Optical and electrochemical properties of copoly(aryl ether)s consisting of alternate 2,5‐distyrylbenzene and electron‐transporting oxadiazole or triazole derivatives

New copoly(aryl ether) P1 consisting of alternate electron‐transporting 2‐(3‐(trifluoromethyl)phenyl)‐5‐(4‐(5‐(3‐(trifluoromethyl)phenyl)‐1,3,4‐oxadiazol‐2‐yl)‐2,5‐bis(hexyloxy)phenyl)‐1,3,4‐oxadiazole and hole‐transporting 2,5‐distyrylbenzene (DSB) was synthesized via nucleophilic substitution polymerization. We investigated the optical and electrochemical properties of alternate copoly(aryl ether)s P1 – P6 , which contain the same hole‐transporting DSB segments, but with different electron transporting segments. The effect of trifluoromethyl groups in electron transporting segments is also discussed. Referencing to the spectra of their model compounds M1 – M4 , the emissions of P1 – P3 are dominated exclusively by the hole‐transporting fluorophores with longer emissive wavelength about 452–453 nm via efficient excitation energy transfer. Furthermore, P1 – P3 also exhibit unique variations in energy transfer in acidic media and solvatochromism in organic solvents. The highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energy levels of P1 – P4 , estimated from electrochemical data, are ?5.12, ?5.15, ?5.18, ?5.00 eV and ?2.93, ?3.39, ?3.49, ?2.76 eV, respectively. The electron and hole affinity of P1 – P6 can be enhanced simultaneously by introducing isolated hole‐ and electron‐transporting segments in backbone. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5083–5096, 2005     

Synthesis and optoelectronic properties of luminescent poly(p‐phenylenevinylene) derivatives containing electron‐transporting 1,3,4‐oxadiazole groups

Three random copolymers ( P1–P3 ) comprising phenylenevinylene and electron‐transporting aromatic 1,3,4‐oxadiazole segments (11, 18, 28 mol %, respectively) were prepared by Gilch polymerization to investigate the influence of oxadiazole content on their photophysical, electrochemical, and electroluminescent properties. For comparative study, homopolymer poly[2‐methoxy‐5‐(2′‐ethylhexyloxy)‐1,4‐p‐phenylenevinylene] ( P0 ) was also prepared by the same process. The polymers ( P0–P3 ) are soluble in common organic solvents and thermally stable up to 410 °C under a nitrogen atmosphere. Their optical properties were investigated by absorption and photoluminescence spectroscopy. The optical results reveal that the aromatic 1,3,4‐oxadiazole chromophores in P1–P3 suppress the intermolecular interactions. The HOMO and LUMO levels of these polymers were estimated from their cyclic voltammograms. The HOMO levels of P0–P3 are very similar (?5.02 to ?5.03 eV), whereas their LUMO levels decrease readily with increasing oxadiazole content (?2.7, ?3.08, ?3.11, and ?3.19 eV, respectively). Therefore, the electron affinity of the poly(p‐phenylenevinylene) chain can be gradually enhanced by incorporating 1,3,4‐oxadiazole segments. Among the polymers, P1 (11 mol % 1,3,4‐oxadiazole) shows the best EL performance (maximal luminance: 3490 cd/m², maximal current efficiency: 0.1 cd/A). Further increase in oxadiazole content results in micro‐phase separation that leads to performance deterioration. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 4377–4388, 2007     

Poly(p‐phenylene vinylene) derivatives containing triazole or oxadiazole segments: Connector effect in optical,electrochemical, and electroluminescent properties

