62507-55-5

Upstream product

• 96237-95-5 1-(p-bromobenzoyl)-2-(p-nitrobenzoyl)hydrazine 
• 1090-82-0 2-(4-nitrophenyl)-5-phenyl-1,3,4-oxadiazole 
• 50907-23-8 1-bromo-4-(2H-tetrazol-5-yl)benzene 
• 122-04-3 4-nitro-benzoyl chloride 
• 339246-84-3 C₁₄H₁₀BrN₃O₃ 
• 5933-32-4 4-bromobenzoic acid hydrazide 
• 62-23-7 4-nitro-benzoic acid 
• 5798-75-4 Ethyl 4-bromobenzoate 
• 619-42-1 4-methoxycarbonylphenyl bromide 
• 636-97-5 N-amino-(4-nitrophenyl)carboxamide 

Relevant academic research and scientific papers

Design, synthesis and characterization of π-conjugated 2,5-diphenylsubstituted-1,3,4-oxadiazole-based D-π-A-π’-D′ form of efficient deep blue functional materials: Photophysical properties and fluorescence “Turn-off” chemsensors approach

This paper primarily deals with the design and synthesis of three novel conjugated organic molecules containing 1,3,4-oxadiazole unit (abbreviated as CHEM-6(a-c)) with Donor-π-Acceptor-π’-Donor’ structures by utilizing palladium catalyzed Suzuki cross coupling reaction. Molecular structures of these compounds were characterized by using various spectroscopic and analytical techniques namely 1H NMR, 13C NMR, FT-IR, GC–MS and elemental analysis. Optical properties of these compounds have been investigated by using UV–visible absorption and fluorescence spectroscopy. Also, the PL investigations on solid state samples (as thin films) were carried out. Furthermore, solvatochromism and Density Functional Theory (DFT) computations are studied in detail. The experimentally measured optical band gap (Egopt) values of compounds CHEM-6a, CHEM-6b and CHEM-6c were determined to be 3.11, 3.03 and 2.70 eV, respectively. The DSC and TGA results revealed that the compounds exhibit good thermal stabilities. Current results indicate that the compounds CHEM-6(a-c) are promising candidates and could play an important role in the field of optoelectronic devices and possibly find potential applications in development of OLEDs. In addition, the compounds CHEM-6(a-c) showed an interesting property of chemical sensing for Hg(II) ion which can be clearly observed by naked eyes from the changes in solution color and fluorescence (under UV excitation).

17O NMR studies of substituted 1,3,4-oxadiazoles

Three series of substituted 1,3,4-oxadiazoles were studied by 17O NMR spectroscopy. Chemical shifts values were correlated with empirical Hammett parameters as well as calculated bond lengths and chemical shielding values.

Convenient preparation of unsymmetrical 2,5-disubstituted 1,3,4-oxadiazoles promoted by Dess-Martin reagent

2,5-Disubstituted 1,3,4-oxadiazoles have been conveniently prepared by oxidative cyclization of N-acyl-N′-aryliden-hydrazines promoted by an excess of Dess-Martin periodinane under mild conditions (23 examples, up to 92% isolated yields).

Preparation of functionalized polystyrene-block-polyisoprene copolymers and their luminescence properties

A series of block copolymers functionalized with aromatic 1,3,4-oxadiazole and stilbene derivatives have been synthesized by the palladium catalyzed reaction between polystyrene-block-polyisoprene and different functional units. These polymers exhibited different emission properties in solution and in the solid state. In chloroform solution, they showed relatively narrow and featured emission bands while, in the solid state, the emission band was broadened and showed a significant red shift. These observations were attributed to the formation of aggregates between the luminophores. After some oxadiazole functionalized copolymers were annealed at elevated temperature, such aggregation was enhanced and there were further changes in the emission spectra. For the bifunctional copolymers, such a shift in the emission band was not significant because the presence of two different chemical species in the same block may prevent the same type of luminophores from aggregating together.

Substitution Reactions of Phenylated Aza-Heterocycles. Part 2. Bromination of Some 2,5-Diaryl-1,3,4-oxadiazoles

Electrophilic bromination of the title compounds may be achieved using either bromine in oleum, or bromine and potassium bromate in a sulphuric-acetic acid mixture.Under the milder reaction conditions provided by the latter, 2-(p-nitrophenyl)-5-phenyl-1,3,4-oxadiazole (2), the model compound used in this study, is mono- and di-brominated in the phenyl ring.In the first bromination step, all three monobromo-isomers are produced in appreciable amount.The orientation of the second bromination is controlled entirely by the first bromine and not by the oxadiazole substituent: this is confirmed by a separate study of the bromination of the three monobromo-compounds (3a-3c).