2,5-双取代-1,3,4-噁二唑类化合物的合成与表征

以3-( 4-氟苯基) -1H-吡唑-5-甲酸乙酯为原料,与H2NNH2?H2O发生肼解生成3-( 4-氟苯基) -1H-吡唑-5-甲酰肼,再与CS2环化生成2-巯基噁二唑中间体,最后在巯基上进行烷基化反应合成了一系列新型的2-硫醚-5-吡唑基-1,3,4-噁二唑类化合物,并利用IR、1H NMR、HRMS等波谱技术对目标化合物结构进行了表征。该合成方法具有原料易得,后处理简便,收率较高的优点。     

Influence of medium acidity upon the luminescence properties of 2,5-diphenyl-1,3,4-oxadiazole and 2,5-diphenyl-1,3-oxazole

The luminescence properties of 2,5-diphenyl-1,3,4-oxadiazole and 2,5-diphenyl-1,3-oxazole in aqueous solutions of sulfuric acid (pH 7 to H_o − 10) were studied. The spectral parameters are essentially acidity dependent, which is due to the acid-base equilibria of these heterocycles both in the ground and in the first excited singlet states. The difference between these two compounds is governed by their dissimilar solvation. The basicity constants of 2,5-diphenyl-1,3,4-oxadiazole in the S₀ state (pK_BH+ = − 2.49) and 2,5-diphenyl-1,3-oxazole in the S₀ and S₁ states (pK_BH+ = −1.93, pK_BH+^* = 1.95) were experimentally obtained. The enthalpies of formation, electron charge density, and geometry of the bases and corresponding conjugate acids in the S₀ and S₁ states were calculated by the MNDO method.     

Reaction of Reformatsky reagents with 2,5-diphenyl-1,3,4-oxadiazole

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Synthesis of a novel β-diketone containing carbazole and 2,5-diphenyl-1,3,4-oxadiazole fragments

A novel β-diketone containing carbazole and 2,5-diphenyl-1,3,4-oxadiazole fragments as hole- and electron-transporting functional groups, respectively, was synthesized via efficient and convenient procedure. The product attracts interest from the viewpoint of its potential applications as optoelectronic material. Published in Russian in Zhurnal Organicheskoi Khimii, 2009, Vol. 45, No. 4, pp. 573–577. The text was submitted by the authors in English.     

Synthesis and optical properties of β-arylethylene derivatives of 2,5-diphenyloxazole

A series of arylethylene derivatives of 2,5-diphenyloxazole derivatives is synthesized, and the absorption and fluorescent spectra of their toluene solutions are investigated. Joining in one molecule of 2,5-diphenyloxazole and arylethylene groups leads to long wave displacement of the absorption and fluorescence bands, and in most cases to greater intensity of absorption and increase in the photoluminescence quantum yield.     

Synthesis of substituted 1,3,4-oxadiazole derivatives

Monosubstituted oxadiazoles were synthesized by the reaction of hydrazides with triethyl orthoformate. Their reactions with benzoyl chloride gave benzoylcarbohydrazides, which under the action of thionyl chloride were cyclized to the respective 2,5-disubstituted oxadiazoles. 1-Aryl-4-(5-thioxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-pyrrolidin-2-ones were synthesized from acid hydrazides using carbon disulfide under basic conditions. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 269-272, February, 2009.     

Molecular wires comprising pi-extended ethynyl- and butadiynyl-2,5-diphenyl-1,3,4-oxadiazole derivatives: synthesis, redox, structural, and optoelectronic properties