To study the effect of connector structure between hole‐ and electron‐transporting segments, we synthesized and characterized new electroluminescent polymers P 1 – P 7 consisting of hole‐transporting 1,4‐bis(hexyloxy)‐2,5‐distyrylbenzene (DSB: P 1 and P 2 ) and electron‐transporting 4‐(4‐(hexyloxy)phenyl)‐3,5‐diphenyl‐4H‐1,2,4‐triazole (TAZ: P 3 and P 4 ) or 2‐(2,5‐bis(hexyloxy)‐4‐(5‐phenyl‐1,3,4‐oxadiazol)phenyl)‐5‐phenyl‐1,3,4‐oxadiazole (DIOXD: P 5 – P 7 ) segments linked by different connectors. The connectors between hole‐ and electron‐transporting segments are (1) 1,4‐phenylene in P 3 and P 5 , (2) 1,4‐divinylbenzene in P 4 and P 6 , and (3) 4,4′‐biphenyl in P 7 . Three corresponding end‐capped model polymers P 1‐M , P 2‐M , and P 3‐M were also synthesized to evaluate the effect of end groups. From optimized semiempirical MNDO calculations, the adjacent benzene rings between DSB and TAZ or DIOXD chromophores in P 3 , P 5 , and P 7 twist about 81°–89°. The effect of twisted architectures and connectors in optical and electrochemical properties for P 1 – P 7 have been discussed by comparing with copolymers P 1 and P 2 , which possess single bond or ether spacer as connectors. From cyclic voltammograms, the torsion in P 3 , P 5 , and P 7 confines electron delocalization and leads to simultaneously enhanced hole and electron affinity as compared to those of P 1 and P 2 . Furthermore, double‐layer light‐emitting diodes with a configuration of ITO/PEDOT:PSS/ P 1 – P 7 /Al all reveal green–yellow electroluminescence with maximum luminance at 8–320 cd/m² and their performances are greatly influenced by the connector's structure. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4514–4531, 2006     

Luminescent copoly(aryl ether)s consisting of alternate oxadiazole and 1,4‐distyrylbenzene derivatives: Synthesis and characterization

In an effort to decrease the electron‐injection barrier from the anode electrode, four copoly(aryl ether)s ( P1 – P4 ), consisting of alternating isolated electron‐transporting [2,5‐diphenyl‐1,3,4‐oxadiazole for P1 and P3 and 5,5′‐diphenyl‐2,2′‐p‐(2,5‐bishexyloxyphenylene)‐bis‐1,3,4‐oxadiazole for P2 and P4 ] and emitting chromophores (1,4‐distyryl‐2,5‐dihexyloxybenzene for P1 and P2 and 1,4‐distyryl‐2,5‐dihexylbenzene for P3 and P4 ), have been synthesized by the nucleophilic displacement reaction between bisfluoride and bisphenol monomers. They are basically amorphous materials with 5% weight‐loss temperature above 400 °C. The photoluminescence spectra and quantum yields of these copolymers are dependent on the compositions of the two isolated fluorophores. The highest occupied molecular orbital and lowest unoccupied molecular orbital energy levels of these copolymers have been estimated from their cyclic voltammograms. All the observations directly prove that the oxidation starts at the hole‐transporting segments. The electron affinity can be enhanced by the introduction of isolated electron‐transporting segments that lead to a charge‐injection balance. Single‐layer light‐emitting diodes (Al/ P1 – P4 /ITO glass) have been fabricated. P1 and P2 reveal blue electroluminescence, and P3 and P4 reveal purple‐blue electroluminescence. Moreover, the incorporation of bisoxadiazole units increases the electron affinity and reduces the turn‐on electric field better than one oxadiazole unit. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 2765–2777, 2003     

Synthesis of electroluminescent copoly(aryl ether)s containing alternate 1,4‐distyrylbenzene derivatives and aromatic 1,3,4‐oxadiazole or 3,3″‐terphenyldicarbonitrile segments

New copoly(aryl ether)s ( P1 – P3 ) containing alternate 2,5‐dihexyloxy‐1,4‐di(m‐ethoxystyryl)benzene ( P1 , P2 ) or 2,5‐dihexyloxy‐1,4‐distyrylbenzene ( P3 ) chromophores and aromatic 1,3,4‐oxadiazole ( P1 ) or 3,3″‐terphenyldicarbonitrile ( P2 , P3 ) segments were prepared by Horner reaction ( P1 and P2 ) or nucleophilic displacement reaction ( P3 ). They are basically amorphous materials with 5% weight‐loss temperature above 410 °C. Their absorption, photoluminescence spectra, and quantum yields are dependent on the composition of the isolated fluorophores. The emissions are exclusively dominated by 1,4‐distyrylbenzene segments via excitation energy transfer from electron‐transporting 1,3,4‐oxadiazole ( P1 ) or 3,3″‐terphenyldicarbonitrile ( P2 , P3 ) chromophores. The HOMO and LUMO energy levels have been estimated from their cyclic voltammograms, and the observations confirm that oxidation and reduction start from the emitting 1,4‐distyrylbenzene and electron‐transporting segments, respectively, indicating that both carriers affinity can be enhanced simultaneously. Among the two‐layer PLED devices (ITO/PEDOT/ P1 – P3 /Al), P1 exhibits the best performance with a turn‐on field of 4 × 10⁵ V/cm and a maximum luminance of 225 cd/m². However, P2 emits green–yellow light (555 nm), owing to the excimer emission. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5009–5022, 2005     

