Preparation of phosphorus-containing polymers—XVI. Synthesis of phosphorus-containing polyanhydride-imides

Phosphorus-containing polyanhydride-imides were synthesized from N,N-bis(4-carboxyphthalimido)-3,3′-diphenylalkylphosphine oxide, 3,3′-[N,N′-bis(4-carboxyphthalimido)]benzophenone and their mixtures in two steps via the diacetyl derivatives of the bisimide-carboxylic acids. The resulting polymers have reduced viscosities of 0.06–0.14 dl/g and are soluble in polar aprotic solvents such as DMA, DMF and DMSO, and conc. H₂SO₄ etc. They have good hydrolytic stability for moisture and water. Phosphorus-containing polymers have little heat-resistance and poor flame-retardance. The benefit of incorporating phosphorus in the polymers is small.     

Hydrazine‐based polyimides from isomeric bis(chlorophthalimide)s

3,3′‐Dichloro‐N,N′‐biphthalimide (3,3′‐DCBPI), 3,4′‐dichloro‐N,N′‐biphthalimide (3,4′‐DCBPI), and 4,4′‐dichloro‐N,N′‐biphthalimide (4,4′‐DCBPI) were synthesized from 3‐ or 4‐chlorophthalic anhydrides and hydrazine in glacial acetic acid. The yield of 3,3′‐DCBPI (90%) was much higher than that of 4,4′‐DCBPI (33%) because of the better stability of the intermediate, 3‐chloro‐N‐aminophthalimide, and 3,3′‐DCBPI. A series of hydrazine‐based polyimides were prepared from isomeric DCBPIs and 4,4′‐thiobisbenzenethiol (TBBT) in N,N‐dimethylacetamide in the presence of tributylamine. Inherent viscosity of these polymers was in the range of 0.51–0.69 dL/g in 1‐methyl‐2‐pyrrolidinone (NMP) at 30 °C. These polyimides were soluble in 1,1,2,2‐terachloroethane, NMP, and phenols. The 5% weight‐loss temperatures (T_5%s) of the polymers were near 450 °C in N₂. Their glass‐transition temperatures (T_gs) determined by dynamic mechanical thermal analysis and differential scanning calorimetry increased according to the order of polyimides based on 4,4′‐DCBPI, 3,4′‐DCBPI, and 3,3′‐DCBPI. The hydrolytic stability of these polymers was measured under acid, basic, and neutral conditions and the results indicated that the order was 3,3′‐DCBPI/TBBT > 3,4′‐DCBPI/TBBT > 4,4′‐DCBPI/TBBT. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 4933–4940, 2007     

Improved Synthesis of Indirubin Derivatives by Sequential Build‐Up of the Indoxyl Unit: First Preparation of Fluorescent Indirubins

Indirubin, present in extracts of Isatis tinctoria and some other plant species, has promising cytotoxicity against a variety of cell lines by inhibition of cyclin‐dependent kinases. Chemical synthesis of its derivatives relies on the combination of isatins and 2,3‐dihydro‐1H‐indol‐3‐one (‘indoxyl’) derivatives and usually yields indigo as well as other by‐products. Inspection of the hydrolysis of the long‐known condensation products of 2‐thioxothiazolidin‐4‐one with isatins gave useful hints for an improved synthesis of indirubins: this reaction does not yield quinoline derivatives but 2‐(2,3‐dihydro‐2‐oxo‐1H‐indol‐3‐ylidene)‐2‐sulfanyl acetic acids. By substitution of the sulfanyl group in this oxindoles with anilines and straightforward cyclization under Nazarov conditions, a broad variety of indirubins substituted in the indoxyl ring system are thus available, usually in very good purity and yield. Use of naphthylamines in this reaction sequence yields various fluorescent substances with λ_fl at ca. 630 nm.     

