Synthesis of N-methyl-N-(2,2,2-trichloro-1-arylaminoethyl)formamides and related compounds as potential fungicides

1980 ◽  
Vol 33 (3) ◽  
pp. 613 ◽  
Author(s):  
HG Grant ◽  
LA Summers
Keyword(s):  
Room Temperature ◽  
Amide Bond ◽  
Restricted Rotation ◽  
Related Compounds

The synthesis of several analogues of the chloralformamide fungicides is reported. The compounds, which comprise N-methyl-N-(2,2,2-trichloro- 1-arylaminoethyl)formamides and related alkoxyethyl and aryloxyethyl derivatives, exist at room temperature as two isomers due to restricted rotation about the C-N amide bond. The results of their evaluation as fungicides are reported.

Intrinsic doping limit and defect-assisted luminescence in Cs4PbBr6

2019 ◽  
Author(s):  
Young-Kwang Jung ◽  
Joaquin Calbo ◽  
Ji-Sang Park ◽  
Lucy D. Wahlley ◽  
Sunghyun Kim ◽  
...  
Keyword(s):  
First Principles ◽  
Room Temperature ◽  
Stokes Shift ◽  
Green Luminescence ◽  
Counter Ions ◽  
Self Consistent ◽  
Deep Ultraviolet ◽  
Halide Perovskite ◽  
Related Compounds ◽  
Level Analysis

Cs<sub>4</sub>PbBr<sub>6 </sub>is a member of the halide perovskite family that is built from isolated (zero-dimensional) PbBr<sub>6</sub><sup>4-</sup> octahedra with Cs<sup>+</sup> counter ions. The material exhibits anomalous optoelectronic properties: optical absorption and weak emission in the deep ultraviolet (310 - 375 nm) with efficient luminescence in the green region (~ 540 nm). Several hypotheses have been proposed to explain the giant Stokes shift including: (i) phase impurities; (ii) self-trapped exciton; (iii) defect emission. We explore, using first-principles theory and self-consistent Fermi level analysis, the unusual defect chemistry and physics of Cs<sub>4</sub>PbBr<sub>6</sub>. We find a heavily compensated system where the room-temperature carrier concentrations (< 10<sup>9</sup> cm<sup>-3</sup>) are more than one million times lower than the defect concentrations. We show that the low-energy Br-on-Cs antisite results in the formation of a polybromide (Br<sub>3</sub>) species that can exist in a range of charge states. We further demonstrate from excited-state calculations that tribromide moieties are photoresponsive and can contribute to the observed green luminescence. Photoactivity of polyhalide molecules is expected to be present in other halide perovskite-related compounds where they can influence light absorption and emission. <br>

Intrinsic doping limit and defect-assisted luminescence in Cs4PbBr6

2019 ◽  
Author(s):  
Young-Kwang Jung ◽  
Joaquin Calbo ◽  
Ji-Sang Park ◽  
Lucy D. Wahlley ◽  
Sunghyun Kim ◽  
...  
Keyword(s):  
First Principles ◽  
Room Temperature ◽  
Stokes Shift ◽  
Green Luminescence ◽  
Counter Ions ◽  
Self Consistent ◽  
Deep Ultraviolet ◽  
Halide Perovskite ◽  
Related Compounds ◽  
Level Analysis

Cs<sub>4</sub>PbBr<sub>6 </sub>is a member of the halide perovskite family that is built from isolated (zero-dimensional) PbBr<sub>6</sub><sup>4-</sup> octahedra with Cs<sup>+</sup> counter ions. The material exhibits anomalous optoelectronic properties: optical absorption and weak emission in the deep ultraviolet (310 - 375 nm) with efficient luminescence in the green region (~ 540 nm). Several hypotheses have been proposed to explain the giant Stokes shift including: (i) phase impurities; (ii) self-trapped exciton; (iii) defect emission. We explore, using first-principles theory and self-consistent Fermi level analysis, the unusual defect chemistry and physics of Cs<sub>4</sub>PbBr<sub>6</sub>. We find a heavily compensated system where the room-temperature carrier concentrations (< 10<sup>9</sup> cm<sup>-3</sup>) are more than one million times lower than the defect concentrations. We show that the low-energy Br-on-Cs antisite results in the formation of a polybromide (Br<sub>3</sub>) species that can exist in a range of charge states. We further demonstrate from excited-state calculations that tribromide moieties are photoresponsive and can contribute to the observed green luminescence. Photoactivity of polyhalide molecules is expected to be present in other halide perovskite-related compounds where they can influence light absorption and emission. <br>

scholarly journals Recyclable Self-Healing Polyurethane Cross-Linked by Alkyl Diselenide with Enhanced Mechanical Properties