Optical and electroluminescent properties of novel poly(aryl ether)s with isolated carbazole and p‐quaterphenyl fluorophores

We report the optical and electroluminescent properties of four novel poly(aryl ether)s ( P1 – P4 ) consisting of alternate isolated hole‐transporting [carbazole or 3,6‐bis(styryl)carbazole] and electron‐transporting [dicyano‐p‐quaterphenyl or bis(trifluoromethyl)‐p‐quaterphenyl] fluorophores. The photoluminescence (PL) spectra of the four polymeric films show maximum peaks around 407–413 nm for P1 , P2 and 442–447 nm for P3 , P4 . The PL spectra of P1 ～ P4 are dependent on the composition of the two isolated fluorophores. According to the observation of relative quantum yield in poor solvent (cyclohexane), P2 containing more bulky trifluoromethyl groups in p‐quaterphenyl segments prevented aggregate quenching processes more than P1 . Compared with P1 and P2 with carbazole segments, P3 and P4 with 3,6‐bis(styryl)carbazole segments exhibited less interchain interaction and a low threshold electric field in a single‐layer device. The p‐quaterphenyl and carbazole [or 3,6‐bis(styryl)carbazole] segments were regarded as electron‐transporting and hole‐transporting units, respectively, in the single‐layer light‐emitting diodes (Al/ P1 – P4 /ITO). In the double‐layer device (ITO/MEH‐PPV/ P2 /Al), the maximum luminance was doubled, and the threshold electric fields diminished because P2 functioned as an electron‐transporting and hole‐blocking layer. Furthermore, the voltage‐tunable multicolor emission from orange to green was observed. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 333–340, 2004     

Synthesis and characterization of novel polyimide from bis‐(3‐aminophenyl)‐4‐(trifluoromethyl)phenyl phosphine oxide

A novel diamine, bis‐(3‐aminophenyl)‐4‐(trifluoromethyl)phenyl phosphine oxide (mDA3FPPO), containing phosphine oxide and fluorine moieties was prepared via the Grignard reaction from an intermediate, 4‐(trifluoromethyl)phenyl diphenyl phosphine oxide, that was synthesized from diphenylphosphinic chloride and 4‐(trifluoromethyl)bromobenzene, followed by nitration and reduction. The monomer was characterized by Fourier transform infrared (FTIR), ¹H NMR, ³¹P NMR, ¹⁹F NMR spectroscopies; elemental analysis; melting point measurements; and titration and was used to prepare polyimides with a number of dianhydrides such as pyromellitic dianhydride (PMDA), 5,5′‐[2,2,2‐trifluoro‐1‐(trifluoromethyl)ethyliden]‐bis‐1,3‐isobenzofuranedione (6FDA), 3,3′,4,4′‐benzophenone tetracarboxylic dianhydride (BTDA), and 4,4′‐oxydiphthalic dianhydride (ODPA). Polyimides were synthesized via a conventional two‐step route; preparation of polyamic acids, followed by solution imidization, and the molecular weight were controlled to 20,000 g/mol. Resulting polyimides were characterized by FTIR, NMR, DSC, and intrinsic viscosity measurements. Refractive‐index, dielectric constant, and adhesive properties were also determined. The properties of polyimides were compared with those of polyimides prepared from 1,1‐bis‐(4‐aminophenyl)‐1‐phenyl‐2,2,2‐trifluoroethane (3FDAm) and bis‐(3‐aminophenyl) phenyl phosphine oxide (mDAPPO). The polyimides prepared from mDA3FPPO provided high glass‐transition temperatures (248–311 °C), good thermal stability, excellent solubility, low birefringence (0.0030–0.0036), low dielectric constants (2.9–3.1), and excellent adhesive properties with Cu foils (107 g/mm). © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 3335–3347, 2001     