Oxidative Asymmetric Aza‐Friedel–Crafts Alkylation of Indoles with 3‐Indolinone‐2‐carboxylates Catalyzed by a BINOL Phosphoric Acid and Promoted by DDQ

An asymmetric aza‐Friedel–Crafts alkylation reaction between indoles and indolenines that were derived in situ from 3‐indolinone‐2‐carboxylates has been developed by using 3,3′‐bis(triphenylsilyl)‐1,1′‐binaphthyl‐2,2′‐diyl hydrogen phosphate as a catalyst. The reaction proceeded under mild conditions and provided chiral indol‐3‐yl‐3‐indolinone‐2‐carboxylate derivatives in good yields with excellent ee values (up to 98.6 %). Similarly, the Mannich‐type addition of indoline‐3‐ones to indolenines provided heterodimers with vicinal chiral quaternary centers. This method was successfully applied to the construction of the core structure of trigonoliimine C.     

Direct copolymerization of sulfonated poly(phthalazinone arylene ether)s for proton‐exchange‐membrane materials

Sulfonated poly(phthalazinone ether ketone) (SPPEK) copolymers and sulfonated poly(phthalazinone ether sulfone) (SPPES) copolymers containing pendant sodium sulfonate groups were prepared by direct copolymerization. The reaction of disodium 3,3′‐disulfonate‐4,4′‐difluorobenzophenone (SDFB‐Na), 4,4′‐difluorobenzophenone (DFB), and 4‐(4‐hydroxyphenyl)‐1(2H)‐phthalazinone (DHPZ) at 170 °C in N‐methyl‐2‐pyrrolidione containing anhydrous potassium carbonate gave SPPEKs. SPPESs were similarly obtained with 3,3′‐disulfonate‐4,4′‐difluorophenyl sulfone, 4‐fluorophenyl sulfone (DFS), and DHPZ as monomers. The sulfonic acid groups, being on deactivated positions of the polymer backbone, were expected to be hydrolytically more stable than postsulfonated polymers. Fourier transform infrared and ¹H NMR were used to characterize the structures and degrees of sulfonation of the sulfonated polymers. Membrane films of SPPEKs with SDFB‐Na/DFB molar feed ratios of up to 60/40 and SPPESs with sulfonated 4‐fluorophenyl sulfone/DFS molar feed ratios of up to 50/50 were cast from N,N‐dimethylacetamide polymer solutions. Membrane films in acid form were then obtained by the treatment of the sodium‐form membrane films in 2 N sulfuric acid at room temperature. An increase in the number of sulfonate groups in the copolymers resulted in an increased glass‐transition temperature and enhanced membrane hydrophilicity. The sodium‐form copolymers were thermally more stable than their acid forms. The proton conductivities of the acid‐form copolymers with sulfonated monomer/unsulfonated monomer molar feed ratios of 0.5 and 0.6 were higher than 10^?2 S/cm and increased with temperature; they were less temperature‐dependent than those of the postsulfonated products. SPPESH‐50 showed higher conductivity than the corresponding postsulfonated poly(phthalazinone ether sulfone). © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 2731–2742, 2003     

Syntheses and properties of organosoluble polyimides based on 5,5′‐bis[4‐(4‐aminophenoxy)phenyl]‐4, 7‐methanohexahydroindan

A series of organosoluble aromatic polyimides (PIs) was synthesized from 5,5′‐bis[4‐(4‐aminophenoxy)phenyl]‐4,7‐methanohexahydroindan (3) and commercial available aromatic dianhydrides such as 3,3′,4,4′‐biphenyltetracarboxylic dianhydride (BPDA), 4,4′‐oxydiphthalic anhydride (ODPA), 4,4′‐sulfonyl diphthalic anhydride (SDPA), or 2,2′‐bis(3,4‐dicarboxyphenyl) hexafluoropropanic dianhydride (6FDA). PIs (III_c–f), which were synthesized by direct polymerization in m‐cresol, had inherent viscosities of 0.83–1.05 dL/g. These polymers could easily be dissolved in N,N′‐dimethylacetamide (DMAc), N‐methyl‐2‐pyrrolidone (NMP), N,N‐dimethylformamide (DMF), pyridine, m‐cresol, and dichloromethane. Whereas copolymerization was proceeded with equivalent molar ratios of pyromellitic dianhydride (PMDA)/6FDA, 3,3′,4,4′‐benzophenonetetracarboxylic dianhydride (BTDA)/6FDA, or BTDA/SDPA, or ½ for PMDA/SDPA, copolyimides (co‐PIs), derived from 3 and mixed dianhydrides, were soluble in NMP. All the soluble PIs could form transparent, flexible, and tough films, and they showed amorphous characteristics. These films had tensile strengths of 88–111 MPa, elongations at break of 5–10% and initial moduli of 2.01–2.67 GPa. The glass transition temperatures of these polymers were in the range of 252–311°C. Except for III_e, the 10% weight loss temperatures (T_d) of PIs were above 500°C, and the amount of carbonized residues of the PIs at 800°C in nitrogen atmosphere were above 50%. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 1681–1691, 1999     