Polymers ◽  
2019 ◽  
Vol 11 (5) ◽  
pp. 773 ◽  
Author(s):  
Yuqing Qian ◽  
Xiaowei An ◽  
Xiaofei Huang ◽  
Xiangqiang Pan ◽  
Jian Zhu ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Room Temperature ◽  
Amide Bond ◽  
Self Healing ◽  
Healing Efficiency ◽  
Polyurethane Networks ◽  
Combined Action ◽  
Cross Linker ◽  
Dynamic Structures ◽  
External Interventions

Dynamic structures containing polymers can behave as thermosets at room temperature while maintaining good mechanical properties, showing good reprocessability, repairability, and recyclability. In this work, alkyl diselenide is effectively used as a dynamic cross-linker for the design of self-healing poly(urea–urethane) elastomers, which show quantitative healing efficiency at room temperature, without the need for any catalysts or external interventions. Due to the combined action of the urea bond and amide bond, the material has better mechanical properties. We also compared the self-healing effect of alkyl diselenide-based polyurethanes and alkyl disulfide-based polyurethanes. The alkyl diselenide has been incorporated into polyurethane networks using a para-substituted amine diphenyl alkyl diselenide. The resulting materials not only exhibit faster self-healing properties than the corresponding disulfide-based materials, but also show the ability to be processed at temperatures as low as 60 °C.

Studies on hydrolysis and radiolysis of N,N,N′,N′-tetraoctyl-3-oxapentane-1,5-diamide

2002 ◽  
Vol 90 (3) ◽  
Author(s):  
Y. Sugo ◽  
Y. Sasaki ◽  
S. Tachimori
Keyword(s):  
Gamma Irradiation ◽  
Room Temperature ◽  
Degradation Products ◽  
Liquid Waste ◽  
Amide Bond ◽  
Radioactive Liquid Waste ◽  
Ether Bond ◽  
Nuclear Fuel Reprocessing ◽  
High Level ◽  
Fuel Reprocessing

SummaryHydrolytic and radiolytic stabilities of a promising extractant, N,N,N′,N′-tetraoctyl-3-oxapentane-1,5-diamide (TODGA), for actinides in high-level radioactive liquid waste from nuclear fuel reprocessing were investigated in air at room temperature. Hydrolysis by nitric acid was not observed, whereas radiolysis by gamma irradiation was notably observed. The radiolysis study showed that an amide-bond, an ether-bond, and a bond adjacent to the ether-bond tended to be broken by gamma irradiation, and dioctylamine and various N,N-dioctylmonoamides were identified as the main degradation products by GC/MS and NMR analyses. The

Green Amide Bond Formation in Water via Direct Coupling of Metal Carboxylate Salts with Ammonium Salts at Room Temperature

2021 ◽  
Author(s):  
Truong Thanh Tung ◽  
John Nielsen
Keyword(s):  
Room Temperature ◽  
Bond Formation ◽  
Direct Coupling ◽  
Ammonium Salts ◽  
Amide Bond ◽  
Metal Carboxylate ◽  
Amide Bond Formation ◽  
Simple Protocol

Herein, we report the green, expedite, and practically simple protocol for direct coupling of carboxylate salts and ammonium salts under ACN/H2O conditions at room temperature without the addition of tertiary...

The reaction of benzonorbornadiene and related compounds with iron carbonyls

1974 ◽  
Vol 27 (1) ◽  
pp. 143 ◽  
Author(s):  
L Lombardo ◽  
D Wege ◽  
SP Wilkinson
Keyword(s):  
Room Temperature ◽  
Iron Carbonyls ◽  
Related Compounds

