scholarly journals A new benzothiazin-functionalized calix[4]arene-based fluorescent chemosensor for the selective and sensitive detection of Co2+ ion

2021 ◽  
Author(s):  
Fatimah Fateh ◽  
Ayşe Yildirim ◽  
Asif Ali Bhatti ◽  
Mustafa YILMAZ
Keyword(s):  
Organic Chemistry ◽  
Detection Limit ◽  
Ir Spectroscopy ◽  
Binding Constant ◽  
Spectroscopic Methods ◽  
Macrocyclic Compounds ◽  
H Nmr ◽  
Ft Ir ◽  
Ft Ir Spectroscopy ◽  
C Nmr

Abstract Calixarenes, which have a great place in supramolecular chemistry, has become the most prominent macrocyclic compounds in synthetic organic chemistry due to their easy synthesis and functionalization. In this study, p-tert-butyl calix[4]arene dihydrazide derivative was synthesized and then reacted with 3-oxo-3,4-dihydro-2H-benzo[b][1, 4] thiazin-2-ylideneacetyl chloride to prepare new calixarene based chromophore compound 4. The structure of the synthesized compound was elucidated by spectroscopic methods such as 1H-NMR 13C-NMR and FT-IR spectroscopy. Chromogenic and fluorescence properties of compound 4 were evaluated. It was observed from both studies that compound 4 was Co2+ selective and shows fluorescence Switched-off behavior. Stoichiometry, binding constant and the detection limit was calculated. The stoichiometry between compound 4 and Co2+ was found to be 1:1. The binding constant value (K) was calculated as 666.67 M− 1 using Benesi–Hildebrand equation, while the detection limit for Co2+ ion was calculated as 0.0465 µM.

Electrochemically Synthesis and Characterization of Copolymers Based on 1, 4-Diethoxybenzene and 3, 4-Ethylenedioxythiophene

2011 ◽  
Vol 335-336 ◽  
pp. 989-993
Author(s):  
Mi Ouyang ◽  
Zhen Wei Yu ◽  
Yi Xu ◽  
Yu Jian Zhang ◽  
Cheng Zhang
Keyword(s):  
Cyclic Voltammetry ◽  
Ir Spectroscopy ◽  
Feed Ratio ◽  
Synthesis And Characterization ◽  
Monomer Mixture ◽  
Long Wavelength ◽  
H Nmr ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

Copolymers based on 1, 4-diethoxybenzene (DEB) and 3, 4-ethylenedioxythiophene (EDOT) were electrochemically synthesized and characterized. The structures of the copolymers were established by 1H NMR and FT-IR spectroscopy. The results indicated the final product was a copolymer instead of a blend or a composite. The physical properties were systematically investigated by cyclic voltammetry, UV-vis absorption and fluorescence. The PL maximum of copolymers presented obviously red-shift to long wavelength as the feed ratio of EDOT in monomer mixture increased.

Synthesis, in vitro inhibition effect of novel phthalocyanine complexes as carbonic anhydrase and paraoxonase enzyme inhibitors

2020 ◽  
Vol 24 (08) ◽  
pp. 1047-1053
Author(s):  
Emre Güzel ◽  
Barış Seçkin Arslan ◽  
Kübra Çıkrıkçı ◽  
Adem Ergün ◽  
Nahit Gençer ◽  
...  
Keyword(s):  
Carbonic Anhydrase ◽  
Enzyme Inhibitors ◽  
Inhibition Effect ◽  
H Nmr ◽  
Vis Spectroscopy ◽  
Ft Ir ◽  
First Time ◽  
Ft Ir Spectroscopy ◽  
C Nmr

The preparation and assessment of carbonic anhydrase and paraoxonase enzyme inhibition properties of 3-(2-(5-amino-4-(4-bromophenyl)-3-methyl-1H-pyrazol-1-yl)ethoxy)phthalonitrile (2) and its nitrogen-containing non-peripheral phthalocyanine derivatives (3 and 4) are reported for the first time. The new phthalonitrile and its phthalocyanine derivatives have been elucidated by FT-IR spectroscopy, 1H-NMR, [Formula: see text]C-NMR, mass and UV-vis spectroscopy. The results demonstrated that all synthesized compounds moderately inhibited carbonic anhydrase and paraoxonase enzymes. Among the compounds, the most active ones were found to be compound 4 for PON (Ki : 0.14 [Formula: see text]M), compound 3 for hCA I (Ki : 22.52 [Formula: see text]M) and compound 1 for hCA II (Ki : 13.62 [Formula: see text]M).

scholarly journals A facile and concise route to (hydroxybenzoyl)pyrido[2,3-d]pyrimidine heterocycle derivatives: synthesis, and structural, spectral and computational exploration