Asymmetric Friedel-Crafts alkylation of indoles with methyl (E)-2-oxo-4-aryl-3-butenoates catalyzed by Sc(OTf)3/pybox

The asymmetric Friedel–Crafts reaction between a series of substituted indoles 2 a – l and methyl (E)‐2‐oxo‐4‐aryl‐3‐butenoates 3 a – c has been efficiently catalyzed by the scandium(III) triflate complex of (4′S,5′S)‐2,6‐bis[4′‐(triisopropylsilyl)oxymethyl‐5′‐phenyl‐1′,3′‐oxazolin‐2′‐yl]pyridine (pybox; 1 ). Substituted 4‐(indol‐3‐yl)‐2‐oxo‐4‐arylbutyric acid methyl esters 4 a – n were usually formed in excellent yields and the enantioselectivity was up to 99 % ee, irrespective of the electronic character of the substituent and its location on the indole ring, albeit with the exclusion of position 2. The adducts could be obtained as stable enol tautomers and the equilibrium with the keto structure is discussed. The X‐ray crystal structure determination of 4 m indicated the 4R absolute configuration, thus confirming the proposal of Jørgensen for 4 i . The sense of the stereoinduction can be rationalized by the same octahedral complex 5 between 3 , pybox 1 , and scandium triflate already proposed for the Diels–Alder/hetero‐Diels–Alder and the Mukaiyama–aldol reactions of pyruvates.     

Organosoluble polyimides and copolyimides based on 1,1‐bis[4‐(4‐aminophenoxy)phenyl]‐1‐phenylethane and aromatic dianhydrides

1,1‐Bis[4‐(4‐aminophenoxy)phenyl]‐1‐phenylethane (BAPPE) was prepared through nucleophilic substitution reaction of 1,1‐bis(4‐hydroxyphenyl)‐1‐phenylethane and p‐chloronitrobenzene in the presence of K₂CO₃ in N,N‐dimethylformamide, followed by catalytic reduction with hydrazine and Pd/C. Novel organosoluble polyimides and copolyimides were synthesized from BAPPE and six kinds of commercial dianhydrides, including pyromellitic dianhydride (PMDA, I_a ), 3,3′,4,4′‐benzophenonetetracarboxylic dianhydride (BTDA, I_b ), 3,3′,4,4′‐ biphenyltetracarboxylic dianhydride (BPDA, I_c ), 4,4′‐oxydiphthalic anhydride (ODPA, I_d ), 3,3′,4,4′‐diphenylsulfonetetracarboxylic dianhydride (DSDA, I_e ) and 4,4′‐hexafluoroisopropylidenediphthalic anhydride (6FDA, I_f ). Differing with the conventional polyimide process by thermal cyclodehydration of poly(amic acid), when polyimides were prepared by chemical cyclodehydration with N‐methyl‐2‐pyrrolidone as used solvent, resulted polymers showed good solubility. Additional, I_a,b were mixed respectively with the rest of dianhydrides (I_c–f) and BAPPE at certain molar ratios to prepare copolyimides with arbitrary solubilities. These polyimides and copolyimides were characterized by good mechanical properties together with good thermal stability. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 2082–2090, 2000     