Reaction of benzonorbornadiene, 7-isopropylidenebenzonorbornadiene (1,4-dihydro-9-isopropylidene-1,4-methanonaphthalene) and 1,4-dihydro-1,4-epoxynaphthalene (7-oxabenzonorbornadiene) with dicarbonyldinitrosyliron, Fe(CO)2(NO)2, gave in good yields the corresponding dimers having the exo-trans-exo configuration. Treatment of a mixture of benzonorbornadiene and norbornadiene with Fe(CO)2(NO)2 gave a 'crossed dimer', in addition to the dimers derived from benzonorbornadiene and norbornadiene. The reaction of benzonorbornadiene with pentacarbonyliron at 100� gave the exo-trans-exo dimer and a ketone derived by dimerization and carbonyl insertion. This ketone, and the analogous ketone obtained from 7-isopropylidenebenzonorbornadiene, have been assigned the exo-trans-exo configuration. Reaction of 1,4-dihydro-1,4-epoxynaphthalene with enneacarbonyldiiron, Fe2(CO)9, at room temperature gave tetracarbonyl(l,4-dihydro-l,4-epoxynaphthalene)iron(0), in which the olefinic ח-bond is bonded to the metal. In solution at 63� this complex gave naphthalene.

Polydentate Ligands Containing Phosphorus, III [1]. Synthesis and Nuclear Magnetic Resonance Studies of Some Unsymmetrical Potentially Tridentate Phosphine Chalcogenide Ligands

1980 ◽  
Vol 35 (7) ◽  
pp. 832-837 ◽  
Author(s):  
Samuel O. Grim ◽  
Larry C. Satek ◽  
J. Dale Mitchell
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Room Temperature ◽  
Electron Pair ◽  
Nmr Spectrum ◽  
Magnetic Resonance Studies ◽  
Polydentate Ligands ◽  
Nmr Data ◽  
Type C ◽  
Related Compounds ◽  
Reduced Temperature

The synthesis via the useful lithium reagent intermediate, (C6H5)2P(S)CH2Li, is reported for eight compounds of the type [(C6H5)2P(X)][R2P(X)]2CH, where R is methyl or phenyl and X is an electron pair, oxygen, or sulfur in various combinations. Two related compounds with three and four phosphorus atoms, respectively, per molecule have also been prepared from the same lithium reagent. Tris(diphenylthiophosphoryl)methane has three equivalent phosphorus atoms as indicated by the room temperature phosphorus-31 NMR spectrum, but at reduced temperature a favored conformation exists which has two equivalent phosphorus atoms and a unique one. Other phosphorus-31 and proton NMR data are reported

scholarly journals Sintering Behavior of BST Nanoparticles at Low Temperature and Electrical Properties of their Ceramics

2020 ◽  
Author(s):  
Jianquan Qi ◽  
Yan Li ◽  
Mengyin Li ◽  
Jiahui Xie ◽  
Tianchi Yu ◽  
...  
Keyword(s):  
Mass Transfer ◽  
Dielectric Constant ◽  
Alkaline Earth ◽  
Room Temperature ◽  
Sintering Temperature ◽  
Sintering Behavior ◽  
Sintering Aids ◽  
Bst Ceramics ◽  
Related Compounds ◽  
Alkaline Earth Cations

Abstract The powders of the Ba0.75Sr0.25TiO3 (BST) nanoparticles were directly synthesized by milling of Ba(OH)2·8H2O, Sr(OH)2·8H2O and Ti(BuO)4 in ethanol at room temperature. They have homogenous grains of ~15 nm and the high sintering activity. The dense ceramics with the density >90% can be obtained at a sintering temperature of ≤950 oC by them with adding 3 wt% sintering aids of Bi2O3 and Li2CO3. The sintering behavior of the BST nanoparticles by adding the aids of Bi2O3 and Li2CO3 is studied carefully. Several Bi-related compounds are involved in the sintering procedure at a different temperature. They enhance the mass transfer and promote the sintering densification. These compounds such as Ba2BiO4 and SrBiO4 appear at 800 oC, LiBa4Bi3O11 and Sr1.2Bi0.8O3 appear over 830 oC, and Bi8.11Ba0.89O13.05 appears at 950 oC. The cation Bi in the ceramics has mixture valences of 3+ and 5+. It makes the ceramics as semiconducting state with the dark gray color and decreases the ceramics resistivities. With the sintering temperature increase, especially at 950 oC, the cation Bi tends back to single valence of +3 in the ceramics. The most of alkaline earth cations in Bi-related compounds will release and resorb into the lattice of BST and drive the densification of the nanoparticles. The BST ceramics can have a peak dielectric constant >6500 at 53 oC, loss <0.025, and resistivity >1012 W·cm when sintered at a temperature of ≥900 oC with 3 wt% sintering aids. They have a potential application for multiple layer ceramic capacitors (MLCC) with silver inner-electrodes.

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