scholarly journals Photochemical Preparation of 1,2-Dihydro-3H-indazol-3-ones in Aqueous Solvent at Room Temperature

2018 ◽  
Vol 83 (24) ◽  
pp. 15493-15498 ◽  
Author(s):  
Jie S. Zhu ◽  
Niklas Kraemer ◽  
Clarabella J. Li ◽  
Makhluf J. Haddadin ◽  
Mark J. Kurth
Symmetry ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 733
Author(s):  
Domenica Donia ◽  
Elvira Maria Bauer ◽  
Mauro Missori ◽  
Ludovica Roselli ◽  
Daniele Cecchetti ◽  
...  

ZnO has many technological applications which largely depend on its properties, which can be tuned by controlled synthesis. Ideally, the most convenient ZnO synthesis is carried out at room temperature in an aqueous solvent. However, the correct temperature values are often loosely defined. In the current paper, we performed the synthesis of ZnO in an aqueous solvent by varying the reaction and drying temperatures by 10 °C steps, and we monitored the synthesis products primarily by XRD). We found out that a simple direct synthesis of ZnO, without additional surfactant, pumping, or freezing, required both a reaction (TP) and a drying (TD) temperature of 40 °C. Higher temperatures also afforded ZnO, but lowering any of the TP or TD below the threshold value resulted either in the achievement of Zn(OH)2 or a mixture of Zn(OH)2/ZnO. A more detailed Rietveld analysis of the ZnO samples revealed a density variation of about 4% (5.44 to 5.68 gcm−3) with the synthesis temperature, and an increase of the nanoparticles’ average size, which was also verified by SEM images. The average size of the ZnO synthesized at TP = TD = 40 °C was 42 nm, as estimated by XRD, and 53 ± 10 nm, as estimated by SEM. For higher synthesis temperatures, they vary between 76 nm and 71 nm (XRD estimate) or 65 ± 12 nm and 69 ± 11 nm (SEM estimate) for TP =50 °C, TD = 40 °C, or TP = TD = 60 °C, respectively. At TP = TD = 30 °C, micrometric structures aggregated in foils are obtained, which segregate nanoparticles of ZnO if TD is raised to 40 °C. The optical properties of ZnO obtained by UV-Vis reflectance spectroscopy indicate a red shift of the band gap by ~0.1 eV.


2003 ◽  
Vol 775 ◽  
Author(s):  
Glenn E. Lawson ◽  
Alok Singh

AbstractFormation of lipid based hollow, spherical nanocapsules is reported. N-acylphosphotidylethanolamine (egg) derivatives equipped with divinylbenzoyl functionality in their headgroup region were synthesized to explore their polymerization behavior in vesicles. Polymerizable phospholipids alone produced vesicles as an aqueous dispersion and produced stable nanocapsules upon polymerization at room temperature. These structures survived a redispersed cycle following lyophilization and maintained their structural integrity in non-aqueous solvent.


Cellulose ◽  
2016 ◽  
Vol 24 (1) ◽  
pp. 49-59 ◽  
Author(s):  
Wei Wei ◽  
Fanbin Meng ◽  
Yuhu Cui ◽  
Man Jiang ◽  
Zuowan Zhou

2017 ◽  
Vol 1 (1) ◽  
Author(s):  
Braja Gopal Bag ◽  
Subhajit Das

A solution of oleanolic acid, a renewable nano-sized monohydroxy triterpenic acid in tetrahydrofuran, transformed into a gel instantly at room temperature on treatment with aqueous ammonia. Study of the self-assembly properties of ammonium oleanolate in water and aqueous solvent mixtures indicated that it self-assembles in the aqueous solvent mixtures forming gels in DMSO-water and DMF-water. Fibrillar networks with optical birefringence properties were observed by polarized optical microscopy. Scanning electron microscopy of the dried gel samples indicated fibrillar networks with fibers of nano to micrometer diameters. The thermodynamic parameters calculated from the gel to sol transition temperatures indicated the stability of the gels. A gel-gold nanoparticles hybrid material has also been prepared and characterized by HRTEM, EDX, SAED and surface Plasmon resonance studies.


2011 ◽  
Vol 361-363 ◽  
pp. 1827-1831 ◽  
Author(s):  
Yan Qi Liu ◽  
Xin Xin Xiao ◽  
Hong Li ◽  
Xue Hong Li ◽  
Liu Zhi Yang

By means of non-aqueous solvent, V-type amylose-hexanol complex which B-type microcrystalline starch made a combination with hexanol was prepared. Study the influence of the reaction temperature, dropping time and cooling temperature on the V-type complexes’ crystallinity. The optimal synthetic conditions were found through the single factor experiment as follows:reaction temperature at 70°C, dropping time of 6min, cooling to room temperature. V-type complex was prepared under optimum conditions, the highest crystallinity reached 73.7%.