New organo‐soluble aromatic polyimides based on 3,3′,5,5′‐tetrabromo‐2,2‐bis[4‐(3,4‐dicarboxyphenoxy)phenyl]propane dianhydride and aromatic diamines

New aromatic tetracarboxylic dianhydride, having isopropylidene and bromo‐substituted arylene ether structure 3,3′,5,5′‐tetrabromo‐2,2‐bis[4‐(3,4‐dicarboxyphenoxy)phenyl]propane dianhydride, was synthesized by the reaction of 4‐nitrophthalonitrile with 3,3′,5,5′‐tetrabromobisphenol A, followed by alkaline hydrolysis of the intermediate bis(ether dinitrile) and subsequent dehydration of the resulting bis(ether diacid). The novel aromatic polyetherimides having inherent viscosities up to 1.04 dL g⁻¹ were obtained by either a one‐step or a conventional two‐step polymerization process starting from the bis(ether anhydride) and various aromatic diamines. All the polyimides showed typical amorphous diffraction patterns. Most of the polyimides were readily soluble in common organic solvents such as N,N‐dimethylacetamide (DMAc), N‐methyl‐2‐pyrrolidone (NMP), pyridine, and even in less polar solvents like chloroform and tetrahydrofuran (THF). These aromatic polyimides had glass transition temperatures in the range of 256–303°C, depending on the nature of the diamine moiety. Thermogravimetric analysis (TGA) showed that all polymers were stable, with 10% weight loss recorded above 470°C in nitrogen. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 1673–1680, 1999     

Construction and photoluminescence properties of a three‐dimensional ZnII coordination network based on naphthalene‐1,4‐dicarboxylic acid and 1,6‐bis(pyridin‐3‐yl)‐1,3,5‐hexatriene

In recent years, coordination polymers constructed from multidentate carboxylate and pyridyl ligands have attracted much attention because these ligands can adopt a rich variety of coordination modes and thus lead to the formation of crystalline products with intriguing structures and interesting properties. A new coordination polymer, namely poly[[μ₂‐1,6‐bis(pyridin‐3‐yl)‐1,3,5‐hexatriene‐κ²N:N′](μ₃‐naphthalene‐1,4‐dicarboxylato‐κ⁴O¹,O^1′:O⁴:O^4′)zinc(II)], [Zn(C₁₂H₆O₄)(C₁₆H₁₄N₂)]_n, has been prepared by the self‐assembly of Zn(NO₃)₂·6H₂O, naphthalene‐1,4‐dicarboxylic acid (1,4‐H₂ndc) and 1,6‐bis(pyridin‐3‐yl)‐1,3,5‐hexatriene (3,3′‐bphte) under hydrothermal conditions. The title compound has been structurally characterized by IR spectroscopy, elemental analysis, powder X‐ray diffraction and single‐crystal X‐ray diffraction analysis. Each Zn^II ion is six‐coordinated by four O atoms from three 1,4‐ndc²⁻ ligands and by two N atoms from two 3,3′‐bphte ligands, forming a distorted octahedral ZnO₄N₂ coordination geometry. Pairs of Zn^II ions are linked by 1,4‐ndc²⁻ ligands, leading to the formation of a two‐dimensional square lattice ( sql ) layer extending in the ab plane. In the crystal, adjacent layers are further connected by 3,3′‐bphte bridges, generating a three‐dimensional architecture. From a topological viewpoint, if each dinuclear zinc unit is considered as a 6‐connected node and the 1,4‐ndc²⁻ and 3,3′‐bphte ligands are regarded as linkers, the structure can be simplified as a unique three‐dimensional 6‐connected framework with the point symbol 4⁴6¹⁰8. The thermal stability and solid‐state photoluminescence properties have also been investigated.     

