Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

English (EN)·Polski (PL)·Yкраїнський (UK)
Przejdź do strony domowej biblioteki Centralna Biblioteka Wojskowa Link otwiera się w nowym oknie Logo biblioteki Prolib Integro - strona głównaCentralna Biblioteka Wojskowa

Wyszukujesz frazę "NMR spectra" wg kryterium: Wszystkie pola

  Lista filtrów
Wyrównaj
    Wyświetlanie 1-8 z 8
    Tytuł:
    Hammett spectral correlations in benzofuranyl flavonols
    Autorzy:
    Thirunarayanan, G.
    Sekar, K. G.
    Powiązania:
    https://bibliotekanauki.pl/articles/412326.pdf
    Data publikacji:
    2014
    Wydawca:
    Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
    Tematy:
    Benzofuranyl flavonols
    Hammett equation
    IR spectra
    NMR spectra
    Regression analysis
    Opis:
    A series containing eleven benzofuranyl flavonols have been prepared by cyclization of 3-hydroxybenzofuranyl chalcones with 30 % hydrogen peroxide in the presence of sodium bicarbonate. The synthesized flavonols were characterized by their physical constants, analytical and spectroscopic data. The infrared spectral νOH, CO stretches(cm-1), NMR chemical shifts of OH, CO(δ, ppm) of these flavonols were assigned and correlated with Hammett substituent constants, F and R parameters using single and multi linear regression analysis. From the results of statistical analyses, the effects of substituents on the above group frequencies were discussed.
    Źródło:
    International Letters of Chemistry, Physics and Astronomy; 2014, 6; 39-47
    2299-3843
    Pojawia się w:
    International Letters of Chemistry, Physics and Astronomy
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Infrared and NMR spectral Hammett correlations in 4-(2-naphthyl)-5,6-dihydro-6-(substituted phenyl)-4H-1,3-oxazine-2-amines
    Autorzy:
    Thirunarayanan, G.
    Pazhamalai, S.
    Sekar, K. G.
    Powiązania:
    https://bibliotekanauki.pl/articles/411654.pdf
    Data publikacji:
    2014
    Wydawca:
    Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
    Tematy:
    Oxazine-2-amines
    IR and NMR spectra
    Hammett equation
    Correlation analysis
    Opis:
    A series containing ten titled compounds have been synthesised and recorded the IR and NMR spectra. From the spectra the infrared νNH, C=N, C-O-C stretches, NMR chemical shifts of (δ, ppm) NH and C=N were assigned and correlated with Hammett substituent constants, F and R parameters using single regression analysis. From the results, the effects of substituent on the above spectral frequencies were discussed.
    Źródło:
    International Letters of Chemistry, Physics and Astronomy; 2014, 8; 38-46
    2299-3843
    Pojawia się w:
    International Letters of Chemistry, Physics and Astronomy
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Synthesis, spectral studies and antimicrobial activities of some substituted (E)-1-benzylidene-2-(4-bromophenyl)hydrazines
    Autorzy:
    Rajarajan, M.
    Senbagam, R.
    Vijayakumar, R.
    Manikandan, V.
    Balaji, S.
    Vanangamudi, G.
    Thirunarayanan, G.
    Powiązania:
    https://bibliotekanauki.pl/articles/1194024.pdf
    Data publikacji:
    2015
    Wydawca:
    Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
    Tematy:
    Antimicrobial study
    Hammett equation
    Hydrazone
    IR spectra
    NMR spectra
    Synthesis
    UV
    Opis:
    A series of nine number of (E)-1-benzylidene-2-(4-bromophenyl)hydrazine compounds have been synthesized by the condensation reaction of 4-bromo phenylhydrazine with varies m- and p- substituted benzaldehydes using acetic acid catalyst were refluxed for 4h with 20 mL of absolute ethanol. The yield of synthesized (E)-1-benzylidene-2-(4-bromophenyl)hydrazine compounds are more than 80%. The synthesized (E)-1-benzylidene-2-(4-bromophenyl)hydrazines have been characterized by UV, IR, 1H and 13C spectral data. These UV, IR and NMR spectral data have been correlated with varies Hammett substituted constant and Swain-Lupton F and R parameters using single and multi- regression analysis. From the results of statistical analysis, the effects of substituent have been studied. The antimicrobial activity of all the synthesized substituted (E)-1-benzylidene-2-(4-bromophenyl)hydrazines have been evaluated using Bayer-Kirby method.
    Źródło:
    World Scientific News; 2015, 9; 144-160
    2392-2192
    Pojawia się w:
    World Scientific News
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Spectral correlations in some substituted styryl (E)-4-((2-oxopropyl) diazenyl) benzoic acids
    Autorzy:
    Sathiyendiran, V.
    Sekar, K. G.
    Thirunarayanan, G.
    Arulkumaran, R.
    Sundararajan, R.
    Kamalakkannan, D.
    Suresh, R.
    Manikanadan, V.
    Vijayakumar, R.
    Vanangamudi, G.
    Powiązania:
    https://bibliotekanauki.pl/articles/412199.pdf
    Data publikacji:
    2014
    Wydawca:
    Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
    Tematy:
    Oxo-propyl diazenyl benzoic acid chalcones
    IR spectra
    NMR spectra
    Hammett equation
    Regression analysis
    Opis:
    A series of titled compounds were prepared and analyzed their purities by literature method. The infrared and NMR spectral group frequencies of the compounds were assigned and correlated with Hammett substituent constants, F and R constants using single and multi linear regression analysis. From the results of statistical analysis, the effect of substituents on the above spectral frequencies was discussed.
    Źródło:
    International Letters of Chemistry, Physics and Astronomy; 2014, 11, 1; 33-43
    2299-3843
    Pojawia się w:
    International Letters of Chemistry, Physics and Astronomy
