyl thiacalix[4] arenes in the cone conformation using 2-chloro-N,N-diethylacetamide is determined by both the nature of the base and the position of the anthraquinone fragment in relation to the amide group: in the case of the 1-amidoanthraquinone derivative, tetrasubstituted products are produced, and in the case of the 2-amidoanthraquinone derivative, trisubstituted macrocycles are formed. It was established that the introduction of N,N-diethylacetamide fragments at the lower rim of 1,3-disubstituted macrocycles leads to an increase in the fluorescence intensity of the synthesized compounds. Β© ISUCT Publishing
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