RSC Advances ◽  
2019 ◽  
Vol 9 (59) ◽  
pp. 34567-34580 ◽  
Author(s):  
Abida Ashraf ◽  
Muhammad Khalid ◽  
Muhammad Nawaz Tahir ◽  
Muhammad Yaqub ◽  
Muhammad Moazzam Naseer ◽  
...  
Keyword(s):  
Electronic Structure ◽  
Ir Spectroscopy ◽  
X Ray Diffraction ◽  
Spectral Techniques ◽  
X Ray ◽  
Chemical Structures ◽  
Computational Exploration ◽  
Ft Ir ◽  
Ft Ir Spectroscopy ◽  
C Nmr

The chemical structures of the title compounds were ascertained by spectral techniques including 1H, 13C NMR, UV-vis and FT-IR spectroscopy as well as single-crystal X-ray diffraction, and DFT computation adopted to analyze the electronic structure.

Synthesis, Characterization and Photophysicochemical Properties of Zinc(Ii) Phthalocyanine With New Benzenesulfonamide Derivative Substituents

2021 ◽  
Author(s):  
Gülen Atiye Öncül ◽  
Ömer Faruk Öztürk ◽  
Mehmet Pişkin
Keyword(s):  
Elemental Analysis ◽  
Mass Spectra ◽  
Spectroscopic Methods ◽  
H Nmr ◽  
Maldi Tof Mass Spectra ◽  
New Type ◽  
Ft Ir ◽  
Photochemical Properties ◽  
Photocatalytic Applications ◽  
C Nmr

Abstract Novel (E)-4-((5-bromo-2-hydroxy-3-methoxybenzylidene)amino)-N-(pyridin-2-yl)benzenesulfonamide 1, (E)-4-((5-bromo-2-(3,4-dicyanophenoxy)-3-methoxybenzylidene)amino)-N-(pyridin-2-yl)benzene sulfonamide 2 and 2(3),9(10),16(17),23(24)-tetra-[(E)-4-((5-bromo-3-methoxy-2-(λ1-oxidanyl)benzyl idene)amino)-N-(pyridine-2-yl)benzenesulfonamide]phthalocyaninato zinc(II) phthalocyanine 3 were synthesized. Their (1-3) structures were illuminated with spectroscopic methods such as FT-IR, 1H NMR,13C NMR, UV–vis, MALDI-TOF mass spectra and also elemental analysis. The spectroscopic, photophysical and photochemical properties of the zinc(II) phthalocyanine 3 were investigated in dimethyl sulfoxide and its effects on the above mentioned properties were reported as a result of containing new type benzenesulfonamide derivatives as substituents. In addition, its above-mentioned properties were reported by comparing different species with those of their substituted and/or unsubstituted counterparts. The zinc(II) phthalocyanine 3 has photosensitizing abilities suitable and sufficient especially for photocatalytic applications.

scholarly journals Structure and excitation-dependent emission of novel zinc complexes with pyridyltriazoles

RSC Advances ◽  
2019 ◽  
Vol 9 (38) ◽  
pp. 22143-22152 ◽  
Author(s):  
Alexey Gusev ◽  
Elena Braga ◽  
Ekaterina Zamnius ◽  
Mikhail Kiskin ◽  
Mariya Kryukova ◽  
...  
Keyword(s):  
Ir Spectroscopy ◽  
Single Crystal ◽  
Zinc Complexes ◽  
X Ray Diffraction ◽  
X Ray ◽  
Esi Ms ◽  
H Nmr ◽  
Elemental Analyses ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

A series of Zn(ii) complexes with 5-(4-R-phenyl)-3-(pyridin-2-yl)-1,2,4-triazoles have been synthesized and subsequently characterized by single crystal X-ray diffraction, 1H-NMR, FT-IR spectroscopy, elemental analyses, ESI-MS, and PXRD.

scholarly journals Synthesis of new pyrazolone and pyrazole-based adamantyl chalcones and antimicrobial activity

2020 ◽  
Vol 40 (9) ◽  
Author(s):  
Rawan Al-Saheb ◽  
Sami Makharza ◽  
Feras Al-battah ◽  
Rajab Abu-El-Halawa ◽  
Tawfeq Kaimari ◽  
...  
Keyword(s):  
High Dose ◽  
Moderate Activity ◽  
Dependent Manner ◽  
H Nmr ◽  
Ft Ir ◽  
Bacteria And Fungi ◽  
New Compounds ◽  
Dose Dependent ◽  
Ft Ir Spectroscopy ◽  
C Nmr

Abstract Chalcones and their derivatives are becoming increasingly popular due to their various pharmacological effects. Chalcone molecules may be extracted from natural resources, entirely synthesised, or biosynthesised by modifying the natural ones. In the present study, five pyrazole-based adamantyl heterocyclic compounds were synthesised by condensation of 1-adamantyl chalcone with substituted phenylhydrazine. The products were characterised by using ¹H NMR, ¹³C NMR and FT-IR spectroscopy. The microbiological activity of these compounds was investigated against bacteria and fungi. The new compounds showed good to moderate activity against the microbial species used for screening. All developed molecules showed antibacterial activity against Gram-negative and Gram-positive. These molecules showed antifungal activities against Fusarium oxysporum fungus and in a dose-dependent manner, apart from RS-1 molecules which showed compromised antifungal activity and even at a high dose.