Synthesis of Functionalized Polynorbornanes Employing 2,5‐Bis(trifluoromethyl)‐1,3,4‐oxadiazole

Cycloaddition reaction of 2,5‐bis(trifluoromethyl)‐1,3,4‐oxadiazole with strained olefinic bonds of norbornenes was used to synthetize functionalized polynorbornanes. This simple, one step procedure was more effective when reaction was carried out by classical heating, in comparison to microwave‐assisted reactions. Various functional groups were stable in the reaction conditions (ester, imide, phthalimide, piperidyl, and carboxylic acid), whereas anhydride, N‐Boc, or TMS functionalities do not withstand reaction conditions.     

Antibacterial and Antifungal Activities of 2‐(substituted ether)‐5‐(1‐phenyl‐5‐(trifluoromethyl)‐1H‐pyrazol‐4‐yl)‐1,3,4‐oxadiazole Derivatives

By replacing the amide bond into 1,3,4‐oxadiazole moiety, a series of 1‐phenyl‐5‐(trifluoromethyl)‐1H‐pyrazole derivatives bearing 1,3,4‐oxadiazole were synthesized and evaluated their antibacterial and antifungal activity. The bioassay results revealed that compounds 7a and 7b showed the strongest antibacterial activity toward pathogen Xanthomonas oryzae pv. oryzae with the EC50 values of 15.0 and 6.4 µg/mL, respectively; compound 6a exhibited comprehensive antifungal activity toward six kinds of fungi; compound 6f could selectively inhibit the growth of Sclertinia sclerotiorum and Rhizoctonia solani with the inhibition rates of 82.5 and 80.3% at the concentrate of 100 µg/mL, respectively; compound 7b exerted good antifungal activity toward Fusarium oxysporum, Cytospora mandshurica, and Rhizoctonia solani with the inhibition rates of 70.8, 69.5, and 71.5%, respectively. The results suggested that this kind of compounds could be further studied as promising antimicrobial agents.     

Photoluminescent and electrochemical properties of novel copoly(aryl ether)s with isolated fluorophores

Two, novel copoly(aryl ether)s ( P1 and P2 ) consisting of alternate, isolated electron‐ and hole‐transporting fluorophores were synthesized and characterized. Furthermore, we investigated the optical, photoluminescent (PL), and electrochemical properties of copoly(aryl ether)s P1 – P5 . The PL spectra of these polymers in film states showed maximum peaks around 420–498 nm. However, compared with the PL spectra of corresponding model compounds M1 – M5 , the emissions of P1 and P2 were compositions of the two isolated fluorophores, and that of P3 was dominated by the fluorophores with a longer emissive wavelength via the energy transfer. The formation of an interchain interaction in P4 and P5 was also observed. The highest occupied molecular orbital and lowest unoccupied molecular orbital energy levels of these copolymers were measured by cyclic voltammetry. Both the electron and hole affinities could be enhanced simultaneously because of the introduction of isolated hole‐transporting naphthalene (or fluorene) and electron‐transporting bis‐1,3,4‐oxadiazole segments. The single‐layer devices (Al/polymer/indium tin oxide) of P1 , P2 , and P4 revealed blue or blue‐green electroluminescence, but that of P3 emitted yellow light because of the excimer emission. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 883–893, 2004     

Vinyl copolymers containing pendant 1,4‐distyrylbenzene and 1,3,4‐oxadiazole chromophores: Preparation and optoelectronic properties