Aromatic poly(1,3,4‐oxadiazole)s and poly(amide‐1,3,4‐oxadiazole)s containing ether sulfone linkages

Polyhydrazides and poly(amide‐hydrazide)s were prepared from two ether‐sulfone‐dicarboxylic acids, 4,4′‐[sulfonylbis(1,4‐phenylene)dioxy]dibenzoic acid and 4,4′‐[sulfonylbis(2,6‐dimethyl‐1,4‐phenylene)dioxy]dibenzoic acid, or their diacyl chlorides with terephthalic dihydrazide, isophthalic dihydrazide, and p‐aminobenzhydrazide via a phosphorylation reaction or a low‐temperature solution polycondensation. All the hydrazide polymers were found to be amorphous according to X‐ray diffraction analysis. They were readily soluble in polar organic solvents such as N‐methyl‐2‐pyrrolidone and N,N‐dimethylacetamide and could afford colorless, flexible, and tough films with good mechanical strengths via solvent casting. These hydrazide polymers exhibited glass‐transition temperatures of 149–207 °C and could be thermally cyclodehydrated into the corresponding oxadiazole polymers in the solid state at elevated temperatures. Although the oxadiazole polymers showed a significantly decreased solubility with respect to their hydrazide prepolymers, some oxadiazole polymers were still organosoluble. The thermally converted oxadiazole polymers had glass‐transition temperatures of 217–255 °C and softening temperatures of 215–268 °C and did not show significant weight loss before 400 °C in nitrogen or air. For a comparative study, related sulfonyl polymers without the ether groups were also synthesized from 4,4′‐sulfonyldibenzoic acid and the hydrazide monomers by the same synthetic routes. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 2271–2286, 2001     

Novel polyimides obtained from a new aromatic diamine (BAPO) containing pyridine and 1,3,4‐oxadiazole moieties for removal of Co(II) and Ni(II) ions

Novel, thermally stable polyimides (PIs) containing a 1,3,4‐oxadiazole and pyridine moieties based on a new aromatic diamine 2,5‐bis‐(aminopyridine‐2‐yl)‐1,3,4‐oxadiazole, BAPO, were synthesized. The prepared polymers were soluble in dimethysulfoxide (DMSO) and concentrated sulfuric acid at room temperature as well as in polar and aprotic solvents, such as, N‐methylpyrrolidone (NMP) and N,N‐dimethylacetamide (DMAc) at elevated temperature. Thermal behaviors of the PIs were studied by thermogravimetric analysis/dynamic thermal analysis (TGA‐DTA) and differential scanning calorimetry (DSC). The inherent viscosities of the PI solutions were in the range of 0.38–0.61 dl/g (in DMSO with a concentration of 0.125 g/dl at 25 ± 0.5°C). The removal of Co(II) and Ni(II) ions from aqueous solutions was performed using polymer 6, which was obtained from BAPO and 3,3′,4,4′‐benzophenonetetracarboxylic dianhydride (BTDA). The maximum adsorption capacity was observed for Co(II) ion at pH = 7.0 (110.4 mg g^?1, 1.87 mmol g^?1). Copyright © 2015 John Wiley & Sons, Ltd.     

Thermally stable and organosoluble binaphthylene‐based poly(urea‐ether‐imide)s: one‐pot preparation and characterization