2,5-Diphenyl-1,3,4-oxadiazole (OXD) derivatives with terminal ethynyl- (4a,b) and butadiynyl- (8a,b) substituents have been synthesized in high yields. 2-Methyl-3,5-hexadiyn-2-ol has not been exploited previously in the synthesis of terminal butadiynes. Crystals of 8a and 8b are remarkably stable to long-term storage under ambient conditions. The X-ray crystal structure of 8a reveals that the butadiyne moieties are spatially isolated by the aromatic moieties, which explains the high stability. Two series of derived pi-conjugated molecules, Donor-(C[triple bond]C)(n)-OXD (n = 1, 2) and OXD-(C[triple bond]C)(n)-Donor-(C[triple bond]C)(n)-OXD (n = 1) [Donor = tetrathiafulvalene (TTF), bithiophene, 9-(4,5-dimethyl-1,3-dithiol-2-ylidene)fluorene, and triphenylamine], have been synthesized using Sonogashira reactions and characterized by X-ray crystallography, cyclic voltammetry, and optical absorption/emission spectroscopy. The electron-withdrawing effect of the OXD units is manifested by a positive shift of the donor oxidation waves in these systems: the butadiynylene spacer (n = 2) further shifts the first oxidation waves by 40-80 mV compared to analogues n = 1. The absorption spectra of TTF-OXD hybrids 10d and 11 are blue-shifted by 80 nm compared to the bithienyl-bridged derivative 10f and are similar to the butadiynyl-OXD building-block 8a, demonstrating that conjugation is disrupted by a neutral TTF unit. Solutions of the TTF-OXD and 9-(4,5-dimethyl-1,3-dithiol-2-ylidene)fluorene-OXD hybrids, 10d, 10g, 11, and 13, are only very weakly fluorescent due to quenching from the electron-donor moieties. In contrast, the triphenylamine-OXD hybrids 12a, 12b, 14a, and 14b are fluorescent; the PLQYs of the butadiynylene derivatives 14a and 14b are lower than those of the ethynylene-bridged analogues 12a and 12b.     

Synthesis of nitrophenyl derivatives of 1,3,4-oxadiazole

Acylation of nitrobenzhydrazides with nitrobenzoyl chlorides and ethyl chlorocarbonate yielded a number of corresponding 1,2-diacylhydrazines, which were converted by the action of phosphorus oxychloride to nitro-substituted 2,5-diphenyl- and 2-phenyl-5-ethoxy-1, 3,4-oxidazoles.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 741–743, June, 1977.     

Hetarylethylene derivatives of 2,5-diphenyloxazole

A number of new effective luminophores were synthesized by PO olefination from 2-(4-bromomethylphenyl)-5-phenyloxazole and various heterocyclic aldehydes containing a furan ring. All of the compounds obtained have intense fluorescence in toluene and, depending on the nature of the substituents, the color of the luminescence changes from blue to green. It is shown that chloro, bromo, and methyl substituents have little effect on the spectral-luminescence properties of the compounds obtained, whereas a nitro group causes a decrease in the fluorescence quantum yield.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1616–1618, December, 1977.     

Electrochromic tetrathiafulvalene derivatives functionalised with 2,5-diaryl-1,3,4-oxadiazole chromophores

Electrochromism has been demonstrated by three novel electrochemically-reversible compounds and, which were synthesised by Pd catalysed cross-coupling of iodotrimethylTTF (6) and 2,6(7)-diiodoTTF (7) with the 2,5-diaryl-1,3,4-oxadiazole derivatives 1 and 2 containing terminal ethyne and butadiyne groups.     

Synthesis and antiviral evaluation of new 2,5-disubstituted 1,3,4-oxadiazole derivatives and their acyclic nucleoside analogues

Abstract  

A number of new 5-[(naphthalen-1-yloxy)-methyl]-1,3,4-oxadiazole derivatives were synthesized. Sugar 2-[5-[(naphthalen-1-yloxy)methyl]-1,3,4-oxadiazol-2-ylthio]acetohydrazones were prepared by condensation of the hydrazide with the corresponding monosaccharides. Cyclization of the sugar hydrazones with acetic anhydride afforded the substituted oxadiazoline derivatives. The synthesized compounds displayed different degrees of antiviral activities or inhibitory actions against HCV and HIV viruses.     

对称双-1,3,4-噁二唑化合物的合成及性质

首先以苯氧乙酰肼和二酰氯为原料反应得到对称双酰肼化合物,再以POCl3合环得到系列对称双-1,3,4-噁二唑化合物。考察了该系列化合物的紫外-可见吸收光谱,其中,间苯双-1,3,4-噁二唑化合物在250nm附近有明显的最大吸收峰,对苯双-1,3,4-噁二唑化合物的最大吸收峰则红移至290nm附近;而脂肪族双-1,3,4-噁二唑化合物没有明显的最大吸收峰,说明没有大的共轭体系,与结构相符合。所有化合物的结构均经元素分析、IR、1H NMR和MS确证。     

Unusual dinuclear and mononuclear cyclometalated iridium complexes of 2,5-diaryl-1,3,4-oxadiazole derivatives