We prepared two vinyl copolymers P1 and P2 containing pendant distyrylbenzene and aromatic 1,3,4‐oxadiazole derivatives, respectively, from their precursor poly(styrene‐ran‐4‐vinylbenzyl chloride) (M_w = 11,400, PDI = 1.18), which had been prepared by the controlled radical polymerization (RAFT). Two main chain polymers containing similar isolated distyrylbenzene ( P3) and aromatic 1,3,4‐oxadiazole ( P4 ) chromophores were also synthesized for comparative study. The resulted copolymers ( P1 – P4 ) are soluble in common organic solvents and are basically amorphous materials with 5% weight‐loss temperature higher than 360 °C. The PL spectral results reveal that the architecture of P1 prevents the formation of inter‐ or intramolecular interaction. The HOMO and LUMO levels of P2 , estimated from cyclic voltammetric data, are ?5.96 and ?3.81 eV, respectively, which are much lower than those of P1 (?5.12 and ?3.11 eV). The emission of blend from P1 and P2 are contributed mainly from distyrylbenzene fluorophore (～450 nm) owing to efficient energy transfer. Moreover, the blend exhibits three kinds of redox behavior depending on their weight ratios. The luminance and current efficiency of the EL device lpar;ITO/PEDOT/ MEH ‐ PPV + P2 /Al) are 503 cd/m² and 0.11 cd/A, which can be improved to 1285 cd/m² and 0.44 cd/A, respectively, as the weight ratio of P2 increases from 0 to 20%. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 5362–5377, 2006     

Synthesis and characterization of novel polyimides with 2,2‐bis[4(4‐aminophenoxy)phenyl]phthalein‐3′,5′‐bis(trifluoromethyl)anilide

2,2‐Bis[4(4‐aminophenoxy)phenyl]phthalein‐3′,5′‐bis(trifluoromethyl)anilide (6FADAP), containing fluorine and phthalimide moieties, was synthesized via the Williamson ether condensation reaction from 1‐chloro‐4‐nitrobenzene and phenolphthalein‐3′,5′‐bis(trifluoromethyl)anilide, which was followed by hydrogenation. Monomers such as 2,2‐bis[4(4‐aminophenoxy)phenyl]phthalein‐anilide containing phthalimide groups and 2,2‐bis[4(4‐aminophenoxy)phenyl]phthalein containing only phthalein moieties were also synthesized for comparison. The monomers were first characterized by Fourier transform infrared (FTIR), ¹H NMR, ¹⁹F NMR, elemental analysis, and titration and were then used to prepare polyimides with 2,2‐bis(3,4‐dicarboxyphenyl)hexafluoropropane dianhydride. The polyimides were designed to have molecular weights of 20,000 g/mol via off‐stoichiometry and were characterized by FTIR, NMR, gel permeation chromatography (GPC), differential scanning calorimetry, and thermogravimetric analysis. Their solubility, water absorption, dielectric constant, and refractive index were also evaluated. The polyimides prepared with 6FADAP, containing fluorine and phthalimide moieties, had excellent solubility in N‐methylpyrrolidinone, N,N‐dimethylacetamide, tetrahydrofuran, CHCl₃, tetrachloroethane, and acetone, and GPC analysis showed a molecular weight of 18,700 g/mol. The polyimides also exhibited a high glass‐transition temperature (290 °C), good thermal stability (～500 °C in air), low water absorption (1.9 wt %), a low dielectric constant (2.81), a low refractive index, and low birefringence (0.0041). © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 3361–3374, 2003     

Click Inspired Synthesis of 1,2,3‐Triazole‐linked 1,3,4‐Oxadiazole Glycoconjugates

The glycoconjugation of biologically privileged 1,3,4‐oxadiazole scaffold is described via Cu(I)‐catalyzed azide–alkyne cycloaddition. A series of glycosyl alkynes 1b – i , obtained from various commercial sugars, were treated with azide functionalized 1,3,4‐oxadiazole using click chemistry to access triazole‐linked glycosylated 1,3,4‐oxadiazoles 10b – i in good yields. The structure of the developed glycoconjugates has been ascertained by extensive spectroscopic analysis (¹H &¹³C NMR, IR, and MS).     

Synthesis and Antibacterial Activity of Some New 2,5‐Disubstituted‐1,3,4‐oxadiazole Derivatives

Synthesis of some new oxadiazole derivatives starting from 1,2,3-benzo[d]triazole-1-acetic hydrazide (1) is described. The target compounds 2-(N-substituted-aminocarbonylmethylthio)-5-(1,2,3-benzo[d]triazol-1-ylmethyl)- 1,3,4-oxadiazole (4a—4i) and 2-[2-(N-substituted-aminocarbonyl)ethylthio]-5-(1,2,3-benzo[d]triazol-1-ylmethyl)- 1,3,4-oxadiazole (5a—5i) were obtained in good yields via cyclisation of 1 and subjected to antibacterial activity test against pathogenic bacteria. The halogen containing mono- and di-substituted derivatives showed excellent antibacterial activity compared to other analogues.     

