Fangzhong Hu

Synthesis and nonvolatile memory behaviors of dioxatetraazapentacene derivatives.

Two novel heteroacenes 2,3,9,10-tetra(furan-2-yl)-1,4,8,11-tetraaza-6,13-dioxapentacene (FAOP, 1) and 2,3,9,10-tetra(thiophen-2-yl)-1,4,8,11-tetraaza-6,13-dioxapentacene (TAOP, 2) was successfully synthesized through a one-step condensation reaction, which have been fully characterized by (1)H NMR (nuclear magnetic resonance), (13)C NMR, FT-IR (Fourier transform infrared spectroscopy), and HRMS (high-resolution mass spectrum). The sandwich-structure memory devices have been fabricated using FAOP (1) and TAOP (2) as active layers, showing a typical bipolar resistive switching (RS) behavior in positive and negative regions.

Crystal structure and phototransistor behavior of N-substituted heptacence.

6,8,15,17-Tetraaza-1.18,4.5,9.10,13.14-tetrabenzoheptacene (TTH, 1) has been prepared and characterized by single-crystal X-ray structure analysis. A phototransistor device based on TTH single crystal demonstrated that TTH showed a good performance in signal amplification under the photoconductive effect as well as photocontrolled switches.

Mesoporous Ni0.85Se Nanospheres Grown in Situ on Graphene with High Performance in Dye-Sensitized Solar Cells

Mesoporous Ni0.85Se nanospheres grown on graphene were synthesized via the hydrothermal approach. Because of the exceptional electron-transfer pathway of graphene and the excellent catalytic ability of the mesoporous Ni0.85Se nanospheres, the nanocomposites exhibited excellent electrocatalytic property as the counter electrode (CE) of dye-sensitized solar cells. More catalytic active sites, better charge-transfer ability and faster reaction velocity of Ni0.85Se@RGO (RGO = reduced graphene oxide) CE led to faster and more complete I3(-) reduction than Pt, Ni0.85Se, and RGO CEs. Furthermore, the power conversion efficiency of Ni0.85Se@RGO CE reached 7.82%, which is higher than that of Pt CE (7.54%). Electrochemical impedance spectra, cyclic voltammetry, and Tafel polarization were obtained to demonstrate positive synergetic effect between Ni0.85Se and RGO, as well as the higher catalytic activity and the better charge-transfer ability of Ni0.85Se@RGO compared with Pt CE.

Synthesis and insecticidal activities of novel pyrazole oxime ether derivatives with different substituted pyridyl rings

BACKGROUND Pyrazole oxime ether derivatives with different substituted pyridyl rings represent new types of compounds that possess good insecticidal and acarcidal activity against Aphis laburni Kaltenbach and Tetranychus cinnabarinus. RESULTS In total, 82 novel pyrazole oxime ether derivatives were synthesized and identified by (1) H NMR, elemental analysis or high-resolution mass spectrometry, and their insecticidal and acarcidal activities were tested against A. laburni Kaltenbach and T. cinnabarinus. Bioassays showed that at a 200 mg L(-1) dosage, one-third of the compounds displayed high insecticidal activity against A. laburni Kaltenbach (> 90%), whereas most of of the compound II series exhibited excellent acarcidal activity against T. cinnabarinus (> 92%). Most compound II series exhibited good activity in both insecticidal and acarcidal tests. In addition, at a low concentration of 10 mg L(-1) , the insecticidal activity of compounds IB9 and IE4 exceeded 90%, and the acarcidal activity of compounds IIB1 and IIB2 was ≥ 95%. CONCLUSION Structure-activity relationships were also examined. Results suggested that the tert-butoxycarbonyl group, as well as the position between tert-butoxycarbonyl and the atom N of the pyridyl ring, were essential to obtaining the acarcidal activity of the title compounds.

Novel protoporphyrinogen oxidase inhibitors: 3H-pyrazolo[3,4-d][1,2,3]triazin-4-one derivatives.

A series of 3 H-pyrazolo[3,4-d][1,2,3]triazin-4-one derivatives were synthesized as candidate herbicides by diazotization of different 5(3)-amino- N-phenyl-1 H-pyrazole-4-carboxamide derivatives prepared by the reaction of substituted 5(3)-amino-pyrazole-4-carbonyl chloride with a substituted aniline. Their structures were identified by (1)H NMR and elemental analyses. The isomers D and E were isolated, and their structures were identified by two-dimensional NMR analyses (heteronuclear single quantum coherence and heteronuclear multiple-bond correlation) and single-crystal X-ray diffraction analysis. The bioassay results showed that some of the title compounds exhibited both excellent herbicidal activity at a dose of 93.75 g/ha and strong inhibition against protoporphyrinogen oxidase activity in vitro. The structure-activity relationship showed that D16 possessed the highest activities both in vivo and in vitro when the N-substituted group of the pyrazole ring was allyl and the N-substituted group of benzooxazinone was propargyl.

Ultralong In2S3 Nanotubes on Graphene Substrate with Enhanced Electrocatalytic Activity.

Ultralong one-dimensional (1D) nanostructures including nanowires or nanotubes have been extensively studied because of their widespread applications in many fields. Although a lot of methods have been reported to prepare In2S3 nanotubes, approaching these nanotubes through one-pot solution synthesis is still extremely difficult, probably because of the intrinsic isotropic crystal growth characteristic of In2S3. In this article, we demonstrated a self-assembly approach for hydrothermal synthesis of In2S3 nanotubes/graphene composites, which contain ultralong (up to 10 μm) In2S3 nanotubes on graphene substrate. The influence of several important synthetic parameters on the final products has been systematically investigated. Importantly, the as-prepared In2S3 nanotubes/graphene composites can be easily cast on FTO to form a film, which can be used as a counter electrode. Our research indicates that the as-fabricated counter electrode exhibits excellent electrocatalytic activity toward the iodide species (I-/I3-) reduction reaction and very high energy conversion efficiency (8.01%) in dye-sensitized solar cells.

Synthesis and herbicidal activities of novel 3-N-substituted amino-6-methyl-4-(3-trifluoromethylphenyl)pyridazine derivatives.

4-(3-Trifluoromethylphenyl)pyridazine is a new series of compounds with bleaching and herbicidal activities. Starting from ethyl 2-(3-trifluoromethylphenyl)acetate, an important intermediate 7 was synthesized in five steps with a moderate total yield of 51.5% in a safe and practical way. Twenty-six novel 3-N-substituted amino-6-methyl-4-(3-trifluoromethylphenyl)pyridazine derivatives were synthesized and evaluated through a Spirodela polyrrhiza test and greenhouse test. Some compounds can completely inhibit Chl at 1 microg/mL and exhibit equal or higher herbicidal activities with the commercial bleaching herbicide diflufenican against dicotyledonous plants at a rate of 75 g/ha.

The Synthesis and Herbicidal Activity of 1-Alkyl-3-(α-hydroxysubstituted benzylidene)pyrrolidine-2,4-diones

In the search for better herbicides a series of 1-alkyl-3-(α-hydroxy-(un)substituted benzylidene)pyrrolidine-2,4-diones were prepared and their structure-activity relationships studied. All their structures have been confirmed by 1H-NMR and elemental analysis. The preliminary bioassay results indicated that some of them have high herbicidal activity against annual dicotyledonous and monocotyledonous plants.

Base-promoted intramolecular cyclization of N-alkyl, N-propargylic β-enaminones for the synthesis of polysubstituted pyrroles

An efficient, mild, metal-free, base-mediated intramolecular cyclization of N-alkyl, N-propargylic β-enaminones has been realized for the generation of polysubstituted pyrrole derivatives. This synthetic transformation tolerates a range of substituted N-alkyl, N-propargylic β-enaminones in moderate to good yields.

Synthesis and herbicidal activities of novel 3-(substituted benzyloxy or phenoxy)-6-methyl-4-(3-trifluoromethylphenyl)pyridazine derivatives.

BACKGROUND 4-(3-Trifluoromethylphenyl)pyridazine represents a new series of compounds with bleaching and herbicidal activities. RESULTS A total of 43 novel 3-(substituted benzyloxy or phenoxy)-6-methyl-4-(3-trifluoromethylphenyl)pyridazine derivatives were synthesised, and their bleaching and herbicidal activities were evaluated through Spirodela polyrrhiza and greenhouse tests. Some compounds exhibited excellent herbicidal activities, even at a dose of 7.5 g ha(-1). CONCLUSION The results showed that a substituted phenoxy group at the 3-position of the pyridazine ring and the electron-withdrawing group at the para-position on the benzene ring were essential for high herbicidal activity.