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Study of IR and NMR spectral correlations and biological evaluation of 4-(6-ethyl-2-(substituted phenyl)-6H-pyrido[3,2-b]carbazol-4-yl) aniline derivatives
    Autorzy:
    Thirunarayanan, Ganesamoorthy
    Powiązania:
    https://bibliotekanauki.pl/articles/1189992.pdf
    Data publikacji:
    2016
    Wydawca:
    Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
    Tematy:
    IR and NMR spectra
    Substituent effects
    Hammett equation
    Antibacterial activity
    Antifungal activity
    pyrido[3
    2-b]carbazol-4-yl) aniline
    Opis:
    A series of seven titled compounds have been prepared and their purities were examined by literature method. The characteristic infrared stretching frequencies (, cm-1) and the NMR chemical shifts (, ppm) of these anilines were assigned. These assigned spectral data were correlated with Hammett substituent constants, F and R parameters using single and multi-regression analysis. From the statistical results the effect of substituents on the spectral data have been discussed. The antimicrobial activities of these aniline derivatives have been evaluated by Bauer-Kirby disc-diffusion method.
    Źródło:
    World Scientific News; 2016, 52; 228-246
    2392-2192
    Pojawia się w:
    World Scientific News
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    FT-IR, 1H and 13C NMR QSAR and molecular docking study on some (E)-2-(2-((aryl)(phenyl)methylene) hydrazinyl)benzo[d]thiazoles
    Autorzy:
    Muthuvel, I.
    Thirunarayanan, G.
    Manikandan, S.
    Powiązania:
    https://bibliotekanauki.pl/articles/1066169.pdf
    Data publikacji:
    2019
    Wydawca:
    Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
    Tematy:
    (E)-2-(2-((aryl)(phenyl)methylene)hydrazinyl)benzo[d]thiazoles
    Docking analysis
    Hammett equation
    IR spectra
    NMR spectra
    QSAR study
    Schiff’s bases
    Opis:
    About six (E)-2-(2-((aryl)(phenyl)methylene)hydrazinyl)benzo[d]thiazoles have been synthesized and characterized by literature data. The infra-red stretching frequencies (ν, cm-1) of NH, CN, C=C and the NMR chemical shifts (δ, ppm) of NH, C=N and ipso carbons were assigned. These spectroscopic data were correlated for studying the QSAR employing Hammett equation with various Hammett substituent constants, Swain-Lupton’s F and R parameters using single and multi-regression analysis. From the results of regression analysis, the QSAR will be predicted by means of effects of substituents on the spectroscopic data of the functional group frequencies. The molecular docking character was evaluated by Schrodinger program, probing analogue docking in Topoisomerase enzymes. The crystallographic enzyme ligand complex (PDB entry 3TTZ) was obtained from the RCSB Protein Data Bank.
    Źródło:
    World Scientific News; 2019, 131; 54-74
    2392-2192
    Pojawia się w:
    World Scientific News
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    QSAR study of infrared and nuclear magnetic resonance spectra of 1-(3-chloro-4-nitrophenyl)-2-(substituted benzylidene) hydrazines
    Autorzy:
    Ananthi, V.
    Rajalakshmi, K.
    Thiruarayanan, G.
    Powiązania:
    https://bibliotekanauki.pl/articles/1178520.pdf
    Data publikacji:
    2017
    Wydawca:
    Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
    Tematy:
    1-(3-chloro-4-nitrophenyl)-2-(substituted benzylidene) hydrazines
    FeCl3/Bentonite
    Hammett equation
    IR and NMR spectra
    QSAR study
    Solvent-free synthesis
    Opis:
    Ten 1-(3-chloro-4-nitrophenyl)-2-(substituted benzylidene) hydrazines have been synthesized by FeCl3/Bentonite catalyzed solvent-free condensation of substituted phenyl hydrazine and aldehydes under microwave irradiation. The synthesized hydrazides are characterized by the physical constants, micro analysis and spectroscopic data. The assigned characteristic spectroscopic data of these 1-(3-chloro-4-nitrophenyl)-2-(substituted benzylidene) hydrazines were correlated with Hammett substituent constants, F and R parameters using Hammett equation through single and multi-regression analysis. With the results of statistical analysis results, the quantitative structure activity relationships were studied and finding the effect of substituents on the spectral data.
    Źródło:
    World Scientific News; 2017, 70, 2; 122-139
    2392-2192
    Pojawia się w:
    World Scientific News
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Spectral Quantitative Structure activity relationships in 3-(substituted phenyl) bicyclo[2.2.1]hept-5-en-2-yl-(pyrene-1-yl) methanone derivatives
    Autorzy:
    Thirunarayanan, Ganesamoorthy
    Powiązania:
    https://bibliotekanauki.pl/articles/1191973.pdf
    Data publikacji:
    2016
    Wydawca:
    Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
    Tematy:
    2
    3-Diarylbicyclo[2.2.1]-hept-5-ene-2-yl methanones; Greener synthesis
    Correlation analysis
    Hammett equation
    IR and NMR spectra
    QSAR study
    Opis:
    About nine titled compounds were synthesized by greener method and the purities of these methanones have been examined using their analytical and spectral data reported in literature. The infrared and NMR spectral data of these methanones were assigned and correlated with Hammett substituent constants, F and R parameters using single and multi-linear regression analysis. From the results of statistical analyses, the effects of substituents in terms of spectral quantitative structure activity on the spectral frequencies were studied.
    Źródło:
    World Scientific News; 2016, 50; 74-94
    2392-2192
    Pojawia się w:
    World Scientific News
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
      Wyświetlanie 1-8 z 8

      Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies