Synthesis of Methyl-substituted Phthalazinone-based Aromatic Poly(amide imide)s

A series of novel aromatic poly ( amide imide)s containing phthalazinone moieties were prepared from 2-(4-aminophenyl)-4-[3-methyl-4-(4-aminophenoxy)-2,3-phthalazinone-1], a novel diamine 1 with four diimide-dicarboxylic acids by Yamazaki phosphorylation method with the inherent viscosity of 0.36~0.65 dL/g. These polymers had high glass transition temperatures above 300C and they lost 10% weight between 426~475C in N2. The structure of diamine 1 and the polymers was confirmed by IR, 1H NMR and MS. The obtained polymers were readily soluble in polar solvents such as NMP, m-cresol etc. and easily cast into tough, flexible films. The X-ray indicated that they are all amorphous.

Synthesis and Characterization of Poly(ether imide)s Containing m-Methyl and Phthalazinone Moieties

Three novel poly(ether imide)s were synthesized by one-step solution polymerization from 2-(3, 4-dicarboxyl-N-phenyl)-4-(3, 4-dicarboxyl-phenoxyl-4-(2-methyl)-phenyl)-2, 3- phthal-azin-1-one dianhydride and three amines, and characterized. The polymers show good solubility and thermal properties.

Synthesis and Characterization of Poly (ether imide)s Containing Phthalazinone and Isopropyl Moieties

A novel poly(ether imide)s containing phthalazinone and isopropyl moieties derived from 2-(4-aminophenyl)-4-[4-(4-aminophenoxy)phenyl]-phthalazin-1-one and bisphenol-A diphthalic anhydride was synthesized by one-step solution condensation polymerization in nr-cresol. The polymer was characterized by FTIR, NMR, molecular weights, glass transition temperature, thermal degradation temperature and WAXD.

SYNTHESIS OF NEW AROMATIC POLY(AMIDE IMIDE)S FROM UNSYMMETRICAL EXTENDED DIAMINE CONTAINING A PHTHALAZINONE MOIETY

The direct polymerization of an unsymmetrical kink non-coplanar heterocyclic diamine (1) with various aromatic bis(trimellitimide)s (2a-e) using triphenyl phosphite and pyridine as condensing agents could generate a series of new aromatic poly(amide imide)s (3a-e) containing the kink non-coplanar phthalazinone heterocyclic units in the polymer main chains with inherent viscosities of 0.58-0.66 dL/g. The polymers are readily soluble in a variety of solvents such as N,N- dimethylformamide, N,N-dimethylacetamide, dimethyl sulfoxide, N-methyl-2-pyrrolidinone, pyridine and m-cresol and can be cast to form flexible and tough films. The glass transition temperatures of polymers (Tg) are in the range of 301-327°C, and the temperatures for 5% weight loss in nitrogen are in the range of 498-521 'C.

Synthesis of Poly(aryl amide imide)s Derived from o-diphenyltrimellitic Anhydride

The synthesis and characterization of a series of novel poly(aryl amide imide)s based on o diphenyltrimellitic anhydride are described.The poly(aryl amide imide)s having inherent viscosities of 0.39-1.43dL/g in N methyl 2 pyrrolidinone at 30℃,were prepared by polymerization with aromatic diamines in N,N-dimethylacetamide and subsequent chemical imidization.All the polymers were amorphous,readily soluble in aprotic polar solvents such as DMAC,NMP,DMF,DMSO,and m cresol,and could be cast to form flexible and tough films.The glass trsanition temperatures were in the range of 284-336℃,and the temperatures for 5% weight loss in nitrogen were above 468℃.

Advances in poly(heptazine imide)/poly(triazine imide) photocatalyst

Polymeric carbon nitride(PCN)has garnered increasing attention as a metal-free photocatalyst with a suitable band gap.In efforts to enhance its photocatalytic performance,researchers have examined various PCN materials,including poly(heptazine imide)(PHI)and poly(triazine imide)(PTI),two isomers within the PCN family that exhibit distinct and superior photocatalytic activity compared to other forms.The challenge,however,lies in the common practice among researchers to categorize PHI and PTI along with other PCN types under the overarching term“g-C_(3)N_(4),”which significantly impedes optimization efforts.The objective of this review is to provide comprehensive insights into the structural features,photoelectrochemical properties,and effective characterization methods employed for distinguishing between PHI and PTI materials.The review also summarizes various optimization strategies,such as crystallinity adjustments,defect engineering,morphology control,constructing heterojunction,and atomic-level metal loading dispersion,to elevate the photocatalytic activity of PHI and PTI,in addition to summarizing the history of carbon nitride development.Furthermore,this review highlights the primary applications of PHI and PTI,encompassing nitrogen fixation,biomass conversion,organic synthesis,CO_(2)reduction,pollutant degradation,H_(2)O_(2)production,and photocatalytic water splitting.Lastly,the prospects and challenges associated with further advancing PHI and PTI are thoroughly examined.