Synthesis of 4‐(5‐aryl‐1,3,4‐oxadiazol‐2‐yl)phenyl‐hydrazine derivatives from 3‐(4‐hydrazinocarbonyl‐phenyl)sydnones

The synthesis of potential fluorescent active 4‐(5‐aryl‐1,3,4‐oxadiazol‐2‐yl)phenylhydrazine derivatives was accomplished in three steps. The key step was the dehydration cyclization of 1,2‐diacylhydrazines to form the 1,3,4‐oxadiazole ring by use of acetic anhydride/perchloric acid mixture as the dehydrating agent. The sydnone moiety served as the masked hydrazines, which could be demasked by HCl for further application. © 2007 Wiley Periodicals, Inc. Heteroatom Chem 18:438–442, 2007; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/hc.20318     

ZnII and CuII complexes generated from 5‐(pyridin‐4‐yl)‐3‐[2‐(pyridin‐4‐yl)ethyl]‐1,3,4‐oxadiazole‐2(3H)‐thione

A new 1,3,4‐oxadiazole‐containing bispyridyl ligand, namely 5‐(pyridin‐4‐yl)‐3‐[2‐(pyridin‐4‐yl)ethyl]‐1,3,4‐oxadiazole‐2(3H)‐thione (L), has been used to create the novel complexes tetranitratobis{μ‐5‐(pyridin‐4‐yl)‐3‐[2‐(pyridin‐4‐yl)ethyl]‐1,3,4‐oxadiazole‐2(3H)‐thione}zinc(II), [Zn₂(NO₃)₄(C₁₄H₁₂N₄OS)₂], (I), and catena‐poly[[[dinitratocopper(II)]‐bis{μ‐5‐(pyridin‐4‐yl)‐3‐[2‐(pyridin‐4‐yl)ethyl]‐1,3,4‐oxadiazole‐2(3H)‐thione}] nitrate acetonitrile sesquisolvate dichloromethane sesquisolvate], {[Cu(NO₃)(C₁₄H₁₂N₄OS)₂]NO₃·1.5CH₃CN·1.5CH₂Cl₂}_n, (II). Compound (I) presents a distorted rectangular centrosymmetric Zn₂L₂ ring (dimensions 9.56 × 7.06 Å), where each Zn^II centre lies in a {ZnN₂O₄} coordination environment. These binuclear zinc metallocycles are linked into a two‐dimensional network through nonclassical C—H...O hydrogen bonds. The resulting sheets lie parallel to the ac plane. Compound (II), which crystallizes as a nonmerohedral twin, is a coordination polymer with double chains of Cu^II centres linked by bridging L ligands, propagating parallel to the crystallographic a axis. The Cu^II centres adopt a distorted square‐pyramidal CuN₄O coordination environment with apical O atoms. The chains in (II) are interlinked via two kinds of π–π stacking interactions along [01]. In addition, the structure of (II) contains channels parallel to the crystallographic a direction. The guest components in these channels consist of dichloromethane and acetonitrile solvent molecules and uncoordinated nitrate anions.     

2,5‐Bis(2‐(diphenylphosphino)phenyl)‐1,3,4‐oxadiazole ligands and their Cu(I) complexes for Sonogashira coupling reaction

Two diphosphane ligands – 2,5‐bis(2‐(diphenylphosphino)‐5‐R)phenyl)‐1,3,4‐oxadiazole ( L1 , R = H, L2 , R = OMe) and their binuclear complexes, L1Cu and L2Cu , were prepared and characterized. The molecular structures of L1Cu and L2Cu , as perchlorate salts, were established by X‐ray crystallography, which showed them to be binuclear complexes with each Cu atom tetrahedrally coordinated by two P atoms and two N atoms. The ligands and their Cu(I) complexes catalyzed Sonogashira coupling reactions of iodobenzene with phenylacetylene in the presence of K₂CO₃ under Pd‐free conditions. Coupling reactions catalyzed by L1 or L2 with Cu(MeCN)₄ClO₄ in situ exhibited better yields than those by the corresponding Cu(I) complexes L1Cu or L2Cu . Detailed studies showed L1 or L2 with Cu(MeCN)₄ClO₄ to be suitable catalysts for the coupling reaction of terminal alkynes and aryl halides. The coupling reactions of aryl iodides with electron‐withdrawing groups showed better results. Copyright © 2014 John Wiley & Sons, Ltd.     