2019 ◽  
Vol 21 (19) ◽  
pp. 5267-5273 ◽  
Author(s):  
Junjuan Yang ◽  
Yuanyuan Wu ◽  
Xiaowei Wu ◽  
Wenjing Liu ◽  
Yaofang Wang ◽  
...  

We report a heterogeneous catalyst based on N-heterocyclic carbene-functionalized covalent organic framework, which shows high activity in the C–C cross coupling reaction at room temperature in pure/ethanol aqueous solvent even with multiple reuse.


2002 ◽  
Vol 736 ◽  
Author(s):  
Douglas L. Schulz

ABSTRACTThe research objective of this project was the spray deposition of CdSe films using a nanoparticle CdSe suspension as the precursor ink. This ink consisted of CdSe nanoparticles (nano-CdSe) mixed with a “reactive dispersant” in a non-aqueous solvent. The reactive dispersant, a metal-organic molecule, served two purposes; (1) to form a dispersed CdSe suspension at room temperature, and (2) to thermally “unzip” giving CdSe and a byproduct. The CdSe thereby formed could be deposited at the grain boundaries and serve to physically and electrically connect the CdSe nanoparticles at moderate, plastic-compatible temperatures. If electronics-grade CdSe layers could be produced at low deposition temperatures, this approach may be applicable to printed CdSe-based thin film field-effect transistors (TFTs) on flexible substrates.


2020 ◽  
Vol 17 (1) ◽  
pp. 65-72
Author(s):  
Jasmin Sultana ◽  
Diganta Sarma

Introduction: An effective Cu-complex, [Cu(NH3)4SO4 • H2O] was prepared conveniently from the inexpensive and easily available starting reagents in a simple route. Materials and Methods: Excellent reactivity of the catalyst was observed towards two competent clickcycloadditions: (a) oxidative cycloaddition of azides with electron-poor olefins and (b) one-pot cycloaddition of alkynes with boronic acid and sodium azide under “click-appropriate” conditions. Results: No external oxidant, short reaction time, high product yield, wide substrate scope, and aqueous solvent media make the azide-olefin cycloaddition approach a greener route in contrast to the reported methods. Conclusion: The newly developed mild, green, and rapid three-component strategy shows product diversity with superb yields at room temperature by reducing the synthetic process time and using only 1 mol % of the synthesized copper complex.


Author(s):  
Domenica Donia ◽  
Elvira Maria Bauer ◽  
Mauro Missori ◽  
Ludovica Roselli ◽  
Daniele Cecchetti ◽  
...  

ZnO has many technological applications which largely depend on its properties that can be tuned by controlled synthesis. Ideally, the most convenient ZnO synthesis is carried out at room temperature in aqueous solvent. However, the correct temperature values are often loosely defined. In the current paper we performed synthesis of ZnO in aqueous solvent, by varying reaction and drying temperature by 10°C steps and monitored the synthesis products primarily by XRD. We found out that a simple direct synthesis of ZnO, without additional surfactant, pumping of freezing, required both a reaction (TP) and a drying (TD) temperature of 40°C. Higher temperatures also afford ZnO, but lowering any of the TP or TD below the threshold value results either in the achievement of Zn(OH)2 or in a mixture of Zn(OH)2/ZnO. A more detailed Rietveld analysis of the ZnO samples reveals a density variation with the synthesis temperature and an increase of the nanoparticles average size also verified by SEM images. The optical properties of ZnO obtained by UV-Vis reflectance spectroscopy indicate a red shift of the band gap by ~0.1 eV.


1977 ◽  
Vol 32 (6) ◽  
pp. 544-554 ◽  
Author(s):  
Rainer Kimmich

Abstract Nuclear magnetic relaxation formulae are given for dipolar nuclei interacting with quadrupolar nuclei. The following cases are distinguished: High-and low-field case with respect to the quadrupole energy levels and, on the other hand, quasi rigid lattices and tumbling lattices with respect to molecular motions.As examples of these cases, the proton T1-dispersion of Polyvinylchloride (quasi rigid lattice) and of protein solutions (tumbling lattice) are discussed and compared with theory. It is shown that the influence of the interaction with quadrupole nuclei is normally not negligible.PVC shows a quadrupolar dip below room temperature as an especially remarkable consequence of the interaction with chlorine. An oscillator model is discussed in order to explain the molecular motion at low temperatures.Proteins contain imino-groups acting as relaxation centers and mediating the contact to the aqueous solvent via hydrogen bonds. These relaxation centers can explain the low absolute values of the longitudinal relaxation times in protein solutions. Furthermore, several effects in such systems, reported previously, can easily be interpreted on the basis of the presented formalism.


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