Salt-melt synthesis of poly(heptazine imide)in binary alkali metal bromides for enhanced visible-light photocatalytic hydrogen production

Poly(heptazine imide)(PHI),a semicrystalline version of carbon nitride photocatalyst based on heptazine units,has gained significant attention for solar H_(2)production benefiting from its advantages including molecular synthetic versatility,excellent physicochemical stability and suitable energy band structure to capture visible photons.Typically,PHI is obtained in saltmelt synthesis in the presence of alkali metal chlorides.Herein,we examined the role of binary alkali metal bromides(LiBr/NaBr)with diverse compositions and melting points to rationally modulate the polymerization process,structure,and properties of PHI.Solid characterizations revealed that semicrystalline PHI with a condensedπ-conjugated system and rapid charge separation rates were obtained in the presence of LiBr/NaBr.Accordingly,the apparent quantum yield of hydrogen using the optimized PHI reaches up to 62.3%at 420 nm.The density functional theory calculation shows that the dehydrogenation of the ethylene glycol has a lower energy barrier than the dehydrogenation of the other alcohols from the thermodynamic point of view.This study holds great promise for rational modulation of the structure and properties of conjugated polymeric materials.

Poly(heptazine imide)nanocrystal for hydrogen peroxide evolution in the dark by accumulating photo-generated electrons

Organic conjugated polymers have received extensive attention due to their unique electronic properties.However,there have been relatively few reports on the dark photocatalytic reactions utilizing organic conjugated polymers.Herein,we report the successful synthesis of an organic conjugated polymer based on poly(heptazine imide)nanocrystals(CNNCs)for H_(2)O_(2)evolution and biomedical applications using a simple salt molten method and sonication-centrifugation process.The results show that these colloid CNNCs have the characteristics of photogenerated electrons accumulation and realize dark photocatalysis with high reducibility under visible light irradiation.Notably,these accumulating photogenerated electrons can reduce O_(2)in darkness to produce H_(2)O_(2).In addition,cytotoxicity tests were conducted and it was found that H_(2)O_(2)produced under dark conditions could oxidize L-arginine(L-Arg)to NO,which effectively killed tumors in the dark.This work provides an important strategy to construct organic conjugated semiconductor nanocrystals and applying them to future energy and biomedical fields.

Molecular Chain Flexibility and Dielectric Loss at High-Frequency:Impact of Ester Bond Arrangement in Poly(ester imide)s

The evolution of high-frequency communication has accentuated the significance of controlling dielectric properties in polymer media.Traditionally,it has been theorized that rigid molecular chains lead to lower dielectric loss.However,the validity of this proposition at high frequencies remains uncertain.To scrutinize the correlation between chain flexibility and dielectric properties,we synthesized six poly(ester imide)s(PEIs)with systematically varied molecular chain flexibilities by modifying the ester's substitution on the aromatic ring.The introduction of ester bonds bestowed all PEI films with a low dielectric dissipation factor(D_(f)),ranging from 0.0021 to 0.0038 at 10 GHz in dry conditions.The dry D_(f)displayed a pattern consistent with volume polarizability(P/V).Unexpectedly,PI-mmm-T,featu ring the most flexible molecular chain,exhibited the lowest dielectric loss under both dry(0.0021@10 GHz)and hygroscopic(0.0029@10 GHz)conditions.Furthermore,the observed increase in D_(f)after humidity absorption suggests that the high dielectric loss of PEI in applications may be attributed to its hygroscopic nature.Molecular simulations and characterization of the aggregation structure revealed that the smaller cavities within flexible molecular chains,after close stacking,impede the entry of water molecules.Despite sacrificing high-temperature resistance,the precursor exhibited enhanced solubility properties and could be processed into high-quality films.Our research unveils new insights into the relationship between flexibility and highfrequency dielectric loss,offering innovative perspectives on synthesizing aromatic polymers with exceptional dielectric properties.

