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Autor:
Yilmaz, ZT, Odabasoglu, HY, Senel, P, Adimcilar, V, Erdogan, T, Ozdemir, AD, Golcu, A, Odabasoglu, M, Buyukgungor, O
In this report, 3((4,6-dimethylpyrimidin-2-yeamino)isobenzofuran-1(3H)-one have been synthesized via reaction between phthalaldehydic acid and 2-amino-4,6-dimethylpyrimidine in 90% yields and characterized by Infrared (IR), Nuclear Magnetic Resonance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::9ef5f7dfe98786f192e8a7c823ffdb72
This work includes the syntheses, molecular and electronic structure analyses of two novel secondary amide compounds 3-acetoxy-2-methyl-N-(2-methoxyphenyl)benzamide, 1 and 3-acetoxy-2-methyl-N-(3-methylphenyl)benzamide, 2. The title compounds were ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::9ab83d1aa15e80f11ef71dd685116664
This study treats about two successfully synthesized secondary amide compounds 3-Acetoxy-2-methyl-N-(phenyl)benzamide, I and 3-Acetoxy-2-methyl-N-(4-methylphenyl)benzamide, II. Compounds were characterized by FTIR, H-1 NMR, C-13 NMR and X-ray single
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::b267e8ca67e1baa6a911918e282df8fe
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/24546
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/24546
The main purpose of this study is to characterize a new organic material, (E)-5-methoxy-2-[(3,4-dimethylphenylimino) methyl] phenol, which was synthesized and grown as a single crystal. The molecular structure and spectroscopic properties of the orth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::71e2f52120433ccbd1bf38ddb190cf41
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/16070
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/16070
In this study, a series of substituted secondary amide compounds were synthesized starting from 2,3-dimethoxybenzoic acid and aniline derivatives. The structures of these synthesized compounds were determined using IR, H-1 NMR and C-13 NMR spectrosco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::364af5d9b12037a04d132da9f8093354
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/23502
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/23502
o-Hydroxy Schiff bases have two tautomers known as phenol-imine and keto-amine forms. In the present work, the tautomerism in (E)-4-Bromo-2-[(2,3-dihydroxypropylimino)methyl]phenol compound has been investigated by experimental (XRD, FT-IR and UV-vis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::c6294cda57047196259e4eb92d27339c
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/21987
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/21987
In this study, the molecular structure and spectroscopic properties of the title compound were characterized by X-ray diffraction, FT-IR and UV-vis spectroscopies. These properties were also investigated using OFT method. The most convenient conforma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::023e0b5e5668d8143fd21bba76a78676
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/13808
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/13808
This work presents a combined experimental and theoretical study on an ortho-hydroxy Schiff base compound, (E)-5-(diethylamino)-2-[(4-propylphenylimino)methyl]phenol. The crystal structure and spectroscopic properties of the compound have been determ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6895a2aaa0ac9ef3c31f7a392adb3069
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/20896
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/20896
In this study, (E)-2-[(4-bromophenylimino)methyl]-6-ethoxyphenol compound was investigated by mainly focusing on stacking interactions assembling the supramolecular network of the compound and on tautomerism in solvent media and in the solid state. I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0fe5bb7f3c9d3fa78c36f7150207d27a
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/13312
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/13312