A new family of wholly aromatic poly(urea‐ether‐imide)s ( 4a–4f ) possessing binaphthylene‐twisted rings was prepared by diphenyl azidophosphate (DPAP)‐activated one‐pot polyaddition reaction of a preformed imide heterocyclic ring‐containing dicarboxylic acid, 2,2′‐bis(4‐trimellitimidophenoxy)‐ 1,1′‐binaphthyl ( 1 ) with various kinds of aromatic diamines ( 3a–3f ). At first, with due attention to structural similarity and to compare the characterization data, a model compound 2 was synthesized by the reaction of diimide‐dicarboxylic acid 1 with two mole equivalents of aniline. In this direct method, the polymers were prepared by polyaddition reactions of the in situ‐formed diisocyanate with the aromatic diamines. Molecular weights of the poly(urea‐ether‐imide)s obtained were evaluated viscometrically, and the inherent viscosities (η_inh) measured were in the range 0.10– 0.25 dl/g. All of the polymers were characterized by FT‐IR spectroscopic method and elemental analysis. All of the resulting polymers exhibited an excellent solubility in common polar solvents such as N‐methyl‐2‐pyrrolidone (NMP), dimethyl sulfoxide (DMSO), N,N‐dimethylformamide (DMF), and N,N‐dimethylacetamide (DMAc). Crystallinity of the resulted polymers was evaluated by wide‐angle X‐ray diffraction (WXRD) method, and they exhibited nearly a non‐crystalline nature as evidenced by their diffractograms. The glass transition temperatures (T_g) of the polymers determined by differential scanning calorimetry (DSC) thermograms were in the range of 274–302°C. The temperatures at 10% weight loss (T_d10%) from their thermogravimetric analysis (TGA/DTG) curves were found to be in the range of 389–414°C in nitrogen atmosphere. Copyright © 2008 John Wiley & Sons, Ltd.     

Synthesis and crystal structures of some bis(3‐methyl‐1H‐indol‐2‐yl)(salicyl)methanes

Four 2,2′‐bisindolylmethanes (BIMs), a useful class of polyindolyl species joined to a central carbon, were synthesized using salicylaldehyde derivatives and simple acid catalysis; these are 2‐[bis(3‐methyl‐1H‐indol‐2‐yl)methyl]‐6‐methylphenol, (IIa), 2‐[bis(3‐methyl‐1H‐indol‐2‐yl)methyl]‐4,6‐dichlorophenol, (IIb), 2‐[bis(3‐methyl‐1H‐indol‐2‐yl)methyl]‐4‐nitrophenol, (IIc), and 2‐[bis(3‐methyl‐1H‐indol‐2‐yl)methyl]‐4,6‐di‐tert‐butylphenol, (IId). BIMs (IIa) and (IIb) were characterized crystallographically as the dimethyl sulfoxide (DMSO) disolvates, i.e. C₂₆H₂₄N₂O·2C₂H₆OS and C₂₅H₂₀Cl₂N₂O·2C₂H₆OS, respectively. Both form strikingly similar one‐dimensional hydrogen‐bonding chain motifs with the DMSO solvent molecules. BIM (IIa) packs into double layers of chains whose orientations alternate every double layer, while (IIb) forms more simply packed chains along the a axis. BIM (IIa) has a remarkably long c axis.     

One‐dimensional CuII coordination polymers containing C2h‐symmetric 1,1′:4′,1′′‐terphenyl‐3,3′‐dicarboxylate linkers

Two new one‐dimensional Cu^II coordination polymers (CPs) containing the C_2h‐symmetric terphenyl‐based dicarboxylate linker 1,1′:4′,1′′‐terphenyl‐3,3′‐dicarboxylate (3,3′‐TPDC), namely catena‐poly[[bis(dimethylamine‐κN)copper(II)]‐μ‐1,1′:4′,1′′‐terphenyl‐3,3′‐dicarboxylato‐κ⁴O,O′:O′′:O′′′] monohydrate], {[Cu(C₂₀H₁₂O₄)(C₂H₇N)₂]·H₂O}_n, (I), and catena‐poly[[aquabis(dimethylamine‐κN)copper(II)]‐μ‐1,1′:4′,1′′‐terphenyl‐3,3′‐dicarboxylato‐κ²O³:O^3′] monohydrate], {[Cu(C₂₀H₁₂O₄)(C₂H₇N)₂(H₂O)]·H₂O}_n, (II), were both obtained from two different methods of preparation: one reaction was performed in the presence of 1,4‐diazabicyclo[2.2.2]octane (DABCO) as a potential pillar ligand and the other was carried out in the absence of the DABCO pillar. Both reactions afforded crystals of different colours, i.e. violet plates for (I) and blue needles for (II), both of which were analysed by X‐ray crystallography. The 3,3′‐TPDC bridging ligands coordinate the Cu^II ions in asymmetric chelating modes in (I) and in monodenate binding modes in (II), forming one‐dimensional chains in each case. Both coordination polymers contain two coordinated dimethylamine ligands in mutually trans positions, and there is an additional aqua ligand in (II). The solvent water molecules are involved in hydrogen bonds between the one‐dimensional coordination polymer chains, forming a two‐dimensional network in (I) and a three‐dimensional network in (II).     