Synthesis, characterization and photochemical properties of metallo porphyrazines substituted with alkyl linked carbazole, benzoazepine and phenothiazine moieties

2017 ◽  
Vol 21 (09) ◽  
pp. 599-610 ◽  
Author(s):  
Remziye Olgaç ◽  
Yasemin Baygu ◽  
Burak Yıldız ◽  
Yaşar Gök ◽  
Baybars Köksoy ◽  
...  
Keyword(s):  
Spectroscopic Methods ◽  
The Novel ◽  
Oxygen Generation ◽  
H Nmr ◽  
Singlet Oxygen Generation ◽  
One Step ◽  
Ft Ir ◽  
Photochemical Properties ◽  
C Nmr

Novel octa-phenotiazine, octa-benzoazepine and octa-carbazole substituted magnesium(II) (MgPz-I-III) and zinc(II) (ZnPz-I-III) porphyrazines were synthesized from 2,3-bis[6-(4a,10a-dihydro-phenothiazin-10-yl)-hexylsulfanyl]-but-2-enedinitrile (5), 2,3-bis [6-(4a,11a-dihydro-dibenzo[b,f]azepin-5-yl)-hexysulfan-yl]-but-2-enedinitrile (8) and 2,3-bis(6-carbazol-9-yl-hexylsulfanyl)-but-2-enedinitrile (10), respectively. These dinitrile derivatives 5, 8 and 10 were also prepared by the reaction of 1,2-dicyano-1,2-ethylenedithiolate di-sodium salt (4) with 10-(6-bromohexyl)-10H-phenothiazine (3), 5-(6-bromohexyl)-5H-diben-zo[b,f]azepine (7) and 9-(6-bromo-hexyl)-9H-carbazole (9), respectively. Porphyrazino-zinc(II) complexes were synthesized by one-step reaction using Zn(BuO)[Formula: see text] as a template agent. All the novel compounds were characterized by elemental analysis and different spectroscopic methods such as [Formula: see text]H NMR, [Formula: see text]C NMR, FT-IR, UV-Vis and mass. The photochemical properties including photodegradation and singlet oxygen generation for magnesium(II) and zinc (II) porphyrazine complexes were studied in dimethylsulfoxide solutions for determination of their photosensitizer behaviors.

scholarly journals Synthesis of gemini basic ionic liquids and their application in anion exchange membranes

RSC Advances ◽  
2018 ◽  
Vol 8 (19) ◽  
pp. 10185-10196 ◽  
Author(s):  
Dan Wang ◽  
Yifu Wang ◽  
Heting Wan ◽  
Jilin Wang ◽  
Lulu Wang
Keyword(s):  
Ionic Liquid ◽  
Ionic Liquids ◽  
Ir Spectroscopy ◽  
Anion Exchange ◽  
Raw Materials ◽  
Anion Exchange Membranes ◽  
Step Method ◽  
H Nmr ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

A gemini-type basic morpholine ionic liquid ([Nbmd][OH]) was synthesizedviaa two-step method with morpholine, bromododecane and 1,4-dibromobutane as raw materials, and its structure was characterized by1H NMR and FT-IR spectroscopy.

scholarly journals Homogeneous Esterification of Cellulose in the Mixture N-Butylpyridinium Chloride/Dimethylsulfoxide

2016 ◽  
Vol 2016 ◽  
pp. 1-7 ◽  
Author(s):  
Lahcen El Hamdaoui ◽  
Mohammed El Moussaouiti ◽  
Said Gmouh
Keyword(s):  
Reaction Medium ◽  
Reaction Parameters ◽  
Reaction Conditions ◽  
Cellulose Esters ◽  
Short Reaction Time ◽  
H Nmr ◽  
Mild Conditions ◽  
Ft Ir ◽  
Ft Ir Spectroscopy ◽  
C Nmr

The present study deals with the homogeneous acylation of cellulose withp-nitrobenzoyl chloride in a reaction medium composed of a mixture of 1-butylpyridinium chloride and dimethylsulfoxide (BPyCl/DMSO), in the presence of different bases and under mild conditions. The preparation of cellulosep-nitrobenzoate depending on the reaction conditions, the influences of reaction parameters such as the base type, and the types of cellulose (kraft and microcrystalline) on the products were investigated. Cellulosep-nitrobenzoate with a degree of substitution (DS) in the range from 0.12 to 1.5 was accessible, with a low excess of reagent and for a short reaction time. The cellulose esters were characterized by1H-NMR,13C NMR, and FT-IR spectroscopy, thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and solubility tests.

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