A family of new 2,5-diphenyl-1,3,4-oxadiazole (OXD) derivatives 8-11 bearing ortho-alkyl substituents on one of the phenyl rings is reported. The reactions of these OXDs with IrCl(3) under standard cyclometalating conditions did not give the usual μ-dichloro bridged diiridium OXD complexes. Instead, the novel diiridium complexes 12-14 and the monoiridium complex 15 were isolated and characterized by X-ray crystallography. It is proposed that the unusual structures arise because of the ortho-alkyl substituents leading to a substantial twisting of part of the OXD system which, for steric reasons, changes the normal course of the metal-ligand coordination reactions. Subsequent reactions of 13 and 15 gave the mononuclear complexes 16-18 with acac and picolinate anciliary ligands. The crystal structures of 16 and 18 are reported. Photoluminescence is observed in the green (16) and blue-green regions (17 and 18) at room temperature. Complexes 16-18 are phosphorescent at low temperature, with triplet lifetimes of 4.2-5.7 μs at 77 K.     

含1,3,4-噁二唑的葡萄糖苷衍生物的合成及抑菌活性

糖苷类化合物广泛存在于生物体内,并担负着重要生物功能,天然药物及中草药中的许多活性成分是糖苷化合物[1].糖苷类化合物的良好抗菌、抗癌活性激发了广大研究者的浓厚兴趣[2-3],启发人们通过糖苷化反应作为改变或增加生物活性的重要结构修饰方法[4],以增加化合物的水溶性和导向性,改进药理学性质.     

New mesogenic 1,3,4-oxadiazole derivatives

The synthesis of novel liquid-crystalline heteroaromatic compounds incorporating the five membered 1,3,4-oxadiazole ring is described. Due to the bent molecular structure of the oxadiazole ring their mesophase stability is low if the heterocyclic ring occupies a central position, but it is increased if this ring is shifted to a terminal position. Dielectric measurements indicate that the 2-n-alkylthio substitutes 1,3,4-oxadiazole derivatives change the sign of the dielectric anisotropy at the phase transition from the nematic to the smectic A phase. This effect is explained by the increase of the antiparallel correlation of the molecules on formation of the smectic layers.     

Synthesis and antimicrobial screening of 1,3,4-oxadiazole and clubbed thiophene derivatives

In the present study, a novel series of 2-{5-[4-(1-aza-2-(2-thienyl)vinyl)phenyl](1,3,4-oxadiazol-2-ylthio)}-N-arylacetamides (IV)_1–12 were synthesized and tested for their antimicrobial activity. Newly synthesized compounds were screened for their antibacterial and antifungal activities on Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, Staphylococcus pyogenes, Candida albicans, Aspergillus niger and Aspergillus clavatus. The chemical structures of newly synthesized compounds were elicited by IR, ¹H NMR, ¹³C NMR and mass spectral data. The synthesized bio-active compounds exhibited excellent to moderate antimicrobial activity. Compounds (IV)₅, (IV)₆ and (IV)₇ possess excellent antibacterial activity whereas compounds (IV)₆, (IV)₉ and (IV)₁₁ possess excellent antifungal activity.     

Synthesis and characterisation of asymmetrical mesogenic materials based on 2,5-disubstituted-1,3,4-oxadiazole

New mesogenic homologous series bearing 1,3,4-oxadiazole ring with a nitro terminal group, 4-(5-(4-nitrophenyl)-1,3,4-oxadiazol-2-yl)phenyl 4-((4-methoxybenzylidene)amino)benzoate (G₁–G₁₁), were synthesised. Their chemical structures are identified by fourier transform infrared spectroscopy (FT-IR), proton nuclear magnetic resonance (¹H-NMR) and elemental analysis. The liquid crystalline properties of the series G_n and their precursory F_n were screened by differential scanning calorimetry and optical polarising microscopy (OPM). The compounds of the series G_n were screened by thermogravimetric analysis to observe their thermal stability. The target compounds (G_n) in this study, were displayed different liquid crystalline mesophase, the first two homologous (G₁ and G₂) did not show any liquid crystalline behaviour, the homologous (G₃–G₁₀) which have an alkoxy terminal group (n = 3–10) exhibited nematic phase, whilst the last derivative of the series (G₁₁), n = 12, displayed SmA phase. The mesomorphic properties of these derivatives were affected by the presence of the nitro group at the end of the molecules which was classified as a strong polar group. Also, the role of alkoxy terminal chain and the bent heterocyclic ring (1,3,4-oxadiazole) in the liquid crystalline properties of these molecules were debated.