Synthesis,characterization, and electroluminescence of PPV copolymers containing electron and hole‐transporting units

Three series of poly(phenylene vinylene) (PPV) derivatives containing hole‐transporting triphenylamine derivatives [N‐(4‐octoxylphenyl)diphenylamine, N,N′‐di(4‐octyloxylphenyl)‐N,N′‐diphenyl‐1,4‐phenylenediamine, and N,N′‐di(4‐octoxylphenyl)‐N,N′‐diphenylbenzidine] (donor) and electron‐transporting oxadiazole unit (2,5‐diphenyl‐1,3,4‐oxadiazole) (acceptor) in the main chain were synthesized by improved Wittig copolymerization. The resulting donor–acceptor (D‐A) polymers are readily soluble in common organic solvents, such as chloroform, dichloroethane, THF, and toluene. The polymers containing oxadiazole group exhibit good thermal stability with 5% weight loss above 400 °C. The intramolecular charge‐transfer was observed in these D‐A polymers. In comparison with corresponding polymers without oxadiazole unit, the single‐layer devices based on the D‐A polymers showed much improved electroluminescent properties, because of the balanced charge injection and transport. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 1566–1576, 2008     

Thermotropic liquid‐crystalline polymers containing five‐membered heterocyclic groups. X. Relationships between structures of semirigid polyesters based on three disubstituted 2,5‐diphenyl‐1,3,4‐thiadiazoles and thermotropic liquid‐crystalline and optical properties

Thermotropic liquid‐crystalline (LC) semirigid polyesters based on three terphenyl analogues of 1,3,4‐thiadiazole (2,5‐diphenyl‐1,3,4‐thiadiazole)s (DPTD) linking undecamethyleneoxy chain at different substituted positions were synthesized from three disubstituted (4,4′‐, 3,4′‐, and 3,3′‐) dioxydiundecanols of DPTD and four diesters, and the relationships between polymer structures and LC and optical properties were investigated. DSC measurements, texture observations, and wide‐angle X‐ray analyses revealed that the polymers composed of DPTD moiety having a more linear molecular structure and 1,4‐phenylene unit or short aliphatic chain tend to exhibit LC smectic C and/or A phases. The following observations were made: (1) the emergence of smectic C and/or A phases in all the polymers on the basis of 4,4′‐disubstituted DPTD, (2) formation of enantiotropic smectic C and/or A phases in the polymers containing a 1,4‐phenylene unit in the main chain, (3) formation of a more stable smectic C phase in the polymers having a short aliphatic [(CH₂)₄] chain, and (4) a decrease of the mesomorphic property of the polyesters in the order of 4,4′‐DPTD > 3,4′‐DPTD > 3,3′‐DPTD. Solution and solid‐state ultraviolet–visible and photoluminescent spectra indicated that all the polyesters display maximum absorbances and blue emissions arising from the DPTD moiety, whose peak maxima were shifted to lower wavelengths in the order of 4,4′‐DPTD > 3,4′‐DPTD > 3,3′‐DPTD as well as the aforementioned LC property. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 2676–2687, 2003     

Polymerization of 4,4′‐(hexafluoroisopropylidene)‐N,N′‐bis(phthaloyl‐L‐leucine) diacid chloride with aromatic diamines by microwave irradiation