Construction of tantalum/poly(ether imide)coatings on magnesium implants with both corrosion protection and osseointegration properties

Poly(ether imide)(PEI)has shown satisfactory corrosion protection capability with good adhesion strength as a coating for magnesium(Mg),a potential candidate of biodegradable orthopedic implant material.However,its innate hydrophobic property causes insufficient osteoblast affinity and a lack of osseointegration.Herein,we modify the physical and chemical properties of a PEI-coated Mg implant.A plasma immersion ion implantation technique is combined with direct current(DC)magnetron sputtering to introduce biologically compatible tantalum(Ta)onto the surface of the PEI coating.The PEI-coating layer is not damaged during this process owing to the extremely short processing time(30 s),retaining its high corrosion protection property and adhesion stability.The Ta-implanted layer(roughly 10-nm-thick)on the topmost PEI surface generates long-term surface hydrophilicity and favorable surface conditions for pre-osteoblasts to adhere,proliferate,and differentiate.Furthermore,in a rabbit femur study,the Ta/PEI-coated Mg implant demonstrates significantly enhanced bone tissue affinity and osseointegration capability.These results indicate that Ta/PEI-coated Mg is promising for achieving early mechanical fixation and long-term success in biodegradable orthopedic implant applications.

Enhancement of Resistance to Protein Fouling of Poly(ether imide) Membrane by Surface Grafting with PEG under Organic Solvent-free Condition

Poly（ether imide） （PEI） membrane with enhanced antifouling property was successfully prepared in a mild and simple procedure. The virgin membrane was firstly functionalized with an aqueous solution of diamino-terminated poly（ethylene oxide） block copolymer （PEG-diamine）. Glutaraldehyde was used in a second step as a linker to chemically attach additional PEG-diamine to the primary amine groups grafted on PEI membrane surface. Immobilization of PEG segments was confirmed using Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy and atomic force microscopy. Ultrafiltration experiments revealed that the enhancement of a PEG coverage on the membrane surface provided superior anti-protein-fouling property. Cycles of protein filtration also demonstrated that the antifouling surface was stable over time and excellent ultrafiltration performance could be maintained without the need of harsh cleansing operation.

Extended light absorption and accelerated charge migration in ultrathin twisted carbon nitride nanoplates for efficient solar hydrogen production

Polymeric carbon nitride has been widely developed as a promising photocatalyst for solar hydrogen production via photocatalytic water splitting.However,pristine carbon nitride prepared by traditional solid-state polymerization usually encounters issues such as rapid carrier recombination and insufficient absorption of visible light below 460 nm.Herein,poly(heptazine imide)with a distinctive nanoplate structure was synthesized in a binary molten salt of NaCl–CaCl_(2).The salt template allows the formation of the thin nanoplate structure,which promotes the charge separation and migration.Besides,the intercalation of Ca^(2+)ions between the conjugated layers endows the activation of n–π*electron transition due to the distortion of in-plane heptazine layers.Accordingly,the optimized poly(heptazine imide)nanoplates achieve an apparent quantum efficiency of up to 17.3%at 500 nm for photocatalytic hydrogen production from water.This work shares new idea for rational control of the optical absorption and charge carrier dynamics of poly(heptazine imide).

Boosting photocatalytic hydrogen production by creating isotype heterojunctions and single-atom active sites in highly-crystallized carbon nitride

Carbon nitride-based photocatalysts hold an enormous potential in producing hydrogen.A strategy to simultaneously create isotype heterojunctions and active sites in highly-crystallized carbon nitride is anticipated to significantly boost the photocatalytic activity,but is yet to be realized.Herein,we find that cobalt salt added in the ionothermal synthesis can promote the phase transition of heptazine-based crystalline carbon nitride(CCN)to triazine-based poly(triazine imide)(PTI),rendering the creation of singleatom cobalt coordinated isotype CCN/PTI heterojunction.Co-CCN/PTI exhibits an appreciable apparent quantum yield of 20.88%at 425 nm for photocatalytic hydrogen production with a rate achieving3538μmol h^(-1)g^(-1)(λ>420 nm),which is 4.8 times that of CCN and 27.6 times that of PTI.The high photocatalytic activity is attributed to the Type II isotype highly-crystallized CCN/PTI heterojunction for promoting charge carrier migration,and the single-atom Co sites for accelerating surface oxidation reaction.