2,5‐Bis[4‐methyl‐3‐(pyridin‐3‐yl)phenyl]‐1,3,4‐oxadiazole and its one‐dimensional polymeric complex with ZnCl2

2,5‐Bis[4‐methyl‐3‐(pyridin‐3‐yl)phenyl]‐1,3,4‐oxadiazole (L), C₂₆H₂₀N₄O, forms one‐dimensional chains via two types of intermolecular π–π interactions. In catena‐poly[[dichloridozinc(II)]‐μ‐2,5‐bis[4‐methyl‐3‐(pyridin‐3‐yl)phenyl]‐1,3,4‐oxadiazole], [ZnCl₂(C₂₆H₂₀N₄O)]_n, synthesized by the combination of L with ZnCl₂, the Zn^II centres are coordinated by two Cl atoms and two N atoms from two L ligands. [ZnCl₂L]_n forms one‐dimensional P (plus) and M (minus) helical chains, where the L ligand has different directions of twist. The helical chains stack together via interchain π–π and C—H...π interactions.     

Synthesis of Some Novel 3,6‐Bis(1,2,3‐triazolyl)‐s‐triazolo[3,4‐b]‐1,3,4‐thiadiazole Derivatives

The cyclization of 1‐amino‐2‐mercapto‐5‐[1‐(4‐ethoxyphenyl)‐5‐methyl‐1,2,3‐triazol‐4‐yl]‐1,3,4‐triazole which was synthesized from p‐ethoxyaniline with various triazole acid in absolute phosphorus oxychloride yields 3,6‐bis(1,2,3‐triazolyl)‐s‐triazolo[3,4‐b]‐1,3,4‐thiadiazole derivatives 9a?j , and their structures are established by MS, IR, CHN and ¹H NMR spectral data.     

Three AgI,CuI and CdII coordination polymers based on the new asymmetrical ligand 2‐{4‐[(1H‐imidazol‐1‐yl)methyl]phenyl}‐5‐(pyridin‐4‐yl)‐1,3,4‐oxadiazole: syntheses,characterization and emission properties

The new asymmetrical organic ligand 2‐{4‐[(1H‐imidazol‐1‐yl)methyl]phenyl}‐5‐(pyridin‐4‐yl)‐1,3,4‐oxadiazole ( L , C₁₇H₁₃N₅O), containing pyridine and imidazole terminal groups, as well as potential oxdiazole coordination sites, was designed and synthesized. The coordination chemistry of L with soft Ag^I, Cu^I and Cd^II metal ions was investigated and three new coordination polymers (CPs), namely, catena‐poly[[silver(I)‐μ‐2‐{4‐[(1H‐imidazol‐1‐yl)methyl]phenyl}‐5‐(pyridin‐4‐yl)‐1,3,4‐oxadiazole] hexafluoridophosphate], {[Ag( L )]PF₆}_n, catena‐poly[[copper(I)‐di‐μ‐iodido‐copper(I)‐bis(μ‐2‐{4‐[(1H‐imidazol‐1‐yl)methyl]phenyl}‐5‐(pyridin‐4‐yl)‐1,3,4‐oxadiazole)] 1,4‐dioxane monosolvate], {[Cu₂I₂( L )₂]·C₄H₈O₂}_n, and catena‐poly[[[dinitratocopper(II)]‐bis(μ‐2‐{4‐[(1H‐imidazol‐1‐yl)methyl]phenyl}‐5‐(pyridin‐4‐yl)‐1,3,4‐oxadiazole)]–methanol–water (1/1/0.65)], {[Cd( L )₂(NO₃)₂]·2CH₄O·0.65H₂O}_n, were obtained. The experimental results show that ligand L coordinates easily with linear Ag^I, tetrahedral Cu^I and octahedral Cd^II metal atoms to form one‐dimensional polymeric structures. The intermediate oxadiazole ring does not participate in the coordination interactions with the metal ions. In all three CPs, weak π–π interactions between the nearly coplanar pyridine, oxadiazole and benzene rings play an important role in the packing of the polymeric chains.