A new facile and rapid polycondensation reaction of 4,4′‐(hexafluoroisopropylidene)‐N,N′‐bis(phthaloyl‐L‐leucine) diacid chloride (1) with several aromatic diamines, including benzidine (2a), 4,4′‐diaminodiphenyl methane (2b), 1,5‐diaminoanthraquinone (2c), 4,4′‐sulfonyldianiline (2d), 3,3′‐diaminobenzophenone (2e), P‐phenylenediamine (2f), 2,6‐diaminopyridine (2g), 4,4′‐diaminobenzophenone (2h), 2,4‐diaminotoluene (2i), and 4,4′‐diaminodiphenylether (2j), was developed with a domestic microwave oven in the presence of a small amount of a polar organic medium such as o‐cresol. The polymerization reactions proceeded rapidly compared to conventional solution polycondensation and finished within 12 min, producing a series of optically active poly(amide‐imide)s with quantitative yields and high inherent viscosities of 0.50–1.93 dL/g. All of the polymers were fully characterized by IR, elemental analyses, and specific rotation. Some structural characterization and physical properties of these optically active poly(amide‐imide)s are reported. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 1154–1160, 2000     

Hydrogen‐bonded supramolecular polymers containing dimethylsilane groups: Synthesis,crystal structure,and characterization

Bis[N‐(4‐carboxyphenyl)phtalimidyl]dimethylsilane prepared by the reaction between bis(3,4‐dicarboxyphenyl)dimethylsilane anhydride and p‐aminobenzoic acid has been used to built three novel hydrogen‐bonded supramolecular polymers as a result of cocrystallization with pyridine derivatives: 4,4′‐bipyridyl ( SP1 ), 1,2‐bis(4‐pyridyl)ethylene ( SP2 ), and 4,4′‐azopyridine ( SP3 ). The structures of the dianhydride, diacid, and derived supramolecular polymers were investigated by Fourier transform infrared (FTIR) and proton magnetic resonance (¹H NMR) spectroscopy. Self‐assembling was proved by the presence of the IR absorption bands around 1900 and 2400 cm^?1 specific for hydrogen bond. The association constant values were estimated by using FTIR spectroscopy in solid state. According to X‐ray diffraction study, the bis(3,4‐dicarboxyphenyl)dimethylsilane anhydride ( 1 ) has an isolated molecular structure. Bis[N‐(4‐carboxyphenyl)phtalimidyl]dimethylsilane ( 2 ) molecules are associated in the crystal structure via dimeric O? H … O hydrogen bonds resulting in the wavy 1D supramolecular chain. The main packing motif for SP1 and SP3 is represented by wavy chain formed by alternating sequences of 4,4′‐bipyridyl or 4,4′‐azopyridine and bis[N(4‐carboxyphenyl)phtalimidyl]dimethylsilane molecules linked by O? H … N hydrogen bonds. Thermal behavior was studied by differential scanning calorimetry and thermogravimetric analysis. The ability for the structuration in film was emphasized by atomic force microscopy. The molecular transport ability of the reversible associations was estimated by dynamic water vapor sorption (DVS) analysis. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012     

Copper(II) Complexes with N‐(9‐anthracenyl)‐N′‐(3‐pyridyl)urea (L) and a Derivative of L: Synthesis,Structure, and Fluorescent Properties

Three copper(II) complexes, [Cu₂(OAc)₄L₂] · 2CH₃OH ( 1 ), [CuBr₂L′₂(CH₃OH)] · CH₃OH ( 2a ), and [CuBr₂L′₂(DMSO)] · 0.5CH₃OH ( 2b ) {L = N‐(9‐anthracenyl)‐N′‐(3‐pyridyl)urea and L′ = N‐[10‐(10‐methoxy‐anthronyl)]‐N′‐(3‐pyridyl)urea} have been synthesized by the reaction of L with the corresponding copper(II) salts. Complex 1 shows a dinuclear structure with a conventional “paddlewheel” motif, in which four acetate units bridge the two Cu^II ions. In complexes 2a and 2b , the anthracenyl ligand L has been converted to an anthronyl derivative L′, and the central metal ion exhibits a distorted square pyramidal arrangement, with two pyridyl nitrogen atoms and two bromide ions defining the basal plane and the apical position is occupied by a solvent molecule (CH₃OH in 2a and DMSO in 2b ).